Item | Value |
---|---|
geneid | 56244 |
ensemblid | ENSG00000204290.11 |
hgncid | 1142 |
symbol | BTNL2 |
name | butyrophilin like 2 |
refseq_nuc | NM_001304561.2 |
refseq_prot | NP_001291490.1 |
ensembl_nuc | ENST00000454136.8 |
ensembl_prot | ENSP00000390613.3 |
mane_status | MANE Select |
chr | chr6 |
start | 32393339 |
end | 32407181 |
strand | - |
ver | v1.2 |
region | chr6:32393339-32407181 |
region5000 | chr6:32388339-32412181 |
regionname0 | BTNL2_chr6_32393339_32407181 |
regionname5000 | BTNL2_chr6_32388339_32412181 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 482 | 213 | 55 | 38 | 85 | 11 | 23 | 57 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(477): Show |
chr6 | 32388339 | 32412181 |
a0002 | 0/0 | 482 | 77 | 16 | 26 | 20 | 4 | 11 | 19 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(477): Show |
chr6 | 32388339 | 32412181 |
a0003 | 0/0 | 245 | 52 | 20 | 6 | 24 | 0 | 2 | 18 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(240): Show |
chr6 | 32388339 | 32412181 |
a0004 | 0/0 | 453 | 45 | 0 | 0 | 39 | 0 | 6 | 35 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(448): Show |
chr6 | 32388339 | 32412181 |
a0005 | 0/0 | 482 | 22 | 0 | 5 | 12 | 3 | 2 | 12 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(477): Show |
chr6 | 32388339 | 32412181 |
a0006 | 0/0 | 245 | 17 | 0 | 1 | 15 | 0 | 1 | 15 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(240): Show |
chr6 | 32388339 | 32412181 |
a0007 | 0/0 | 482 | 16 | 0 | 1 | 15 | 0 | 0 | 15 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(477): Show |
chr6 | 32388339 | 32412181 |
a0008 | 0/0 | 283 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(278): Show |
chr6 | 32388339 | 32412181 |
a0009 | 0/0 | 482 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(477): Show |
chr6 | 32388339 | 32412181 |
a0010 | 0/0 | 482 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(477): Show |
chr6 | 32388339 | 32412181 |
a0011 | 0/0 | 482 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(477): Show |
chr6 | 32388339 | 32412181 |
a0012 | 0/0 | 482 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(477): Show |
chr6 | 32388339 | 32412181 |
a0013 | 0/0 | 482 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(477): Show |
chr6 | 32388339 | 32412181 |
a0014 | 0/0 | 482 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | MVDFP others(477): Show |
chr6 | 32388339 | 32412181 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1446 | 179 | 47 | 33 | 68 | 7 | 23 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0001c0005 | 0/0 | 1446 | 24 | 8 | 5 | 7 | 4 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0001c0010 | 0/0 | 1446 | 10 | 0 | 0 | 10 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0002c0002 | 0/0 | 1446 | 77 | 16 | 26 | 20 | 4 | 11 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0003c0004 | 0/0 | 1445 | 31 | 18 | 5 | 6 | 0 | 2 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1440): Show |
chr6 | 32388339 | 32412181 | ||
a0003c0008 | 0/0 | 1445 | 17 | 0 | 0 | 17 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1440): Show |
chr6 | 32388339 | 32412181 | ||
a0003c0012 | 0/0 | 1445 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1440): Show |
chr6 | 32388339 | 32412181 | ||
a0003c0020 | 0/0 | 1445 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1440): Show |
chr6 | 32388339 | 32412181 | ||
a0003c0021 | 0/0 | 1445 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1440): Show |
chr6 | 32388339 | 32412181 | ||
a0004c0003 | 0/0 | 1446 | 45 | 0 | 0 | 39 | 0 | 6 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0005c0006 | 0/0 | 1446 | 22 | 0 | 5 | 12 | 3 | 2 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0006c0007 | 0/0 | 1445 | 17 | 0 | 1 | 15 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1440): Show |
chr6 | 32388339 | 32412181 | ||
a0007c0009 | 0/0 | 1446 | 15 | 0 | 1 | 14 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0007c0018 | 0/0 | 1446 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0008c0011 | 0/0 | 1446 | 5 | 2 | 3 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0009c0017 | 0/0 | 1446 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0010c0019 | 0/0 | 1446 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0011c0016 | 0/0 | 1446 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0012c0015 | 0/0 | 1446 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0013c0014 | 0/0 | 1446 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 | ||
a0014c0013 | 0/0 | 1446 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | ATGGT others(1441): Show |
chr6 | 32388339 | 32412181 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 1564 | 179 | 47 | 33 | 68 | 7 | 23 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0001c0005t0001 | 0/0 | 1564 | 24 | 8 | 5 | 7 | 4 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0001c0010t0001 | 0/0 | 1564 | 10 | 0 | 0 | 10 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0002c0002t0001 | 0/0 | 1564 | 77 | 16 | 26 | 20 | 4 | 11 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0003c0004t0002 | 0/0 | 1562 | 31 | 18 | 5 | 6 | 0 | 2 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1557): Show |
chr6 | 32388339 | 32412181 |
a0003c0008t0001 | 0/0 | 1563 | 17 | 0 | 0 | 17 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1558): Show |
chr6 | 32388339 | 32412181 |
a0003c0012t0002 | 0/0 | 1562 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1557): Show |
chr6 | 32388339 | 32412181 |
a0003c0020t0002 | 0/0 | 1562 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1557): Show |
chr6 | 32388339 | 32412181 |
a0003c0021t0002 | 0/0 | 1562 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1557): Show |
chr6 | 32388339 | 32412181 |
a0004c0003t0003 | 0/0 | 1563 | 45 | 0 | 0 | 39 | 0 | 6 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1558): Show |
chr6 | 32388339 | 32412181 |
a0005c0006t0002 | 0/0 | 1563 | 22 | 0 | 5 | 12 | 3 | 2 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1558): Show |
chr6 | 32388339 | 32412181 |
a0006c0007t0001 | 0/0 | 1563 | 17 | 0 | 1 | 15 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1558): Show |
chr6 | 32388339 | 32412181 |
a0007c0009t0001 | 0/0 | 1564 | 15 | 0 | 1 | 14 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0007c0018t0001 | 0/0 | 1564 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0008c0011t0004 | 0/0 | 1564 | 5 | 2 | 3 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0009c0017t0001 | 0/0 | 1564 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0010c0019t0001 | 0/0 | 1564 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0011c0016t0001 | 0/0 | 1564 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0012c0015t0001 | 0/0 | 1564 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0013c0014t0001 | 0/0 | 1564 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
a0014c0013t0001 | 0/0 | 1564 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | CCGGG others(1559): Show |
chr6 | 32388339 | 32412181 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 21 | 0 | 4 | 17 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0007 | 0/0 | 8 | 0 | 0 | 6 | 0 | 2 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0009 | 0/0 | 8 | 2 | 3 | 1 | 0 | 2 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0010 | 0/0 | 8 | 1 | 2 | 5 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0011 | 0/0 | 8 | 3 | 5 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0013 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0014 | 0/0 | 6 | 0 | 0 | 1 | 0 | 5 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0015 | 0/0 | 6 | 0 | 3 | 3 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0016 | 0/0 | 6 | 0 | 2 | 3 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0020 | 0/0 | 5 | 3 | 1 | 0 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0021 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0022 | 0/0 | 5 | 0 | 3 | 0 | 1 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0028 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0030 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0032 | 0/0 | 4 | 0 | 1 | 0 | 0 | 3 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0033 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0037 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0038 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0039 | 0/1 | 3 | 0 | 0 | 1 | 1 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0040 | 0/0 | 3 | 1 | 0 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0053 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0056 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0057 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0059 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0060 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0064 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0065 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0066 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0019 | 0/0 | 5 | 2 | 1 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0024 | 0/0 | 4 | 0 | 1 | 0 | 3 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0026 | 0/0 | 4 | 3 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0052 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0005t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0010t0001g0025 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0010t0001g0036 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0010t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0010t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0001c0010t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0002 | 0/0 | 23 | 0 | 10 | 11 | 0 | 2 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0012 | 0/0 | 7 | 1 | 0 | 1 | 1 | 4 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0018 | 0/0 | 5 | 2 | 1 | 0 | 1 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0023 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0034 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0035 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0044 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0046 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0047 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0049 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0050 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0043 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0071 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0072 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0073 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0074 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0075 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0076 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0004t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0008t0001g0006 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0008t0001g0027 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0008t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0008t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0008t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0008t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0008t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0012t0002g0070 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0020t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0003c0021t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0004c0003t0003g0001 | 0/0 | 27 | 0 | 0 | 24 | 0 | 3 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0004c0003t0003g0017 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0004c0003t0003g0041 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0004c0003t0003g0067 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0004c0003t0003g0068 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0004c0003t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0004c0003t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0004c0003t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0004c0003t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0004c0003t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0005c0006t0002g0008 | 0/0 | 8 | 0 | 1 | 5 | 1 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0005c0006t0002g0031 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0005c0006t0002g0061 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0005c0006t0002g0062 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0005c0006t0002g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0005c0006t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0005c0006t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0005c0006t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0005c0006t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0005c0006t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0006c0007t0001g0005 | 0/0 | 10 | 0 | 0 | 9 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0006c0007t0001g0029 | 0/0 | 4 | 0 | 1 | 3 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0006c0007t0001g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0006c0007t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0007c0009t0001g0004 | 0/0 | 14 | 0 | 1 | 13 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0007c0009t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0007c0018t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0008c0011t0004g0042 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0008c0011t0004g0069 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0009c0017t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0010c0019t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0011c0016t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0012c0015t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0013c0014t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
a0014c0013t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0005 | t0001 | g0024 | EUR | GBR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0134 | EUR | GBR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00140 | hp1 | a0001 | c0005 | t0001 | g0024 | EUR | GBR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00140 | hp2 | a0005 | c0006 | t0002 | g0062 | EUR | GBR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00280 | hp1 | a0001 | c0005 | t0001 | g0024 | EUR | FIN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0064 | EUR | FIN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00323 | hp1 | a0001 | c0005 | t0001 | g0108 | EUR | FIN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0155 | EUR | FIN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00423 | hp1 | a0003 | c0008 | t0001 | g0027 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00438 | hp2 | a0004 | c0003 | t0003 | g0068 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00609 | hp2 | a0001 | c0005 | t0001 | g0052 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00621 | hp2 | a0009 | c0017 | t0001 | g0152 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00639 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00639 | hp2 | a0010 | c0019 | t0001 | g0162 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00642 | hp2 | a0008 | c0011 | t0004 | g0042 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00673 | hp1 | a0003 | c0008 | t0001 | g0027 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | CHS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00735 | hp2 | a0005 | c0006 | t0002 | g0031 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00738 | hp1 | a0011 | c0016 | t0001 | g0107 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00738 | hp2 | a0003 | c0004 | t0002 | g0074 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01069 | hp1 | a0001 | c0005 | t0001 | g0024 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01069 | hp2 | a0002 | c0002 | t0001 | g0050 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01070 | hp1 | a0001 | c0005 | t0001 | g0106 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01074 | hp2 | a0002 | c0002 | t0001 | g0101 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01081 | hp2 | a0008 | c0011 | t0004 | g0042 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01106 | hp2 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01175 | hp2 | a0005 | c0006 | t0002 | g0031 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01192 | hp1 | a0006 | c0007 | t0001 | g0029 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01243 | hp1 | a0001 | c0005 | t0001 | g0019 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01243 | hp2 | a0003 | c0004 | t0002 | g0075 | AMR | PUR | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01255 | hp1 | a0003 | c0004 | t0002 | g0074 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01255 | hp2 | a0008 | c0011 | t0004 | g0069 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01256 | hp2 | a0005 | c0006 | t0002 | g0061 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01346 | hp1 | a0001 | c0005 | t0001 | g0051 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01346 | hp2 | a0003 | c0004 | t0002 | g0071 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01358 | hp2 | a0007 | c0009 | t0001 | g0004 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01433 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01496 | hp2 | a0005 | c0006 | t0002 | g0008 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0103 | EUR | IBS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01516 | hp2 | a0005 | c0006 | t0002 | g0062 | EUR | IBS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | IBS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0102 | EUR | IBS | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01884 | hp2 | a0003 | c0004 | t0002 | g0043 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01934 | hp1 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01952 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01952 | hp2 | a0003 | c0020 | t0002 | g0175 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01978 | hp2 | a0002 | c0002 | t0001 | g0088 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01981 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01981 | hp2 | a0002 | c0002 | t0001 | g0095 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01993 | hp2 | a0005 | c0006 | t0002 | g0061 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02015 | hp1 | a0001 | c0005 | t0001 | g0127 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02015 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02027 | hp1 | a0003 | c0008 | t0001 | g0120 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02055 | hp1 | a0012 | c0015 | t0001 | g0144 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0099 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02071 | hp2 | a0003 | c0008 | t0001 | g0122 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0047 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02083 | hp2 | a0003 | c0008 | t0001 | g0119 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02129 | hp1 | a0001 | c0005 | t0001 | g0112 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02129 | hp2 | a0004 | c0003 | t0003 | g0172 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02132 | hp2 | a0004 | c0003 | t0003 | g0017 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02135 | hp2 | a0003 | c0008 | t0001 | g0121 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0164 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02145 | hp2 | a0003 | c0004 | t0002 | g0077 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02148 | hp1 | a0001 | c0005 | t0001 | g0109 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CDX | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | CDX | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0087 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02280 | hp2 | a0003 | c0004 | t0002 | g0081 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02293 | hp1 | a0002 | c0002 | t0001 | g0094 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02300 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0066 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02615 | hp1 | a0001 | c0005 | t0001 | g0113 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02615 | hp2 | a0003 | c0004 | t0002 | g0084 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02622 | hp2 | a0003 | c0004 | t0002 | g0079 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0093 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0035 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02683 | hp2 | a0004 | c0003 | t0003 | g0041 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02717 | hp2 | a0003 | c0004 | t0002 | g0184 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02723 | hp2 | a0002 | c0002 | t0001 | g0012 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02735 | hp1 | a0002 | c0002 | t0001 | g0047 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02735 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02809 | hp1 | a0002 | c0002 | t0001 | g0092 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02809 | hp2 | a0002 | c0002 | t0001 | g0100 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02818 | hp2 | a0003 | c0004 | t0002 | g0181 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02895 | hp2 | a0003 | c0004 | t0002 | g0073 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02896 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02897 | hp2 | a0003 | c0004 | t0002 | g0073 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02922 | hp1 | a0001 | c0005 | t0001 | g0026 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02922 | hp2 | a0008 | c0011 | t0004 | g0042 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02965 | hp1 | a0001 | c0005 | t0001 | g0026 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0034 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02976 | hp2 | a0003 | c0004 | t0002 | g0078 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03017 | hp2 | a0006 | c0007 | t0001 | g0005 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03041 | hp1 | a0001 | c0005 | t0001 | g0019 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03098 | hp2 | a0003 | c0004 | t0002 | g0083 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03139 | hp1 | a0001 | c0005 | t0001 | g0026 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03209 | hp2 | a0003 | c0012 | t0002 | g0070 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03239 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03453 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03486 | hp2 | a0001 | c0005 | t0001 | g0019 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03490 | hp2 | a0004 | c0003 | t0003 | g0001 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03516 | hp2 | a0003 | c0004 | t0002 | g0180 | AFR | ESN | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03540 | hp2 | a0003 | c0004 | t0002 | g0082 | AFR | GWD | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0018 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03669 | hp1 | a0013 | c0014 | t0001 | g0091 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03669 | hp2 | a0004 | c0003 | t0003 | g0041 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0046 | SAS | STU | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | STU | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03704 | hp2 | a0003 | c0004 | t0002 | g0076 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03831 | hp2 | a0004 | c0003 | t0003 | g0041 | SAS | BEB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0012 | SAS | BEB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03834 | hp2 | a0005 | c0006 | t0002 | g0008 | SAS | BEB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | STU | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | BEB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | BEB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0002 | SAS | STU | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG04199 | hp2 | a0005 | c0006 | t0002 | g0138 | SAS | STU | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0023 | SAS | STU | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG04204 | hp2 | a0004 | c0003 | t0003 | g0001 | SAS | STU | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18522 | hp1 | a0003 | c0004 | t0002 | g0179 | AFR | YRI | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18522 | hp2 | a0003 | c0004 | t0002 | g0043 | AFR | YRI | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18612 | hp1 | a0001 | c0010 | t0001 | g0036 | EAS | CHB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18612 | hp2 | a0001 | c0005 | t0001 | g0051 | EAS | CHB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18747 | hp1 | a0001 | c0010 | t0001 | g0110 | EAS | CHB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | CHB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18940 | hp1 | a0006 | c0007 | t0001 | g0029 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18940 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18942 | hp1 | a0014 | c0013 | t0001 | g0125 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18942 | hp2 | a0004 | c0003 | t0003 | g0017 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18943 | hp1 | a0006 | c0007 | t0001 | g0054 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18943 | hp2 | a0003 | c0008 | t0001 | g0006 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18944 | hp1 | a0006 | c0007 | t0001 | g0029 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18944 | hp2 | a0003 | c0004 | t0002 | g0072 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18945 | hp1 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18948 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18948 | hp2 | a0005 | c0006 | t0002 | g0008 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18949 | hp2 | a0005 | c0006 | t0002 | g0130 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18950 | hp1 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18950 | hp2 | a0005 | c0006 | t0002 | g0008 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18951 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18952 | hp2 | a0005 | c0006 | t0002 | g0031 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18953 | hp1 | a0006 | c0007 | t0001 | g0005 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18953 | hp2 | a0004 | c0003 | t0003 | g0068 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18954 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18957 | hp1 | a0001 | c0010 | t0001 | g0025 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18957 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18959 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18960 | hp2 | a0004 | c0003 | t0003 | g0017 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18961 | hp2 | a0004 | c0003 | t0003 | g0017 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18962 | hp1 | a0005 | c0006 | t0002 | g0008 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18962 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18963 | hp2 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18968 | hp2 | a0001 | c0010 | t0001 | g0025 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18969 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18969 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18972 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18973 | hp1 | a0001 | c0010 | t0001 | g0025 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18973 | hp2 | a0003 | c0008 | t0001 | g0027 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18975 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18975 | hp2 | a0005 | c0006 | t0002 | g0008 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18978 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18978 | hp2 | a0003 | c0004 | t0002 | g0076 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18979 | hp1 | a0004 | c0003 | t0003 | g0067 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18979 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18981 | hp2 | a0006 | c0007 | t0001 | g0005 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18982 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18983 | hp2 | a0003 | c0004 | t0002 | g0176 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18984 | hp1 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18984 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18985 | hp2 | a0004 | c0003 | t0003 | g0017 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18987 | hp1 | a0003 | c0008 | t0001 | g0006 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18987 | hp2 | a0003 | c0004 | t0002 | g0178 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18988 | hp1 | a0003 | c0021 | t0002 | g0185 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18988 | hp2 | a0005 | c0006 | t0002 | g0008 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18989 | hp1 | a0006 | c0007 | t0001 | g0123 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18989 | hp2 | a0004 | c0003 | t0003 | g0171 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18990 | hp1 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18991 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18992 | hp1 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18992 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18993 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18993 | hp2 | a0006 | c0007 | t0001 | g0054 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18994 | hp1 | a0006 | c0007 | t0001 | g0005 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18994 | hp2 | a0005 | c0006 | t0002 | g0139 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18995 | hp2 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18997 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18998 | hp1 | a0001 | c0010 | t0001 | g0036 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18998 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19000 | hp1 | a0005 | c0006 | t0002 | g0140 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19000 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19001 | hp1 | a0004 | c0003 | t0003 | g0174 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19001 | hp2 | a0005 | c0006 | t0002 | g0141 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19002 | hp2 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19003 | hp1 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19003 | hp2 | a0003 | c0008 | t0001 | g0006 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19004 | hp1 | a0003 | c0004 | t0002 | g0071 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19004 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19005 | hp1 | a0001 | c0005 | t0001 | g0026 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19005 | hp2 | a0001 | c0010 | t0001 | g0036 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19007 | hp1 | a0003 | c0008 | t0001 | g0006 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19010 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19011 | hp2 | a0005 | c0006 | t0002 | g0031 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | LWK | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19030 | hp2 | a0008 | c0011 | t0004 | g0069 | AFR | LWK | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19054 | hp1 | a0003 | c0008 | t0001 | g0006 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19054 | hp2 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19055 | hp1 | a0005 | c0006 | t0002 | g0137 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19055 | hp2 | a0003 | c0004 | t0002 | g0072 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19056 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19058 | hp2 | a0003 | c0008 | t0001 | g0006 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19060 | hp1 | a0006 | c0007 | t0001 | g0005 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19060 | hp2 | a0001 | c0010 | t0001 | g0104 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19062 | hp1 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19064 | hp1 | a0002 | c0002 | t0001 | g0045 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19064 | hp2 | a0003 | c0008 | t0001 | g0006 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19065 | hp1 | a0006 | c0007 | t0001 | g0005 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0012 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19066 | hp2 | a0004 | c0003 | t0003 | g0173 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19068 | hp1 | a0006 | c0007 | t0001 | g0005 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19070 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19072 | hp1 | a0001 | c0005 | t0001 | g0019 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19072 | hp2 | a0004 | c0003 | t0003 | g0170 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19074 | hp1 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19074 | hp2 | a0006 | c0007 | t0001 | g0005 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19076 | hp1 | a0006 | c0007 | t0001 | g0029 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19076 | hp2 | a0004 | c0003 | t0003 | g0067 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19078 | hp1 | a0003 | c0008 | t0001 | g0027 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19078 | hp2 | a0007 | c0018 | t0001 | g0153 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19079 | hp1 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19079 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19080 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19080 | hp2 | a0001 | c0005 | t0001 | g0019 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19081 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19083 | hp1 | a0001 | c0010 | t0001 | g0025 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19083 | hp2 | a0007 | c0009 | t0001 | g0131 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19084 | hp1 | a0003 | c0008 | t0001 | g0118 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19084 | hp2 | a0003 | c0008 | t0001 | g0006 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19085 | hp1 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19085 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19086 | hp2 | a0006 | c0007 | t0001 | g0005 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19087 | hp1 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19087 | hp2 | a0007 | c0009 | t0001 | g0004 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19088 | hp1 | a0001 | c0010 | t0001 | g0111 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19088 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19091 | hp1 | a0006 | c0007 | t0001 | g0005 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19091 | hp2 | a0004 | c0003 | t0003 | g0017 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA19240 | hp2 | a0003 | c0004 | t0002 | g0177 | AFR | YRI | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA20129 | hp1 | a0001 | c0005 | t0001 | g0052 | AFR | ASW | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ASW | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA20752 | hp1 | a0002 | c0002 | t0001 | g0012 | EUR | TSI | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA20752 | hp2 | a0005 | c0006 | t0002 | g0008 | EUR | TSI | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0022 | EUR | TSI | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0018 | EUR | TSI | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA20905 | hp1 | a0004 | c0003 | t0003 | g0001 | SAS | GIH | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA20905 | hp2 | a0003 | c0004 | t0002 | g0183 | SAS | GIH | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG01123 | hp2 | a0003 | c0004 | t0002 | g0075 | AMR | CLM | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02109 | hp1 | a0003 | c0004 | t0002 | g0182 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02109 | hp2 | a0003 | c0012 | t0002 | g0070 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02559 | hp1 | a0002 | c0002 | t0001 | g0090 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG02559 | hp2 | a0003 | c0004 | t0002 | g0080 | AFR | ACB | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG03471 | hp2 | a0002 | c0002 | t0001 | g0018 | AFR | MSL | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | USA | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | USA | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA18955 | hp2 | a0004 | c0003 | t0003 | g0001 | EAS | JPT | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | USA | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | USA | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0105 | AFR | LWK | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0039 | REF | REF | BTNL2_chr6_32388339_32412181 | BTNL2 | chr6 | 32388339 | 32412181 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32393972 | G | C | 2 | a0003 a0005 |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
missense_variant | MODERATE | c.1446C>G | p.Ser482Arg | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/8 | 1504/1564 | 1446/1449 | 482/482 | chr6 | 32393972 | |||
chr6:32393985 | G | A | 3 | a0003 a0004 a0005 |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
missense_variant | MODERATE | c.1433C>T | p.Pro478Leu | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/8 | 1491/1564 | 1433/1449 | 478/482 | chr6 | 32393985 | |||
chr6:32394022 | C | G | 1 | a0004 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
missense_variant | MODERATE | c.1396G>C | p.Val466Leu | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/8 | 1454/1564 | 1396/1449 | 466/482 | chr6 | 32394022 | |||
chr6:32394744 | C | A | 1 | a0004 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
stop_gained&splice_region_variant | HIGH | c.1360G>T | p.Glu454* | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1418/1564 | 1360/1449 | 454/482 | chr6 | 32394744 | |||
chr6:32394744 | C | G | 1 | a0011 | 1 | HG00738.hp1 | missense_variant&splice_region_variant | MODERATE | c.1360G>C | p.Glu454Gln | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1418/1564 | 1360/1449 | 454/482 | chr6 | 32394744 | |||
chr6:32394755 | A | G | 1 | a0008 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.1349T>C | p.Phe450Ser | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1407/1564 | 1349/1449 | 450/482 | chr6 | 32394755 | |||
chr6:32394902 | G | A | 1 | a0008 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.1202C>T | p.Thr401Met | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1260/1564 | 1202/1449 | 401/482 | chr6 | 32394902 | |||
chr6:32394926 | G | T | 3 | a0003 a0004 a0005 |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
missense_variant | MODERATE | c.1178C>A | p.Pro393Gln | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1236/1564 | 1178/1449 | 393/482 | chr6 | 32394926 | |||
chr6:32394964 | C | T | 3 | a0003 a0004 a0005 |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
missense_variant | MODERATE | c.1140G>A | p.Met380Ile | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1198/1564 | 1140/1449 | 380/482 | chr6 | 32394964 | |||
chr6:32394968 | G | A | 4 | a0003 a0004 a0005 others(1): Show |
103 | HG00140.hp2 HG00438.hp2 HG00621.hp2 others(100): Show |
missense_variant | MODERATE | c.1136C>T | p.Pro379Leu | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1194/1564 | 1136/1449 | 379/482 | chr6 | 32394968 | |||
chr6:32394992 | C | T | 1 | a0008 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.1112G>A | p.Gly371Glu | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1170/1564 | 1112/1449 | 371/482 | chr6 | 32394992 | |||
chr6:32395025 | C | A | 1 | a0007 | 1 | NA19078.hp2 | missense_variant&splice_region_variant | MODERATE | c.1079G>T | p.Ser360Ile | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1137/1564 | 1079/1449 | 360/482 | chr6 | 32395025 | |||
chr6:32396039 | T | C | 7 | a0002 a0003 a0004 others(4): Show |
200 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(197): Show |
missense_variant&splice_region_variant | MODERATE | c.1078A>G | p.Ser360Gly | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 1136/1564 | 1078/1449 | 360/482 | chr6 | 32396039 | |||
chr6:32396063 | C | T | 1 | a0008 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.1054G>A | p.Ala352Thr | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 1112/1564 | 1054/1449 | 352/482 | chr6 | 32396063 | |||
chr6:32396111 | C | T | 1 | a0004 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
missense_variant | MODERATE | c.1006G>A | p.Asp336Asn | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 1064/1564 | 1006/1449 | 336/482 | chr6 | 32396111 | |||
chr6:32396116 | G | A | 2 | a0008 a0010 |
6 | HG00639.hp2 HG00642.hp2 HG01081.hp2 others(3): Show |
missense_variant | MODERATE | c.1001C>T | p.Ser334Leu | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 1059/1564 | 1001/1449 | 334/482 | chr6 | 32396116 | |||
chr6:32396234 | T | C | 1 | a0004 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
missense_variant | MODERATE | c.883A>G | p.Met295Val | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 941/1564 | 883/1449 | 295/482 | chr6 | 32396234 | |||
chr6:32396267 | G | A | 1 | a0008 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
stop_gained | HIGH | c.850C>T | p.Arg284* | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 908/1564 | 850/1449 | 284/482 | chr6 | 32396267 | |||
chr6:32396269 | T | A | 2 | a0004 a0008 |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
missense_variant | MODERATE | c.848A>T | p.Asp283Val | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 906/1564 | 848/1449 | 283/482 | chr6 | 32396269 | |||
chr6:32396275 | C | T | 1 | a0004 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
missense_variant | MODERATE | c.842G>A | p.Arg281Lys | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 900/1564 | 842/1449 | 281/482 | chr6 | 32396275 | |||
chr6:32396299 | G | A | 1 | a0008 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.818C>T | p.Ala273Val | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 876/1564 | 818/1449 | 273/482 | chr6 | 32396299 | |||
chr6:32396371 | T | A | 1 | a0008 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.746A>T | p.Asn249Ile | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 804/1564 | 746/1449 | 249/482 | chr6 | 32396371 | |||
chr6:32401785 | C | G | 1 | a0003 | 2 | HG02109.hp2 HG03209.hp2 |
missense_variant&splice_region_variant | MODERATE | c.730G>C | p.Ala244Pro | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/8 | 788/1564 | 730/1449 | 244/482 | chr6 | 32401785 | |||
chr6:32403039 | G | A | 4 | a0003 a0004 a0006 others(1): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
missense_variant | MODERATE | c.605C>T | p.Ala202Val | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 663/1564 | 605/1449 | 202/482 | chr6 | 32403039 | |||
chr6:32403058 | T | C | 6 | a0002 a0003 a0004 others(3): Show |
197 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(194): Show |
missense_variant | MODERATE | c.586A>G | p.Lys196Glu | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 644/1564 | 586/1449 | 196/482 | chr6 | 32403058 | |||
chr6:32403069 | C | T | 1 | a0008 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.575G>A | p.Arg192His | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 633/1564 | 575/1449 | 192/482 | chr6 | 32403069 | |||
chr6:32403082 | C | T | 1 | a0012 | 1 | HG02055.hp1 | missense_variant | MODERATE | c.562G>A | p.Val188Met | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 620/1564 | 562/1449 | 188/482 | chr6 | 32403082 | |||
chr6:32403102 | C | T | 2 | a0003 a0006 |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
missense_variant | MODERATE | c.542G>A | p.Arg181Gln | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 600/1564 | 542/1449 | 181/482 | chr6 | 32403102 | |||
chr6:32403150 | G | A | 1 | a0004 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
missense_variant | MODERATE | c.494C>T | p.Thr165Ile | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 552/1564 | 494/1449 | 165/482 | chr6 | 32403150 | |||
chr6:32403192 | TG | T | 2 | a0003 a0006 |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
frameshift_variant | HIGH | c.451delC | p.His151fs | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 509/1564 | 451/1449 | 151/482 | chr6 | 32403192 | |||
chr6:32403198 | C | T | 3 | a0003 a0006 a0008 |
74 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(71): Show |
missense_variant | MODERATE | c.446G>A | p.Ser149Asn | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 504/1564 | 446/1449 | 149/482 | chr6 | 32403198 | |||
chr6:32403210 | C | A | 1 | a0008 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.434G>T | p.Gly145Val | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 492/1564 | 434/1449 | 145/482 | chr6 | 32403210 | |||
chr6:32403211 | C | T | 1 | a0008 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
missense_variant | MODERATE | c.433G>A | p.Gly145Arg | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 491/1564 | 433/1449 | 145/482 | chr6 | 32403211 | |||
chr6:32403216 | C | T | 1 | a0006 | 17 | HG01192.hp1 HG03017.hp2 NA18940.hp1 others(14): Show |
missense_variant&splice_region_variant | MODERATE | c.428G>A | p.Gly143Asp | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 486/1564 | 428/1449 | 143/482 | chr6 | 32403216 | |||
chr6:32405014 | C | T | 1 | a0013 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.352G>A | p.Asp118Asn | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/8 | 410/1564 | 352/1449 | 118/482 | chr6 | 32405014 | |||
chr6:32405086 | A | T | 2 | a0003 a0006 |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
missense_variant | MODERATE | c.280T>A | p.Trp94Arg | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/8 | 338/1564 | 280/1449 | 94/482 | chr6 | 32405086 | |||
chr6:32405185 | C | T | 2 | a0008 a0014 |
6 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(3): Show |
missense_variant | MODERATE | c.181G>A | p.Val61Met | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/8 | 239/1564 | 181/1449 | 61/482 | chr6 | 32405185 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32393975 | C | T | 5 | a0003c0004 a0003c0012 a0003c0020 others(2): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
synonymous_variant | LOW | c.1443G>A | p.Arg481Arg | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/8 | 1501/1564 | 1443/1449 | 481/482 | chr6 | 32393975 | |||
chr6:32394032 | T | C | 5 | a0003c0004 a0003c0012 a0003c0020 others(2): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
synonymous_variant | LOW | c.1386A>G | p.Lys462Lys | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/8 | 1444/1564 | 1386/1449 | 462/482 | chr6 | 32394032 | |||
chr6:32394044 | C | T | 3 | a0001c0005 a0001c0010 a0011c0016 |
35 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(32): Show |
synonymous_variant | LOW | c.1374G>A | p.Thr458Thr | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/8 | 1432/1564 | 1374/1449 | 458/482 | chr6 | 32394044 | |||
chr6:32394862 | G | A | 6 | a0003c0004 a0003c0012 a0003c0020 others(3): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
synonymous_variant | LOW | c.1242C>T | p.His414His | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1300/1564 | 1242/1449 | 414/482 | chr6 | 32394862 | |||
chr6:32394892 | T | G | 6 | a0003c0004 a0003c0012 a0003c0020 others(3): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
synonymous_variant | LOW | c.1212A>C | p.Ser404Ser | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1270/1564 | 1212/1449 | 404/482 | chr6 | 32394892 | |||
chr6:32394925 | T | C | 6 | a0003c0004 a0003c0012 a0003c0020 others(3): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
synonymous_variant | LOW | c.1179A>G | p.Pro393Pro | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1237/1564 | 1179/1449 | 393/482 | chr6 | 32394925 | |||
chr6:32395008 | G | A | 1 | a0004c0003 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
synonymous_variant | LOW | c.1096C>T | p.Leu366Leu | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/8 | 1154/1564 | 1096/1449 | 366/482 | chr6 | 32395008 | |||
chr6:32396067 | C | T | 2 | a0002c0002 a0013c0014 |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
synonymous_variant | LOW | c.1050G>A | p.Gln350Gln | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 1108/1564 | 1050/1449 | 350/482 | chr6 | 32396067 | |||
chr6:32396178 | T | C | 9 | a0002c0002 a0003c0004 a0003c0012 others(6): Show |
185 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(182): Show |
synonymous_variant | LOW | c.939A>G | p.Val313Val | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 997/1564 | 939/1449 | 313/482 | chr6 | 32396178 | |||
chr6:32396196 | C | T | 1 | a0004c0003 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
synonymous_variant | LOW | c.921G>A | p.Glu307Glu | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 979/1564 | 921/1449 | 307/482 | chr6 | 32396196 | |||
chr6:32396280 | C | T | 1 | a0004c0003 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
synonymous_variant | LOW | c.837G>A | p.Glu279Glu | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/8 | 895/1564 | 837/1449 | 279/482 | chr6 | 32396280 | |||
chr6:32403014 | G | A | 2 | a0004c0003 a0008c0011 |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
synonymous_variant | LOW | c.630C>T | p.Asn210Asn | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 688/1564 | 630/1449 | 210/482 | chr6 | 32403014 | |||
chr6:32403017 | C | T | 6 | a0003c0004 a0003c0008 a0003c0012 others(3): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
synonymous_variant | LOW | c.627G>A | p.Arg209Arg | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 685/1564 | 627/1449 | 209/482 | chr6 | 32403017 | |||
chr6:32403083 | G | A | 1 | a0004c0003 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
synonymous_variant | LOW | c.561C>T | p.Ala187Ala | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 619/1564 | 561/1449 | 187/482 | chr6 | 32403083 | |||
chr6:32403131 | T | A | 6 | a0003c0004 a0003c0008 a0003c0012 others(3): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
synonymous_variant | LOW | c.513A>T | p.Pro171Pro | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 571/1564 | 513/1449 | 171/482 | chr6 | 32403131 | |||
chr6:32403149 | A | G | 1 | a0003c0020 | 1 | HG01952.hp2 | synonymous_variant | LOW | c.495T>C | p.Thr165Thr | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 553/1564 | 495/1449 | 165/482 | chr6 | 32403149 | |||
chr6:32403209 | C | A | 6 | a0003c0004 a0003c0008 a0003c0012 others(3): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
synonymous_variant | LOW | c.435G>T | p.Gly145Gly | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/8 | 493/1564 | 435/1449 | 145/482 | chr6 | 32403209 | |||
chr6:32405015 | G | A | 1 | a0001c0010 | 10 | NA18612.hp1 NA18747.hp1 NA18957.hp1 others(7): Show |
synonymous_variant | LOW | c.351C>T | p.Ser117Ser | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/8 | 409/1564 | 351/1449 | 117/482 | chr6 | 32405015 | |||
chr6:32405186 | G | A | 6 | a0003c0004 a0003c0008 a0003c0012 others(3): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
synonymous_variant | LOW | c.180C>T | p.His60His | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/8 | 238/1564 | 180/1449 | 60/482 | chr6 | 32405186 | |||
chr6:32405282 | G | A | 1 | a0008c0011 | 5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
synonymous_variant | LOW | c.84C>T | p.Asp28Asp | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/8 | 142/1564 | 84/1449 | 28/482 | chr6 | 32405282 | |||
chr6:32407088 | T | C | 1 | a0003c0021 | 1 | NA18988.hp1 | synonymous_variant | LOW | c.36A>G | p.Ala12Ala | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/8 | 94/1564 | 36/1449 | 12/482 | chr6 | 32407088 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32393353 | C | T | 6 | a0003c0004t0002 a0003c0012t0002 a0003c0020t0002 others(3): Show |
62 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*43G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 8/8 | 616 | chr6 | 32393353 | ||||||
chr6:32393356 | A | G | 1 | a0004c0003t0003 | 45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*40T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 8/8 | 613 | chr6 | 32393356 | ||||||
chr6:32393965 | CT | C | 6 | a0003c0004t0002 a0003c0012t0002 a0003c0020t0002 others(3): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
3_prime_UTR_variant | MODIFIER | c.*3delA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/8 | 3 | chr6 | 32393965 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:32393446 | C | T | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*7-57G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393446 | |||||||
chr6:32393462 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.*7-73G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393462 | |||||||
chr6:32393474 | G | A | 39 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(36): Show |
62 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.*7-85C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393474 | |||||||
chr6:32393478 | A | G | 39 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(36): Show |
62 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.*7-89T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393478 | |||||||
chr6:32393537 | G | A | 1 | a0002c0002t0001g0087 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.*7-148C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393537 | |||||||
chr6:32393564 | CCAA | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.*7-178_*7-176delTT others(1): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393564 | |||||||
chr6:32393592 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
9 | HG00423.hp2 HG00621.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.*7-203C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393592 | |||||||
chr6:32393611 | C | T | 49 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(46): Show |
107 | HG00140.hp2 HG00438.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.*7-222G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393611 | |||||||
chr6:32393631 | C | T | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*7-242G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393631 | |||||||
chr6:32393647 | T | C | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*7-258A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393647 | |||||||
chr6:32393668 | T | C | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*7-279A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393668 | |||||||
chr6:32393672 | C | A | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*7-283G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393672 | |||||||
chr6:32393673 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.*7-284T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393673 | |||||||
chr6:32393678 | TTTC | T | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*6+282_*6+284delGA others(1): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393678 | |||||||
chr6:32393692 | C | T | 49 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(46): Show |
107 | HG00140.hp2 HG00438.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.*6+271G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393692 | |||||||
chr6:32393705 | T | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.*6+258A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393705 | |||||||
chr6:32393708 | G | A | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*6+255C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393708 | |||||||
chr6:32393748 | T | C | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*6+215A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393748 | |||||||
chr6:32393789 | A | G | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*6+174T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393789 | |||||||
chr6:32393803 | G | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.*6+160C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393803 | |||||||
chr6:32393806 | T | A | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*6+157A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393806 | |||||||
chr6:32393833 | C | T | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*6+130G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393833 | |||||||
chr6:32393835 | T | C | 49 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(46): Show |
107 | HG00140.hp2 HG00438.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.*6+128A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393835 | |||||||
chr6:32393836 | G | A | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.*6+127C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393836 | |||||||
chr6:32393866 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.*6+97C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393866 | |||||||
chr6:32393900 | G | A | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*6+63C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393900 | |||||||
chr6:32393903 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.*6+60C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393903 | |||||||
chr6:32393916 | C | T | 4 | a0001c0001t0001g0159 a0001c0001t0001g0160 a0008c0011t0004g0042 others(1): Show |
7 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.*6+47G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393916 | |||||||
chr6:32393917 | G | A | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.*6+46C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 7/7 | chr6 | 32393917 | |||||||
chr6:32394064 | T | C | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
splice_region_variant&intron_variant | LOW | c.1361-7A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394064 | |||||||
chr6:32394065 | G | A | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
splice_region_variant&intron_variant | LOW | c.1361-8C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394065 | |||||||
chr6:32394081 | C | T | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1361-24G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394081 | |||||||
chr6:32394082 | T | G | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1361-25A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394082 | |||||||
chr6:32394088 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1361-31G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394088 | |||||||
chr6:32394108 | T | G | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1361-51A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394108 | |||||||
chr6:32394117 | A | G | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1361-60T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394117 | |||||||
chr6:32394166 | C | T | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1361-109G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394166 | |||||||
chr6:32394176 | A | G | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1361-119T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394176 | |||||||
chr6:32394178 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1361-121G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394178 | |||||||
chr6:32394233 | C | T | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1361-176G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394233 | |||||||
chr6:32394234 | A | G | 49 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(46): Show |
107 | HG00140.hp2 HG00438.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.1361-177T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394234 | |||||||
chr6:32394243 | C | T | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1361-186G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394243 | |||||||
chr6:32394272 | A | AGTT | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1361-218_1361-216d others(5): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394272 | |||||||
chr6:32394285 | C | G | 10 | a0001c0005t0001g0051 a0001c0005t0001g0052 a0001c0005t0001g0105 others(7): Show |
17 | HG00323.hp1 HG00609.hp2 HG01346.hp1 others(14): Show |
intron_variant | MODIFIER | c.1361-228G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394285 | |||||||
chr6:32394298 | A | G | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1361-241T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394298 | |||||||
chr6:32394308 | C | T | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1361-251G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394308 | |||||||
chr6:32394351 | G | A | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1361-294C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394351 | |||||||
chr6:32394396 | A | G | 1 | a0010c0019t0001g0162 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1361-339T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394396 | |||||||
chr6:32394405 | T | C | 49 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(46): Show |
107 | HG00140.hp2 HG00438.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.1360+339A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394405 | |||||||
chr6:32394410 | G | C | 1 | a0004c0003t0003g0171 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1360+334C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394410 | |||||||
chr6:32394440 | A | G | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1360+304T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394440 | |||||||
chr6:32394463 | G | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1360+281C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394463 | |||||||
chr6:32394468 | TAA | T | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1360+274_1360+275d others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394468 | |||||||
chr6:32394470 | A | AAG | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1360+272_1360+273d others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394470 | |||||||
chr6:32394485 | A | G | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1360+259T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394485 | |||||||
chr6:32394495 | A | T | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1360+249T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394495 | |||||||
chr6:32394541 | C | T | 2 | a0002c0002t0001g0092 a0013c0014t0001g0091 |
2 | HG02809.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.1360+203G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394541 | |||||||
chr6:32394612 | G | A | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1360+132C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394612 | |||||||
chr6:32394631 | G | A | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1360+113C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394631 | |||||||
chr6:32394639 | T | G | 153 | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0013 others(150): Show |
365 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(362): Show |
intron_variant | MODIFIER | c.1360+105A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394639 | |||||||
chr6:32394656 | C | A | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1360+88G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394656 | |||||||
chr6:32394670 | C | T | 1 | a0001c0001t0001g0014 | 6 | HG02080.hp2 HG02602.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.1360+74G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394670 | |||||||
chr6:32394676 | A | G | 49 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(46): Show |
107 | HG00140.hp2 HG00438.hp2 HG00642.hp2 others(104): Show |
intron_variant | MODIFIER | c.1360+68T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 6/7 | chr6 | 32394676 | |||||||
chr6:32395055 | G | A | 47 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(44): Show |
102 | HG00140.hp2 HG00438.hp2 HG00735.hp2 others(99): Show |
intron_variant | MODIFIER | c.1079-30C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395055 | |||||||
chr6:32395056 | G | A | 1 | a0002c0002t0001g0034 | 3 | HG02970.hp2 HG03098.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1079-31C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395056 | |||||||
chr6:32395101 | G | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-76C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395101 | |||||||
chr6:32395108 | A | T | 1 | a0001c0001t0001g0169 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1079-83T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395108 | |||||||
chr6:32395125 | A | G | 2 | a0003c0004t0002g0182 a0003c0004t0002g0184 |
2 | HG02109.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1079-100T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395125 | |||||||
chr6:32395143 | G | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079-118C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395143 | |||||||
chr6:32395153 | C | T | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1079-128G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395153 | |||||||
chr6:32395187 | CTTATT | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-167_1079-163d others(7): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395187 | |||||||
chr6:32395190 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079-165T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395190 | |||||||
chr6:32395235 | T | C | 18 | a0003c0004t0002g0071 a0003c0004t0002g0072 a0003c0004t0002g0073 others(15): Show |
25 | HG00738.hp2 HG01123.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.1079-210A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395235 | |||||||
chr6:32395240 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079-215C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395240 | |||||||
chr6:32395268 | A | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-243T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395268 | |||||||
chr6:32395306 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1079-281A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395306 | |||||||
chr6:32395307 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079-282G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395307 | |||||||
chr6:32395323 | C | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079-298G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395323 | |||||||
chr6:32395344 | C | G | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-319G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395344 | |||||||
chr6:32395370 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079-345G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395370 | |||||||
chr6:32395386 | T | C | 1 | a0001c0001t0001g0168 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1079-361A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395386 | |||||||
chr6:32395409 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079-384G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395409 | |||||||
chr6:32395435 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1079-410G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395435 | |||||||
chr6:32395438 | T | C | 17 | a0001c0005t0001g0019 a0001c0005t0001g0024 a0001c0005t0001g0026 others(14): Show |
34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.1079-413A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395438 | |||||||
chr6:32395442 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1079-417T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395442 | |||||||
chr6:32395479 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1079-454C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395479 | |||||||
chr6:32395523 | C | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1079-498G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395523 | |||||||
chr6:32395542 | C | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078+497G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395542 | |||||||
chr6:32395546 | G | A | 2 | a0003c0004t0002g0177 a0003c0012t0002g0070 |
3 | HG02109.hp2 HG03209.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1078+493C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395546 | |||||||
chr6:32395558 | C | T | 4 | a0001c0005t0001g0019 a0001c0005t0001g0026 a0001c0005t0001g0112 others(1): Show |
11 | HG01243.hp1 HG02129.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.1078+481G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395558 | |||||||
chr6:32395574 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+465C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395574 | |||||||
chr6:32395610 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+429A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395610 | |||||||
chr6:32395614 | C | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+425G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395614 | |||||||
chr6:32395615 | CCT | C | 3 | a0001c0001t0001g0032 a0001c0001t0001g0147 a0001c0001t0001g0150 |
6 | HG01070.hp2 HG01071.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.1078+422_1078+423d others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395615 | |||||||
chr6:32395671 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+368A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395671 | |||||||
chr6:32395714 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+325A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395714 | |||||||
chr6:32395716 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.1078+323A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395716 | |||||||
chr6:32395750 | C | T | 81 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(78): Show |
185 | HG00140.hp2 HG00438.hp2 HG00639.hp1 others(182): Show |
intron_variant | MODIFIER | c.1078+289G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395750 | |||||||
chr6:32395768 | G | A | 2 | a0001c0001t0001g0038 a0001c0001t0001g0148 |
4 | NA18941.hp2 NA18961.hp1 NA18965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1078+271C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395768 | |||||||
chr6:32395781 | A | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+258T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395781 | |||||||
chr6:32395862 | T | G | 7 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(4): Show |
17 | HG00423.hp1 HG00673.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.1078+177A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395862 | |||||||
chr6:32395872 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+167C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395872 | |||||||
chr6:32395935 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+104T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395935 | |||||||
chr6:32395939 | A | G | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.1078+100T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395939 | |||||||
chr6:32395945 | A | G | 10 | a0002c0002t0001g0035 a0002c0002t0001g0047 a0002c0002t0001g0048 others(7): Show |
16 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.1078+94T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395945 | |||||||
chr6:32395995 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+44G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395995 | |||||||
chr6:32395997 | G | A | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.1078+42C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32395997 | |||||||
chr6:32396009 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+30C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32396009 | |||||||
chr6:32396013 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.1078+26T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 5/7 | chr6 | 32396013 | |||||||
chr6:32396413 | A | G | 10 | a0002c0002t0001g0035 a0002c0002t0001g0047 a0002c0002t0001g0048 others(7): Show |
16 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.731-27T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396413 | |||||||
chr6:32396417 | A | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-31T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396417 | |||||||
chr6:32396437 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-51A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396437 | |||||||
chr6:32396455 | C | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-69G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396455 | |||||||
chr6:32396496 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-110C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396496 | |||||||
chr6:32396508 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-122T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396508 | |||||||
chr6:32396509 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-123C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396509 | |||||||
chr6:32396528 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-142A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396528 | |||||||
chr6:32396545 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-159G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396545 | |||||||
chr6:32396559 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-173G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396559 | |||||||
chr6:32396579 | A | G | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.731-193T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396579 | |||||||
chr6:32396588 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-202A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396588 | |||||||
chr6:32396600 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-214A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396600 | |||||||
chr6:32396601 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-215C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396601 | |||||||
chr6:32396604 | T | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-218A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396604 | |||||||
chr6:32396609 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-223G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396609 | |||||||
chr6:32396642 | T | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-256A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396642 | |||||||
chr6:32396675 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-289A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396675 | |||||||
chr6:32396695 | G | GA | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-310dupT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396695 | |||||||
chr6:32396706 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-320A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396706 | |||||||
chr6:32396707 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-321C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396707 | |||||||
chr6:32396719 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-333C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396719 | |||||||
chr6:32396747 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-361C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396747 | |||||||
chr6:32396790 | G | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-404C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396790 | |||||||
chr6:32396810 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-424C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396810 | |||||||
chr6:32396814 | CTACAGAA others(1): Show |
C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-436_731-429del others(8): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396814 | |||||||
chr6:32396825 | C | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-439G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396825 | |||||||
chr6:32396835 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-449A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396835 | |||||||
chr6:32396837 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-451C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396837 | |||||||
chr6:32396841 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-455T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396841 | |||||||
chr6:32396872 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-486G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396872 | |||||||
chr6:32396873 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-487T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396873 | |||||||
chr6:32396890 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(175): Show |
440 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(437): Show |
intron_variant | MODIFIER | c.731-504T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396890 | |||||||
chr6:32396895 | G | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-509C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396895 | |||||||
chr6:32396898 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-512G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396898 | |||||||
chr6:32396905 | G | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-519C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396905 | |||||||
chr6:32396928 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-542A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396928 | |||||||
chr6:32396941 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-555G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396941 | |||||||
chr6:32396942 | T | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-556A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396942 | |||||||
chr6:32396957 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
9 | HG00423.hp2 HG00621.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.731-571C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396957 | |||||||
chr6:32396967 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-581C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396967 | |||||||
chr6:32396973 | T | TTGTC | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-588_731-587ins others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396973 | |||||||
chr6:32396976 | AAAAC | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-594_731-591del others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396976 | |||||||
chr6:32396990 | A | AACAAGCA others(7): Show |
10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-605_731-604ins others(14): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396990 | |||||||
chr6:32396999 | C | T | 4 | a0001c0001t0001g0013 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
9 | HG00423.hp2 HG00621.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.731-613G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32396999 | |||||||
chr6:32397114 | GCA | G | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.731-730_731-729del others(2): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397114 | |||||||
chr6:32397134 | T | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-748A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397134 | |||||||
chr6:32397187 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-801T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397187 | |||||||
chr6:32397207 | A | G | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.731-821T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397207 | |||||||
chr6:32397239 | G | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-853C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397239 | |||||||
chr6:32397272 | C | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-886G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397272 | |||||||
chr6:32397286 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-900G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397286 | |||||||
chr6:32397298 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-912A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397298 | |||||||
chr6:32397309 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-923T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397309 | |||||||
chr6:32397314 | A | G | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-928T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397314 | |||||||
chr6:32397316 | T | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-930A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397316 | |||||||
chr6:32397336 | C | T | 3 | a0003c0004t0002g0073 a0003c0004t0002g0180 a0003c0004t0002g0181 |
4 | HG02818.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.731-950G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397336 | |||||||
chr6:32397343 | C | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-957G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397343 | |||||||
chr6:32397359 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-973T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397359 | |||||||
chr6:32397360 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-974A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397360 | |||||||
chr6:32397373 | GT | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-988delA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397373 | |||||||
chr6:32397425 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1039A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397425 | |||||||
chr6:32397475 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1089C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397475 | |||||||
chr6:32397481 | G | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1095C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397481 | |||||||
chr6:32397485 | G | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1099C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397485 | |||||||
chr6:32397503 | T | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-1117A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397503 | |||||||
chr6:32397507 | A | T | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.731-1121T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397507 | |||||||
chr6:32397512 | G | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1126C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397512 | |||||||
chr6:32397527 | AGTCT | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1145_731-1142d others(6): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397527 | |||||||
chr6:32397538 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1152T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397538 | |||||||
chr6:32397557 | C | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1171G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397557 | |||||||
chr6:32397558 | A | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1172T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397558 | |||||||
chr6:32397558 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1172T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397558 | |||||||
chr6:32397582 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1196A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397582 | |||||||
chr6:32397592 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1206A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397592 | |||||||
chr6:32397612 | C | T | 1 | a0004c0003t0003g0017 | 6 | HG02132.hp2 NA18942.hp2 NA18960.hp2 others(3): Show |
intron_variant | MODIFIER | c.731-1226G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397612 | |||||||
chr6:32397629 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-1243C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397629 | |||||||
chr6:32397654 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1268T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397654 | |||||||
chr6:32397669 | A | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1283T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397669 | |||||||
chr6:32397690 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1304A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397690 | |||||||
chr6:32397714 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-1328G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397714 | |||||||
chr6:32397716 | T | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1330A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397716 | |||||||
chr6:32397726 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1340A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397726 | |||||||
chr6:32397737 | G | GTC | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.731-1352_731-1351i others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397737 | |||||||
chr6:32397752 | G | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1366C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397752 | |||||||
chr6:32397755 | G | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1369C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397755 | |||||||
chr6:32397762 | TC | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1377delG | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397762 | |||||||
chr6:32397776 | C | T | 18 | a0003c0004t0002g0043 a0003c0004t0002g0078 a0003c0004t0002g0079 others(15): Show |
31 | HG00140.hp2 HG00735.hp2 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.731-1390G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397776 | |||||||
chr6:32397787 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1401C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397787 | |||||||
chr6:32397803 | A | G | 145 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
349 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.731-1417T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397803 | |||||||
chr6:32397855 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1469C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397855 | |||||||
chr6:32397857 | A | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1471T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397857 | |||||||
chr6:32397881 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1495C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397881 | |||||||
chr6:32397888 | C | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1502G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397888 | |||||||
chr6:32397889 | G | A | 13 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(10): Show |
51 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.731-1503C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397889 | |||||||
chr6:32397890 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1504G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397890 | |||||||
chr6:32397911 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1525G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397911 | |||||||
chr6:32397930 | T | C | 60 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(57): Show |
141 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.731-1544A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397930 | |||||||
chr6:32397943 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1557C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397943 | |||||||
chr6:32397969 | A | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1583T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397969 | |||||||
chr6:32397971 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1585A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397971 | |||||||
chr6:32397975 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1589T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32397975 | |||||||
chr6:32398008 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1622G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398008 | |||||||
chr6:32398014 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1628T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398014 | |||||||
chr6:32398063 | T | C | 145 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(142): Show |
349 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(346): Show |
intron_variant | MODIFIER | c.731-1677A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398063 | |||||||
chr6:32398119 | A | G | 60 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(57): Show |
141 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.731-1733T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398119 | |||||||
chr6:32398129 | C | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1743G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398129 | |||||||
chr6:32398138 | T | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1752A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398138 | |||||||
chr6:32398151 | G | A | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
96 | HG00140.hp2 HG00423.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.731-1765C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398151 | |||||||
chr6:32398154 | C | CT | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.731-1769_731-1768i others(3): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398154 | |||||||
chr6:32398155 | C | A | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.731-1769G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398155 | |||||||
chr6:32398156 | A | AT | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1771dupA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398156 | |||||||
chr6:32398164 | T | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1778A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398164 | |||||||
chr6:32398178 | A | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1792T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398178 | |||||||
chr6:32398194 | G | A | 60 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(57): Show |
141 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.731-1808C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398194 | |||||||
chr6:32398220 | A | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-1834T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398220 | |||||||
chr6:32398245 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-1859G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398245 | |||||||
chr6:32398262 | T | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-1876A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398262 | |||||||
chr6:32398293 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-1907G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398293 | |||||||
chr6:32398320 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-1934C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398320 | |||||||
chr6:32398355 | C | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-1969G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398355 | |||||||
chr6:32398364 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-1978T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398364 | |||||||
chr6:32398367 | A | C | 1 | a0003c0021t0002g0185 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.731-1981T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398367 | |||||||
chr6:32398400 | G | C | 2 | a0003c0004t0002g0073 a0003c0004t0002g0181 |
3 | HG02818.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.731-2014C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398400 | |||||||
chr6:32398405 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2019G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398405 | |||||||
chr6:32398449 | G | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0133 |
5 | HG02486.hp1 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-2063C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398449 | |||||||
chr6:32398554 | G | C | 60 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(57): Show |
141 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.731-2168C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398554 | |||||||
chr6:32398565 | G | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2179C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398565 | |||||||
chr6:32398615 | C | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-2229G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398615 | |||||||
chr6:32398644 | T | C | 49 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(46): Show |
95 | HG00140.hp2 HG00423.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.731-2258A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398644 | |||||||
chr6:32398651 | T | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-2265A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398651 | |||||||
chr6:32398653 | T | TG | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2268dupC | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398653 | |||||||
chr6:32398655 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0063 others(7): Show |
39 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.731-2269G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398655 | |||||||
chr6:32398711 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-2325T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398711 | |||||||
chr6:32398760 | C | T | 10 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0063 others(7): Show |
39 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(36): Show |
intron_variant | MODIFIER | c.731-2374G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398760 | |||||||
chr6:32398779 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2393G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398779 | |||||||
chr6:32398792 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2406T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398792 | |||||||
chr6:32398839 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2453T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398839 | |||||||
chr6:32398848 | T | C | 60 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(57): Show |
141 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.731-2462A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398848 | |||||||
chr6:32398857 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2471C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398857 | |||||||
chr6:32398874 | G | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.731-2488C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398874 | |||||||
chr6:32398889 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2503T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398889 | |||||||
chr6:32398904 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-2518G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398904 | |||||||
chr6:32398905 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2519T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398905 | |||||||
chr6:32398920 | C | CTT | 42 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(39): Show |
123 | HG00438.hp2 HG00639.hp1 HG01069.hp2 others(120): Show |
intron_variant | MODIFIER | c.731-2536_731-2535d others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398920 | |||||||
chr6:32398958 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2572A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398958 | |||||||
chr6:32398991 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2605T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398991 | |||||||
chr6:32398997 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2611G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32398997 | |||||||
chr6:32399029 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.731-2643G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399029 | |||||||
chr6:32399030 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2644G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399030 | |||||||
chr6:32399056 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2670C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399056 | |||||||
chr6:32399059 | G | A | 11 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(8): Show |
49 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(46): Show |
intron_variant | MODIFIER | c.731-2673C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399059 | |||||||
chr6:32399079 | T | TC | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.731-2694dupG | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399079 | |||||||
chr6:32399142 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2643G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399142 | |||||||
chr6:32399147 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2638G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399147 | |||||||
chr6:32399148 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2637T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399148 | |||||||
chr6:32399155 | C | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2630G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399155 | |||||||
chr6:32399232 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2553C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399232 | |||||||
chr6:32399240 | G | A | 166 | a0001c0001t0001g0003 a0001c0001t0001g0007 a0001c0001t0001g0009 others(163): Show |
390 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(387): Show |
intron_variant | MODIFIER | c.730+2545C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399240 | |||||||
chr6:32399269 | T | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2516A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399269 | |||||||
chr6:32399271 | G | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+2514C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399271 | |||||||
chr6:32399274 | T | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2511A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399274 | |||||||
chr6:32399280 | G | GA | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2504dupT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399280 | |||||||
chr6:32399300 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2485G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399300 | |||||||
chr6:32399325 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2460G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399325 | |||||||
chr6:32399462 | C | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2323G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399462 | |||||||
chr6:32399482 | T | G | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.730+2303A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399482 | |||||||
chr6:32399576 | G | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2209C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399576 | |||||||
chr6:32399600 | G | A | 1 | a0002c0002t0001g0092 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.730+2185C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399600 | |||||||
chr6:32399611 | T | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+2174A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399611 | |||||||
chr6:32399624 | C | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2161G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399624 | |||||||
chr6:32399635 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.730+2150G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399635 | |||||||
chr6:32399674 | T | A | 60 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(57): Show |
141 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.730+2111A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399674 | |||||||
chr6:32399700 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2085A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399700 | |||||||
chr6:32399738 | T | C | 60 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(57): Show |
141 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.730+2047A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399738 | |||||||
chr6:32399774 | T | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+2011A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399774 | |||||||
chr6:32399795 | A | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1990T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399795 | |||||||
chr6:32399798 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1987T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399798 | |||||||
chr6:32399817 | C | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1968G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399817 | |||||||
chr6:32399821 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1964T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399821 | |||||||
chr6:32399827 | T | C | 60 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(57): Show |
141 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.730+1958A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399827 | |||||||
chr6:32399854 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1931C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399854 | |||||||
chr6:32399872 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1913A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399872 | |||||||
chr6:32399873 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1912A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399873 | |||||||
chr6:32399879 | T | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1906A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399879 | |||||||
chr6:32399882 | C | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1903G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399882 | |||||||
chr6:32399888 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1897T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399888 | |||||||
chr6:32399896 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1889C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399896 | |||||||
chr6:32399905 | G | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.730+1880C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399905 | |||||||
chr6:32399916 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1869G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399916 | |||||||
chr6:32399920 | C | G | 2 | a0002c0002t0001g0095 a0002c0002t0001g0097 |
2 | HG00639.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.730+1865G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399920 | |||||||
chr6:32399945 | A | G | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.730+1840T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399945 | |||||||
chr6:32399953 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1832C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399953 | |||||||
chr6:32399954 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1831A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399954 | |||||||
chr6:32399955 | G | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1830C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399955 | |||||||
chr6:32399970 | C | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+1815G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399970 | |||||||
chr6:32399975 | G | GA | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1809dupT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399975 | |||||||
chr6:32399980 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1805A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32399980 | |||||||
chr6:32400000 | A | T | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.730+1785T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400000 | |||||||
chr6:32400008 | G | A | 7 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(4): Show |
17 | HG00423.hp1 HG00673.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.730+1777C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400008 | |||||||
chr6:32400018 | G | T | 80 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(77): Show |
169 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.730+1767C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400018 | |||||||
chr6:32400070 | T | C | 43 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(40): Show |
127 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(124): Show |
intron_variant | MODIFIER | c.730+1715A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400070 | |||||||
chr6:32400120 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1665C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400120 | |||||||
chr6:32400125 | T | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1660A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400125 | |||||||
chr6:32400150 | A | G | 60 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(57): Show |
141 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(138): Show |
intron_variant | MODIFIER | c.730+1635T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400150 | |||||||
chr6:32400193 | C | T | 1 | a0001c0001t0001g0158 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.730+1592G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400193 | |||||||
chr6:32400194 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.730+1591C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400194 | |||||||
chr6:32400220 | T | A | 12 | a0002c0002t0001g0002 a0002c0002t0001g0044 a0002c0002t0001g0046 others(9): Show |
36 | HG00639.hp1 HG01167.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.730+1565A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400220 | |||||||
chr6:32400239 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1546C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400239 | |||||||
chr6:32400246 | C | A | 5 | a0001c0010t0001g0025 a0001c0010t0001g0036 a0001c0010t0001g0104 others(2): Show |
10 | NA18612.hp1 NA18747.hp1 NA18957.hp1 others(7): Show |
intron_variant | MODIFIER | c.730+1539G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400246 | |||||||
chr6:32400298 | C | A | 2 | a0001c0001t0001g0030 a0001c0001t0001g0133 |
5 | HG02486.hp1 HG02886.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+1487G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400298 | |||||||
chr6:32400310 | T | C | 42 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(39): Show |
123 | HG00438.hp2 HG00639.hp1 HG01069.hp2 others(120): Show |
intron_variant | MODIFIER | c.730+1475A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400310 | |||||||
chr6:32400357 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+1428A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400357 | |||||||
chr6:32400407 | A | G | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+1378T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400407 | |||||||
chr6:32400537 | C | A | 34 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(31): Show |
83 | HG00639.hp1 HG00642.hp2 HG01069.hp2 others(80): Show |
intron_variant | MODIFIER | c.730+1248G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400537 | |||||||
chr6:32400575 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.730+1210C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400575 | |||||||
chr6:32400578 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.730+1207C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400578 | |||||||
chr6:32400594 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0116 |
7 | HG00423.hp2 HG02040.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.730+1191T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400594 | |||||||
chr6:32400610 | T | G | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+1175A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400610 | |||||||
chr6:32400655 | TC | T | 80 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(77): Show |
169 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.730+1129delG | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400655 | |||||||
chr6:32400659 | A | T | 80 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(77): Show |
169 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(166): Show |
intron_variant | MODIFIER | c.730+1126T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400659 | |||||||
chr6:32400661 | CA | C | 82 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(79): Show |
174 | HG00140.hp2 HG00423.hp1 HG00639.hp1 others(171): Show |
intron_variant | MODIFIER | c.730+1123delT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400661 | |||||||
chr6:32400682 | G | A | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.730+1103C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400682 | |||||||
chr6:32400685 | G | A | 3 | a0001c0005t0001g0024 a0001c0005t0001g0106 a0011c0016t0001g0107 |
6 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+1100C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400685 | |||||||
chr6:32400706 | G | A | 58 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(55): Show |
136 | HG00140.hp2 HG00423.hp1 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.730+1079C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400706 | |||||||
chr6:32400736 | C | T | 34 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(31): Show |
83 | HG00639.hp1 HG00642.hp2 HG01069.hp2 others(80): Show |
intron_variant | MODIFIER | c.730+1049G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400736 | |||||||
chr6:32400745 | T | TA | 8 | a0001c0001t0001g0028 a0001c0001t0001g0053 a0001c0001t0001g0117 others(5): Show |
14 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.730+1039dupT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400745 | T | TAAAAAAA others(4): Show |
1 | a0013c0014t0001g0091 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.730+1029_730+1039d others(13): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400745 | T | TAAAAATA others(5): Show |
10 | a0002c0002t0001g0012 a0002c0002t0001g0023 a0002c0002t0001g0034 others(7): Show |
22 | HG01123.hp1 HG01167.hp1 HG01981.hp2 others(19): Show |
intron_variant | MODIFIER | c.730+1039_730+1040i others(14): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400745 | T | TAAAAATA others(6): Show |
18 | a0002c0002t0001g0002 a0002c0002t0001g0018 a0002c0002t0001g0035 others(15): Show |
51 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.730+1039_730+1040i others(15): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400745 | T | TAAAAATA others(7): Show |
2 | a0002c0002t0001g0046 a0002c0002t0001g0099 |
3 | HG02055.hp2 HG03688.hp1 NA18993.hp1 |
intron_variant | MODIFIER | c.730+1039_730+1040i others(16): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400745 | T | TAAAAATA others(8): Show |
1 | a0005c0006t0002g0137 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.730+1039_730+1040i others(17): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400745 | T | TAAAAATA others(9): Show |
15 | a0003c0004t0002g0043 a0003c0004t0002g0078 a0003c0004t0002g0079 others(12): Show |
28 | HG00140.hp2 HG00735.hp2 HG01175.hp2 others(25): Show |
intron_variant | MODIFIER | c.730+1039_730+1040i others(18): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400745 | T | TAAAAATA others(10): Show |
18 | a0003c0004t0002g0071 a0003c0004t0002g0072 a0003c0004t0002g0073 others(15): Show |
25 | HG00738.hp2 HG01123.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.730+1039_730+1040i others(19): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400745 | T | TAAAAATA others(11): Show |
2 | a0003c0004t0002g0178 a0003c0004t0002g0180 |
2 | HG03516.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.730+1039_730+1040i others(20): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400745 | T | TAAAATAC others(5): Show |
1 | a0002c0002t0001g0089 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.730+1039_730+1040i others(14): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400745 | TA | T | 7 | a0001c0001t0001g0145 a0001c0001t0001g0151 a0001c0001t0001g0165 others(4): Show |
9 | HG00642.hp2 HG01070.hp1 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+1039delT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400745 | |||||||
chr6:32400750 | A | ATAC | 10 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(7): Show |
32 | HG00423.hp1 HG00673.hp1 HG01192.hp1 others(29): Show |
intron_variant | MODIFIER | c.730+1034_730+1035i others(5): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400750 | |||||||
chr6:32400760 | A | ACAAAAAA others(3): Show |
1 | a0003c0021t0002g0185 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.730+1024_730+1025i others(12): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400760 | |||||||
chr6:32400760 | A | C | 36 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(33): Show |
56 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(53): Show |
intron_variant | MODIFIER | c.730+1025T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400760 | |||||||
chr6:32400763 | ATTAGCTG others(271): Show |
A | 11 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(8): Show |
34 | HG00423.hp1 HG00673.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.730+744_730+1021de others(1): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400763 | |||||||
chr6:32400767 | G | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+1018C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400767 | |||||||
chr6:32400781 | C | T | 93 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(90): Show |
209 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(206): Show |
intron_variant | MODIFIER | c.730+1004G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400781 | |||||||
chr6:32400783 | C | T | 69 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(66): Show |
135 | HG00140.hp2 HG00639.hp1 HG00735.hp2 others(132): Show |
intron_variant | MODIFIER | c.730+1002G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400783 | |||||||
chr6:32400784 | A | C | 2 | a0007c0009t0001g0004 a0007c0009t0001g0131 |
15 | HG01358.hp2 NA18945.hp1 NA18963.hp2 others(12): Show |
intron_variant | MODIFIER | c.730+1001T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400784 | |||||||
chr6:32400784 | A | G | 71 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(68): Show |
140 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(137): Show |
intron_variant | MODIFIER | c.730+1001T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400784 | |||||||
chr6:32400794 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+991A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400794 | |||||||
chr6:32400800 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+985A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400800 | |||||||
chr6:32400816 | A | G | 134 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0014 others(131): Show |
315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.730+969T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400816 | |||||||
chr6:32400827 | A | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+958T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400827 | |||||||
chr6:32400844 | T | C | 37 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(34): Show |
57 | HG00140.hp2 HG00735.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.730+941A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400844 | |||||||
chr6:32400844 | T | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+941A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400844 | |||||||
chr6:32400854 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+931T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400854 | |||||||
chr6:32400856 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+929A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400856 | |||||||
chr6:32400886 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+899A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400886 | |||||||
chr6:32400892 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+893T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400892 | |||||||
chr6:32400894 | CAG | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+889_730+890del others(2): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400894 | |||||||
chr6:32400908 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+877C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400908 | |||||||
chr6:32400912 | C | CA | 4 | a0001c0001t0001g0030 a0001c0001t0001g0133 a0001c0010t0001g0025 others(1): Show |
7 | HG02486.hp1 HG02886.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.730+872dupT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400912 | |||||||
chr6:32400912 | C | CAA | 17 | a0001c0005t0001g0019 a0001c0005t0001g0024 a0001c0005t0001g0026 others(14): Show |
32 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.730+871_730+872dup others(2): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400912 | |||||||
chr6:32400912 | C | CAAAAA | 18 | a0003c0004t0002g0071 a0003c0004t0002g0072 a0003c0004t0002g0073 others(15): Show |
25 | HG00738.hp2 HG01123.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.730+868_730+872dup others(5): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400912 | |||||||
chr6:32400912 | C | CAAAAAA | 21 | a0003c0004t0002g0043 a0003c0004t0002g0077 a0003c0004t0002g0081 others(18): Show |
36 | HG00140.hp2 HG00642.hp2 HG00735.hp2 others(33): Show |
intron_variant | MODIFIER | c.730+867_730+872dup others(6): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400912 | |||||||
chr6:32400912 | C | CAAAAAAA others(2): Show |
10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
42 | HG00438.hp2 HG02129.hp2 HG02132.hp2 others(39): Show |
intron_variant | MODIFIER | c.730+864_730+872dup others(9): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400912 | |||||||
chr6:32400912 | C | CAAAAAAA others(3): Show |
1 | a0004c0003t0003g0001 | 2 | HG02015.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.730+863_730+872dup others(10): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400912 | |||||||
chr6:32400912 | CA | C | 11 | a0002c0002t0001g0035 a0002c0002t0001g0047 a0002c0002t0001g0048 others(8): Show |
17 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.730+872delT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400912 | |||||||
chr6:32400927 | T | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+858A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400927 | |||||||
chr6:32400931 | C | T | 6 | a0001c0001t0001g0014 a0001c0001t0001g0016 a0001c0001t0001g0040 others(3): Show |
18 | HG00558.hp2 HG01257.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.730+854G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400931 | |||||||
chr6:32400932 | G | A | 5 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0022 others(2): Show |
13 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.730+853C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400932 | |||||||
chr6:32400932 | G | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+853C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400932 | |||||||
chr6:32400935 | G | A | 1 | a0004c0003t0003g0001 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.730+850C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400935 | |||||||
chr6:32400936 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+849A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400936 | |||||||
chr6:32400938 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+847C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400938 | |||||||
chr6:32400953 | A | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+832T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400953 | |||||||
chr6:32400960 | G | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+825C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400960 | |||||||
chr6:32400968 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+817C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400968 | |||||||
chr6:32400980 | G | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+805C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400980 | |||||||
chr6:32400983 | G | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
3 | HG02572.hp2 HG02818.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.730+802C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400983 | |||||||
chr6:32400990 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+795G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400990 | |||||||
chr6:32400994 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+791T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32400994 | |||||||
chr6:32401012 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+773A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401012 | |||||||
chr6:32401017 | G | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+768C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401017 | |||||||
chr6:32401022 | C | T | 1 | a0002c0002t0001g0002 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.730+763G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401022 | |||||||
chr6:32401024 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+761G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401024 | |||||||
chr6:32401032 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+753A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401032 | |||||||
chr6:32401034 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+751A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401034 | |||||||
chr6:32401035 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+750G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401035 | |||||||
chr6:32401036 | G | C | 1 | a0001c0001t0001g0028 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.730+749C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401036 | |||||||
chr6:32401043 | C | A | 4 | a0006c0007t0001g0005 a0006c0007t0001g0029 a0006c0007t0001g0054 others(1): Show |
17 | HG01192.hp1 HG03017.hp2 NA18940.hp1 others(14): Show |
intron_variant | MODIFIER | c.730+742G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401043 | |||||||
chr6:32401043 | CT | C | 7 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(4): Show |
17 | HG00423.hp1 HG00673.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.730+741delA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401043 | |||||||
chr6:32401044 | T | C | 4 | a0006c0007t0001g0005 a0006c0007t0001g0029 a0006c0007t0001g0054 others(1): Show |
17 | HG01192.hp1 HG03017.hp2 NA18940.hp1 others(14): Show |
intron_variant | MODIFIER | c.730+741A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401044 | |||||||
chr6:32401050 | T | A | 11 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(8): Show |
34 | HG00423.hp1 HG00673.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.730+735A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401050 | |||||||
chr6:32401052 | C | A | 11 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(8): Show |
34 | HG00423.hp1 HG00673.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.730+733G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401052 | |||||||
chr6:32401055 | A | C | 11 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(8): Show |
34 | HG00423.hp1 HG00673.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.730+730T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401055 | |||||||
chr6:32401064 | C | T | 11 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(8): Show |
34 | HG00423.hp1 HG00673.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.730+721G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401064 | |||||||
chr6:32401065 | G | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.730+720C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401065 | |||||||
chr6:32401068 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+717G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401068 | |||||||
chr6:32401077 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.730+708C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401077 | |||||||
chr6:32401080 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+705A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401080 | |||||||
chr6:32401081 | G | A | 3 | a0004c0003t0003g0172 a0008c0011t0004g0042 a0008c0011t0004g0069 |
6 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+704C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401081 | |||||||
chr6:32401092 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+693G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401092 | |||||||
chr6:32401122 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.730+663C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401122 | |||||||
chr6:32401132 | T | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+653A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401132 | |||||||
chr6:32401134 | G | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+651C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401134 | |||||||
chr6:32401157 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+628T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401157 | |||||||
chr6:32401165 | G | A | 15 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0167 others(12): Show |
60 | HG00438.hp2 HG00558.hp2 HG00642.hp2 others(57): Show |
intron_variant | MODIFIER | c.730+620C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401165 | |||||||
chr6:32401191 | G | C | 2 | a0003c0004t0002g0073 a0003c0004t0002g0181 |
3 | HG02818.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.730+594C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401191 | |||||||
chr6:32401195 | A | G | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+590T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401195 | |||||||
chr6:32401207 | C | CA | 8 | a0001c0001t0001g0157 a0001c0001t0001g0166 a0001c0005t0001g0019 others(5): Show |
13 | HG01175.hp1 HG01243.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.730+577dupT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAA | 10 | a0001c0005t0001g0026 a0003c0004t0002g0074 a0003c0004t0002g0176 others(7): Show |
21 | HG00738.hp2 HG01255.hp1 HG01952.hp2 others(18): Show |
intron_variant | MODIFIER | c.730+576_730+577dup others(2): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAA | 6 | a0001c0005t0001g0051 a0003c0004t0002g0071 a0003c0004t0002g0075 others(3): Show |
12 | HG00423.hp1 HG00673.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.730+575_730+577dup others(3): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAA | 9 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0056 others(6): Show |
16 | HG00323.hp1 HG02109.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.730+574_730+577dup others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAA | 9 | a0001c0001t0001g0007 a0001c0001t0001g0117 a0001c0001t0001g0124 others(6): Show |
18 | HG00408.hp2 HG00609.hp1 HG01256.hp2 others(15): Show |
intron_variant | MODIFIER | c.730+573_730+577dup others(5): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAA | 6 | a0001c0001t0001g0053 a0001c0001t0001g0058 a0003c0012t0002g0070 others(3): Show |
16 | HG01496.hp2 HG01891.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.730+572_730+577dup others(6): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA | 4 | a0003c0004t0002g0078 a0003c0004t0002g0177 a0005c0006t0002g0031 others(1): Show |
7 | HG00735.hp2 HG01175.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.730+571_730+577dup others(7): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(1): Show |
6 | a0001c0001t0001g0059 a0002c0002t0001g0047 a0002c0002t0001g0048 others(3): Show |
9 | HG01884.hp1 HG02080.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.730+570_730+577dup others(8): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(2): Show |
4 | a0001c0001t0001g0128 a0001c0010t0001g0036 a0001c0010t0001g0110 others(1): Show |
7 | HG01106.hp2 HG02723.hp1 NA18612.hp1 others(4): Show |
intron_variant | MODIFIER | c.730+569_730+577dup others(9): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(3): Show |
3 | a0001c0001t0001g0116 a0003c0004t0002g0178 a0005c0006t0002g0141 |
3 | NA18987.hp2 NA19001.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.730+568_730+577dup others(10): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(4): Show |
3 | a0001c0001t0001g0114 a0001c0005t0001g0105 a0003c0004t0002g0080 |
3 | HG02559.hp2 NA18964.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.730+567_730+577dup others(11): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(5): Show |
4 | a0001c0001t0001g0115 a0001c0005t0001g0052 a0001c0010t0001g0025 others(1): Show |
9 | HG00140.hp2 HG00609.hp2 HG00621.hp1 others(6): Show |
intron_variant | MODIFIER | c.730+566_730+577dup others(12): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(6): Show |
5 | a0001c0005t0001g0109 a0001c0010t0001g0104 a0001c0010t0001g0111 others(2): Show |
6 | HG01884.hp2 HG02148.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.730+565_730+577dup others(13): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(7): Show |
1 | a0002c0002t0001g0050 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.730+564_730+577dup others(14): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(8): Show |
1 | a0002c0002t0001g0035 | 3 | HG01361.hp1 HG01433.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.730+563_730+577dup others(15): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(9): Show |
2 | a0002c0002t0001g0101 a0003c0004t0002g0082 |
2 | HG01074.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.730+562_730+577dup others(16): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(10): Show |
1 | a0002c0002t0001g0102 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.730+561_730+577dup others(17): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(12): Show |
2 | a0002c0002t0001g0103 a0003c0004t0002g0083 |
2 | HG01516.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.730+559_730+577dup others(19): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | C | CAAAAAAA others(15): Show |
1 | a0003c0004t0002g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.730+556_730+577dup others(22): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CA | C | 6 | a0001c0001t0001g0039 a0001c0001t0001g0066 a0001c0001t0001g0133 others(3): Show |
11 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.730+577delT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAA | C | 11 | a0001c0001t0001g0011 a0001c0001t0001g0030 a0001c0001t0001g0037 others(8): Show |
27 | HG00099.hp2 HG00733.hp1 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.730+576_730+577del others(2): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAA | C | 14 | a0001c0001t0001g0009 a0001c0001t0001g0021 a0001c0001t0001g0032 others(11): Show |
38 | HG00558.hp1 HG00642.hp1 HG00673.hp2 others(35): Show |
intron_variant | MODIFIER | c.730+575_730+577del others(3): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAA | C | 11 | a0001c0001t0001g0010 a0001c0001t0001g0022 a0001c0001t0001g0060 others(8): Show |
23 | HG00438.hp1 HG00621.hp2 HG00639.hp2 others(20): Show |
intron_variant | MODIFIER | c.730+574_730+577del others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAAA | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0015 a0001c0001t0001g0020 others(5): Show |
40 | HG00280.hp2 HG00408.hp1 HG00741.hp2 others(37): Show |
intron_variant | MODIFIER | c.730+573_730+577del others(5): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAAAA | C | 11 | a0001c0001t0001g0158 a0001c0001t0001g0159 a0002c0002t0001g0023 others(8): Show |
17 | HG01123.hp1 HG01978.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.730+572_730+577del others(6): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAAAAA | C | 12 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(9): Show |
46 | HG00639.hp1 HG01167.hp1 HG01168.hp1 others(43): Show |
intron_variant | MODIFIER | c.730+571_730+577del others(7): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAAAAA others(1): Show |
C | 2 | a0001c0001t0001g0013 a0002c0002t0001g0094 |
7 | HG00423.hp2 HG02040.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.730+570_730+577del others(8): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAAAAA others(8): Show |
C | 1 | a0001c0001t0001g0014 | 6 | HG02080.hp2 HG02602.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.730+563_730+577del others(15): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAAAAA others(9): Show |
C | 1 | a0007c0009t0001g0131 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.730+562_730+577del others(16): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAAAAA others(10): Show |
C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0040 a0001c0001t0001g0167 others(4): Show |
30 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(27): Show |
intron_variant | MODIFIER | c.730+561_730+577del others(17): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAAAAA others(11): Show |
C | 2 | a0004c0003t0003g0173 a0004c0003t0003g0174 |
2 | NA19001.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.730+560_730+577del others(18): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAAAAA others(12): Show |
C | 8 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(5): Show |
44 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(41): Show |
intron_variant | MODIFIER | c.730+559_730+577del others(19): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401207 | CAAAAAAA others(13): Show |
C | 1 | a0004c0003t0003g0170 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.730+558_730+577del others(20): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401207 | |||||||
chr6:32401249 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+536A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401249 | |||||||
chr6:32401257 | C | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+528G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401257 | |||||||
chr6:32401260 | T | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+525A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401260 | |||||||
chr6:32401300 | T | C | 11 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(8): Show |
34 | HG00423.hp1 HG00673.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.730+485A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401300 | |||||||
chr6:32401302 | G | T | 1 | a0002c0002t0001g0089 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.730+483C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401302 | |||||||
chr6:32401303 | T | G | 1 | a0002c0002t0001g0089 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.730+482A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401303 | |||||||
chr6:32401319 | G | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+466C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401319 | |||||||
chr6:32401346 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+439G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401346 | |||||||
chr6:32401361 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+424C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401361 | |||||||
chr6:32401362 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+423T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401362 | |||||||
chr6:32401396 | T | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.730+389A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401396 | |||||||
chr6:32401461 | C | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+324G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401461 | |||||||
chr6:32401472 | C | T | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.730+313G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401472 | |||||||
chr6:32401481 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+304A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401481 | |||||||
chr6:32401516 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+269T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401516 | |||||||
chr6:32401535 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+250A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401535 | |||||||
chr6:32401539 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+246T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401539 | |||||||
chr6:32401546 | T | A | 10 | a0002c0002t0001g0035 a0002c0002t0001g0047 a0002c0002t0001g0048 others(7): Show |
16 | HG01069.hp2 HG01071.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.730+239A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401546 | |||||||
chr6:32401559 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+226G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401559 | |||||||
chr6:32401574 | G | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.730+211C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401574 | |||||||
chr6:32401578 | C | T | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.730+207G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401578 | |||||||
chr6:32401604 | C | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+181G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401604 | |||||||
chr6:32401651 | T | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+134A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401651 | |||||||
chr6:32401662 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+123C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401662 | |||||||
chr6:32401677 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+108C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401677 | |||||||
chr6:32401689 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+96A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401689 | |||||||
chr6:32401711 | G | A | 12 | a0002c0002t0001g0002 a0002c0002t0001g0044 a0002c0002t0001g0046 others(9): Show |
36 | HG00639.hp1 HG01167.hp1 HG01168.hp1 others(33): Show |
intron_variant | MODIFIER | c.730+74C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401711 | |||||||
chr6:32401740 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.730+45C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401740 | |||||||
chr6:32401777 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
splice_region_variant&intron_variant | LOW | c.730+8C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 4/7 | chr6 | 32401777 | |||||||
chr6:32401809 | GAA | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
splice_region_variant&intron_variant | LOW | c.710-6_710-5delTT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32401809 | |||||||
chr6:32401817 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-12T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32401817 | |||||||
chr6:32401819 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-14T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32401819 | |||||||
chr6:32401824 | T | C | 4 | a0003c0004t0002g0074 a0003c0004t0002g0075 a0003c0004t0002g0076 others(1): Show |
7 | HG00738.hp2 HG01123.hp2 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.710-19A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32401824 | |||||||
chr6:32401828 | A | G | 2 | a0007c0009t0001g0004 a0007c0009t0001g0131 |
15 | HG01358.hp2 NA18945.hp1 NA18963.hp2 others(12): Show |
intron_variant | MODIFIER | c.710-23T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32401828 | |||||||
chr6:32401866 | A | G | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.710-61T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32401866 | |||||||
chr6:32401904 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-99C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32401904 | |||||||
chr6:32401925 | AT | A | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.710-121delA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32401925 | |||||||
chr6:32401969 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.710-164A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32401969 | |||||||
chr6:32402078 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-273T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402078 | |||||||
chr6:32402079 | G | GT | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-275_710-274ins others(1): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402079 | |||||||
chr6:32402080 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-275G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402080 | |||||||
chr6:32402094 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-289T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402094 | |||||||
chr6:32402100 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-295G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402100 | |||||||
chr6:32402109 | A | G | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.710-304T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402109 | |||||||
chr6:32402120 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-315C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402120 | |||||||
chr6:32402123 | C | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-318G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402123 | |||||||
chr6:32402132 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-327T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402132 | |||||||
chr6:32402154 | A | AT | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-350_710-349ins others(1): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402154 | |||||||
chr6:32402166 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-361T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402166 | |||||||
chr6:32402174 | G | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-369C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402174 | |||||||
chr6:32402217 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-412C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402217 | |||||||
chr6:32402281 | A | G | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.710-476T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402281 | |||||||
chr6:32402335 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.710-530C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402335 | |||||||
chr6:32402409 | AT | A | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
91 | HG00140.hp2 HG00423.hp1 HG00673.hp1 others(88): Show |
intron_variant | MODIFIER | c.709+525delA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402409 | |||||||
chr6:32402443 | C | CCT | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+491_709+492ins others(2): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402443 | |||||||
chr6:32402448 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+487A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402448 | |||||||
chr6:32402488 | G | T | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG02027.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.709+447C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402488 | |||||||
chr6:32402500 | T | TGGGGG | 9 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(6): Show |
43 | HG02015.hp2 HG02129.hp2 HG02132.hp2 others(40): Show |
intron_variant | MODIFIER | c.709+430_709+434dup others(5): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402500 | |||||||
chr6:32402541 | A | G | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.709+394T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402541 | |||||||
chr6:32402570 | G | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.709+365C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402570 | |||||||
chr6:32402594 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+341T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402594 | |||||||
chr6:32402629 | C | T | 19 | a0003c0004t0002g0071 a0003c0004t0002g0072 a0003c0004t0002g0073 others(16): Show |
26 | HG00738.hp2 HG01123.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.709+306G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402629 | |||||||
chr6:32402656 | T | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+279A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402656 | |||||||
chr6:32402658 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+277A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402658 | |||||||
chr6:32402685 | A | G | 8 | a0001c0001t0001g0011 a0001c0001t0001g0039 a0001c0001t0001g0132 others(5): Show |
16 | HG00099.hp2 HG00733.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.709+250T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402685 | |||||||
chr6:32402708 | AATGC | A | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.709+223_709+226del others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402708 | |||||||
chr6:32402712 | C | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.709+223G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402712 | |||||||
chr6:32402743 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+192G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402743 | |||||||
chr6:32402744 | G | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.709+191C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402744 | |||||||
chr6:32402745 | C | G | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.709+190G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402745 | |||||||
chr6:32402747 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+188C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402747 | |||||||
chr6:32402748 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+187C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402748 | |||||||
chr6:32402749 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+186G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402749 | |||||||
chr6:32402782 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+153C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402782 | |||||||
chr6:32402791 | C | T | 1 | a0001c0001t0001g0016 | 6 | HG00558.hp2 HG01257.hp1 HG01258.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+144G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402791 | |||||||
chr6:32402797 | T | C | 1 | a0001c0005t0001g0113 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.709+138A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402797 | |||||||
chr6:32402810 | G | C | 5 | a0001c0001t0001g0021 a0001c0001t0001g0037 a0001c0001t0001g0142 others(2): Show |
11 | HG01109.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.709+125C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402810 | |||||||
chr6:32402826 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.709+109C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402826 | |||||||
chr6:32402839 | T | C | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.709+96A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402839 | |||||||
chr6:32402847 | C | T | 1 | a0001c0001t0001g0155 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.709+88G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402847 | |||||||
chr6:32402869 | A | G | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.709+66T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402869 | |||||||
chr6:32402907 | A | G | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.709+28T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 3/7 | chr6 | 32402907 | |||||||
chr6:32403292 | G | A | 7 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(4): Show |
17 | HG00423.hp1 HG00673.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.428-76C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403292 | |||||||
chr6:32403303 | G | A | 1 | a0003c0008t0001g0119 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.428-87C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403303 | |||||||
chr6:32403353 | T | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-137A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403353 | |||||||
chr6:32403355 | C | T | 2 | a0004c0003t0003g0067 a0004c0003t0003g0170 |
3 | NA18979.hp1 NA19072.hp2 NA19076.hp2 |
intron_variant | MODIFIER | c.428-139G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403355 | |||||||
chr6:32403402 | G | C | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.428-186C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403402 | |||||||
chr6:32403417 | G | A | 1 | a0014c0013t0001g0125 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.428-201C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403417 | |||||||
chr6:32403458 | C | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-242G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403458 | |||||||
chr6:32403476 | T | C | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.428-260A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403476 | |||||||
chr6:32403489 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0063 others(5): Show |
36 | HG00438.hp1 HG00558.hp1 HG00621.hp2 others(33): Show |
intron_variant | MODIFIER | c.428-273G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403489 | |||||||
chr6:32403492 | C | T | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.428-276G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403492 | |||||||
chr6:32403515 | A | T | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.428-299T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403515 | |||||||
chr6:32403517 | C | G | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.428-301G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403517 | |||||||
chr6:32403595 | T | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-379A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403595 | |||||||
chr6:32403596 | CTGGT | C | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-384_428-381del others(4): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403596 | |||||||
chr6:32403613 | G | T | 11 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(8): Show |
34 | HG00423.hp1 HG00673.hp1 HG01192.hp1 others(31): Show |
intron_variant | MODIFIER | c.428-397C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403613 | |||||||
chr6:32403617 | T | C | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-401A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403617 | |||||||
chr6:32403629 | T | TA | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-414_428-413ins others(1): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403629 | |||||||
chr6:32403632 | T | C | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-416A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403632 | |||||||
chr6:32403634 | G | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-418C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403634 | |||||||
chr6:32403637 | G | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-421C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403637 | |||||||
chr6:32403646 | C | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-430G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403646 | |||||||
chr6:32403667 | A | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-451T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403667 | |||||||
chr6:32403723 | G | A | 19 | a0003c0004t0002g0071 a0003c0004t0002g0072 a0003c0004t0002g0073 others(16): Show |
26 | HG00738.hp2 HG01123.hp2 HG01243.hp2 others(23): Show |
intron_variant | MODIFIER | c.428-507C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403723 | |||||||
chr6:32403751 | C | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-535G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403751 | |||||||
chr6:32403756 | C | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-540G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403756 | |||||||
chr6:32403761 | C | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-545G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403761 | |||||||
chr6:32403762 | G | A | 40 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(37): Show |
74 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.428-546C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403762 | |||||||
chr6:32403795 | A | G | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-579T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403795 | |||||||
chr6:32403822 | C | G | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-606G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403822 | |||||||
chr6:32403827 | G | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-611C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403827 | |||||||
chr6:32403842 | A | G | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.428-626T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403842 | |||||||
chr6:32403843 | A | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.428-627T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403843 | |||||||
chr6:32403863 | G | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-647C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403863 | |||||||
chr6:32403875 | C | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-659G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403875 | |||||||
chr6:32403890 | G | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-674C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403890 | |||||||
chr6:32403902 | C | T | 1 | a0001c0005t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.428-686G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403902 | |||||||
chr6:32403920 | C | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-704G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403920 | |||||||
chr6:32403940 | A | G | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-724T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403940 | |||||||
chr6:32403947 | T | C | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-731A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403947 | |||||||
chr6:32403950 | A | G | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-734T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403950 | |||||||
chr6:32403954 | C | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-738G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403954 | |||||||
chr6:32403962 | T | G | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-746A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403962 | |||||||
chr6:32403966 | C | G | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-750G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32403966 | |||||||
chr6:32404023 | C | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-807G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404023 | |||||||
chr6:32404041 | G | C | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-825C>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404041 | |||||||
chr6:32404054 | GTATTCCT others(4): Show |
G | 1 | a0004c0003t0003g0174 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.428-849_428-839del others(11): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404054 | |||||||
chr6:32404063 | C | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.428-847G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404063 | |||||||
chr6:32404075 | A | T | 2 | a0007c0009t0001g0004 a0007c0009t0001g0131 |
15 | HG01358.hp2 NA18945.hp1 NA18963.hp2 others(12): Show |
intron_variant | MODIFIER | c.428-859T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404075 | |||||||
chr6:32404088 | C | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+851G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404088 | |||||||
chr6:32404090 | G | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+849C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404090 | |||||||
chr6:32404110 | G | GA | 15 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0053 others(12): Show |
31 | HG00408.hp2 HG00609.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.427+828dupT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404110 | |||||||
chr6:32404121 | G | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+818C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404121 | |||||||
chr6:32404138 | C | T | 22 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(19): Show |
62 | HG00639.hp1 HG01123.hp1 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.427+801G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404138 | |||||||
chr6:32404177 | G | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+762C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404177 | |||||||
chr6:32404210 | G | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+729C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404210 | |||||||
chr6:32404230 | T | C | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+709A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404230 | |||||||
chr6:32404246 | A | G | 2 | a0003c0008t0001g0118 a0003c0008t0001g0119 |
2 | HG02083.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.427+693T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404246 | |||||||
chr6:32404255 | A | G | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+684T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404255 | |||||||
chr6:32404269 | A | G | 8 | a0003c0004t0002g0043 a0003c0004t0002g0078 a0003c0004t0002g0079 others(5): Show |
9 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.427+670T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404269 | |||||||
chr6:32404290 | C | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.427+649G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404290 | |||||||
chr6:32404335 | A | C | 1 | a0001c0001t0001g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.427+604T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404335 | |||||||
chr6:32404335 | A | G | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+604T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404335 | |||||||
chr6:32404391 | G | T | 8 | a0003c0004t0002g0043 a0003c0004t0002g0078 a0003c0004t0002g0079 others(5): Show |
9 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.427+548C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404391 | |||||||
chr6:32404409 | CTG | C | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+528_427+529del others(2): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404409 | |||||||
chr6:32404459 | C | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+480G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404459 | |||||||
chr6:32404474 | T | C | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+465A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404474 | |||||||
chr6:32404544 | C | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+395G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404544 | |||||||
chr6:32404551 | G | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+388C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404551 | |||||||
chr6:32404560 | G | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+379C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404560 | |||||||
chr6:32404576 | A | G | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+363T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404576 | |||||||
chr6:32404619 | T | C | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+320A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404619 | |||||||
chr6:32404645 | C | G | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+294G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404645 | |||||||
chr6:32404858 | T | A | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.427+81A>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404858 | |||||||
chr6:32404858 | T | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.427+81A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 2/7 | chr6 | 32404858 | |||||||
chr6:32405287 | C | T | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
splice_acceptor_variant&intron_variant | HIGH | c.80-1G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405287 | |||||||
chr6:32405408 | T | C | 40 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(37): Show |
74 | HG00423.hp1 HG00642.hp2 HG00673.hp1 others(71): Show |
intron_variant | MODIFIER | c.80-122A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405408 | |||||||
chr6:32405455 | G | T | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
114 | HG00423.hp1 HG00438.hp2 HG00673.hp1 others(111): Show |
intron_variant | MODIFIER | c.80-169C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405455 | |||||||
chr6:32405509 | G | A | 4 | a0001c0005t0001g0019 a0001c0005t0001g0026 a0001c0005t0001g0112 others(1): Show |
11 | HG01243.hp1 HG02129.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.80-223C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405509 | |||||||
chr6:32405535 | C | T | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.80-249G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405535 | |||||||
chr6:32405597 | C | T | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.80-311G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405597 | |||||||
chr6:32405601 | A | T | 2 | a0002c0002t0001g0045 a0002c0002t0001g0090 |
3 | HG02559.hp1 NA18970.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.80-315T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405601 | |||||||
chr6:32405752 | A | G | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.80-466T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405752 | |||||||
chr6:32405761 | CT | C | 81 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(78): Show |
196 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(193): Show |
intron_variant | MODIFIER | c.80-476delA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405761 | |||||||
chr6:32405799 | TA | T | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.80-514delT | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405799 | |||||||
chr6:32405805 | C | CTGTTTTT others(4): Show |
12 | a0001c0001t0001g0009 a0001c0001t0001g0015 a0001c0001t0001g0022 others(9): Show |
33 | HG00408.hp1 HG00642.hp1 HG00673.hp2 others(30): Show |
intron_variant | MODIFIER | c.80-530_80-520dupAA others(9): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405805 | |||||||
chr6:32405805 | CTGTTTTT others(4): Show |
C | 4 | a0001c0001t0001g0013 a0001c0001t0001g0114 a0001c0001t0001g0115 others(1): Show |
9 | HG00423.hp2 HG00621.hp1 HG02040.hp1 others(6): Show |
intron_variant | MODIFIER | c.80-530_80-520delAA others(9): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405805 | |||||||
chr6:32405807 | G | GT | 49 | a0001c0001t0001g0007 a0001c0001t0001g0014 a0001c0001t0001g0020 others(46): Show |
109 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(106): Show |
intron_variant | MODIFIER | c.80-522dupA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405807 | |||||||
chr6:32405807 | G | GTT | 4 | a0001c0001t0001g0030 a0001c0001t0001g0056 a0001c0001t0001g0124 others(1): Show |
8 | HG02486.hp1 HG02698.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.80-523_80-522dupAA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405807 | |||||||
chr6:32405807 | GTT | G | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.80-523_80-522delAA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405807 | |||||||
chr6:32405813 | T | TTTG | 28 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(25): Show |
73 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(70): Show |
intron_variant | MODIFIER | c.80-528_80-527insCA others(1): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405813 | |||||||
chr6:32405818 | G | GT | 3 | a0001c0001t0001g0132 a0007c0009t0001g0004 a0007c0009t0001g0131 |
16 | HG01169.hp2 HG01358.hp2 NA18945.hp1 others(13): Show |
intron_variant | MODIFIER | c.80-533dupA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405818 | |||||||
chr6:32405818 | G | T | 33 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(30): Show |
79 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(76): Show |
intron_variant | MODIFIER | c.80-532C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405818 | |||||||
chr6:32405820 | T | G | 3 | a0002c0002t0001g0044 a0002c0002t0001g0087 a0002c0002t0001g0088 |
4 | HG01978.hp2 HG02273.hp1 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.80-534A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405820 | |||||||
chr6:32405821 | T | G | 29 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(26): Show |
74 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(71): Show |
intron_variant | MODIFIER | c.80-535A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405821 | |||||||
chr6:32405822 | T | G | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.80-536A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405822 | |||||||
chr6:32405826 | TTTG | T | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.80-543_80-541delCA others(1): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405826 | |||||||
chr6:32405921 | G | T | 82 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(79): Show |
197 | HG00423.hp1 HG00438.hp2 HG00639.hp1 others(194): Show |
intron_variant | MODIFIER | c.80-635C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405921 | |||||||
chr6:32405997 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.80-711C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32405997 | |||||||
chr6:32406019 | A | G | 1 | a0001c0001t0001g0014 | 6 | HG02080.hp2 HG02602.hp2 HG03704.hp1 others(3): Show |
intron_variant | MODIFIER | c.80-733T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406019 | |||||||
chr6:32406024 | T | G | 70 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(67): Show |
147 | HG00423.hp1 HG00639.hp1 HG00673.hp1 others(144): Show |
intron_variant | MODIFIER | c.80-738A>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406024 | |||||||
chr6:32406052 | G | T | 38 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(35): Show |
69 | HG00423.hp1 HG00673.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.80-766C>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406052 | |||||||
chr6:32406089 | C | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-803G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406089 | |||||||
chr6:32406090 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0116 |
7 | HG00423.hp2 HG02040.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.80-804C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406090 | |||||||
chr6:32406126 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-840A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406126 | |||||||
chr6:32406127 | G | A | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-841C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406127 | |||||||
chr6:32406130 | A | T | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.80-844T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406130 | |||||||
chr6:32406270 | A | C | 1 | a0001c0001t0001g0129 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.79+775T>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406270 | |||||||
chr6:32406308 | A | G | 1 | a0002c0002t0001g0086 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.79+737T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406308 | |||||||
chr6:32406328 | T | C | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.79+717A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406328 | |||||||
chr6:32406354 | C | G | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.79+691G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406354 | |||||||
chr6:32406358 | A | G | 12 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(9): Show |
50 | HG00438.hp2 HG00642.hp2 HG01081.hp2 others(47): Show |
intron_variant | MODIFIER | c.79+687T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406358 | |||||||
chr6:32406379 | C | T | 7 | a0003c0008t0001g0006 a0003c0008t0001g0027 a0003c0008t0001g0118 others(4): Show |
17 | HG00423.hp1 HG00673.hp1 HG02027.hp1 others(14): Show |
intron_variant | MODIFIER | c.79+666G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406379 | |||||||
chr6:32406383 | A | G | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.79+662T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406383 | |||||||
chr6:32406385 | C | T | 1 | a0003c0004t0002g0077 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.79+660G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406385 | |||||||
chr6:32406399 | C | A | 1 | a0001c0001t0001g0168 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.79+646G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406399 | |||||||
chr6:32406404 | C | G | 1 | a0002c0002t0001g0085 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.79+641G>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406404 | |||||||
chr6:32406408 | G | A | 10 | a0004c0003t0003g0001 a0004c0003t0003g0017 a0004c0003t0003g0041 others(7): Show |
45 | HG00438.hp2 HG02015.hp2 HG02129.hp2 others(42): Show |
intron_variant | MODIFIER | c.79+637C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406408 | |||||||
chr6:32406408 | G | GGCGCCGA others(21): Show |
2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+636_79+637insTG others(26): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406408 | |||||||
chr6:32406414 | G | A | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.79+631C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406414 | |||||||
chr6:32406428 | G | A | 50 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(47): Show |
119 | HG00423.hp1 HG00438.hp2 HG00642.hp2 others(116): Show |
intron_variant | MODIFIER | c.79+617C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406428 | |||||||
chr6:32406439 | C | T | 14 | a0001c0001t0001g0007 a0001c0001t0001g0028 a0001c0001t0001g0053 others(11): Show |
30 | HG00408.hp2 HG00609.hp1 HG01891.hp1 others(27): Show |
intron_variant | MODIFIER | c.79+606G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406439 | |||||||
chr6:32406447 | C | T | 1 | a0001c0001t0001g0055 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.79+598G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406447 | |||||||
chr6:32406485 | G | A | 48 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(45): Show |
107 | HG00438.hp2 HG00642.hp2 HG00738.hp2 others(104): Show |
intron_variant | MODIFIER | c.79+560C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406485 | |||||||
chr6:32406512 | A | AT | 21 | a0001c0001t0001g0028 a0001c0001t0001g0053 a0001c0001t0001g0117 others(18): Show |
41 | HG01192.hp1 HG01346.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.79+532dupA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406512 | |||||||
chr6:32406512 | A | ATT | 7 | a0003c0004t0002g0043 a0003c0004t0002g0078 a0003c0004t0002g0079 others(4): Show |
8 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.79+531_79+532dupAA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406512 | |||||||
chr6:32406512 | AT | A | 46 | a0001c0001t0001g0169 a0002c0002t0001g0002 a0002c0002t0001g0012 others(43): Show |
130 | HG00438.hp2 HG00639.hp1 HG00642.hp2 others(127): Show |
intron_variant | MODIFIER | c.79+532delA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406512 | |||||||
chr6:32406523 | T | C | 2 | a0008c0011t0004g0042 a0008c0011t0004g0069 |
5 | HG00642.hp2 HG01081.hp2 HG01255.hp2 others(2): Show |
intron_variant | MODIFIER | c.79+522A>G | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406523 | |||||||
chr6:32406605 | C | A | 27 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(24): Show |
35 | HG00738.hp2 HG01123.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.79+440G>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406605 | |||||||
chr6:32406660 | A | G | 27 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(24): Show |
35 | HG00738.hp2 HG01123.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.79+385T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406660 | |||||||
chr6:32406694 | CTA | C | 6 | a0001c0001t0001g0013 a0001c0001t0001g0114 a0001c0001t0001g0115 others(3): Show |
21 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.79+349_79+350delTA | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406694 | |||||||
chr6:32406818 | A | G | 17 | a0001c0005t0001g0019 a0001c0005t0001g0024 a0001c0005t0001g0026 others(14): Show |
34 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(31): Show |
intron_variant | MODIFIER | c.79+227T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406818 | |||||||
chr6:32406845 | A | T | 32 | a0002c0002t0001g0002 a0002c0002t0001g0012 a0002c0002t0001g0018 others(29): Show |
78 | HG00639.hp1 HG01069.hp2 HG01071.hp1 others(75): Show |
intron_variant | MODIFIER | c.79+200T>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406845 | |||||||
chr6:32406863 | G | A | 27 | a0003c0004t0002g0043 a0003c0004t0002g0071 a0003c0004t0002g0072 others(24): Show |
35 | HG00738.hp2 HG01123.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.79+182C>T | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406863 | |||||||
chr6:32406940 | GGCTTGGC others(4): Show |
G | 8 | a0003c0004t0002g0043 a0003c0004t0002g0078 a0003c0004t0002g0079 others(5): Show |
9 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+94_79+104delTGG others(8): Show |
BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406940 | |||||||
chr6:32406953 | A | G | 8 | a0003c0004t0002g0043 a0003c0004t0002g0078 a0003c0004t0002g0079 others(5): Show |
9 | HG01884.hp2 HG02280.hp2 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.79+92T>C | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32406953 | |||||||
chr6:32407041 | C | T | 1 | a0003c0004t0002g0077 | 1 | HG02145.hp2 | splice_region_variant&intron_variant | LOW | c.79+4G>A | BTNL2 | ENSG00000204290.11 | transcript | ENST00000454136.8 | protein_coding | 1/7 | chr6 | 32407041 |