Item | Value |
---|---|
geneid | 153579 |
ensemblid | ENSG00000165810.17 |
hgncid | 24176 |
symbol | BTNL9 |
name | butyrophilin like 9 |
refseq_nuc | NM_152547.5 |
refseq_prot | NP_689760.2 |
ensembl_nuc | ENST00000327705.14 |
ensembl_prot | ENSP00000330200.9 |
mane_status | MANE Select |
chr | chr5 |
start | 181040266 |
end | 181061521 |
strand | + |
ver | v1.2 |
region | chr5:181040266-181061521 |
region5000 | chr5:181035266-181066521 |
regionname0 | BTNL9_chr5_181040266_181061521 |
regionname5000 | BTNL9_chr5_181035266_181066521 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 535 | 246 | 48 | 42 | 104 | 11 | 40 | 78 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
a0002 | 1/0 | 535 | 130 | 11 | 38 | 68 | 7 | 5 | 59 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
a0003 | 0/0 | 535 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
a0004 | 0/0 | 535 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
a0005 | 0/0 | 535 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
a0006 | 0/0 | 535 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
a0007 | 0/0 | 535 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
a0008 | 0/0 | 535 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDFS others(530): Show |
chr5 | 181035266 | 181066521 |
a0009 | 0/0 | 535 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
a0010 | 0/0 | 535 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
a0011 | 0/0 | 535 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
a0012 | 0/0 | 535 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | MVDLS others(530): Show |
chr5 | 181035266 | 181066521 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1605 | 149 | 10 | 33 | 75 | 8 | 22 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0004 | 0/0 | 1605 | 22 | 6 | 2 | 10 | 0 | 4 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0005 | 0/0 | 1605 | 20 | 1 | 3 | 10 | 3 | 3 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0006 | 0/0 | 1605 | 20 | 19 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0007 | 0/0 | 1605 | 10 | 0 | 1 | 4 | 0 | 5 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0008 | 0/0 | 1605 | 8 | 3 | 0 | 2 | 0 | 3 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0009 | 0/0 | 1605 | 7 | 7 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0013 | 0/0 | 1605 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0014 | 0/0 | 1605 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0016 | 0/0 | 1605 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0018 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0019 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0020 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0001c0021 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0002c0002 | 0/0 | 1605 | 63 | 6 | 23 | 29 | 3 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0002c0003 | 0/0 | 1605 | 60 | 5 | 14 | 35 | 4 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0002c0010 | 1/0 | 1605 | 3 | 0 | 0 | 1 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0002c0012 | 0/0 | 1605 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0002c0027 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0002c0029 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0003c0011 | 0/0 | 1605 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0004c0017 | 0/0 | 1605 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0005c0015 | 0/0 | 1605 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0006c0026 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0007c0028 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0008c0023 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0009c0030 | 0/0 | 1605 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0010c0025 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0011c0024 | 0/0 | 1605 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 | ||
a0012c0022 | 0/0 | 1605 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | ATGGT others(1600): Show |
chr5 | 181035266 | 181066521 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3462 | 141 | 7 | 31 | 75 | 7 | 21 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0001t0011 | 0/0 | 3461 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3456): Show |
chr5 | 181035266 | 181066521 |
a0001c0001t0014 | 0/0 | 3462 | 2 | 1 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0001t0017 | 0/1 | 3462 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0001t0019 | 0/0 | 3462 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0001t0020 | 0/0 | 3479 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3474): Show |
chr5 | 181035266 | 181066521 |
a0001c0001t0021 | 0/0 | 3462 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0004t0005 | 0/0 | 3461 | 20 | 6 | 2 | 10 | 0 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3456): Show |
chr5 | 181035266 | 181066521 |
a0001c0004t0012 | 0/0 | 3461 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3456): Show |
chr5 | 181035266 | 181066521 |
a0001c0005t0004 | 0/0 | 3458 | 19 | 1 | 2 | 10 | 3 | 3 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3453): Show |
chr5 | 181035266 | 181066521 |
a0001c0005t0023 | 0/0 | 3458 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3453): Show |
chr5 | 181035266 | 181066521 |
a0001c0006t0001 | 0/0 | 3462 | 8 | 7 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0006t0004 | 0/0 | 3458 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3453): Show |
chr5 | 181035266 | 181066521 |
a0001c0006t0006 | 0/0 | 3457 | 7 | 7 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0001c0006t0010 | 0/0 | 3458 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3453): Show |
chr5 | 181035266 | 181066521 |
a0001c0007t0007 | 0/0 | 3462 | 9 | 0 | 0 | 4 | 0 | 5 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0007t0008 | 0/0 | 3462 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0008t0001 | 0/0 | 3462 | 7 | 2 | 0 | 2 | 0 | 3 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0008t0018 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0009t0008 | 0/0 | 3462 | 6 | 6 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0009t0022 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0013t0002 | 0/0 | 3457 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0001c0014t0001 | 0/0 | 3462 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0016t0009 | 0/0 | 3458 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3453): Show |
chr5 | 181035266 | 181066521 |
a0001c0018t0001 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0019t0001 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0001c0020t0005 | 0/0 | 3461 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3456): Show |
chr5 | 181035266 | 181066521 |
a0001c0021t0001 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0002c0002t0002 | 0/0 | 3457 | 45 | 2 | 15 | 24 | 3 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0002c0002t0004 | 0/0 | 3458 | 13 | 0 | 8 | 4 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3453): Show |
chr5 | 181035266 | 181066521 |
a0002c0002t0006 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0002c0002t0013 | 0/0 | 3457 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0002c0002t0015 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0002c0002t0016 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0002c0003t0002 | 0/0 | 3457 | 5 | 0 | 2 | 1 | 2 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0002c0003t0003 | 0/0 | 3457 | 55 | 5 | 12 | 34 | 2 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0002c0010t0002 | 0/0 | 3457 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0002c0010t0003 | 1/0 | 3457 | 2 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0002c0012t0002 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0002c0012t0004 | 0/0 | 3458 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3453): Show |
chr5 | 181035266 | 181066521 |
a0002c0027t0004 | 0/0 | 3458 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3453): Show |
chr5 | 181035266 | 181066521 |
a0002c0029t0002 | 0/0 | 3457 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0003c0011t0006 | 0/0 | 3457 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0004c0017t0009 | 0/0 | 3458 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3453): Show |
chr5 | 181035266 | 181066521 |
a0005c0015t0004 | 0/0 | 3458 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3453): Show |
chr5 | 181035266 | 181066521 |
a0006c0026t0002 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0007c0028t0002 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0008c0023t0001 | 0/0 | 3462 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
a0009c0030t0003 | 0/0 | 3457 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0010c0025t0005 | 0/0 | 3461 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3456): Show |
chr5 | 181035266 | 181066521 |
a0011c0024t0002 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3452): Show |
chr5 | 181035266 | 181066521 |
a0012c0022t0001 | 0/0 | 3462 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | AATTC others(3457): Show |
chr5 | 181035266 | 181066521 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 11 | 0 | 3 | 7 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0006 | 0/0 | 5 | 0 | 3 | 0 | 0 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0012 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0020 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0021 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0039 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0040 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0044 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0046 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0011g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0011g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0014g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0014g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0017g0164 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0019g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0020g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0001t0021g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0050 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0051 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0053 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0005g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0004t0012g0047 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0004 | 0/0 | 7 | 1 | 0 | 6 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0004g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0005t0023g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0006g0009 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0010g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0006t0010g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0007t0007g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0007t0007g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0007t0007g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0007t0007g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0007t0007g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0007t0007g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0007t0007g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0007t0007g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0007t0007g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0007t0008g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0008t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0008t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0008t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0008t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0008t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0008t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0008t0001g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0008t0018g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0009t0008g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0009t0008g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0009t0008g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0009t0008g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0009t0008g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0009t0008g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0009t0022g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0013t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0013t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0014t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0014t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0016t0009g0049 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0018t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0019t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0020t0005g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0001c0021t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0001 | 0/0 | 11 | 2 | 7 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0003 | 0/0 | 7 | 0 | 0 | 6 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0016 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0027 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0004g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0004g0011 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0004g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0004g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0004g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0004g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0004g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0006g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0013g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0013g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0015g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0002t0016g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0002g0015 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0005 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0007 | 0/0 | 5 | 0 | 0 | 4 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0008 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0014 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0017 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0022 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0010t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0010t0003g0188 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0010t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0012t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0012t0004g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0027t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0002c0029t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0003c0011t0006g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0003c0011t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0004c0017t0009g0048 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0005c0015t0004g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0006c0026t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0007c0028t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0008c0023t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0009c0030t0003g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0010c0025t0005g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0011c0024t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
a0012c0022t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0002 | g0076 | EUR | GBR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00099 | hp2 | a0002 | c0002 | t0002 | g0078 | EUR | GBR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00140 | hp1 | a0002 | c0003 | t0003 | g0008 | EUR | GBR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00140 | hp2 | a0001 | c0001 | t0014 | g0153 | EUR | GBR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00280 | hp1 | a0001 | c0005 | t0004 | g0031 | EUR | FIN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0020 | EUR | FIN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0162 | EUR | FIN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00323 | hp2 | a0002 | c0003 | t0002 | g0015 | EUR | FIN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00438 | hp1 | a0001 | c0007 | t0007 | g0177 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00544 | hp1 | a0001 | c0005 | t0004 | g0004 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00558 | hp2 | a0002 | c0002 | t0002 | g0073 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00597 | hp1 | a0001 | c0005 | t0004 | g0124 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00597 | hp2 | a0006 | c0026 | t0002 | g0062 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00609 | hp2 | a0007 | c0028 | t0002 | g0001 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00642 | hp1 | a0002 | c0002 | t0002 | g0072 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0237 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00733 | hp2 | a0001 | c0016 | t0009 | g0049 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00735 | hp1 | a0002 | c0002 | t0002 | g0016 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00735 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00741 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG00741 | hp2 | a0002 | c0003 | t0003 | g0005 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01069 | hp2 | a0002 | c0003 | t0002 | g0015 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01070 | hp1 | a0002 | c0003 | t0003 | g0022 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01071 | hp1 | a0002 | c0003 | t0003 | g0022 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01074 | hp2 | a0001 | c0016 | t0009 | g0049 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01081 | hp1 | a0001 | c0001 | t0020 | g0165 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01081 | hp2 | a0002 | c0003 | t0003 | g0022 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01099 | hp1 | a0002 | c0003 | t0003 | g0005 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01106 | hp1 | a0002 | c0003 | t0002 | g0015 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01106 | hp2 | a0001 | c0004 | t0005 | g0256 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01109 | hp1 | a0002 | c0029 | t0002 | g0079 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01168 | hp1 | a0002 | c0002 | t0002 | g0027 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01168 | hp2 | a0002 | c0003 | t0003 | g0008 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0187 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01169 | hp2 | a0002 | c0003 | t0003 | g0008 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01175 | hp1 | a0001 | c0001 | t0019 | g0045 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0016 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01192 | hp1 | a0001 | c0005 | t0023 | g0031 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01192 | hp2 | a0002 | c0003 | t0003 | g0005 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01243 | hp2 | a0001 | c0006 | t0001 | g0067 | AMR | PUR | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01255 | hp1 | a0001 | c0007 | t0008 | g0019 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01256 | hp2 | a0002 | c0002 | t0004 | g0028 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01257 | hp2 | a0002 | c0002 | t0002 | g0092 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01261 | hp2 | a0001 | c0004 | t0005 | g0264 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01346 | hp2 | a0002 | c0002 | t0002 | g0082 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01358 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01361 | hp1 | a0004 | c0017 | t0009 | g0048 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01433 | hp1 | a0001 | c0005 | t0004 | g0131 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01433 | hp2 | a0004 | c0017 | t0009 | g0048 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01496 | hp1 | a0002 | c0002 | t0004 | g0011 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0081 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01515 | hp1 | a0001 | c0005 | t0004 | g0125 | EUR | IBS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01515 | hp2 | a0002 | c0002 | t0002 | g0027 | EUR | IBS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0095 | EUR | IBS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | IBS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01517 | hp2 | a0001 | c0005 | t0004 | g0126 | EUR | IBS | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01891 | hp1 | a0001 | c0009 | t0008 | g0123 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01891 | hp2 | a0001 | c0001 | t0014 | g0154 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01928 | hp1 | a0002 | c0002 | t0004 | g0091 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01928 | hp2 | a0002 | c0003 | t0003 | g0005 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01943 | hp2 | a0002 | c0002 | t0004 | g0011 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0214 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01975 | hp2 | a0002 | c0002 | t0004 | g0011 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01978 | hp1 | a0002 | c0002 | t0004 | g0090 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01978 | hp2 | a0001 | c0005 | t0004 | g0242 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01981 | hp2 | a0002 | c0002 | t0004 | g0089 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02004 | hp1 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02015 | hp1 | a0001 | c0005 | t0004 | g0140 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02015 | hp2 | a0002 | c0002 | t0004 | g0087 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02027 | hp1 | a0001 | c0005 | t0004 | g0004 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02056 | hp1 | a0002 | c0002 | t0002 | g0077 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02071 | hp1 | a0001 | c0004 | t0005 | g0266 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02074 | hp1 | a0002 | c0003 | t0003 | g0104 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02074 | hp2 | a0002 | c0003 | t0003 | g0007 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02129 | hp1 | a0008 | c0023 | t0001 | g0213 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02129 | hp2 | a0002 | c0003 | t0003 | g0110 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02132 | hp1 | a0001 | c0005 | t0004 | g0004 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02135 | hp2 | a0001 | c0005 | t0004 | g0004 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02145 | hp1 | a0001 | c0006 | t0004 | g0137 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02148 | hp1 | a0002 | c0003 | t0003 | g0005 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0001 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CDX | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02165 | hp2 | a0002 | c0003 | t0003 | g0055 | EAS | CDX | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02257 | hp1 | a0001 | c0006 | t0004 | g0139 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0219 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02273 | hp2 | a0002 | c0002 | t0004 | g0011 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02280 | hp1 | a0001 | c0006 | t0010 | g0128 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02280 | hp2 | a0001 | c0004 | t0005 | g0053 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02293 | hp1 | a0002 | c0003 | t0003 | g0005 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02451 | hp1 | a0001 | c0009 | t0008 | g0120 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02451 | hp2 | a0001 | c0009 | t0022 | g0117 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02523 | hp1 | a0001 | c0005 | t0004 | g0004 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02572 | hp1 | a0001 | c0006 | t0006 | g0009 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02572 | hp2 | a0001 | c0013 | t0002 | g0251 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02602 | hp1 | a0001 | c0004 | t0005 | g0265 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02622 | hp1 | a0002 | c0003 | t0003 | g0100 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02622 | hp2 | a0001 | c0006 | t0006 | g0066 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02630 | hp1 | a0001 | c0006 | t0001 | g0010 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02683 | hp1 | a0001 | c0008 | t0001 | g0001 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02683 | hp2 | a0002 | c0010 | t0002 | g0149 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02698 | hp2 | a0001 | c0008 | t0001 | g0132 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02717 | hp2 | a0003 | c0011 | t0006 | g0142 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02723 | hp1 | a0003 | c0011 | t0006 | g0033 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02723 | hp2 | a0001 | c0006 | t0001 | g0010 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0235 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02809 | hp1 | a0001 | c0006 | t0010 | g0127 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02809 | hp2 | a0003 | c0011 | t0006 | g0033 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02818 | hp1 | a0001 | c0004 | t0005 | g0257 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02818 | hp2 | a0002 | c0002 | t0015 | g0001 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02922 | hp1 | a0001 | c0013 | t0002 | g0250 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02922 | hp2 | a0001 | c0004 | t0005 | g0252 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02965 | hp1 | a0001 | c0006 | t0006 | g0063 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02965 | hp2 | a0002 | c0003 | t0003 | g0032 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02970 | hp1 | a0001 | c0008 | t0018 | g0141 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02970 | hp2 | a0001 | c0006 | t0001 | g0010 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03017 | hp1 | a0009 | c0030 | t0003 | g0008 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03041 | hp1 | a0001 | c0006 | t0001 | g0064 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03041 | hp2 | a0010 | c0025 | t0005 | g0255 | AFR | GWD | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03098 | hp1 | a0002 | c0002 | t0013 | g0070 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0001 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03130 | hp1 | a0001 | c0006 | t0006 | g0009 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03130 | hp2 | a0001 | c0009 | t0008 | g0116 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03195 | hp1 | a0001 | c0001 | t0011 | g0245 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03195 | hp2 | a0001 | c0006 | t0001 | g0069 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03209 | hp1 | a0001 | c0008 | t0001 | g0135 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03209 | hp2 | a0001 | c0006 | t0001 | g0010 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03225 | hp1 | a0002 | c0002 | t0006 | g0114 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03225 | hp2 | a0001 | c0001 | t0011 | g0244 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03239 | hp2 | a0001 | c0020 | t0005 | g0173 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03453 | hp1 | a0002 | c0003 | t0003 | g0103 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03453 | hp2 | a0001 | c0009 | t0008 | g0121 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03486 | hp1 | a0001 | c0009 | t0008 | g0119 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03486 | hp2 | a0002 | c0002 | t0013 | g0071 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03491 | hp1 | a0001 | c0008 | t0001 | g0259 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03491 | hp2 | a0001 | c0004 | t0012 | g0047 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03492 | hp1 | a0001 | c0004 | t0012 | g0047 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03516 | hp1 | a0002 | c0003 | t0003 | g0032 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03579 | hp1 | a0001 | c0006 | t0001 | g0068 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03579 | hp2 | a0001 | c0009 | t0008 | g0118 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0241 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0269 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03669 | hp2 | a0001 | c0007 | t0007 | g0175 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03688 | hp1 | a0001 | c0014 | t0001 | g0052 | SAS | STU | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03688 | hp2 | a0001 | c0005 | t0004 | g0129 | SAS | STU | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03704 | hp1 | a0001 | c0005 | t0004 | g0136 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03710 | hp1 | a0001 | c0007 | t0007 | g0199 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03831 | hp1 | a0002 | c0002 | t0004 | g0094 | SAS | BEB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0247 | SAS | BEB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0006 | SAS | BEB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03834 | hp2 | a0002 | c0002 | t0002 | g0003 | SAS | BEB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | BEB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03927 | hp2 | a0001 | c0007 | t0007 | g0179 | SAS | BEB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03942 | hp2 | a0001 | c0007 | t0007 | g0180 | SAS | BEB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG04115 | hp1 | a0001 | c0005 | t0004 | g0130 | SAS | STU | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG04115 | hp2 | a0001 | c0014 | t0001 | g0260 | SAS | STU | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG04184 | hp1 | a0001 | c0007 | t0007 | g0151 | SAS | BEB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG04184 | hp2 | a0001 | c0004 | t0005 | g0053 | SAS | BEB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG04199 | hp2 | a0002 | c0003 | t0003 | g0243 | SAS | STU | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG04204 | hp1 | a0001 | c0001 | t0021 | g0228 | SAS | STU | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | STU | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | STU | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | STU | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18522 | hp1 | a0001 | c0004 | t0005 | g0263 | AFR | YRI | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18522 | hp2 | a0001 | c0006 | t0004 | g0138 | AFR | YRI | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18612 | hp1 | a0002 | c0012 | t0004 | g0215 | EAS | CHB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18612 | hp2 | a0001 | c0019 | t0001 | g0018 | EAS | CHB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | CHB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18747 | hp2 | a0002 | c0003 | t0003 | g0057 | EAS | CHB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18940 | hp2 | a0001 | c0004 | t0005 | g0052 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18942 | hp2 | a0001 | c0005 | t0004 | g0004 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18944 | hp1 | a0001 | c0004 | t0005 | g0050 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18944 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18948 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18948 | hp2 | a0001 | c0007 | t0007 | g0178 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18950 | hp1 | a0002 | c0003 | t0003 | g0097 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18950 | hp2 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18953 | hp1 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18954 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18956 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18956 | hp2 | a0002 | c0003 | t0003 | g0096 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18957 | hp2 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18959 | hp1 | a0002 | c0027 | t0004 | g0028 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18959 | hp2 | a0001 | c0021 | t0001 | g0002 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18960 | hp1 | a0002 | c0002 | t0002 | g0025 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18961 | hp1 | a0002 | c0002 | t0002 | g0085 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18962 | hp1 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18962 | hp2 | a0002 | c0003 | t0003 | g0014 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18963 | hp1 | a0002 | c0003 | t0003 | g0246 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18964 | hp2 | a0002 | c0012 | t0002 | g0221 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18966 | hp1 | a0001 | c0005 | t0004 | g0133 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18967 | hp2 | a0002 | c0003 | t0003 | g0023 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18969 | hp2 | a0002 | c0003 | t0003 | g0106 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18970 | hp1 | a0002 | c0002 | t0004 | g0003 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18972 | hp1 | a0002 | c0003 | t0003 | g0058 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18974 | hp1 | a0002 | c0003 | t0002 | g0084 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18975 | hp1 | a0002 | c0003 | t0003 | g0111 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18977 | hp1 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18979 | hp2 | a0002 | c0010 | t0003 | g0190 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18980 | hp1 | a0001 | c0008 | t0001 | g0234 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18980 | hp2 | a0001 | c0007 | t0007 | g0181 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18983 | hp1 | a0002 | c0003 | t0003 | g0102 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18983 | hp2 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18988 | hp1 | a0002 | c0002 | t0002 | g0086 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18990 | hp1 | a0002 | c0002 | t0002 | g0093 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18991 | hp1 | a0002 | c0002 | t0002 | g0059 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18991 | hp2 | a0005 | c0015 | t0004 | g0030 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18992 | hp2 | a0002 | c0003 | t0003 | g0113 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18993 | hp1 | a0002 | c0003 | t0003 | g0029 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18994 | hp1 | a0001 | c0004 | t0005 | g0051 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18994 | hp2 | a0002 | c0002 | t0002 | g0115 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18997 | hp1 | a0002 | c0003 | t0003 | g0107 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18998 | hp1 | a0002 | c0003 | t0003 | g0017 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18998 | hp2 | a0001 | c0004 | t0005 | g0262 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19000 | hp2 | a0002 | c0003 | t0003 | g0101 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0080 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19002 | hp2 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19004 | hp1 | a0002 | c0003 | t0003 | g0105 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0026 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19009 | hp2 | a0002 | c0003 | t0003 | g0108 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19011 | hp1 | a0002 | c0002 | t0002 | g0061 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19012 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19054 | hp1 | a0001 | c0005 | t0004 | g0134 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19054 | hp2 | a0001 | c0004 | t0005 | g0253 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0001 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19056 | hp2 | a0002 | c0003 | t0003 | g0109 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19058 | hp1 | a0002 | c0003 | t0003 | g0054 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19064 | hp2 | a0001 | c0004 | t0005 | g0051 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19066 | hp1 | a0002 | c0003 | t0003 | g0023 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19066 | hp2 | a0001 | c0004 | t0005 | g0050 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19067 | hp1 | a0002 | c0003 | t0003 | g0056 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19068 | hp1 | a0011 | c0024 | t0002 | g0075 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19070 | hp1 | a0002 | c0002 | t0016 | g0026 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19072 | hp1 | a0001 | c0004 | t0005 | g0254 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19072 | hp2 | a0005 | c0015 | t0004 | g0030 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19074 | hp2 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19078 | hp1 | a0002 | c0003 | t0003 | g0017 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19078 | hp2 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19079 | hp1 | a0002 | c0003 | t0003 | g0007 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19082 | hp2 | a0001 | c0004 | t0005 | g0261 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19083 | hp1 | a0002 | c0002 | t0002 | g0060 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19083 | hp2 | a0001 | c0008 | t0001 | g0002 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19084 | hp1 | a0002 | c0003 | t0003 | g0099 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19085 | hp2 | a0002 | c0002 | t0004 | g0088 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19086 | hp2 | a0001 | c0007 | t0007 | g0176 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19087 | hp1 | a0001 | c0018 | t0001 | g0204 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19088 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19088 | hp2 | a0002 | c0003 | t0003 | g0112 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19091 | hp1 | a0002 | c0002 | t0002 | g0003 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19240 | hp1 | a0002 | c0002 | t0002 | g0001 | AFR | YRI | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA19240 | hp2 | a0001 | c0006 | t0006 | g0009 | AFR | YRI | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA20129 | hp1 | a0001 | c0004 | t0005 | g0258 | AFR | ASW | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA20129 | hp2 | a0002 | c0003 | t0003 | g0098 | AFR | ASW | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | TSI | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0160 | EUR | TSI | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA20805 | hp2 | a0002 | c0003 | t0003 | g0007 | EUR | TSI | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA20905 | hp1 | a0002 | c0003 | t0003 | g0017 | SAS | GIH | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | GIH | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01123 | hp1 | a0002 | c0003 | t0003 | g0008 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02486 | hp1 | a0001 | c0008 | t0001 | g0074 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | ACB | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03471 | hp1 | a0001 | c0006 | t0006 | g0065 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG03471 | hp2 | a0001 | c0004 | t0005 | g0267 | AFR | MSL | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | USA | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
HG06807 | hp2 | a0001 | c0006 | t0006 | g0009 | AFR | USA | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA20300 | hp1 | a0012 | c0022 | t0001 | g0006 | AFR | USA | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
NA20300 | hp2 | a0001 | c0005 | t0004 | g0004 | AFR | USA | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
homoSapiens | chm13v2 | a0001 | c0001 | t0017 | g0164 | REF | REF | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
homoSapiens | grch38p0 | a0002 | c0010 | t0003 | g0188 | REF | REF | BTNL9_chr5_181035266_181066521 | BTNL9 | chr5 | 181035266 | 181066521 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:181045499 | C | T | 1 | a0008 | 1 | HG02129.hp1 | missense_variant | MODERATE | c.10C>T | p.Leu4Phe | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/11 | 200/3457 | 10/1608 | 4/535 | chr5 | 181045499 | |||
chr5:181050139 | T | C | 1 | a0011 | 1 | NA19068.hp1 | missense_variant | MODERATE | c.506T>C | p.Ile169Thr | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/11 | 696/3457 | 506/1608 | 169/535 | chr5 | 181050139 | |||
chr5:181053275 | C | T | 1 | a0009 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.812C>T | p.Ala271Val | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 5/11 | 1002/3457 | 812/1608 | 271/535 | chr5 | 181053275 | |||
chr5:181059306 | C | T | 1 | a0005 | 2 | NA18991.hp2 NA19072.hp2 |
missense_variant | MODERATE | c.1052C>T | p.Ser351Phe | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1242/3457 | 1052/1608 | 351/535 | chr5 | 181059306 | |||
chr5:181059329 | C | T | 1 | a0010 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.1075C>T | p.Pro359Ser | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1265/3457 | 1075/1608 | 359/535 | chr5 | 181059329 | |||
chr5:181059383 | G | A | 1 | a0012 | 1 | NA20300.hp1 | missense_variant | MODERATE | c.1129G>A | p.Glu377Lys | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1319/3457 | 1129/1608 | 377/535 | chr5 | 181059383 | |||
chr5:181059404 | C | T | 1 | a0004 | 2 | HG01361.hp1 HG01433.hp2 |
missense_variant | MODERATE | c.1150C>T | p.His384Tyr | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1340/3457 | 1150/1608 | 384/535 | chr5 | 181059404 | |||
chr5:181059471 | C | T | 1 | a0007 | 1 | HG00609.hp2 | missense_variant | MODERATE | c.1217C>T | p.Pro406Leu | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1407/3457 | 1217/1608 | 406/535 | chr5 | 181059471 | |||
chr5:181059578 | C | G | 1 | a0003 | 3 | HG02717.hp2 HG02723.hp1 HG02809.hp2 |
missense_variant | MODERATE | c.1324C>G | p.Leu442Val | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1514/3457 | 1324/1608 | 442/535 | chr5 | 181059578 | |||
chr5:181059785 | G | C | 6 | a0001 a0004 a0005 others(3): Show |
252 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
missense_variant | MODERATE | c.1531G>C | p.Gly511Arg | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1721/3457 | 1531/1608 | 511/535 | chr5 | 181059785 | |||
chr5:181059797 | G | A | 1 | a0006 | 1 | HG00597.hp2 | missense_variant | MODERATE | c.1543G>A | p.Glu515Lys | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1733/3457 | 1543/1608 | 515/535 | chr5 | 181059797 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:181045498 | C | T | 19 | a0001c0004 a0001c0005 a0001c0006 others(16): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
synonymous_variant | LOW | c.9C>T | p.Asp3Asp | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/11 | 199/3457 | 9/1608 | 3/535 | chr5 | 181045498 | |||
chr5:181045513 | A | G | 19 | a0001c0004 a0001c0005 a0001c0006 others(16): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
synonymous_variant | LOW | c.24A>G | p.Pro8Pro | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/11 | 214/3457 | 24/1608 | 8/535 | chr5 | 181045513 | |||
chr5:181047991 | G | A | 1 | a0001c0018 | 1 | NA19087.hp1 | synonymous_variant | LOW | c.174G>A | p.Pro58Pro | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/11 | 364/3457 | 174/1608 | 58/535 | chr5 | 181047991 | |||
chr5:181048043 | C | A | 1 | a0001c0019 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.226C>A | p.Arg76Arg | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/11 | 416/3457 | 226/1608 | 76/535 | chr5 | 181048043 | |||
chr5:181048195 | T | C | 1 | a0001c0013 | 2 | HG02572.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.378T>C | p.Ser126Ser | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/11 | 568/3457 | 378/1608 | 126/535 | chr5 | 181048195 | |||
chr5:181053213 | C | T | 2 | a0001c0016 a0004c0017 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
synonymous_variant | LOW | c.750C>T | p.Pro250Pro | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 5/11 | 940/3457 | 750/1608 | 250/535 | chr5 | 181053213 | |||
chr5:181058353 | G | A | 4 | a0001c0004 a0001c0014 a0001c0020 others(1): Show |
26 | HG01106.hp2 HG01261.hp2 HG02071.hp1 others(23): Show |
splice_region_variant&synonymous_variant | LOW | c.957G>A | p.Glu319Glu | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/11 | 1147/3457 | 957/1608 | 319/535 | chr5 | 181058353 | |||
chr5:181058374 | T | C | 1 | a0001c0009 | 7 | HG01891.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
synonymous_variant | LOW | c.978T>C | p.Tyr326Tyr | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/11 | 1168/3457 | 978/1608 | 326/535 | chr5 | 181058374 | |||
chr5:181059247 | G | T | 19 | a0001c0001 a0001c0006 a0001c0008 others(16): Show |
261 | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(258): Show |
synonymous_variant | LOW | c.993G>T | p.Thr331Thr | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1183/3457 | 993/1608 | 331/535 | chr5 | 181059247 | |||
chr5:181059403 | C | T | 1 | a0002c0029 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.1149C>T | p.Arg383Arg | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1339/3457 | 1149/1608 | 383/535 | chr5 | 181059403 | |||
chr5:181059811 | C | T | 1 | a0001c0013 | 2 | HG02572.hp2 HG02922.hp1 |
synonymous_variant | LOW | c.1557C>T | p.Asp519Asp | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1747/3457 | 1557/1608 | 519/535 | chr5 | 181059811 | |||
chr5:181059841 | C | T | 9 | a0001c0001 a0001c0008 a0001c0014 others(6): Show |
164 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(161): Show |
synonymous_variant | LOW | c.1587C>T | p.Asp529Asp | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1777/3457 | 1587/1608 | 529/535 | chr5 | 181059841 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:181040394 | C | A | 1 | a0001c0006t0010 | 2 | HG02280.hp1 HG02809.hp1 |
5_prime_UTR_variant | MODIFIER | c.-62C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/11 | 5096 | chr5 | 181040394 | ||||||
chr5:181059891 | C | CG | 28 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0019 others(25): Show |
232 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*35dupG | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 36 | INFO_REALIGN_3_PRIME | chr5 | 181059891 | |||||
chr5:181060085 | G | A | 16 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(13): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*223G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 223 | chr5 | 181060085 | ||||||
chr5:181060137 | C | T | 16 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(13): Show |
172 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(169): Show |
3_prime_UTR_variant | MODIFIER | c.*275C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 275 | chr5 | 181060137 | ||||||
chr5:181060144 | C | A | 18 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(15): Show |
176 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(173): Show |
3_prime_UTR_variant | MODIFIER | c.*282C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 282 | chr5 | 181060144 | ||||||
chr5:181060449 | C | T | 1 | a0001c0001t0021 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*587C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 587 | chr5 | 181060449 | ||||||
chr5:181060567 | A | ATTAAAGA others(61): Show |
1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*706_*707insTAAAGA others(62): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 707 | INFO_REALIGN_3_PRIME | chr5 | 181060567 | |||||
chr5:181060583 | A | C | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*721A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 721 | chr5 | 181060583 | ||||||
chr5:181060583 | A | G | 1 | a0001c0005t0023 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*721A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 721 | chr5 | 181060583 | ||||||
chr5:181060586 | C | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*724C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 724 | chr5 | 181060586 | ||||||
chr5:181060587 | A | G | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*725A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 725 | chr5 | 181060587 | ||||||
chr5:181060602 | A | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*740A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 740 | chr5 | 181060602 | ||||||
chr5:181060604 | G | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*742G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 742 | chr5 | 181060604 | ||||||
chr5:181060610 | A | G | 1 | a0001c0007t0007 | 9 | HG00438.hp1 HG03669.hp2 HG03710.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*748A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 748 | chr5 | 181060610 | ||||||
chr5:181060611 | C | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*749C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 749 | chr5 | 181060611 | ||||||
chr5:181060617 | G | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*755G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 755 | chr5 | 181060617 | ||||||
chr5:181060637 | T | G | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*775T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 775 | chr5 | 181060637 | ||||||
chr5:181060638 | C | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*776C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 776 | chr5 | 181060638 | ||||||
chr5:181060639 | T | G | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*777T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 777 | chr5 | 181060639 | ||||||
chr5:181060640 | A | G | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*778A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 778 | chr5 | 181060640 | ||||||
chr5:181060650 | G | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*788G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 788 | chr5 | 181060650 | ||||||
chr5:181060651 | A | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*789A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 789 | chr5 | 181060651 | ||||||
chr5:181060652 | G | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*790G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 790 | chr5 | 181060652 | ||||||
chr5:181060653 | A | G | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*791A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 791 | chr5 | 181060653 | ||||||
chr5:181060656 | C | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 794 | chr5 | 181060656 | ||||||
chr5:181060671 | G | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*809G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 809 | chr5 | 181060671 | ||||||
chr5:181060672 | T | G | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*810T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 810 | chr5 | 181060672 | ||||||
chr5:181060674 | T | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*812T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 812 | chr5 | 181060674 | ||||||
chr5:181060675 | C | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*813C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 813 | chr5 | 181060675 | ||||||
chr5:181060676 | C | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*814C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 814 | chr5 | 181060676 | ||||||
chr5:181060678 | G | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*816G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 816 | chr5 | 181060678 | ||||||
chr5:181060682 | C | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*820C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 820 | chr5 | 181060682 | ||||||
chr5:181060683 | A | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*821A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 821 | chr5 | 181060683 | ||||||
chr5:181060694 | C | G | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*832C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 832 | chr5 | 181060694 | ||||||
chr5:181060699 | A | G | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*837A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 837 | chr5 | 181060699 | ||||||
chr5:181060700 | C | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*838C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 838 | chr5 | 181060700 | ||||||
chr5:181060701 | A | C | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*839A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 839 | chr5 | 181060701 | ||||||
chr5:181060705 | C | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*843C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 843 | chr5 | 181060705 | ||||||
chr5:181060706 | T | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*844T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 844 | chr5 | 181060706 | ||||||
chr5:181060711 | AGTTTGAA others(44): Show |
A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*850_*900delGTTTGA others(45): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 850 | chr5 | 181060711 | ||||||
chr5:181060765 | A | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*903A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 903 | chr5 | 181060765 | ||||||
chr5:181060766 | G | C | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*904G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 904 | chr5 | 181060766 | ||||||
chr5:181060769 | A | C | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*907A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 907 | chr5 | 181060769 | ||||||
chr5:181060770 | T | C | 1 | a0001c0001t0014 | 2 | HG00140.hp2 HG01891.hp2 |
3_prime_UTR_variant | MODIFIER | c.*908T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 908 | chr5 | 181060770 | ||||||
chr5:181060773 | A | T | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*911A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 911 | chr5 | 181060773 | ||||||
chr5:181060778 | A | C | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*916A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 916 | chr5 | 181060778 | ||||||
chr5:181060780 | C | A | 1 | a0001c0001t0020 | 1 | HG01081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*918C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 918 | chr5 | 181060780 | ||||||
chr5:181060849 | A | T | 1 | a0002c0002t0013 | 2 | HG03098.hp1 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*987A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 987 | chr5 | 181060849 | ||||||
chr5:181060863 | G | C | 45 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(42): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*1001G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1001 | chr5 | 181060863 | ||||||
chr5:181060905 | T | C | 48 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(45): Show |
331 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(328): Show |
3_prime_UTR_variant | MODIFIER | c.*1043T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1043 | chr5 | 181060905 | ||||||
chr5:181060944 | C | CAGCT | 23 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(20): Show |
212 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*1083_*1084insGCTA | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1084 | INFO_REALIGN_3_PRIME | chr5 | 181060944 | |||||
chr5:181060958 | T | C | 1 | a0001c0009t0022 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1096T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1096 | chr5 | 181060958 | ||||||
chr5:181060967 | C | T | 4 | a0001c0004t0005 a0001c0004t0012 a0001c0020t0005 others(1): Show |
24 | HG01106.hp2 HG01261.hp2 HG02071.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*1105C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1105 | chr5 | 181060967 | ||||||
chr5:181060968 | G | A | 1 | a0002c0002t0016 | 1 | NA19070.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1106G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1106 | chr5 | 181060968 | ||||||
chr5:181061075 | T | C | 26 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(23): Show |
217 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(214): Show |
3_prime_UTR_variant | MODIFIER | c.*1213T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1213 | chr5 | 181061075 | ||||||
chr5:181061260 | T | C | 25 | a0001c0001t0001 a0001c0001t0011 a0001c0001t0014 others(22): Show |
216 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(213): Show |
3_prime_UTR_variant | MODIFIER | c.*1398T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1398 | chr5 | 181061260 | ||||||
chr5:181061297 | G | A | 1 | a0001c0007t0007 | 9 | HG00438.hp1 HG03669.hp2 HG03710.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1435G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1435 | chr5 | 181061297 | ||||||
chr5:181061434 | A | G | 1 | a0001c0001t0019 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1572A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1572 | chr5 | 181061434 | ||||||
chr5:181061477 | T | C | 1 | a0001c0004t0012 | 2 | HG03491.hp2 HG03492.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1615T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1615 | chr5 | 181061477 | ||||||
chr5:181061493 | G | A | 1 | a0001c0008t0018 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1631G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 11/11 | 1631 | chr5 | 181061493 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:181040482 | G | A | 117 | a0001c0001t0001g0122 a0001c0005t0004g0004 a0001c0005t0004g0031 others(114): Show |
173 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.-24+50G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181040482 | |||||||
chr5:181040488 | C | T | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-24+56C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181040488 | |||||||
chr5:181040495 | T | C | 88 | a0001c0006t0001g0010 a0001c0006t0001g0064 a0001c0006t0001g0067 others(85): Show |
137 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.-24+63T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181040495 | |||||||
chr5:181040551 | G | T | 1 | a0001c0005t0004g0140 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-24+119G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181040551 | |||||||
chr5:181040576 | G | A | 1 | a0001c0009t0008g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-24+144G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181040576 | |||||||
chr5:181040625 | C | G | 2 | a0001c0001t0001g0268 a0001c0001t0001g0269 |
2 | HG03669.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-24+193C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181040625 | |||||||
chr5:181040804 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0143 |
3 | HG00609.hp1 HG02056.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-24+372G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181040804 | |||||||
chr5:181041025 | C | T | 134 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(131): Show |
197 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.-24+593C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181041025 | |||||||
chr5:181041096 | A | G | 1 | a0002c0002t0002g0115 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-24+664A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181041096 | |||||||
chr5:181041261 | G | A | 1 | a0001c0005t0004g0124 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-24+829G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181041261 | |||||||
chr5:181041388 | G | A | 1 | a0001c0001t0001g0144 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-24+956G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181041388 | |||||||
chr5:181041519 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0145 |
3 | HG00438.hp2 NA19009.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-24+1087G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181041519 | |||||||
chr5:181041537 | A | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-24+1105A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181041537 | |||||||
chr5:181041615 | G | GTGATTTT others(71): Show |
1 | a0001c0001t0001g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-24+1184_-24+1261d others(80): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 181041615 | ||||||
chr5:181041732 | A | C | 1 | a0001c0001t0001g0248 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.-24+1300A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181041732 | |||||||
chr5:181041738 | A | G | 1 | a0001c0001t0001g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-24+1306A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181041738 | |||||||
chr5:181041964 | G | A | 1 | a0001c0004t0012g0047 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.-24+1532G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181041964 | |||||||
chr5:181042209 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-24+1777G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042209 | |||||||
chr5:181042233 | G | T | 1 | a0002c0003t0003g0246 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.-24+1801G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042233 | |||||||
chr5:181042304 | A | C | 1 | a0001c0009t0008g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-24+1872A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042304 | |||||||
chr5:181042318 | T | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-24+1886T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042318 | |||||||
chr5:181042389 | C | T | 2 | a0001c0001t0011g0244 a0001c0001t0011g0245 |
2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-24+1957C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042389 | |||||||
chr5:181042436 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-24+2004G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042436 | |||||||
chr5:181042444 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-24+2012C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042444 | |||||||
chr5:181042536 | C | T | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-24+2104C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042536 | |||||||
chr5:181042713 | C | T | 143 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(140): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-24+2281C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042713 | |||||||
chr5:181042767 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-24+2335C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042767 | |||||||
chr5:181042905 | G | T | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-24+2473G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042905 | |||||||
chr5:181042908 | G | T | 143 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(140): Show |
211 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(208): Show |
intron_variant | MODIFIER | c.-24+2476G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042908 | |||||||
chr5:181042930 | G | A | 19 | a0001c0005t0004g0004 a0001c0005t0004g0031 a0001c0005t0004g0124 others(16): Show |
26 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.-24+2498G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181042930 | |||||||
chr5:181043059 | G | A | 1 | a0001c0001t0001g0148 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.-23-2408G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181043059 | |||||||
chr5:181043133 | T | C | 199 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0036 others(196): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-23-2334T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181043133 | |||||||
chr5:181043152 | C | A | 7 | a0001c0009t0008g0116 a0001c0009t0008g0118 a0001c0009t0008g0119 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.-23-2315C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181043152 | |||||||
chr5:181043216 | ATCTGTGT others(17): Show |
A | 142 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(139): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-23-2237_-23-2214d others(26): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 181043216 | ||||||
chr5:181043263 | T | A | 142 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(139): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-23-2204T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181043263 | |||||||
chr5:181043266 | C | CTA | 142 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(139): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.-23-2200_-23-2199i others(4): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 181043266 | ||||||
chr5:181043292 | C | CTG | 22 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(19): Show |
26 | HG01106.hp2 HG01261.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-23-2157_-23-2156d others(4): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 181043292 | ||||||
chr5:181043292 | CTG | C | 2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-2157_-23-2156d others(4): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 181043292 | ||||||
chr5:181043301 | T | G | 8 | a0002c0003t0003g0014 a0002c0003t0003g0023 a0002c0003t0003g0054 others(5): Show |
11 | HG02165.hp2 NA18747.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.-23-2166T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181043301 | |||||||
chr5:181043547 | T | G | 146 | a0001c0001t0001g0018 a0001c0001t0001g0144 a0001c0001t0001g0182 others(143): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.-23-1920T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181043547 | |||||||
chr5:181043823 | A | G | 1 | a0001c0001t0001g0241 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-23-1644A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181043823 | |||||||
chr5:181043867 | G | T | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-23-1600G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181043867 | |||||||
chr5:181043913 | C | T | 1 | a0002c0002t0006g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-23-1554C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181043913 | |||||||
chr5:181043970 | C | T | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-23-1497C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181043970 | |||||||
chr5:181044090 | T | C | 4 | a0001c0013t0002g0250 a0001c0013t0002g0251 a0001c0016t0009g0049 others(1): Show |
6 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-1377T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044090 | |||||||
chr5:181044103 | C | A | 4 | a0001c0013t0002g0250 a0001c0013t0002g0251 a0001c0016t0009g0049 others(1): Show |
6 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-1364C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044103 | |||||||
chr5:181044139 | G | C | 145 | a0001c0001t0001g0122 a0001c0001t0001g0150 a0001c0004t0005g0050 others(142): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.-23-1328G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044139 | |||||||
chr5:181044145 | T | C | 4 | a0001c0013t0002g0250 a0001c0013t0002g0251 a0001c0016t0009g0049 others(1): Show |
6 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-1322T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044145 | |||||||
chr5:181044218 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-23-1249T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044218 | |||||||
chr5:181044228 | C | T | 2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.-23-1239C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044228 | |||||||
chr5:181044311 | G | A | 4 | a0001c0013t0002g0250 a0001c0013t0002g0251 a0001c0016t0009g0049 others(1): Show |
6 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.-23-1156G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044311 | |||||||
chr5:181044362 | C | T | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-23-1105C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044362 | |||||||
chr5:181044377 | G | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-23-1090G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044377 | |||||||
chr5:181044380 | G | A | 24 | a0001c0001t0001g0122 a0001c0001t0001g0150 a0001c0004t0005g0050 others(21): Show |
28 | HG01106.hp2 HG01261.hp2 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.-23-1087G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044380 | |||||||
chr5:181044552 | G | A | 141 | a0001c0001t0001g0122 a0001c0001t0001g0150 a0001c0004t0005g0050 others(138): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.-23-915G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044552 | |||||||
chr5:181044691 | C | T | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-23-776C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044691 | |||||||
chr5:181044693 | G | A | 4 | a0001c0001t0001g0185 a0002c0002t0002g0024 a0002c0002t0002g0059 others(1): Show |
5 | HG02698.hp1 NA18956.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.-23-774G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044693 | |||||||
chr5:181044823 | A | G | 145 | a0001c0001t0001g0122 a0001c0001t0001g0150 a0001c0004t0005g0050 others(142): Show |
213 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(210): Show |
intron_variant | MODIFIER | c.-23-644A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044823 | |||||||
chr5:181044841 | G | A | 2 | a0002c0002t0002g0061 a0006c0026t0002g0062 |
2 | HG00597.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.-23-626G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044841 | |||||||
chr5:181044921 | G | A | 1 | a0001c0007t0007g0151 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-23-546G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181044921 | |||||||
chr5:181045155 | A | G | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-23-312A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181045155 | |||||||
chr5:181045405 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.-23-62G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181045405 | |||||||
chr5:181045419 | TC | T | 50 | a0001c0007t0007g0151 a0001c0007t0007g0175 a0001c0007t0007g0176 others(47): Show |
71 | HG00140.hp1 HG00438.hp1 HG00741.hp2 others(68): Show |
intron_variant | MODIFIER | c.-23-43delC | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr5 | 181045419 | ||||||
chr5:181045448 | C | T | 17 | a0001c0007t0007g0151 a0001c0007t0007g0175 a0001c0007t0007g0176 others(14): Show |
17 | HG00438.hp1 HG01891.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.-23-19C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 1/10 | chr5 | 181045448 | |||||||
chr5:181045648 | G | A | 1 | a0001c0001t0001g0143 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.109+50G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045648 | |||||||
chr5:181045719 | C | T | 2 | a0001c0009t0008g0120 a0001c0009t0008g0121 |
2 | HG02451.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.109+121C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045719 | |||||||
chr5:181045751 | C | T | 1 | a0006c0026t0002g0062 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.109+153C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045751 | |||||||
chr5:181045779 | C | G | 1 | a0001c0004t0005g0267 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.109+181C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045779 | |||||||
chr5:181045800 | C | CCAACACC others(858): Show |
1 | a0002c0002t0006g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.109+203_109+204ins others(865): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045800 | ||||||
chr5:181045802 | G | A | 2 | a0001c0001t0001g0186 a0002c0002t0006g0114 |
2 | HG03225.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.109+204G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045802 | |||||||
chr5:181045802 | G | GACACCTC others(472): Show |
2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+223_109+224ins others(479): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045802 | ||||||
chr5:181045802 | G | GACACCTC others(2110): Show |
1 | a0003c0011t0006g0142 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.109+223_109+224ins others(2117): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045802 | ||||||
chr5:181045807 | C | CTCCTCCA others(588): Show |
7 | a0001c0005t0004g0004 a0001c0005t0004g0129 a0001c0005t0004g0130 others(4): Show |
14 | HG00544.hp1 HG02015.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.109+223_109+224ins others(595): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045807 | ||||||
chr5:181045807 | C | CTCCTCCA others(826): Show |
3 | a0001c0005t0004g0124 a0001c0005t0004g0133 a0001c0005t0004g0134 |
3 | HG00597.hp1 NA18966.hp1 NA19054.hp1 |
intron_variant | MODIFIER | c.109+223_109+224ins others(833): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045807 | ||||||
chr5:181045807 | C | CTCCTCCA others(588): Show |
1 | a0001c0008t0001g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.109+223_109+224ins others(595): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045807 | ||||||
chr5:181045807 | C | CTCCTCCA others(5032): Show |
1 | a0001c0001t0001g0186 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.109+223_109+224ins others(5039): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045807 | ||||||
chr5:181045822 | T | C | 75 | a0001c0001t0001g0186 a0001c0004t0005g0252 a0001c0005t0004g0004 others(72): Show |
112 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(109): Show |
intron_variant | MODIFIER | c.109+224T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045822 | |||||||
chr5:181045830 | T | C | 74 | a0001c0001t0001g0186 a0001c0004t0005g0252 a0001c0005t0004g0004 others(71): Show |
111 | HG00140.hp1 HG00280.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.109+232T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045830 | |||||||
chr5:181045830 | T | TCAAAACC others(950): Show |
1 | a0001c0004t0005g0254 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.109+235_109+236ins others(957): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045830 | ||||||
chr5:181045830 | T | TCAAAACC others(2949): Show |
1 | a0001c0004t0005g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.109+235_109+236ins others(2956): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045830 | ||||||
chr5:181045834 | C | A | 19 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(16): Show |
23 | HG01261.hp2 HG02071.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.109+236C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045834 | |||||||
chr5:181045860 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.109+262G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045860 | |||||||
chr5:181045866 | T | TTCCTCCA others(4885): Show |
1 | a0001c0006t0006g0009 | 4 | HG02572.hp1 HG03130.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+292_109+293ins others(4892): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(4557): Show |
1 | a0001c0006t0006g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(4564): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(1933): Show |
1 | a0002c0002t0006g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(1940): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2970): Show |
1 | a0002c0003t0003g0096 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.109+292_109+293ins others(2977): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2946): Show |
1 | a0001c0006t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(2953): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3274): Show |
1 | a0003c0011t0006g0033 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.109+292_109+293ins others(3281): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3095): Show |
1 | a0002c0003t0003g0097 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(3102): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2886): Show |
1 | a0002c0003t0003g0246 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(2893): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3741): Show |
1 | a0002c0003t0003g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.109+292_109+293ins others(3748): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3633): Show |
2 | a0002c0003t0003g0007 a0002c0003t0003g0099 |
6 | HG02074.hp2 NA18957.hp2 NA19074.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+292_109+293ins others(3640): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2887): Show |
1 | a0002c0003t0003g0054 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(2894): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2021): Show |
1 | a0002c0003t0003g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(2028): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2887): Show |
4 | a0002c0003t0003g0014 a0002c0003t0003g0055 a0002c0003t0003g0056 others(1): Show |
6 | HG02165.hp2 NA18747.hp2 NA18950.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+292_109+293ins others(2894): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2976): Show |
8 | a0002c0003t0003g0008 a0002c0003t0003g0017 a0002c0003t0003g0022 others(5): Show |
15 | HG00140.hp1 HG01070.hp1 HG01071.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+292_109+293ins others(2983): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3214): Show |
1 | a0002c0003t0003g0104 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(3221): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2975): Show |
2 | a0001c0006t0001g0010 a0001c0006t0001g0067 |
5 | HG01243.hp2 HG02630.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.109+292_109+293ins others(2982): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2886): Show |
1 | a0002c0003t0003g0105 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(2893): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2893): Show |
1 | a0002c0003t0003g0058 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(2900): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2885): Show |
1 | a0001c0006t0001g0068 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(2892): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(1722): Show |
1 | a0001c0006t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.109+292_109+293ins others(1729): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3660): Show |
2 | a0002c0002t0013g0070 a0002c0002t0013g0071 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.109+292_109+293ins others(3667): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2917): Show |
1 | a0002c0003t0003g0106 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.109+292_109+293ins others(2924): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2916): Show |
2 | a0002c0003t0003g0107 a0002c0003t0003g0108 |
2 | NA18997.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.109+292_109+293ins others(2923): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2916): Show |
1 | a0002c0003t0003g0109 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.109+292_109+293ins others(2923): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2916): Show |
1 | a0002c0003t0003g0110 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.109+292_109+293ins others(2923): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2976): Show |
1 | a0002c0003t0003g0032 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.109+292_109+293ins others(2983): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2977): Show |
1 | a0002c0003t0003g0111 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.109+292_109+293ins others(2984): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3035): Show |
1 | a0002c0003t0003g0005 | 6 | HG00741.hp2 HG01099.hp1 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+292_109+293ins others(3042): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2887): Show |
1 | a0002c0003t0003g0023 | 2 | NA18967.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.109+292_109+293ins others(2894): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3542): Show |
1 | a0002c0003t0003g0029 | 2 | NA18983.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.109+292_109+293ins others(3549): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3542): Show |
1 | a0002c0003t0003g0112 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.109+292_109+293ins others(3549): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3538): Show |
1 | a0002c0003t0003g0113 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.109+292_109+293ins others(3545): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2413): Show |
1 | a0001c0004t0005g0253 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.109+290_109+291ins others(2420): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3368): Show |
2 | a0001c0004t0005g0050 a0001c0004t0005g0051 |
4 | NA18944.hp1 NA18994.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+290_109+291ins others(3375): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2232): Show |
2 | a0001c0004t0005g0267 a0010c0025t0005g0255 |
2 | HG03041.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.109+290_109+291ins others(2239): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3367): Show |
11 | a0001c0004t0005g0052 a0001c0004t0005g0053 a0001c0004t0005g0257 others(8): Show |
13 | HG02280.hp2 HG02818.hp1 HG03491.hp1 others(10): Show |
intron_variant | MODIFIER | c.109+290_109+291ins others(3374): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3337): Show |
1 | a0001c0004t0005g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.109+290_109+291ins others(3344): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3367): Show |
1 | a0001c0004t0005g0265 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.109+290_109+291ins others(3374): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3367): Show |
1 | a0001c0004t0005g0266 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.109+290_109+291ins others(3374): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3991): Show |
1 | a0001c0006t0004g0137 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.109+290_109+291ins others(3998): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2110): Show |
1 | a0001c0006t0004g0138 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.109+290_109+291ins others(2117): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3781): Show |
1 | a0001c0006t0004g0139 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.109+290_109+291ins others(3788): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(4534): Show |
1 | a0004c0017t0009g0048 | 2 | HG01361.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.109+290_109+291ins others(4541): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(4534): Show |
1 | a0001c0016t0009g0049 | 2 | HG00733.hp2 HG01074.hp2 |
intron_variant | MODIFIER | c.109+290_109+291ins others(4541): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(530): Show |
3 | a0001c0005t0004g0125 a0001c0005t0004g0126 a0001c0005t0004g0242 |
3 | HG01515.hp1 HG01517.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.109+290_109+291ins others(537): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2380): Show |
1 | a0002c0002t0002g0073 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.109+289_109+290ins others(2387): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2678): Show |
1 | a0001c0008t0001g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.109+289_109+290ins others(2685): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2887): Show |
1 | a0006c0026t0002g0062 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.109+289_109+290ins others(2894): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2468): Show |
1 | a0002c0002t0002g0025 | 2 | NA18940.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.109+289_109+290ins others(2475): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2708): Show |
2 | a0002c0002t0002g0026 a0002c0002t0016g0026 |
2 | NA19004.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.109+289_109+290ins others(2715): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2887): Show |
1 | a0002c0002t0002g0083 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.109+289_109+290ins others(2894): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2380): Show |
1 | a0002c0003t0002g0084 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.109+289_109+290ins others(2387): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2350): Show |
5 | a0002c0002t0002g0003 a0002c0002t0002g0085 a0002c0002t0002g0086 others(2): Show |
12 | HG02015.hp2 HG03834.hp2 NA18944.hp2 others(9): Show |
intron_variant | MODIFIER | c.109+289_109+290ins others(2357): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(2918): Show |
1 | a0002c0002t0002g0060 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.109+289_109+290ins others(2925): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3036): Show |
1 | a0002c0002t0004g0094 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.109+289_109+290ins others(3043): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(887): Show |
2 | a0002c0002t0002g0016 a0002c0002t0002g0095 |
4 | HG00735.hp1 HG00735.hp2 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+289_109+290ins others(894): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045866 | T | TTCCTCCA others(3663): Show |
1 | a0001c0004t0005g0252 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.109+289_109+290ins others(3670): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045866 | ||||||
chr5:181045888 | C | CCCAACAC others(52): Show |
2 | a0001c0006t0006g0065 a0001c0006t0006g0066 |
2 | HG02622.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.109+292_109+293ins others(59): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045888 | ||||||
chr5:181045888 | C | T | 28 | a0001c0005t0004g0136 a0001c0008t0001g0001 a0002c0002t0002g0001 others(25): Show |
45 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(42): Show |
intron_variant | MODIFIER | c.109+290C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045888 | |||||||
chr5:181045889 | C | T | 4 | a0001c0005t0004g0031 a0001c0005t0004g0131 a0001c0005t0023g0031 others(1): Show |
4 | HG00280.hp1 HG01192.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+291C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045889 | |||||||
chr5:181045891 | G | A | 140 | a0001c0001t0001g0186 a0001c0004t0005g0050 a0001c0004t0005g0051 others(137): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.109+293G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045891 | |||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
3 | a0001c0001t0001g0036 a0001c0001t0001g0147 a0001c0001t0001g0152 |
4 | HG02145.hp2 HG02630.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4794): Show |
1 | a0001c0001t0001g0189 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4801): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(6341): Show |
1 | a0001c0007t0007g0175 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(6348): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(6146): Show |
1 | a0001c0007t0007g0176 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(6153): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(6193): Show |
1 | a0001c0007t0007g0177 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(6200): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(6192): Show |
1 | a0001c0007t0007g0178 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(6199): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(6193): Show |
3 | a0001c0007t0007g0151 a0001c0007t0007g0179 a0001c0007t0007g0180 |
3 | HG03927.hp2 HG03942.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.109+342_109+343ins others(6200): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(2702): Show |
1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(2709): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(1752): Show |
1 | a0002c0010t0003g0190 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(1759): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4801): Show |
1 | a0001c0001t0001g0191 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4808): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0001t0001g0184 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4973): Show |
1 | a0001c0001t0011g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4980): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4853): Show |
1 | a0001c0001t0011g0245 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4860): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0001t0001g0192 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4787): Show |
1 | a0001c0001t0001g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4794): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4704): Show |
1 | a0001c0001t0014g0153 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4711): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4764): Show |
1 | a0001c0001t0001g0195 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4771): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(6107): Show |
1 | a0001c0001t0001g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(6114): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4496): Show |
1 | a0001c0001t0001g0156 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4503): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(3543): Show |
1 | a0002c0010t0002g0149 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(3550): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(7057): Show |
1 | a0001c0001t0001g0182 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(7064): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4853): Show |
1 | a0001c0001t0001g0157 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4860): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(5151): Show |
1 | a0001c0001t0001g0196 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(5158): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(1543): Show |
1 | a0001c0001t0001g0163 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(1550): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4584): Show |
2 | a0001c0001t0001g0042 a0001c0001t0001g0197 |
2 | NA19067.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.109+342_109+343ins others(4591): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4584): Show |
1 | a0001c0001t0001g0158 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4591): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(1752): Show |
2 | a0001c0001t0001g0021 a0001c0001t0001g0229 |
4 | NA18960.hp2 NA18974.hp2 NA19079.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+342_109+343ins others(1759): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(5032): Show |
1 | a0001c0001t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(5039): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4704): Show |
1 | a0001c0001t0001g0198 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4711): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
2 | a0001c0001t0001g0200 a0001c0007t0007g0199 |
2 | HG03017.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4764): Show |
1 | a0001c0001t0001g0202 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4771): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(6104): Show |
1 | a0001c0001t0001g0203 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(6111): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4792): Show |
1 | a0001c0018t0001g0204 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4799): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4794): Show |
1 | a0001c0001t0001g0187 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4801): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(5121): Show |
2 | a0001c0001t0001g0019 a0001c0007t0008g0019 |
3 | HG01255.hp1 HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.109+342_109+343ins others(5128): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4584): Show |
2 | a0001c0001t0001g0043 a0001c0001t0001g0207 |
3 | HG02165.hp1 NA18997.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.109+342_109+343ins others(4591): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
35 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(32): Show |
55 | HG00544.hp2 HG00558.hp1 HG00609.hp1 others(52): Show |
intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4436): Show |
1 | a0001c0001t0001g0162 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4443): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0001t0001g0226 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(7059): Show |
3 | a0001c0001t0001g0018 a0001c0001t0001g0183 a0001c0019t0001g0018 |
3 | NA18612.hp2 NA18953.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.109+342_109+343ins others(7066): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4703): Show |
1 | a0001c0001t0001g0020 | 3 | HG00280.hp2 HG00639.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.109+342_109+343ins others(4710): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0001t0021g0228 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4794): Show |
1 | a0001c0001t0001g0247 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4801): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
9 | a0001c0001t0001g0012 a0001c0001t0001g0035 a0001c0001t0001g0038 others(6): Show |
15 | HG00438.hp2 HG01081.hp1 HG01109.hp2 others(12): Show |
intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0001t0001g0166 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0001t0001g0167 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4106): Show |
1 | a0001c0001t0001g0168 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4113): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
3 | a0001c0001t0001g0169 a0001c0001t0001g0170 a0001c0001t0001g0171 |
3 | HG00673.hp1 NA18965.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0001t0001g0230 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(6163): Show |
1 | a0001c0001t0001g0185 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(6170): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0020t0005g0173 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0001t0001g0046 | 2 | NA18967.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0001t0001g0249 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4673): Show |
1 | a0001c0001t0001g0233 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4680): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4495): Show |
1 | a0001c0008t0001g0234 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4502): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(5867): Show |
1 | a0001c0001t0001g0235 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(5874): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4730): Show |
1 | a0001c0001t0001g0148 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4737): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4972): Show |
1 | a0001c0001t0001g0269 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(4979): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4763): Show |
1 | a0001c0001t0001g0237 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4770): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(6223): Show |
1 | a0001c0007t0007g0181 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(6230): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4822): Show |
1 | a0001c0001t0001g0238 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4829): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4793): Show |
1 | a0001c0001t0001g0239 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045891 | G | GACACCTC others(4913): Show |
1 | a0001c0001t0001g0240 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.109+319_109+320ins others(4920): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045891 | ||||||
chr5:181045893 | C | T | 4 | a0001c0005t0004g0031 a0001c0005t0004g0131 a0001c0005t0023g0031 others(1): Show |
4 | HG00280.hp1 HG01192.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+295C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045893 | |||||||
chr5:181045896 | C | CTCCTCCA others(2469): Show |
1 | a0011c0024t0002g0075 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.109+349_109+350ins others(2476): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045896 | ||||||
chr5:181045896 | C | CTCCTCCA others(2558): Show |
5 | a0002c0002t0004g0011 a0002c0002t0004g0028 a0002c0002t0004g0089 others(2): Show |
8 | HG01256.hp2 HG01496.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.109+349_109+350ins others(2565): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045896 | ||||||
chr5:181045896 | C | CTCCTCCA others(2558): Show |
1 | a0002c0002t0004g0091 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.109+349_109+350ins others(2565): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045896 | ||||||
chr5:181045918 | C | CCCAACAC others(7060): Show |
1 | a0001c0009t0008g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(7067): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045918 | ||||||
chr5:181045918 | C | CCCAACAC others(7060): Show |
2 | a0001c0009t0008g0118 a0001c0009t0008g0119 |
2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.109+342_109+343ins others(7067): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045918 | ||||||
chr5:181045918 | C | CCCAACAC others(7060): Show |
1 | a0001c0009t0008g0116 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(7067): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045918 | ||||||
chr5:181045918 | C | CCCAACAC others(10218): Show |
1 | a0001c0009t0008g0120 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(10225): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045918 | ||||||
chr5:181045918 | C | CCCAACAC others(8578): Show |
1 | a0001c0009t0008g0121 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.109+342_109+343ins others(8585): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045918 | ||||||
chr5:181045918 | C | CTCAACAC others(171): Show |
2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+320_109+321ins others(178): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045918 | |||||||
chr5:181045918 | C | CTCAATAC others(82): Show |
1 | a0001c0005t0004g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.109+320_109+321ins others(89): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045918 | |||||||
chr5:181045919 | C | CCAACACC others(23): Show |
4 | a0001c0001t0001g0174 a0001c0001t0001g0194 a0001c0001t0001g0232 others(1): Show |
4 | HG01891.hp2 HG01952.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+342_109+343ins others(30): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045919 | ||||||
chr5:181045919 | C | CCAACACC others(3007): Show |
1 | a0002c0002t0002g0072 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.109+342_109+343ins others(3014): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045919 | ||||||
chr5:181045941 | C | T | 14 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0042 others(11): Show |
15 | HG02132.hp2 HG02451.hp2 NA18943.hp1 others(12): Show |
intron_variant | MODIFIER | c.109+343C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045941 | |||||||
chr5:181045948 | T | C | 49 | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0042 others(46): Show |
64 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.109+350T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045948 | |||||||
chr5:181045948 | T | TGTAGTGT others(260): Show |
4 | a0001c0005t0004g0031 a0001c0005t0004g0131 a0001c0005t0023g0031 others(1): Show |
4 | HG00280.hp1 HG01192.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+350_109+351ins others(267): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045948 | |||||||
chr5:181045949 | C | T | 9 | a0001c0001t0001g0018 a0001c0001t0001g0144 a0001c0001t0001g0174 others(6): Show |
9 | HG01891.hp2 HG01952.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+351C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045949 | C | TCAACACC others(4584): Show |
1 | a0001c0001t0001g0042 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.109+350_109+351ins others(4591): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045949 | C | TCAACACC others(4764): Show |
1 | a0001c0001t0001g0201 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.109+350_109+351ins others(4771): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045949 | C | TCAACACC others(4704): Show |
1 | a0001c0001t0001g0205 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.109+350_109+351ins others(4711): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045949 | C | TCAACACC others(4793): Show |
1 | a0001c0001t0001g0206 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.109+350_109+351ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045949 | C | TCAACACC others(4793): Show |
2 | a0001c0001t0001g0222 a0002c0012t0002g0221 |
2 | NA18964.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.109+350_109+351ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045949 | C | TCAACACC others(4763): Show |
1 | a0001c0001t0001g0227 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.109+350_109+351ins others(4770): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045949 | C | TCAACACC others(4793): Show |
1 | a0001c0001t0001g0012 | 2 | NA18947.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.109+350_109+351ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045949 | C | TCAACACC others(4790): Show |
1 | a0001c0001t0001g0172 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.109+350_109+351ins others(4797): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045949 | C | TCAACACC others(4793): Show |
1 | a0001c0001t0001g0231 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.109+350_109+351ins others(4800): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045949 | C | TCAACACC others(4823): Show |
1 | a0001c0001t0001g0236 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.109+350_109+351ins others(4830): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045949 | |||||||
chr5:181045950 | C | T | 1 | a0002c0003t0003g0098 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.109+352C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045950 | |||||||
chr5:181045953 | C | T | 4 | a0001c0001t0001g0174 a0001c0001t0001g0194 a0001c0001t0001g0232 others(1): Show |
4 | HG01891.hp2 HG01952.hp2 HG02602.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+355C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045953 | |||||||
chr5:181045978 | T | C | 246 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(243): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.109+380T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045978 | |||||||
chr5:181045978 | T | TCCAACAC others(291): Show |
1 | a0003c0011t0006g0142 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.109+670_109+671ins others(298): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045978 | ||||||
chr5:181045979 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0144 a0001c0009t0022g0117 |
3 | HG02132.hp2 HG02451.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.109+381C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045979 | |||||||
chr5:181045983 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0144 |
2 | HG02132.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.109+385C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045983 | |||||||
chr5:181045983 | C | TACCTCCT others(11475): Show |
1 | a0001c0009t0022g0117 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.109+384_109+385ins others(11482): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181045983 | |||||||
chr5:181045986 | C | CTCCTCCA others(22): Show |
4 | a0002c0002t0002g0115 a0002c0002t0004g0088 a0002c0003t0002g0015 others(1): Show |
6 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+409_109+410ins others(29): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045986 | ||||||
chr5:181045986 | C | CTCCTCCA others(7062): Show |
1 | a0001c0006t0006g0065 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.109+409_109+410ins others(7069): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045986 | ||||||
chr5:181045986 | C | CTCCTCCA others(6525): Show |
1 | a0001c0006t0006g0066 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.109+409_109+410ins others(6532): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045986 | ||||||
chr5:181045986 | C | CTCCTCCA others(2917): Show |
14 | a0001c0008t0001g0001 a0002c0002t0002g0001 a0002c0002t0002g0024 others(11): Show |
26 | HG00099.hp2 HG00609.hp2 HG00639.hp1 others(23): Show |
intron_variant | MODIFIER | c.109+409_109+410ins others(2924): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045986 | ||||||
chr5:181045986 | C | CTCCTCCA others(2887): Show |
1 | a0002c0002t0002g0092 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.109+409_109+410ins others(2894): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045986 | ||||||
chr5:181045986 | C | CTCCTCCA others(2440): Show |
1 | a0002c0002t0002g0093 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.109+409_109+410ins others(2447): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181045986 | ||||||
chr5:181046000 | C | CCCCAGCC others(16829): Show |
1 | a0001c0001t0001g0163 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.109+670_109+671ins others(16836): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046000 | ||||||
chr5:181046000 | C | CCCCAGCC others(202): Show |
1 | a0001c0001t0001g0186 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.109+610_109+611ins others(209): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046000 | ||||||
chr5:181046000 | C | CCCCAGCC others(6582): Show |
1 | a0001c0001t0001g0194 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.109+409_109+410ins others(6589): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046000 | ||||||
chr5:181046000 | C | CCCCAGCC others(4674): Show |
1 | a0001c0001t0014g0154 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.109+409_109+410ins others(4681): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046000 | ||||||
chr5:181046000 | C | CCCCAGCC others(4673): Show |
1 | a0001c0001t0001g0232 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.109+409_109+410ins others(4680): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046000 | ||||||
chr5:181046000 | C | CCCCAGCC others(4616): Show |
1 | a0001c0001t0001g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.109+409_109+410ins others(4623): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046000 | ||||||
chr5:181046000 | C | G | 113 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(110): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.109+402C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046000 | |||||||
chr5:181046008 | C | T | 5 | a0001c0005t0004g0031 a0001c0005t0004g0131 a0001c0005t0004g0136 others(2): Show |
5 | HG00280.hp1 HG01192.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+410C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046008 | |||||||
chr5:181046009 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+411C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046009 | |||||||
chr5:181046025 | C | T | 2 | a0001c0001t0011g0244 a0001c0001t0011g0245 |
2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.109+427C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046025 | |||||||
chr5:181046028 | C | A | 1 | a0001c0001t0001g0208 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.109+430C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046028 | |||||||
chr5:181046045 | T | TTCCTCCA others(1607): Show |
2 | a0001c0006t0010g0127 a0001c0006t0010g0128 |
2 | HG02280.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.109+648_109+649ins others(1614): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046045 | ||||||
chr5:181046045 | T | TTCCTCCA others(2440): Show |
1 | a0002c0002t0004g0088 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.109+648_109+649ins others(2447): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046045 | ||||||
chr5:181046045 | T | TTCCTCCA others(2200): Show |
1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.109+528_109+529ins others(2207): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046045 | ||||||
chr5:181046045 | T | TTCCTCCA others(322): Show |
1 | a0001c0004t0005g0256 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.109+462_109+463ins others(329): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046045 | ||||||
chr5:181046045 | T | TTCCTCCA others(82): Show |
2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+454_109+455ins others(89): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046045 | ||||||
chr5:181046065 | C | CCCCCAAC others(2405): Show |
1 | a0001c0004t0005g0254 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.109+648_109+649ins others(2412): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046065 | ||||||
chr5:181046065 | C | G | 1 | a0001c0001t0001g0144 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.109+467C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046065 | |||||||
chr5:181046067 | C | CCCAACAC others(2590): Show |
2 | a0002c0003t0002g0015 a0002c0003t0002g0076 |
4 | HG00099.hp1 HG00323.hp2 HG01069.hp2 others(1): Show |
intron_variant | MODIFIER | c.109+648_109+649ins others(2597): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046067 | ||||||
chr5:181046067 | C | CCCAACAC others(113): Show |
1 | a0002c0010t0002g0149 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.109+588_109+589ins others(120): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046067 | ||||||
chr5:181046070 | A | G | 2 | a0001c0001t0001g0018 a0001c0001t0001g0144 |
2 | HG02132.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.109+472A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046070 | |||||||
chr5:181046083 | C | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+485C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046083 | |||||||
chr5:181046089 | C | G | 1 | a0001c0001t0001g0193 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.109+491C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046089 | |||||||
chr5:181046090 | C | CCCAGCCT others(380): Show |
1 | a0001c0005t0004g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.109+498_109+499ins others(387): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046090 | ||||||
chr5:181046098 | C | CCAACACC others(231): Show |
4 | a0001c0005t0004g0031 a0001c0005t0004g0131 a0001c0005t0023g0031 others(1): Show |
4 | HG00280.hp1 HG01192.hp1 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+558_109+559ins others(238): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046098 | ||||||
chr5:181046098 | C | T | 1 | a0001c0005t0004g0136 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.109+500C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046098 | |||||||
chr5:181046120 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0144 |
2 | HG02132.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.109+522C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046120 | |||||||
chr5:181046127 | C | T | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.109+529C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046127 | |||||||
chr5:181046128 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0144 |
2 | HG02132.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.109+530C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046128 | |||||||
chr5:181046147 | C | T | 1 | a0001c0001t0020g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.109+549C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046147 | |||||||
chr5:181046150 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0144 |
2 | HG02132.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.109+552C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046150 | |||||||
chr5:181046157 | T | C | 4 | a0001c0001t0001g0018 a0001c0001t0001g0144 a0001c0013t0002g0250 others(1): Show |
4 | HG02132.hp2 HG02572.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.109+559T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046157 | |||||||
chr5:181046157 | T | TCCAACAC others(321): Show |
1 | a0001c0006t0004g0139 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.109+670_109+671ins others(328): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046157 | ||||||
chr5:181046157 | T | TCCAACAC others(349): Show |
1 | a0001c0007t0007g0176 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.109+618_109+619ins others(356): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046157 | ||||||
chr5:181046157 | T | TCCAACAC others(349): Show |
1 | a0001c0007t0007g0178 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.109+618_109+619ins others(356): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046157 | ||||||
chr5:181046157 | T | TCCAACAC others(351): Show |
6 | a0001c0007t0007g0151 a0001c0007t0007g0175 a0001c0007t0007g0177 others(3): Show |
6 | HG00438.hp1 HG03669.hp2 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.109+618_109+619ins others(358): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046157 | ||||||
chr5:181046158 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0144 |
2 | HG02132.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.109+560C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046158 | |||||||
chr5:181046162 | C | T | 2 | a0001c0001t0001g0018 a0001c0001t0001g0144 |
2 | HG02132.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.109+564C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046162 | |||||||
chr5:181046192 | C | CACCTCCT others(12277): Show |
1 | a0001c0001t0001g0144 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.109+641_109+642ins others(12284): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046192 | ||||||
chr5:181046192 | C | CACCTCCT others(7059): Show |
1 | a0001c0001t0001g0018 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.109+641_109+642ins others(7066): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046192 | ||||||
chr5:181046211 | C | CCAGCCCC others(381): Show |
12 | a0001c0005t0004g0004 a0001c0005t0004g0124 a0001c0005t0004g0125 others(9): Show |
19 | HG00544.hp1 HG00597.hp1 HG01515.hp1 others(16): Show |
intron_variant | MODIFIER | c.109+648_109+649ins others(388): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046211 | ||||||
chr5:181046211 | C | T | 5 | a0001c0005t0004g0031 a0001c0005t0004g0131 a0001c0005t0004g0136 others(2): Show |
5 | HG00280.hp1 HG01192.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+613C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046211 | |||||||
chr5:181046219 | C | CCAACACC others(2948): Show |
1 | a0002c0002t0002g0115 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.109+621_109+622ins others(2955): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046219 | |||||||
chr5:181046220 | A | C | 1 | a0002c0002t0002g0115 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.109+622A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046220 | |||||||
chr5:181046244 | G | GCCCCCAA others(24): Show |
2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+648_109+649ins others(31): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046244 | ||||||
chr5:181046247 | T | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+649T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046247 | |||||||
chr5:181046248 | G | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+650G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046248 | |||||||
chr5:181046249 | T | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+651T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046249 | |||||||
chr5:181046251 | G | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+653G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046251 | |||||||
chr5:181046252 | T | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+654T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046252 | |||||||
chr5:181046253 | G | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+655G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046253 | |||||||
chr5:181046254 | T | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+656T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046254 | |||||||
chr5:181046254 | T | TTCCTCCA others(23): Show |
17 | a0001c0005t0004g0004 a0001c0005t0004g0031 a0001c0005t0004g0124 others(14): Show |
24 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.109+670_109+671ins others(30): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046254 | ||||||
chr5:181046269 | T | C | 19 | a0001c0005t0004g0004 a0001c0005t0004g0031 a0001c0005t0004g0124 others(16): Show |
26 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(23): Show |
intron_variant | MODIFIER | c.109+671T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046269 | |||||||
chr5:181046277 | C | CCAACACC others(5244): Show |
1 | a0001c0013t0002g0250 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.109+707_109+708ins others(5251): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046277 | ||||||
chr5:181046277 | C | CCAACACC others(5244): Show |
1 | a0001c0013t0002g0251 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.109+707_109+708ins others(5251): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046277 | ||||||
chr5:181046366 | C | G | 1 | a0001c0008t0001g0074 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.109+768C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046366 | |||||||
chr5:181046396 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+798C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046396 | |||||||
chr5:181046452 | G | A | 6 | a0002c0002t0002g0025 a0002c0003t0003g0014 a0002c0003t0003g0054 others(3): Show |
9 | HG02165.hp2 NA18940.hp1 NA18950.hp2 others(6): Show |
intron_variant | MODIFIER | c.109+854G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046452 | |||||||
chr5:181046468 | C | A | 5 | a0001c0005t0004g0031 a0001c0005t0004g0131 a0001c0005t0004g0136 others(2): Show |
5 | HG00280.hp1 HG01192.hp1 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.109+870C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046468 | |||||||
chr5:181046471 | G | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+873G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046471 | |||||||
chr5:181046601 | G | A | 17 | a0001c0005t0004g0004 a0001c0005t0004g0031 a0001c0005t0004g0124 others(14): Show |
24 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(21): Show |
intron_variant | MODIFIER | c.109+1003G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046601 | |||||||
chr5:181046627 | T | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+1029T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046627 | |||||||
chr5:181046682 | C | G | 1 | a0002c0003t0003g0102 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.109+1084C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046682 | |||||||
chr5:181046694 | AGAGCGAG others(9): Show |
A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.109+1100_109+1115d others(18): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046694 | ||||||
chr5:181046710 | G | GGAGA | 2 | a0001c0001t0001g0012 a0001c0001t0001g0172 |
3 | HG02027.hp2 NA18943.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.109+1127_109+1130d others(6): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr5 | 181046710 | ||||||
chr5:181046717 | G | A | 2 | a0001c0004t0005g0257 a0001c0004t0005g0258 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.109+1119G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046717 | |||||||
chr5:181046783 | A | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.110-1144A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046783 | |||||||
chr5:181046906 | A | G | 1 | a0005c0015t0004g0030 | 2 | NA18991.hp2 NA19072.hp2 |
intron_variant | MODIFIER | c.110-1021A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181046906 | |||||||
chr5:181047080 | T | C | 158 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(155): Show |
226 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(223): Show |
intron_variant | MODIFIER | c.110-847T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047080 | |||||||
chr5:181047109 | G | T | 1 | a0001c0001t0001g0225 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.110-818G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047109 | |||||||
chr5:181047123 | A | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.110-804A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047123 | |||||||
chr5:181047176 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.110-751C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047176 | |||||||
chr5:181047194 | A | G | 1 | a0002c0003t0003g0246 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.110-733A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047194 | |||||||
chr5:181047588 | C | T | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.110-339C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047588 | |||||||
chr5:181047626 | G | A | 1 | a0001c0005t0004g0129 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.110-301G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047626 | |||||||
chr5:181047668 | T | A | 4 | a0001c0006t0006g0009 a0001c0006t0006g0063 a0001c0006t0006g0065 others(1): Show |
7 | HG02572.hp1 HG02622.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.110-259T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047668 | |||||||
chr5:181047687 | A | G | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.110-240A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047687 | |||||||
chr5:181047764 | G | C | 1 | a0002c0003t0003g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.110-163G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047764 | |||||||
chr5:181047814 | C | T | 137 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(134): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.110-113C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047814 | |||||||
chr5:181047815 | A | G | 141 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(138): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.110-112A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047815 | |||||||
chr5:181047815 | A | T | 1 | a0002c0003t0003g0111 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.110-112A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047815 | |||||||
chr5:181047816 | C | G | 1 | a0002c0003t0003g0111 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.110-111C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047816 | |||||||
chr5:181047879 | A | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.110-48A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047879 | |||||||
chr5:181047913 | A | T | 4 | a0001c0001t0001g0046 a0001c0001t0001g0189 a0001c0001t0001g0224 others(1): Show |
5 | NA18947.hp2 NA18967.hp1 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.110-14A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 2/10 | chr5 | 181047913 | |||||||
chr5:181048362 | C | T | 2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+91C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048362 | |||||||
chr5:181048396 | A | C | 1 | a0002c0003t0003g0243 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.454+125A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048396 | |||||||
chr5:181048462 | T | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+191T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048462 | |||||||
chr5:181048543 | T | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+272T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048543 | |||||||
chr5:181048572 | T | C | 2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+301T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048572 | |||||||
chr5:181048634 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+363G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048634 | |||||||
chr5:181048637 | G | A | 1 | a0001c0009t0008g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.454+366G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048637 | |||||||
chr5:181048718 | T | C | 1 | a0001c0001t0001g0203 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.454+447T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048718 | |||||||
chr5:181048723 | ATATCTAT others(9): Show |
A | 1 | a0001c0001t0001g0169 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.454+467_454+482del others(16): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 181048723 | ||||||
chr5:181048727 | C | A | 1 | a0002c0002t0002g0077 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.454+456C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048727 | |||||||
chr5:181048731 | A | C | 1 | a0002c0002t0013g0071 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.454+460A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048731 | |||||||
chr5:181048733 | A | C | 1 | a0002c0002t0004g0090 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.454+462A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048733 | |||||||
chr5:181048735 | A | C | 8 | a0001c0001t0001g0206 a0001c0001t0001g0211 a0001c0001t0001g0236 others(5): Show |
8 | HG00438.hp1 HG02165.hp2 NA18612.hp1 others(5): Show |
intron_variant | MODIFIER | c.454+464A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048735 | |||||||
chr5:181048738 | T | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+467T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048738 | |||||||
chr5:181048739 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+468C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048739 | |||||||
chr5:181048742 | T | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+471T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048742 | |||||||
chr5:181048743 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+472C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048743 | |||||||
chr5:181048748 | T | TATATAG | 139 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(136): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.454+489_454+494dup others(6): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 181048748 | ||||||
chr5:181048754 | G | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+483G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048754 | |||||||
chr5:181048760 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+489G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048760 | |||||||
chr5:181048761 | A | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+490A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048761 | |||||||
chr5:181048766 | T | G | 1 | a0002c0002t0002g0085 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.454+495T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048766 | |||||||
chr5:181048774 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+503G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048774 | |||||||
chr5:181048775 | C | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+504C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048775 | |||||||
chr5:181048790 | ATAGTTAT others(17): Show |
A | 142 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(139): Show |
210 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(207): Show |
intron_variant | MODIFIER | c.454+530_454+553del others(24): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 181048790 | ||||||
chr5:181048797 | T | TATATTAT others(20): Show |
2 | a0001c0001t0001g0217 a0001c0009t0008g0116 |
2 | HG00738.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.454+585_454+611dup others(27): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 181048797 | ||||||
chr5:181048797 | T | TATATTAT others(47): Show |
101 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(98): Show |
127 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.454+558_454+611dup others(54): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 181048797 | ||||||
chr5:181048797 | T | TATATTAT others(74): Show |
24 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0013 others(21): Show |
28 | HG00609.hp1 HG01943.hp1 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.454+531_454+611dup others(81): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 181048797 | ||||||
chr5:181048797 | T | TATATTAT others(101): Show |
1 | a0001c0001t0001g0040 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.454+611_454+612ins others(108): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 181048797 | ||||||
chr5:181048797 | TATATTAT others(20): Show |
T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0145 |
3 | HG00438.hp2 NA19009.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.454+585_454+611del others(27): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 181048797 | ||||||
chr5:181048801 | T | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+530T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048801 | |||||||
chr5:181048843 | A | G | 3 | a0001c0006t0004g0137 a0001c0006t0004g0138 a0001c0006t0004g0139 |
3 | HG02145.hp1 HG02257.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.454+572A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048843 | |||||||
chr5:181048851 | A | AATATTAT others(17): Show |
1 | a0001c0009t0008g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.454+584_454+607dup others(24): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 181048851 | ||||||
chr5:181048873 | TATATA | T | 48 | a0001c0006t0001g0010 a0001c0006t0001g0064 a0001c0006t0001g0067 others(45): Show |
76 | HG00140.hp1 HG00741.hp2 HG01070.hp1 others(73): Show |
intron_variant | MODIFIER | c.454+608_454+612del others(5): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr5 | 181048873 | ||||||
chr5:181048885 | C | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+614C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048885 | |||||||
chr5:181048887 | T | TTATATTA others(22): Show |
2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+616_454+617ins others(29): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048887 | |||||||
chr5:181048910 | T | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+639T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181048910 | |||||||
chr5:181049137 | C | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.454+866C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049137 | |||||||
chr5:181049137 | C | T | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.454+866C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049137 | |||||||
chr5:181049140 | A | T | 1 | a0001c0001t0001g0223 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.454+869A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049140 | |||||||
chr5:181049388 | A | T | 1 | a0001c0004t0005g0254 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.455-700A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049388 | |||||||
chr5:181049451 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-637G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049451 | |||||||
chr5:181049463 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-625G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049463 | |||||||
chr5:181049479 | T | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-609T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049479 | |||||||
chr5:181049531 | T | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-557T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049531 | |||||||
chr5:181049531 | T | G | 1 | a0002c0002t0006g0114 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.455-557T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049531 | |||||||
chr5:181049536 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-552G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049536 | |||||||
chr5:181049537 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-551C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049537 | |||||||
chr5:181049551 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-537C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049551 | |||||||
chr5:181049628 | T | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-460T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049628 | |||||||
chr5:181049629 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-459G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049629 | |||||||
chr5:181049911 | T | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-177T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049911 | |||||||
chr5:181049932 | G | A | 1 | a0001c0007t0007g0199 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.455-156G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049932 | |||||||
chr5:181049942 | G | A | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.455-146G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049942 | |||||||
chr5:181049994 | T | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.455-94T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181049994 | |||||||
chr5:181050068 | A | C | 1 | a0002c0003t0003g0099 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.455-20A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181050068 | |||||||
chr5:181050069 | C | A | 1 | a0002c0003t0003g0099 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.455-19C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 3/10 | chr5 | 181050069 | |||||||
chr5:181050449 | C | G | 139 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(136): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.736+80C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181050449 | |||||||
chr5:181050473 | A | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.736+104A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181050473 | |||||||
chr5:181050505 | G | T | 22 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(19): Show |
26 | HG01106.hp2 HG01261.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.736+136G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181050505 | |||||||
chr5:181050704 | C | T | 1 | a0002c0002t0004g0087 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.736+335C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181050704 | |||||||
chr5:181050960 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.736+591G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181050960 | |||||||
chr5:181050979 | C | T | 6 | a0001c0001t0001g0037 a0001c0001t0001g0160 a0001c0001t0001g0161 others(3): Show |
7 | HG00323.hp1 HG01516.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+610C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181050979 | |||||||
chr5:181051011 | G | A | 4 | a0001c0007t0007g0176 a0001c0007t0007g0177 a0001c0007t0007g0178 others(1): Show |
4 | HG00438.hp1 NA18948.hp2 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.736+642G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051011 | |||||||
chr5:181051012 | G | A | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.736+643G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051012 | |||||||
chr5:181051034 | C | A | 2 | a0001c0004t0005g0257 a0001c0004t0005g0258 |
2 | HG02818.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.736+665C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051034 | |||||||
chr5:181051083 | A | C | 1 | a0001c0004t0005g0258 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.736+714A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051083 | |||||||
chr5:181051089 | C | A | 5 | a0001c0013t0002g0250 a0001c0013t0002g0251 a0001c0016t0009g0049 others(2): Show |
7 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+720C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051089 | |||||||
chr5:181051089 | C | CA | 22 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(19): Show |
29 | HG00280.hp2 HG00558.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.736+734dupA | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 181051089 | ||||||
chr5:181051089 | CA | C | 135 | a0001c0001t0001g0222 a0001c0004t0005g0050 a0001c0004t0005g0051 others(132): Show |
196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.736+734delA | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 181051089 | ||||||
chr5:181051090 | A | C | 3 | a0001c0016t0009g0049 a0002c0003t0003g0058 a0004c0017t0009g0048 |
5 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.736+721A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051090 | |||||||
chr5:181051190 | A | G | 144 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(141): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.736+821A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051190 | |||||||
chr5:181051201 | G | C | 1 | a0002c0002t0002g0086 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.736+832G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051201 | |||||||
chr5:181051300 | A | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.736+931A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051300 | |||||||
chr5:181051349 | A | G | 2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+980A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051349 | |||||||
chr5:181051353 | A | G | 4 | a0001c0006t0006g0009 a0001c0006t0006g0063 a0001c0006t0006g0065 others(1): Show |
7 | HG02572.hp1 HG02622.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+984A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051353 | |||||||
chr5:181051361 | A | G | 2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.736+992A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051361 | |||||||
chr5:181051664 | A | T | 1 | a0001c0005t0004g0134 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.736+1295A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051664 | |||||||
chr5:181051716 | A | G | 45 | a0001c0008t0001g0001 a0002c0002t0002g0001 a0002c0002t0002g0003 others(42): Show |
72 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.736+1347A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051716 | |||||||
chr5:181051754 | AAG | A | 139 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(136): Show |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.736+1388_736+1389d others(4): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 181051754 | ||||||
chr5:181051809 | T | C | 1 | a0001c0006t0001g0069 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.737-1391T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051809 | |||||||
chr5:181051849 | A | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.737-1351A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051849 | |||||||
chr5:181051893 | G | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.737-1307G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051893 | |||||||
chr5:181051947 | G | C | 1 | a0001c0001t0001g0212 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.737-1253G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051947 | |||||||
chr5:181051967 | A | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.737-1233A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181051967 | |||||||
chr5:181052303 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.737-897G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181052303 | |||||||
chr5:181052612 | G | A | 1 | a0001c0001t0001g0225 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.737-588G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181052612 | |||||||
chr5:181052676 | G | A | 5 | a0002c0003t0003g0014 a0002c0003t0003g0054 a0002c0003t0003g0055 others(2): Show |
7 | HG02165.hp2 NA18950.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.737-524G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181052676 | |||||||
chr5:181052869 | C | A | 1 | a0001c0001t0001g0155 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.737-331C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181052869 | |||||||
chr5:181052896 | G | GGACGCGG others(35): Show |
4 | a0001c0007t0007g0151 a0001c0007t0007g0175 a0001c0007t0007g0179 others(1): Show |
4 | HG03669.hp2 HG03927.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-265_737-264ins others(42): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 181052896 | ||||||
chr5:181052896 | G | GGACGCGG others(56): Show |
9 | a0001c0007t0007g0176 a0001c0007t0007g0177 a0001c0007t0007g0178 others(6): Show |
9 | HG00438.hp1 HG01891.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.737-265_737-264ins others(63): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 181052896 | ||||||
chr5:181052911 | G | GCGGGAAG others(56): Show |
2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.737-265_737-264ins others(63): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 181052911 | ||||||
chr5:181052933 | C | T | 1 | a0003c0011t0006g0142 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.737-267C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181052933 | |||||||
chr5:181052991 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.737-209C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181052991 | |||||||
chr5:181052996 | GGCGCGCC others(17): Show |
G | 8 | a0001c0007t0007g0151 a0001c0007t0007g0175 a0001c0007t0007g0176 others(5): Show |
8 | HG00438.hp1 HG03669.hp2 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.737-173_737-150del others(24): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 181052996 | ||||||
chr5:181053017 | CCG | C | 20 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(17): Show |
24 | HG01106.hp2 HG01261.hp2 HG02071.hp1 others(21): Show |
intron_variant | MODIFIER | c.737-175_737-174del others(2): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 181053017 | ||||||
chr5:181053018 | C | G | 1 | a0001c0004t0005g0262 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.737-182C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181053018 | |||||||
chr5:181053020 | C | CGCGCCCC others(13): Show |
1 | a0001c0004t0005g0262 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.737-176_737-175ins others(20): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr5 | 181053020 | ||||||
chr5:181053020 | C | G | 19 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(16): Show |
23 | HG01261.hp2 HG02071.hp1 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.737-180C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181053020 | |||||||
chr5:181053054 | C | G | 4 | a0002c0002t0002g0024 a0002c0002t0002g0059 a0002c0002t0002g0060 others(1): Show |
5 | NA18956.hp1 NA18962.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.737-146C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181053054 | |||||||
chr5:181053135 | G | A | 1 | a0001c0005t0004g0242 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.737-65G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181053135 | |||||||
chr5:181053157 | C | T | 1 | a0001c0009t0008g0123 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.737-43C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181053157 | |||||||
chr5:181053187 | G | T | 19 | a0001c0007t0007g0151 a0001c0007t0007g0175 a0001c0007t0007g0176 others(16): Show |
21 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.737-13G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 4/10 | chr5 | 181053187 | |||||||
chr5:181053363 | A | G | 25 | a0001c0004t0005g0257 a0001c0004t0005g0258 a0001c0004t0005g0266 others(22): Show |
30 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.853+47A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 5/10 | chr5 | 181053363 | |||||||
chr5:181053365 | C | T | 25 | a0001c0004t0005g0257 a0001c0004t0005g0258 a0001c0004t0005g0266 others(22): Show |
30 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.853+49C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 5/10 | chr5 | 181053365 | |||||||
chr5:181053421 | A | T | 3 | a0001c0008t0018g0141 a0001c0016t0009g0049 a0004c0017t0009g0048 |
5 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(2): Show |
intron_variant | MODIFIER | c.854-48A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 5/10 | chr5 | 181053421 | |||||||
chr5:181053682 | G | A | 1 | a0001c0006t0010g0127 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.886+181G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 6/10 | chr5 | 181053682 | |||||||
chr5:181053808 | T | C | 17 | a0001c0007t0007g0151 a0001c0007t0007g0175 a0001c0007t0007g0176 others(14): Show |
17 | HG00438.hp1 HG01891.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.886+307T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 6/10 | chr5 | 181053808 | |||||||
chr5:181053896 | G | A | 2 | a0001c0001t0001g0122 a0001c0001t0001g0150 |
2 | HG01952.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.887-343G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 6/10 | chr5 | 181053896 | |||||||
chr5:181054161 | C | T | 1 | a0001c0004t0005g0252 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.887-78C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 6/10 | chr5 | 181054161 | |||||||
chr5:181054191 | T | C | 1 | a0008c0023t0001g0213 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.887-48T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 6/10 | chr5 | 181054191 | |||||||
chr5:181054216 | C | CT | 14 | a0001c0001t0011g0244 a0001c0001t0011g0245 a0001c0006t0006g0009 others(11): Show |
17 | HG02451.hp1 HG02572.hp1 HG02622.hp2 others(14): Show |
splice_region_variant&intron_variant | LOW | c.887-7dupT | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 181054216 | ||||||
chr5:181054216 | CT | C | 17 | a0001c0001t0001g0157 a0001c0001t0001g0166 a0001c0001t0001g0187 others(14): Show |
22 | HG00140.hp1 HG00558.hp2 HG01070.hp1 others(19): Show |
splice_region_variant&intron_variant | LOW | c.887-7delT | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr5 | 181054216 | ||||||
chr5:181054297 | GC | G | 2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.907+40delC | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 181054297 | ||||||
chr5:181054345 | C | T | 5 | a0001c0001t0001g0203 a0001c0001t0001g0214 a0001c0001t0001g0220 others(2): Show |
5 | HG01361.hp2 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.907+86C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181054345 | |||||||
chr5:181054480 | T | C | 1 | a0002c0002t0002g0027 | 2 | HG01168.hp1 HG01515.hp2 |
intron_variant | MODIFIER | c.907+221T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181054480 | |||||||
chr5:181054574 | C | A | 1 | a0002c0003t0003g0104 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.907+315C>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181054574 | |||||||
chr5:181054626 | G | C | 8 | a0001c0007t0007g0151 a0001c0007t0007g0175 a0001c0007t0007g0176 others(5): Show |
8 | HG00438.hp1 HG03669.hp2 HG03927.hp2 others(5): Show |
intron_variant | MODIFIER | c.907+367G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181054626 | |||||||
chr5:181054629 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.907+370C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181054629 | |||||||
chr5:181054730 | G | C | 17 | a0001c0007t0007g0151 a0001c0007t0007g0175 a0001c0007t0007g0176 others(14): Show |
19 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.907+471G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181054730 | |||||||
chr5:181054749 | T | C | 2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.907+490T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181054749 | |||||||
chr5:181054823 | A | G | 1 | a0001c0004t0005g0258 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.907+564A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181054823 | |||||||
chr5:181054998 | T | G | 49 | a0001c0008t0001g0001 a0002c0002t0002g0001 a0002c0002t0002g0003 others(46): Show |
76 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.908-435T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181054998 | |||||||
chr5:181055033 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.908-400C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181055033 | |||||||
chr5:181055152 | C | G | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.908-281C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181055152 | |||||||
chr5:181055159 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.908-274G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181055159 | |||||||
chr5:181055190 | A | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.908-243A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181055190 | |||||||
chr5:181055191 | T | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.908-242T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181055191 | |||||||
chr5:181055193 | C | T | 1 | a0001c0001t0001g0219 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.908-240C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181055193 | |||||||
chr5:181055250 | G | A | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.908-183G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | chr5 | 181055250 | |||||||
chr5:181055303 | T | TA | 7 | a0001c0001t0001g0038 a0001c0001t0001g0158 a0001c0006t0006g0009 others(4): Show |
13 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.908-117dupA | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr5 | 181055303 | ||||||
chr5:181055495 | T | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.928+42T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055495 | |||||||
chr5:181055508 | A | G | 4 | a0001c0006t0010g0127 a0001c0006t0010g0128 a0001c0013t0002g0250 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+55A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055508 | |||||||
chr5:181055522 | T | A | 2 | a0002c0002t0013g0070 a0002c0002t0013g0071 |
2 | HG03098.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.928+69T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055522 | |||||||
chr5:181055541 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.928+88G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055541 | |||||||
chr5:181055626 | C | T | 2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.928+173C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055626 | |||||||
chr5:181055641 | T | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.928+188T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055641 | |||||||
chr5:181055682 | G | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.928+229G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055682 | |||||||
chr5:181055795 | A | T | 92 | a0001c0006t0006g0009 a0001c0006t0006g0063 a0001c0006t0006g0065 others(89): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.929-194A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055795 | |||||||
chr5:181055838 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.929-151C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055838 | |||||||
chr5:181055899 | C | T | 92 | a0001c0006t0006g0009 a0001c0006t0006g0063 a0001c0006t0006g0065 others(89): Show |
144 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(141): Show |
intron_variant | MODIFIER | c.929-90C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055899 | |||||||
chr5:181055942 | T | C | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.929-47T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 8/10 | chr5 | 181055942 | |||||||
chr5:181056044 | C | T | 2 | a0001c0013t0002g0250 a0001c0013t0002g0251 |
2 | HG02572.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.955+29C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056044 | |||||||
chr5:181056155 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.955+140G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056155 | |||||||
chr5:181056167 | C | G | 1 | a0001c0001t0021g0228 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.955+152C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056167 | |||||||
chr5:181056209 | A | T | 1 | a0001c0001t0021g0228 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.955+194A>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056209 | |||||||
chr5:181056222 | A | G | 5 | a0001c0004t0005g0053 a0001c0004t0005g0263 a0001c0004t0005g0264 others(2): Show |
7 | HG01261.hp2 HG02280.hp2 HG02602.hp1 others(4): Show |
intron_variant | MODIFIER | c.955+207A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056222 | |||||||
chr5:181056319 | A | G | 2 | a0001c0001t0001g0159 a0001c0008t0001g0135 |
2 | HG01243.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.955+304A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056319 | |||||||
chr5:181056441 | C | T | 7 | a0001c0001t0001g0012 a0001c0001t0001g0038 a0001c0001t0001g0158 others(4): Show |
11 | HG00673.hp1 HG02027.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.955+426C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056441 | |||||||
chr5:181056447 | T | G | 1 | a0001c0001t0001g0163 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.955+432T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056447 | |||||||
chr5:181056505 | G | C | 2 | a0001c0016t0009g0049 a0004c0017t0009g0048 |
4 | HG00733.hp2 HG01074.hp2 HG01361.hp1 others(1): Show |
intron_variant | MODIFIER | c.955+490G>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056505 | |||||||
chr5:181056598 | C | G | 1 | a0001c0001t0001g0236 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.955+583C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056598 | |||||||
chr5:181056689 | G | A | 1 | a0001c0014t0001g0260 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.955+674G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056689 | |||||||
chr5:181056744 | G | T | 1 | a0002c0002t0004g0089 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.955+729G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056744 | |||||||
chr5:181056973 | G | T | 42 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(39): Show |
48 | HG00438.hp1 HG00733.hp2 HG01074.hp2 others(45): Show |
intron_variant | MODIFIER | c.955+958G>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181056973 | |||||||
chr5:181057003 | T | A | 7 | a0001c0009t0008g0116 a0001c0009t0008g0118 a0001c0009t0008g0119 others(4): Show |
7 | HG01891.hp1 HG02451.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.955+988T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181057003 | |||||||
chr5:181057008 | C | CTG | 13 | a0001c0001t0001g0013 a0001c0001t0001g0146 a0001c0001t0001g0191 others(10): Show |
19 | HG00544.hp2 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.955+1028_955+1029d others(4): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 181057008 | ||||||
chr5:181057008 | C | T | 1 | a0002c0002t0002g0072 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.955+993C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181057008 | |||||||
chr5:181057008 | CTG | C | 87 | a0001c0001t0001g0012 a0001c0001t0001g0036 a0001c0001t0001g0038 others(84): Show |
122 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(119): Show |
intron_variant | MODIFIER | c.955+1028_955+1029d others(4): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 181057008 | ||||||
chr5:181057008 | CTGTG | C | 47 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0020 others(44): Show |
63 | HG00280.hp2 HG00639.hp2 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.955+1026_955+1029d others(6): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 181057008 | ||||||
chr5:181057008 | CTGTGTG | C | 13 | a0001c0001t0001g0163 a0001c0001t0001g0171 a0001c0007t0007g0175 others(10): Show |
15 | HG00438.hp1 HG00673.hp1 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.955+1024_955+1029d others(8): Show |
BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr5 | 181057008 | ||||||
chr5:181057043 | T | A | 1 | a0001c0001t0001g0216 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.955+1028T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181057043 | |||||||
chr5:181057056 | T | A | 3 | a0001c0001t0001g0044 a0001c0001t0001g0146 a0001c0001t0001g0210 |
4 | HG00544.hp2 HG00558.hp1 NA18963.hp2 others(1): Show |
intron_variant | MODIFIER | c.955+1041T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181057056 | |||||||
chr5:181057172 | T | C | 1 | a0001c0009t0008g0120 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.955+1157T>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181057172 | |||||||
chr5:181057438 | A | G | 1 | a0001c0001t0021g0228 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.956-914A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181057438 | |||||||
chr5:181057784 | G | A | 16 | a0001c0007t0007g0151 a0001c0007t0007g0175 a0001c0007t0007g0176 others(13): Show |
16 | HG00438.hp1 HG01891.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.956-568G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181057784 | |||||||
chr5:181057884 | A | C | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.956-468A>C | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181057884 | |||||||
chr5:181057990 | A | G | 3 | a0002c0002t0002g0061 a0002c0002t0002g0080 a0006c0026t0002g0062 |
3 | HG00597.hp2 NA19001.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.956-362A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 9/10 | chr5 | 181057990 | |||||||
chr5:181058597 | T | A | 1 | a0001c0008t0018g0141 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.982+219T>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/10 | chr5 | 181058597 | |||||||
chr5:181058720 | G | A | 142 | a0001c0004t0005g0050 a0001c0004t0005g0051 a0001c0004t0005g0052 others(139): Show |
208 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(205): Show |
intron_variant | MODIFIER | c.982+342G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/10 | chr5 | 181058720 | |||||||
chr5:181058814 | T | TA | 26 | a0001c0001t0001g0040 a0001c0001t0001g0045 a0001c0001t0001g0046 others(23): Show |
34 | HG00099.hp1 HG00140.hp2 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.983-405dupA | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 181058814 | ||||||
chr5:181058814 | TA | T | 39 | a0001c0001t0001g0163 a0001c0001t0001g0233 a0001c0004t0005g0050 others(36): Show |
43 | HG00438.hp1 HG01070.hp2 HG01106.hp2 others(40): Show |
intron_variant | MODIFIER | c.983-405delA | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr5 | 181058814 | ||||||
chr5:181058820 | A | G | 16 | a0001c0005t0004g0004 a0001c0005t0004g0031 a0001c0005t0004g0124 others(13): Show |
23 | HG00280.hp1 HG00544.hp1 HG00597.hp1 others(20): Show |
intron_variant | MODIFIER | c.983-417A>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/10 | chr5 | 181058820 | |||||||
chr5:181058949 | G | A | 113 | a0001c0005t0004g0004 a0001c0005t0004g0031 a0001c0005t0004g0124 others(110): Show |
172 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(169): Show |
intron_variant | MODIFIER | c.983-288G>A | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/10 | chr5 | 181058949 | |||||||
chr5:181059016 | C | G | 1 | a0002c0003t0003g0100 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.983-221C>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/10 | chr5 | 181059016 | |||||||
chr5:181059155 | C | T | 1 | a0001c0001t0001g0037 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.983-82C>T | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/10 | chr5 | 181059155 | |||||||
chr5:181059224 | T | G | 213 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0012 others(210): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(285): Show |
intron_variant | MODIFIER | c.983-13T>G | BTNL9 | ENSG00000165810.17 | transcript | ENST00000327705.14 | protein_coding | 10/10 | chr5 | 181059224 |