Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 79908 |
| ensemblid | ENSG00000113303.12 |
| hgncid | 26131 |
| symbol | BTNL8 |
| name | butyrophilin like 8 |
| refseq_nuc | NM_001040462.3 |
| refseq_prot | NP_001035552.1 |
| ensembl_nuc | ENST00000340184.9 |
| ensembl_prot | ENSP00000342197.4 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 180899159 |
| end | 180950906 |
| strand | + |
| ver | v1.2 |
| region | chr5:180899159-180950906 |
| region5000 | chr5:180894159-180955906 |
| regionname0 | BTNL8_chr5_180899159_180950906 |
| regionname5000 | BTNL8_chr5_180894159_180955906 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 500 | 78 | 15 | 19 | 27 | 4 | 11 | 18 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0002 | 0/0 | 500 | 43 | 25 | 4 | 9 | 1 | 4 | 5 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0003 | 0/0 | 500 | 28 | 5 | 1 | 14 | 0 | 8 | 9 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0004 | 0/0 | 500 | 17 | 0 | 5 | 4 | 1 | 7 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0005 | 0/0 | 500 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0006 | 0/0 | 500 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0007 | 0/0 | 500 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0008 | 0/0 | 500 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0009 | 0/0 | 500 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0010 | 0/0 | 500 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0011 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0012 | 0/0 | 500 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0013 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0014 | 0/0 | 500 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0015 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| a0016 | 0/0 | 500 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | MALML others(495): Show |
chr5 | 180894159 | 180955906 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1500 | 78 | 15 | 19 | 27 | 4 | 11 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0002c0002 | 0/0 | 1500 | 29 | 15 | 3 | 9 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0002c0005 | 0/0 | 1500 | 9 | 5 | 1 | 0 | 1 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0002c0007 | 0/0 | 1500 | 4 | 4 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0002c0024 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0003c0003 | 0/0 | 1500 | 21 | 2 | 1 | 14 | 0 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0003c0006 | 0/0 | 1500 | 7 | 3 | 0 | 0 | 0 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0004c0004 | 0/0 | 1500 | 15 | 0 | 5 | 4 | 1 | 5 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0004c0010 | 0/0 | 1500 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0005c0009 | 0/0 | 1500 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0005c0012 | 0/0 | 1500 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0005c0021 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0006c0013 | 0/0 | 1500 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0006c0017 | 0/0 | 1500 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0007c0008 | 0/0 | 1500 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0008c0019 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0008c0025 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0009c0018 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0009c0022 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0010c0011 | 0/0 | 1500 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0011c0026 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0012c0015 | 0/0 | 1500 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0013c0016 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0014c0020 | 0/0 | 1500 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0015c0023 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 | ||
| a0016c0014 | 0/0 | 1500 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | ATGGC others(1495): Show |
chr5 | 180894159 | 180955906 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 2017 | 77 | 15 | 19 | 27 | 4 | 10 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0001c0001t0002 | 0/0 | 2017 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0002c0002t0001 | 0/0 | 2017 | 29 | 15 | 3 | 9 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0002c0005t0001 | 0/0 | 2017 | 9 | 5 | 1 | 0 | 1 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0002c0007t0001 | 0/0 | 2017 | 4 | 4 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0002c0024t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0003c0003t0001 | 0/0 | 2017 | 21 | 2 | 1 | 14 | 0 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0003c0006t0001 | 0/0 | 2017 | 7 | 3 | 0 | 0 | 0 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0004c0004t0001 | 0/0 | 2017 | 14 | 0 | 5 | 4 | 1 | 4 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0004c0004t0002 | 0/0 | 2017 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0004c0010t0001 | 0/0 | 2017 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0005c0009t0001 | 0/0 | 2017 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0005c0012t0001 | 0/0 | 2017 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0005c0021t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0006c0013t0001 | 0/0 | 2017 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0006c0017t0001 | 0/0 | 2017 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0007c0008t0001 | 0/0 | 2017 | 3 | 3 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0008c0019t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0008c0025t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0009c0018t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0009c0022t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0010c0011t0001 | 0/0 | 2017 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0011c0026t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0012c0015t0001 | 0/0 | 2017 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0013c0016t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0014c0020t0001 | 0/0 | 2017 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0015c0023t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| a0016c0014t0001 | 0/0 | 2017 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | AGAAC others(2012): Show |
chr5 | 180894159 | 180955906 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0097 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0110 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0005t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0005t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0005t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0005t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0005t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0005t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0005t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0005t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0005t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0007t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0007t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0007t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0007t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0002c0024t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0006t0001g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0006t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0006t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0006t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0006t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0003c0006t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0001g0002 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0004t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0010t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0004c0010t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0005c0009t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0005c0009t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0005c0009t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0005c0012t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0005c0012t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0005c0021t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0006c0013t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0006c0013t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0006c0017t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0007c0008t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0007c0008t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0008c0019t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0008c0025t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0009c0018t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0009c0022t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0010c0011t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0011c0026t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0012c0015t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0013c0016t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0014c0020t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0015c0023t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| a0016c0014t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0004 | c0004 | t0001 | g0153 | EUR | GBR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | GBR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG00280 | hp1 | a0002 | c0005 | t0001 | g0138 | EUR | FIN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | FIN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG00438 | hp2 | a0003 | c0003 | t0001 | g0070 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG00544 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG00621 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01070 | hp2 | a0004 | c0004 | t0001 | g0002 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01071 | hp1 | a0004 | c0004 | t0001 | g0002 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01081 | hp2 | a0004 | c0004 | t0001 | g0002 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01167 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01169 | hp1 | a0004 | c0004 | t0001 | g0152 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01192 | hp1 | a0002 | c0005 | t0001 | g0135 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01243 | hp2 | a0006 | c0017 | t0001 | g0052 | AMR | PUR | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0068 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01884 | hp1 | a0003 | c0003 | t0001 | g0073 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01884 | hp2 | a0005 | c0021 | t0001 | g0029 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01952 | hp2 | a0002 | c0002 | t0001 | g0025 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02027 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02071 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02132 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02132 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | KHV | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02145 | hp1 | a0003 | c0003 | t0001 | g0072 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0051 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | CDX | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02155 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | CDX | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02257 | hp2 | a0002 | c0024 | t0001 | g0062 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02280 | hp1 | a0008 | c0019 | t0001 | g0046 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02451 | hp1 | a0002 | c0005 | t0001 | g0141 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02451 | hp2 | a0002 | c0005 | t0001 | g0060 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02572 | hp2 | a0003 | c0006 | t0001 | g0146 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02602 | hp1 | a0003 | c0003 | t0001 | g0067 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02615 | hp1 | a0005 | c0012 | t0001 | g0039 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02615 | hp2 | a0009 | c0018 | t0001 | g0047 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02622 | hp1 | a0003 | c0006 | t0001 | g0147 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02622 | hp2 | a0005 | c0009 | t0001 | g0035 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02630 | hp1 | a0005 | c0009 | t0001 | g0034 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02698 | hp1 | a0002 | c0005 | t0001 | g0137 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02698 | hp2 | a0003 | c0006 | t0001 | g0021 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02717 | hp2 | a0007 | c0008 | t0001 | g0142 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02723 | hp1 | a0007 | c0008 | t0001 | g0011 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02723 | hp2 | a0002 | c0007 | t0001 | g0042 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02735 | hp1 | a0002 | c0005 | t0001 | g0136 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0093 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02809 | hp1 | a0007 | c0008 | t0001 | g0011 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02809 | hp2 | a0008 | c0025 | t0001 | g0045 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02886 | hp2 | a0003 | c0006 | t0001 | g0145 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02895 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02897 | hp2 | a0002 | c0002 | t0001 | g0057 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02922 | hp1 | a0006 | c0013 | t0001 | g0043 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02922 | hp2 | a0011 | c0026 | t0001 | g0076 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02965 | hp1 | a0002 | c0002 | t0001 | g0049 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02970 | hp1 | a0005 | c0009 | t0001 | g0036 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02970 | hp2 | a0002 | c0005 | t0001 | g0058 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0027 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03017 | hp1 | a0012 | c0015 | t0001 | g0002 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03041 | hp1 | a0013 | c0016 | t0001 | g0064 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03041 | hp2 | a0002 | c0002 | t0001 | g0024 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03130 | hp1 | a0002 | c0007 | t0001 | g0055 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03130 | hp2 | a0002 | c0002 | t0001 | g0056 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03139 | hp1 | a0009 | c0022 | t0001 | g0053 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03139 | hp2 | a0005 | c0012 | t0001 | g0041 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03195 | hp1 | a0002 | c0007 | t0001 | g0044 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03195 | hp2 | a0002 | c0002 | t0001 | g0007 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03209 | hp1 | a0002 | c0005 | t0001 | g0085 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03209 | hp2 | a0002 | c0007 | t0001 | g0040 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0007 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03225 | hp2 | a0002 | c0002 | t0001 | g0028 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03239 | hp1 | a0003 | c0006 | t0001 | g0021 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03490 | hp1 | a0003 | c0006 | t0001 | g0156 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03490 | hp2 | a0004 | c0004 | t0001 | g0148 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03492 | hp1 | a0003 | c0006 | t0001 | g0149 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03492 | hp2 | a0004 | c0004 | t0001 | g0155 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03516 | hp2 | a0002 | c0002 | t0001 | g0050 | AFR | ESN | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03540 | hp2 | a0002 | c0005 | t0001 | g0061 | AFR | GWD | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03579 | hp1 | a0006 | c0013 | t0001 | g0037 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03579 | hp2 | a0002 | c0002 | t0001 | g0054 | AFR | MSL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03669 | hp1 | a0004 | c0004 | t0002 | g0150 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03688 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03688 | hp2 | a0003 | c0003 | t0001 | g0012 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03831 | hp1 | a0004 | c0004 | t0001 | g0157 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03927 | hp1 | a0004 | c0004 | t0001 | g0154 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG03927 | hp2 | a0014 | c0020 | t0001 | g0124 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG04115 | hp1 | a0002 | c0002 | t0001 | g0008 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG04115 | hp2 | a0003 | c0003 | t0001 | g0012 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG04184 | hp1 | a0004 | c0010 | t0001 | g0120 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG04184 | hp2 | a0003 | c0003 | t0001 | g0069 | SAS | BEB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG04199 | hp2 | a0004 | c0010 | t0001 | g0119 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0063 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | STU | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18522 | hp1 | a0002 | c0002 | t0001 | g0048 | AFR | YRI | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18522 | hp2 | a0015 | c0023 | t0001 | g0038 | AFR | YRI | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18952 | hp2 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18964 | hp2 | a0010 | c0011 | t0001 | g0014 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18966 | hp1 | a0002 | c0002 | t0001 | g0032 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18980 | hp1 | a0003 | c0003 | t0001 | g0130 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18980 | hp2 | a0004 | c0004 | t0001 | g0143 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18984 | hp1 | a0003 | c0003 | t0001 | g0001 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA18986 | hp2 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19002 | hp1 | a0004 | c0004 | t0001 | g0151 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19010 | hp1 | a0003 | c0003 | t0001 | g0071 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | LWK | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19043 | hp2 | a0016 | c0014 | t0001 | g0144 | AFR | LWK | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19054 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0003 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19063 | hp2 | a0010 | c0011 | t0001 | g0014 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19064 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19065 | hp1 | a0003 | c0003 | t0001 | g0006 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19072 | hp1 | a0003 | c0003 | t0001 | g0140 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19072 | hp2 | a0002 | c0002 | t0001 | g0031 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19082 | hp2 | a0003 | c0003 | t0001 | g0139 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19086 | hp1 | a0004 | c0004 | t0001 | g0022 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0082 | EUR | TSI | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | TSI | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01123 | hp1 | a0004 | c0004 | t0001 | g0002 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0110 | REF | REF | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0097 | REF | REF | BTNL8_chr5_180894159_180955906 | BTNL8 | chr5 | 180894159 | 180955906 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180908846 | A | G | 1 | a0014 | 1 | HG03927.hp2 | missense_variant | MODERATE | c.310A>G | p.Ile104Val | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/8 | 462/2017 | 310/1503 | 104/500 | chr5 | 180908846 | |||
| chr5:180911368 | A | G | 8 | a0002 a0005 a0006 others(5): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
missense_variant | MODERATE | c.427A>G | p.Thr143Ala | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/8 | 579/2017 | 427/1503 | 143/500 | chr5 | 180911368 | |||
| chr5:180911566 | C | T | 1 | a0013 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.625C>T | p.Arg209Trp | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/8 | 777/2017 | 625/1503 | 209/500 | chr5 | 180911566 | |||
| chr5:180947523 | G | A | 5 | a0002 a0005 a0006 others(2): Show |
55 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(52): Show |
missense_variant | MODERATE | c.685G>A | p.Glu229Lys | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/8 | 837/2017 | 685/1503 | 229/500 | chr5 | 180947523 | |||
| chr5:180949972 | C | G | 6 | a0002 a0004 a0008 others(3): Show |
66 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(63): Show |
missense_variant | MODERATE | c.931C>G | p.His311Asp | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1083/2017 | 931/1503 | 311/500 | chr5 | 180949972 | |||
| chr5:180949974 | T | G | 6 | a0002 a0004 a0008 others(3): Show |
66 | HG00140.hp1 HG00280.hp1 HG00544.hp2 others(63): Show |
missense_variant | MODERATE | c.933T>G | p.His311Gln | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1085/2017 | 933/1503 | 311/500 | chr5 | 180949974 | |||
| chr5:180950018 | C | A | 6 | a0003 a0004 a0005 others(3): Show |
56 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(53): Show |
missense_variant | MODERATE | c.977C>A | p.Thr326Lys | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1129/2017 | 977/1503 | 326/500 | chr5 | 180950018 | |||
| chr5:180950407 | C | T | 1 | a0012 | 1 | HG03017.hp1 | missense_variant | MODERATE | c.1366C>T | p.Pro456Ser | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1518/2017 | 1366/1503 | 456/500 | chr5 | 180950407 | |||
| chr5:180950470 | G | A | 5 | a0002 a0006 a0008 others(2): Show |
50 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(47): Show |
missense_variant | MODERATE | c.1429G>A | p.Ala477Thr | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1581/2017 | 1429/1503 | 477/500 | chr5 | 180950470 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180908671 | G | A | 4 | a0003c0006 a0004c0004 a0012c0015 others(1): Show |
24 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
synonymous_variant | LOW | c.135G>A | p.Lys45Lys | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/8 | 287/2017 | 135/1503 | 45/500 | chr5 | 180908671 | |||
| chr5:180908743 | C | T | 11 | a0002c0002 a0002c0007 a0002c0024 others(8): Show |
46 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(43): Show |
synonymous_variant | LOW | c.207C>T | p.Asp69Asp | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/8 | 359/2017 | 207/1503 | 69/500 | chr5 | 180908743 | |||
| chr5:180947534 | G | A | 14 | a0002c0002 a0002c0005 a0002c0007 others(11): Show |
57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
synonymous_variant | LOW | c.696G>A | p.Ser232Ser | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/8 | 848/2017 | 696/1503 | 232/500 | chr5 | 180947534 | |||
| chr5:180949249 | C | T | 4 | a0002c0007 a0005c0009 a0005c0012 others(1): Show |
11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
synonymous_variant | LOW | c.846C>T | p.Asp282Asp | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/8 | 998/2017 | 846/1503 | 282/500 | chr5 | 180949249 | |||
| chr5:180949261 | C | T | 1 | a0002c0024 | 1 | HG02257.hp2 | synonymous_variant | LOW | c.858C>T | p.His286His | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/8 | 1010/2017 | 858/1503 | 286/500 | chr5 | 180949261 | |||
| chr5:180950331 | T | C | 12 | a0002c0002 a0002c0005 a0002c0007 others(9): Show |
54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
synonymous_variant | LOW | c.1290T>C | p.Tyr430Tyr | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 8/8 | 1442/2017 | 1290/1503 | 430/500 | chr5 | 180950331 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180899274 | G | A | 2 | a0001c0001t0002 a0004c0004t0002 |
2 | HG03669.hp1 HG04204.hp2 |
5_prime_UTR_variant | MODIFIER | c.-37G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/8 | 37 | chr5 | 180899274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:180899502 | C | T | 19 | a0003c0006t0001g0021 a0003c0006t0001g0145 a0003c0006t0001g0146 others(16): Show |
24 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.49+143C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899502 | |||||||
| chr5:180899510 | A | G | 1 | a0007c0008t0001g0142 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.49+151A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899510 | |||||||
| chr5:180899568 | C | T | 1 | a0002c0005t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.49+209C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899568 | |||||||
| chr5:180899569 | G | A | 1 | a0002c0002t0001g0023 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.49+210G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899569 | |||||||
| chr5:180899571 | T | A | 67 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(64): Show |
79 | HG00140.hp1 HG00544.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.49+212T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899571 | |||||||
| chr5:180899590 | G | A | 3 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 |
3 | HG01243.hp1 HG01952.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.49+231G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899590 | |||||||
| chr5:180899617 | C | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+258C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899617 | |||||||
| chr5:180899961 | T | C | 1 | a0001c0001t0002g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.49+602T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180899961 | |||||||
| chr5:180900021 | A | G | 3 | a0003c0003t0001g0006 a0003c0003t0001g0139 a0003c0003t0001g0140 |
5 | NA19054.hp1 NA19064.hp1 NA19065.hp1 others(2): Show |
intron_variant | MODIFIER | c.49+662A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900021 | |||||||
| chr5:180900152 | G | A | 25 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(22): Show |
31 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(28): Show |
intron_variant | MODIFIER | c.49+793G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900152 | |||||||
| chr5:180900158 | G | A | 19 | a0003c0006t0001g0021 a0003c0006t0001g0145 a0003c0006t0001g0146 others(16): Show |
24 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.49+799G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900158 | |||||||
| chr5:180900188 | G | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.49+829G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900188 | |||||||
| chr5:180900428 | G | A | 1 | a0004c0004t0001g0143 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.49+1069G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900428 | |||||||
| chr5:180900543 | G | A | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.49+1184G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900543 | |||||||
| chr5:180900780 | C | T | 12 | a0002c0007t0001g0040 a0002c0007t0001g0042 a0002c0007t0001g0044 others(9): Show |
12 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.49+1421C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900780 | |||||||
| chr5:180900855 | A | G | 2 | a0002c0002t0001g0010 a0002c0002t0001g0033 |
3 | HG01167.hp1 HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.49+1496A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900855 | |||||||
| chr5:180900892 | G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+1533G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180900892 | |||||||
| chr5:180901001 | G | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+1642G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901001 | |||||||
| chr5:180901003 | A | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+1644A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901003 | |||||||
| chr5:180901071 | G | A | 1 | a0007c0008t0001g0142 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.49+1712G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901071 | |||||||
| chr5:180901103 | A | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+1744A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901103 | |||||||
| chr5:180901133 | T | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+1774T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901133 | |||||||
| chr5:180901331 | A | G | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.49+1972A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901331 | |||||||
| chr5:180901493 | A | T | 19 | a0003c0006t0001g0021 a0003c0006t0001g0145 a0003c0006t0001g0146 others(16): Show |
24 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.49+2134A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901493 | |||||||
| chr5:180901623 | G | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+2264G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901623 | |||||||
| chr5:180901742 | T | A | 1 | a0013c0016t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.49+2383T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901742 | |||||||
| chr5:180901743 | T | A | 1 | a0013c0016t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.49+2384T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901743 | |||||||
| chr5:180901809 | A | G | 12 | a0003c0006t0001g0156 a0004c0004t0001g0002 a0004c0004t0001g0022 others(9): Show |
16 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+2450A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180901809 | |||||||
| chr5:180902023 | A | G | 1 | a0002c0005t0001g0061 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.49+2664A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902023 | |||||||
| chr5:180902035 | T | C | 2 | a0001c0001t0001g0065 a0001c0001t0001g0066 |
2 | HG03669.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.49+2676T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902035 | |||||||
| chr5:180902041 | T | TAAA | 2 | a0007c0008t0001g0011 a0007c0008t0001g0142 |
3 | HG02717.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.49+2684_49+2686dup others(3): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180902041 | ||||||
| chr5:180902187 | GT | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+2838delT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180902187 | ||||||
| chr5:180902188 | T | G | 37 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0074 others(34): Show |
50 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.49+2829T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902188 | |||||||
| chr5:180902189 | T | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+2830T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902189 | |||||||
| chr5:180902359 | T | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3000T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902359 | |||||||
| chr5:180902448 | G | T | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+3089G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902448 | |||||||
| chr5:180902452 | G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+3093G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902452 | |||||||
| chr5:180902458 | C | G | 15 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.49+3099C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902458 | |||||||
| chr5:180902517 | GT | G | 67 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0074 others(64): Show |
87 | HG00140.hp1 HG00438.hp2 HG00544.hp2 others(84): Show |
intron_variant | MODIFIER | c.49+3169delT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180902517 | ||||||
| chr5:180902536 | C | T | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3177C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902536 | |||||||
| chr5:180902673 | C | T | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3314C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902673 | |||||||
| chr5:180902678 | C | T | 2 | a0002c0005t0001g0060 a0002c0005t0001g0061 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.49+3319C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902678 | |||||||
| chr5:180902682 | T | C | 67 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(64): Show |
79 | HG00140.hp1 HG00544.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.49+3323T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902682 | |||||||
| chr5:180902698 | C | A | 1 | a0006c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.49+3339C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902698 | |||||||
| chr5:180902770 | C | T | 1 | a0002c0007t0001g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.49+3411C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902770 | |||||||
| chr5:180902771 | G | A | 12 | a0003c0006t0001g0156 a0004c0004t0001g0002 a0004c0004t0001g0022 others(9): Show |
16 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.49+3412G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902771 | |||||||
| chr5:180902847 | C | T | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.49+3488C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902847 | |||||||
| chr5:180902848 | A | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3489A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902848 | |||||||
| chr5:180902898 | T | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3539T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902898 | |||||||
| chr5:180902940 | T | C | 1 | a0002c0002t0001g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.49+3581T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902940 | |||||||
| chr5:180902969 | G | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3610G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902969 | |||||||
| chr5:180902973 | C | T | 11 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(8): Show |
11 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(8): Show |
intron_variant | MODIFIER | c.49+3614C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180902973 | |||||||
| chr5:180903081 | T | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3722T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903081 | |||||||
| chr5:180903168 | A | AC | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3809_49+3810ins others(1): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903168 | |||||||
| chr5:180903284 | A | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+3925A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903284 | |||||||
| chr5:180903448 | C | T | 1 | a0002c0005t0001g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.49+4089C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903448 | |||||||
| chr5:180903571 | T | C | 4 | a0002c0005t0001g0060 a0002c0005t0001g0061 a0002c0005t0001g0141 others(1): Show |
4 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.49+4212T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903571 | |||||||
| chr5:180903604 | C | T | 5 | a0001c0001t0001g0020 a0002c0005t0001g0135 a0002c0005t0001g0136 others(2): Show |
6 | HG00280.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.49+4245C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903604 | |||||||
| chr5:180903694 | T | A | 1 | a0002c0007t0001g0044 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.49+4335T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903694 | |||||||
| chr5:180903707 | T | C | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.49+4348T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903707 | |||||||
| chr5:180903789 | C | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+4430C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903789 | |||||||
| chr5:180903790 | C | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+4431C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903790 | |||||||
| chr5:180903791 | C | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.49+4432C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903791 | |||||||
| chr5:180903840 | T | C | 2 | a0002c0005t0001g0141 a0006c0017t0001g0052 |
2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.49+4481T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903840 | |||||||
| chr5:180903846 | G | A | 1 | a0001c0001t0001g0077 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.49+4487G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180903846 | |||||||
| chr5:180904006 | A | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-4580A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904006 | |||||||
| chr5:180904042 | T | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-4544T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904042 | |||||||
| chr5:180904116 | G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-4470G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904116 | |||||||
| chr5:180904256 | T | G | 15 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(12): Show |
15 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.50-4330T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904256 | |||||||
| chr5:180904349 | C | T | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-4237C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904349 | |||||||
| chr5:180904580 | G | C | 47 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.50-4006G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904580 | |||||||
| chr5:180904584 | G | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-4002G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904584 | |||||||
| chr5:180904670 | G | C | 47 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.50-3916G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904670 | |||||||
| chr5:180904673 | A | G | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.50-3913A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904673 | |||||||
| chr5:180904694 | C | T | 7 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0009 others(4): Show |
11 | HG00544.hp2 HG02027.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.50-3892C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904694 | |||||||
| chr5:180904697 | C | G | 5 | a0001c0001t0001g0020 a0002c0005t0001g0135 a0002c0005t0001g0136 others(2): Show |
6 | HG00280.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-3889C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904697 | |||||||
| chr5:180904808 | G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-3778G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904808 | |||||||
| chr5:180904850 | C | G | 1 | a0001c0001t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.50-3736C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904850 | |||||||
| chr5:180904953 | T | C | 1 | a0002c0002t0001g0007 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.50-3633T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180904953 | |||||||
| chr5:180905011 | G | C | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.50-3575G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905011 | |||||||
| chr5:180905033 | A | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3553A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905033 | |||||||
| chr5:180905102 | T | C | 2 | a0002c0005t0001g0141 a0006c0017t0001g0052 |
2 | HG01243.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.50-3484T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905102 | |||||||
| chr5:180905135 | G | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3451G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905135 | |||||||
| chr5:180905170 | T | C | 3 | a0001c0001t0001g0013 a0001c0001t0001g0078 a0001c0001t0001g0079 |
4 | HG01167.hp2 HG01169.hp2 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.50-3416T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905170 | |||||||
| chr5:180905218 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.50-3368G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905218 | |||||||
| chr5:180905233 | C | G | 1 | a0001c0001t0001g0133 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.50-3353C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905233 | |||||||
| chr5:180905259 | G | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3327G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905259 | |||||||
| chr5:180905362 | C | T | 32 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(29): Show |
39 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-3224C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905362 | |||||||
| chr5:180905396 | A | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3190A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905396 | |||||||
| chr5:180905411 | C | T | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3175C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905411 | |||||||
| chr5:180905413 | C | G | 1 | a0002c0002t0001g0059 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.50-3173C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905413 | |||||||
| chr5:180905441 | C | T | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-3145C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905441 | |||||||
| chr5:180905520 | A | C | 2 | a0003c0006t0001g0149 a0004c0004t0001g0148 |
2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.50-3066A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905520 | |||||||
| chr5:180905938 | T | TC | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2646dupC | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180905938 | ||||||
| chr5:180905959 | T | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2627T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180905959 | |||||||
| chr5:180906007 | C | T | 32 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(29): Show |
39 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-2579C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906007 | |||||||
| chr5:180906008 | G | A | 14 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(11): Show |
14 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.50-2578G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906008 | |||||||
| chr5:180906094 | G | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2492G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906094 | |||||||
| chr5:180906102 | A | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2484A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906102 | |||||||
| chr5:180906307 | G | T | 12 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(9): Show |
18 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.50-2279G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906307 | |||||||
| chr5:180906325 | T | C | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.50-2261T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906325 | |||||||
| chr5:180906332 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.50-2254C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906332 | |||||||
| chr5:180906346 | C | T | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2240C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906346 | |||||||
| chr5:180906415 | C | T | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2171C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906415 | |||||||
| chr5:180906424 | G | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-2162G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906424 | |||||||
| chr5:180906446 | A | G | 1 | a0003c0006t0001g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.50-2140A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906446 | |||||||
| chr5:180906528 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.50-2058C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906528 | |||||||
| chr5:180906614 | C | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1972C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906614 | |||||||
| chr5:180906704 | G | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-1882G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906704 | |||||||
| chr5:180906707 | A | G | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.50-1879A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906707 | |||||||
| chr5:180906712 | G | C | 1 | a0006c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.50-1874G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906712 | |||||||
| chr5:180906757 | T | G | 49 | a0001c0001t0001g0081 a0002c0002t0001g0003 a0002c0002t0001g0007 others(46): Show |
56 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(53): Show |
intron_variant | MODIFIER | c.50-1829T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906757 | |||||||
| chr5:180906805 | G | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1781G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906805 | |||||||
| chr5:180906882 | C | T | 18 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0074 others(15): Show |
26 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.50-1704C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906882 | |||||||
| chr5:180906929 | G | A | 1 | a0010c0011t0001g0014 | 2 | NA18964.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.50-1657G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906929 | |||||||
| chr5:180906992 | T | C | 1 | a0002c0002t0001g0023 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.50-1594T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180906992 | |||||||
| chr5:180907036 | G | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1550G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907036 | |||||||
| chr5:180907061 | C | T | 12 | a0003c0006t0001g0156 a0004c0004t0001g0002 a0004c0004t0001g0022 others(9): Show |
16 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.50-1525C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907061 | |||||||
| chr5:180907066 | T | G | 67 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(64): Show |
79 | HG00140.hp1 HG00544.hp2 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.50-1520T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907066 | |||||||
| chr5:180907106 | A | C | 1 | a0001c0001t0001g0066 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.50-1480A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907106 | |||||||
| chr5:180907238 | T | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1348T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907238 | |||||||
| chr5:180907253 | C | T | 18 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0074 others(15): Show |
26 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(23): Show |
intron_variant | MODIFIER | c.50-1333C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907253 | |||||||
| chr5:180907315 | C | T | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1271C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907315 | |||||||
| chr5:180907351 | T | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-1235T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907351 | |||||||
| chr5:180907404 | T | C | 32 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(29): Show |
39 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(36): Show |
intron_variant | MODIFIER | c.50-1182T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907404 | |||||||
| chr5:180907427 | A | AT | 14 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(11): Show |
14 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.50-1151dupT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180907427 | ||||||
| chr5:180907661 | C | T | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-925C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907661 | |||||||
| chr5:180907700 | T | C | 1 | a0006c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.50-886T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907700 | |||||||
| chr5:180907722 | T | TGTTA | 2 | a0003c0003t0001g0067 a0003c0003t0001g0068 |
2 | HG01261.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.50-861_50-860insAG others(2): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180907722 | ||||||
| chr5:180907740 | G | C | 1 | a0003c0003t0001g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.50-846G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907740 | |||||||
| chr5:180907748 | T | G | 1 | a0001c0001t0001g0082 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.50-838T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907748 | |||||||
| chr5:180907760 | C | G | 1 | a0003c0006t0001g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.50-826C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907760 | |||||||
| chr5:180907768 | G | A | 1 | a0003c0003t0001g0067 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.50-818G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907768 | |||||||
| chr5:180907777 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.50-809C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907777 | |||||||
| chr5:180907787 | G | A | 15 | a0001c0001t0001g0013 a0002c0002t0001g0024 a0002c0002t0001g0025 others(12): Show |
16 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.50-799G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907787 | |||||||
| chr5:180907790 | A | G | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.50-796A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907790 | |||||||
| chr5:180907797 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.50-789C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907797 | |||||||
| chr5:180907831 | G | A | 2 | a0001c0001t0001g0015 a0003c0006t0001g0147 |
3 | HG02109.hp1 HG02622.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.50-755G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907831 | |||||||
| chr5:180907847 | G | T | 1 | a0003c0006t0001g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.50-739G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907847 | |||||||
| chr5:180907851 | T | A | 1 | a0003c0006t0001g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.50-735T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907851 | |||||||
| chr5:180907851 | T | C | 57 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0129 others(54): Show |
66 | HG00280.hp1 HG00544.hp2 HG01109.hp1 others(63): Show |
intron_variant | MODIFIER | c.50-735T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907851 | |||||||
| chr5:180907859 | G | A | 1 | a0001c0001t0001g0015 | 2 | HG02109.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.50-727G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907859 | |||||||
| chr5:180907873 | A | C | 3 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0128 |
3 | HG02040.hp2 HG04199.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.50-713A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907873 | |||||||
| chr5:180907873 | A | G | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-713A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180907873 | |||||||
| chr5:180908041 | C | T | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.50-545C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908041 | |||||||
| chr5:180908063 | T | G | 38 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0009 others(35): Show |
43 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.50-523T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908063 | |||||||
| chr5:180908091 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.50-495C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908091 | |||||||
| chr5:180908096 | G | A | 1 | a0002c0002t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.50-490G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908096 | |||||||
| chr5:180908118 | T | C | 1 | a0001c0001t0001g0125 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.50-468T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908118 | |||||||
| chr5:180908185 | T | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-401T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908185 | |||||||
| chr5:180908196 | T | C | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-390T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908196 | |||||||
| chr5:180908280 | G | GC | 5 | a0001c0001t0001g0020 a0002c0005t0001g0135 a0002c0005t0001g0136 others(2): Show |
6 | HG00280.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-305dupC | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr5 | 180908280 | ||||||
| chr5:180908285 | C | T | 5 | a0001c0001t0001g0020 a0002c0005t0001g0135 a0002c0005t0001g0136 others(2): Show |
6 | HG00280.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-301C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908285 | |||||||
| chr5:180908289 | A | G | 5 | a0001c0001t0001g0020 a0002c0005t0001g0135 a0002c0005t0001g0136 others(2): Show |
6 | HG00280.hp1 HG01109.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.50-297A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908289 | |||||||
| chr5:180908376 | C | T | 1 | a0002c0002t0001g0032 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.50-210C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908376 | |||||||
| chr5:180908382 | G | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-204G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908382 | |||||||
| chr5:180908384 | G | A | 48 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(45): Show |
55 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(52): Show |
intron_variant | MODIFIER | c.50-202G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 1/7 | chr5 | 180908384 | |||||||
| chr5:180909022 | T | TCTTTATT others(4): Show |
1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397+89_397+90insCT others(9): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909022 | |||||||
| chr5:180909024 | G | T | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397+91G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909024 | |||||||
| chr5:180909025 | G | T | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397+92G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909025 | |||||||
| chr5:180909027 | C | T | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397+94C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909027 | |||||||
| chr5:180909028 | A | C | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.397+95A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909028 | |||||||
| chr5:180909080 | A | G | 1 | a0004c0004t0001g0157 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.397+147A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909080 | |||||||
| chr5:180909276 | C | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.397+343C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909276 | |||||||
| chr5:180909434 | C | A | 1 | a0001c0001t0001g0083 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.397+501C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909434 | |||||||
| chr5:180909581 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.397+648T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909581 | |||||||
| chr5:180909678 | G | C | 17 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0074 others(14): Show |
25 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(22): Show |
intron_variant | MODIFIER | c.397+745G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909678 | |||||||
| chr5:180909716 | T | TA | 26 | a0001c0001t0001g0016 a0001c0001t0001g0065 a0001c0001t0001g0066 others(23): Show |
35 | HG00438.hp2 HG00621.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.397+799dupA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 180909716 | ||||||
| chr5:180909716 | T | TAA | 6 | a0002c0002t0001g0033 a0002c0002t0001g0057 a0006c0013t0001g0043 others(3): Show |
7 | HG01167.hp1 HG02280.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.397+798_397+799dup others(2): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 180909716 | ||||||
| chr5:180909716 | T | TAAA | 31 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(28): Show |
37 | HG00544.hp2 HG01243.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.397+797_397+799dup others(3): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr5 | 180909716 | ||||||
| chr5:180909770 | A | G | 1 | a0003c0003t0001g0071 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.397+837A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909770 | |||||||
| chr5:180909781 | C | T | 1 | a0002c0007t0001g0042 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.397+848C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909781 | |||||||
| chr5:180909782 | G | A | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.397+849G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909782 | |||||||
| chr5:180909849 | C | T | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.397+916C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180909849 | |||||||
| chr5:180910369 | C | T | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.398-970C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910369 | |||||||
| chr5:180910401 | C | T | 1 | a0014c0020t0001g0124 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.398-938C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910401 | |||||||
| chr5:180910541 | A | G | 54 | a0001c0001t0001g0079 a0002c0002t0001g0003 a0002c0002t0001g0007 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.398-798A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910541 | |||||||
| chr5:180910543 | A | G | 48 | a0001c0001t0001g0079 a0002c0002t0001g0003 a0002c0002t0001g0007 others(45): Show |
55 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.398-796A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910543 | |||||||
| chr5:180910634 | A | T | 1 | a0002c0002t0001g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.398-705A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910634 | |||||||
| chr5:180910753 | C | G | 1 | a0001c0001t0001g0123 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.398-586C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180910753 | |||||||
| chr5:180911212 | G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.398-127G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180911212 | |||||||
| chr5:180911300 | G | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.398-39G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180911300 | |||||||
| chr5:180911318 | C | T | 1 | a0001c0001t0001g0122 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.398-21C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 2/7 | chr5 | 180911318 | |||||||
| chr5:180911743 | A | C | 5 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0050 others(2): Show |
5 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+129A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180911743 | |||||||
| chr5:180911754 | G | A | 41 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(38): Show |
48 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.673+140G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180911754 | |||||||
| chr5:180911952 | A | C | 1 | a0002c0005t0001g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.673+338A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180911952 | |||||||
| chr5:180911980 | G | T | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+366G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180911980 | |||||||
| chr5:180912213 | C | T | 36 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(33): Show |
43 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.673+599C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912213 | |||||||
| chr5:180912293 | C | T | 1 | a0003c0003t0001g0139 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.673+679C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912293 | |||||||
| chr5:180912415 | A | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.673+801A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912415 | |||||||
| chr5:180912427 | G | GTA | 14 | a0001c0001t0001g0074 a0003c0003t0001g0001 a0003c0003t0001g0006 others(11): Show |
22 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(19): Show |
intron_variant | MODIFIER | c.673+829_673+830dup others(2): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180912427 | ||||||
| chr5:180912427 | GTATATA | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+825_673+830del others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180912427 | ||||||
| chr5:180912830 | G | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+1216G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912830 | |||||||
| chr5:180912912 | C | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+1298C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912912 | |||||||
| chr5:180912939 | G | T | 1 | a0002c0002t0001g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.673+1325G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180912939 | |||||||
| chr5:180913020 | C | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+1406C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913020 | |||||||
| chr5:180913362 | G | A | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+1748G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913362 | |||||||
| chr5:180913378 | T | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+1764T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913378 | |||||||
| chr5:180913503 | A | G | 1 | a0001c0001t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.673+1889A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913503 | |||||||
| chr5:180913541 | T | A | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+1927T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913541 | |||||||
| chr5:180913569 | G | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+1955G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913569 | |||||||
| chr5:180913652 | C | A | 2 | a0001c0001t0001g0004 a0001c0001t0001g0086 |
4 | HG01109.hp2 HG01123.hp2 HG01258.hp1 others(1): Show |
intron_variant | MODIFIER | c.673+2038C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913652 | |||||||
| chr5:180913705 | G | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+2091G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913705 | |||||||
| chr5:180913721 | G | A | 5 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0050 others(2): Show |
5 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+2107G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180913721 | |||||||
| chr5:180914080 | G | A | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+2466G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180914080 | |||||||
| chr5:180914119 | C | T | 47 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.673+2505C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180914119 | |||||||
| chr5:180914751 | A | T | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+3137A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180914751 | |||||||
| chr5:180914845 | G | A | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+3231G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180914845 | |||||||
| chr5:180914895 | C | T | 21 | a0003c0006t0001g0021 a0003c0006t0001g0145 a0003c0006t0001g0146 others(18): Show |
26 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.673+3281C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180914895 | |||||||
| chr5:180915059 | A | T | 3 | a0003c0006t0001g0021 a0003c0006t0001g0149 a0004c0004t0001g0148 |
4 | HG02698.hp2 HG03239.hp1 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+3445A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915059 | |||||||
| chr5:180915085 | G | A | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+3471G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915085 | |||||||
| chr5:180915243 | T | G | 1 | a0003c0003t0001g0071 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.673+3629T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915243 | |||||||
| chr5:180915278 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.673+3664G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915278 | |||||||
| chr5:180915398 | G | C | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+3784G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915398 | |||||||
| chr5:180915506 | G | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+3892G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915506 | |||||||
| chr5:180915568 | G | C | 1 | a0002c0005t0001g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.673+3954G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915568 | |||||||
| chr5:180915600 | A | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+3986A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915600 | |||||||
| chr5:180915620 | A | G | 90 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0002c0002t0001g0003 others(87): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.673+4006A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915620 | |||||||
| chr5:180915626 | G | A | 5 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+4012G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915626 | |||||||
| chr5:180915700 | A | G | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0003c0003t0001g0001 others(12): Show |
23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.673+4086A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915700 | |||||||
| chr5:180915707 | C | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+4093C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915707 | |||||||
| chr5:180915806 | G | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+4192G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915806 | |||||||
| chr5:180915859 | C | T | 46 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(43): Show |
53 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.673+4245C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915859 | |||||||
| chr5:180915889 | C | A | 1 | a0005c0021t0001g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.673+4275C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180915889 | |||||||
| chr5:180916025 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.673+4411C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180916025 | |||||||
| chr5:180916026 | G | A | 2 | a0004c0004t0001g0151 a0004c0004t0001g0157 |
2 | HG03831.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.673+4412G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180916026 | |||||||
| chr5:180916225 | A | G | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+4611A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180916225 | |||||||
| chr5:180916376 | AAAAG | A | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0003c0003t0001g0001 others(12): Show |
23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.673+4768_673+4771d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180916376 | ||||||
| chr5:180916530 | A | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+4916A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180916530 | |||||||
| chr5:180916749 | C | T | 90 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0002c0002t0001g0003 others(87): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.673+5135C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180916749 | |||||||
| chr5:180917048 | T | TCAACAAA others(1097): Show |
1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+5455_673+5456i others(1106): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917048 | ||||||
| chr5:180917048 | T | TCAACAAA others(407): Show |
11 | a0002c0007t0001g0040 a0002c0007t0001g0042 a0002c0007t0001g0044 others(8): Show |
11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.673+5455_673+5456i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917048 | ||||||
| chr5:180917057 | T | C | 1 | a0002c0005t0001g0135 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.673+5443T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917057 | |||||||
| chr5:180917070 | G | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+5456G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917070 | |||||||
| chr5:180917093 | T | C | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+5479T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917093 | |||||||
| chr5:180917095 | T | C | 41 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(38): Show |
48 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.673+5481T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917095 | |||||||
| chr5:180917109 | G | A | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+5495G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917109 | |||||||
| chr5:180917113 | T | C | 20 | a0002c0002t0001g0027 a0002c0005t0001g0058 a0002c0005t0001g0060 others(17): Show |
21 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(18): Show |
intron_variant | MODIFIER | c.673+5499T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917113 | |||||||
| chr5:180917113 | T | TAGGCCAA others(407): Show |
3 | a0002c0002t0001g0032 a0002c0005t0001g0085 a0011c0026t0001g0076 |
3 | HG02922.hp2 HG03209.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.673+5567_673+5568i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917113 | ||||||
| chr5:180917113 | T | TAGGCCAA others(476): Show |
1 | a0002c0005t0001g0135 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.673+5567_673+5568i others(485): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917113 | ||||||
| chr5:180917139 | A | G | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.673+5525A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917139 | |||||||
| chr5:180917164 | CGGCACTA others(131): Show |
C | 2 | a0001c0001t0001g0016 a0001c0001t0001g0083 |
3 | NA18966.hp2 NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.673+5688_673+5825d others(2): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917164 | ||||||
| chr5:180917182 | T | C | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+5568T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917182 | |||||||
| chr5:180917234 | G | A | 2 | a0003c0006t0001g0145 a0003c0006t0001g0146 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.673+5620G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917234 | |||||||
| chr5:180917251 | T | C | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+5637T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917251 | |||||||
| chr5:180917302 | T | C | 57 | a0001c0001t0001g0121 a0002c0002t0001g0003 a0002c0002t0001g0007 others(54): Show |
65 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(62): Show |
intron_variant | MODIFIER | c.673+5688T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917302 | |||||||
| chr5:180917305 | C | G | 1 | a0001c0001t0001g0117 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.673+5691C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917305 | |||||||
| chr5:180917320 | T | C | 37 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(34): Show |
44 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.673+5706T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917320 | |||||||
| chr5:180917332 | C | CTGGATAA others(407): Show |
30 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(27): Show |
37 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(34): Show |
intron_variant | MODIFIER | c.673+5774_673+5775i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917332 | ||||||
| chr5:180917332 | C | CTGGATAA others(269): Show |
1 | a0002c0002t0001g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.673+5774_673+5775i others(278): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917332 | ||||||
| chr5:180917332 | C | T | 14 | a0002c0002t0001g0032 a0002c0005t0001g0085 a0002c0007t0001g0040 others(11): Show |
14 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.673+5718C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917332 | |||||||
| chr5:180917389 | T | C | 7 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.673+5775T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917389 | |||||||
| chr5:180917402 | T | C | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+5788T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917402 | |||||||
| chr5:180917403 | G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+5789G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917403 | |||||||
| chr5:180917403 | G | GGATAACC others(407): Show |
2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+5843_673+5844i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917403 | ||||||
| chr5:180917440 | C | CGGCACTA others(407): Show |
1 | a0002c0005t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.673+5843_673+5844i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917440 | ||||||
| chr5:180917440 | C | CGGCACTA others(407): Show |
2 | a0002c0005t0001g0061 a0006c0017t0001g0052 |
2 | HG01243.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.673+5843_673+5844i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917440 | ||||||
| chr5:180917440 | C | CGGCACTA others(407): Show |
1 | a0002c0005t0001g0141 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.673+5843_673+5844i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917440 | ||||||
| chr5:180917440 | C | CGGCACTA others(407): Show |
1 | a0002c0005t0001g0060 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.673+5843_673+5844i others(416): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917440 | ||||||
| chr5:180917440 | C | T | 47 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.673+5826C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917440 | |||||||
| chr5:180917608 | T | TA | 53 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(50): Show |
60 | HG00280.hp1 HG00544.hp2 HG01192.hp1 others(57): Show |
intron_variant | MODIFIER | c.673+5994_673+5995i others(3): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917608 | |||||||
| chr5:180917609 | T | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+5995T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917609 | |||||||
| chr5:180917609 | T | TA | 36 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0003c0003t0001g0001 others(33): Show |
49 | HG00140.hp1 HG00438.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.673+6003dupA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180917609 | ||||||
| chr5:180917750 | T | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+6136T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917750 | |||||||
| chr5:180917763 | G | A | 1 | a0002c0002t0001g0008 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.673+6149G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917763 | |||||||
| chr5:180917810 | C | T | 1 | a0002c0005t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.673+6196C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917810 | |||||||
| chr5:180917817 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.673+6203A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917817 | |||||||
| chr5:180917830 | C | T | 1 | a0001c0001t0001g0116 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.673+6216C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917830 | |||||||
| chr5:180917877 | G | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+6263G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917877 | |||||||
| chr5:180917920 | T | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+6306T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917920 | |||||||
| chr5:180917986 | G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+6372G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180917986 | |||||||
| chr5:180918028 | C | CA | 50 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(47): Show |
57 | HG00280.hp1 HG00544.hp2 HG01192.hp1 others(54): Show |
intron_variant | MODIFIER | c.673+6429dupA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180918028 | ||||||
| chr5:180918028 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.673+6414C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180918028 | |||||||
| chr5:180918177 | T | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+6563T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180918177 | |||||||
| chr5:180918625 | A | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+7011A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180918625 | |||||||
| chr5:180918810 | A | C | 1 | a0001c0001t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.673+7196A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180918810 | |||||||
| chr5:180918814 | G | T | 1 | a0001c0001t0001g0134 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.673+7200G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180918814 | |||||||
| chr5:180919153 | T | C | 1 | a0006c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.673+7539T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919153 | |||||||
| chr5:180919231 | T | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+7617T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919231 | |||||||
| chr5:180919363 | T | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+7749T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919363 | |||||||
| chr5:180919616 | T | G | 36 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(33): Show |
43 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.673+8002T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919616 | |||||||
| chr5:180919731 | G | T | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+8117G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919731 | |||||||
| chr5:180919794 | A | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+8180A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919794 | |||||||
| chr5:180919907 | G | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+8293G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180919907 | |||||||
| chr5:180920004 | C | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+8390C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180920004 | |||||||
| chr5:180920753 | T | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+9139T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180920753 | |||||||
| chr5:180920980 | C | T | 9 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(6): Show |
9 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.673+9366C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180920980 | |||||||
| chr5:180921220 | T | C | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+9606T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180921220 | |||||||
| chr5:180921239 | A | T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0115 |
2 | HG02080.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.673+9625A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180921239 | |||||||
| chr5:180921459 | T | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+9845T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180921459 | |||||||
| chr5:180921660 | T | TAC | 20 | a0001c0001t0001g0084 a0001c0001t0001g0088 a0001c0001t0001g0121 others(17): Show |
23 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.673+10080_673+1008 others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | ||||||
| chr5:180921660 | T | TACAC | 3 | a0002c0005t0001g0060 a0004c0004t0001g0152 a0011c0026t0001g0076 |
3 | HG01169.hp1 HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.673+10078_673+1008 others(8): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | ||||||
| chr5:180921660 | T | TACACAC | 3 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0050 |
3 | HG02965.hp1 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.673+10076_673+1008 others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | ||||||
| chr5:180921660 | TAC | T | 19 | a0001c0001t0001g0018 a0001c0001t0001g0020 a0001c0001t0001g0065 others(16): Show |
21 | HG00140.hp2 HG00438.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.673+10080_673+1008 others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | ||||||
| chr5:180921660 | TACAC | T | 9 | a0001c0001t0001g0113 a0002c0002t0001g0010 a0002c0002t0001g0033 others(6): Show |
10 | HG01167.hp1 HG02615.hp2 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.673+10078_673+1008 others(8): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | ||||||
| chr5:180921660 | TACACAC | T | 18 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0074 others(15): Show |
28 | HG00438.hp2 HG00621.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.673+10076_673+1008 others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | ||||||
| chr5:180921660 | TACACACA others(1): Show |
T | 3 | a0003c0006t0001g0145 a0003c0006t0001g0146 a0003c0006t0001g0147 |
3 | HG02572.hp2 HG02622.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.673+10074_673+1008 others(12): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180921660 | ||||||
| chr5:180922074 | TA | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+10461delA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922074 | |||||||
| chr5:180922128 | T | A | 11 | a0002c0007t0001g0040 a0002c0007t0001g0042 a0002c0007t0001g0044 others(8): Show |
11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.673+10514T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922128 | |||||||
| chr5:180922352 | C | T | 2 | a0002c0005t0001g0060 a0002c0005t0001g0061 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.673+10738C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922352 | |||||||
| chr5:180922514 | G | A | 6 | a0001c0001t0001g0019 a0001c0001t0001g0082 a0001c0001t0001g0105 others(3): Show |
7 | HG00438.hp1 HG02027.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.673+10900G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922514 | |||||||
| chr5:180922533 | C | T | 7 | a0002c0002t0001g0027 a0002c0005t0001g0135 a0002c0005t0001g0136 others(4): Show |
7 | HG00280.hp1 HG01192.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.673+10919C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922533 | |||||||
| chr5:180922554 | A | G | 1 | a0001c0001t0001g0104 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.673+10940A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922554 | |||||||
| chr5:180922591 | T | TAAGAAGT others(311): Show |
3 | a0002c0005t0001g0141 a0002c0024t0001g0062 a0009c0018t0001g0047 |
3 | HG02257.hp2 HG02451.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.673+10990_673+1099 others(322): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | ||||||
| chr5:180922591 | T | TAAGAAGT others(315): Show |
1 | a0008c0025t0001g0045 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.673+10990_673+1099 others(326): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | ||||||
| chr5:180922591 | T | TAAGAAGT others(316): Show |
6 | a0002c0002t0001g0027 a0002c0005t0001g0135 a0002c0005t0001g0136 others(3): Show |
6 | HG00280.hp1 HG01192.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.673+10990_673+1099 others(327): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | ||||||
| chr5:180922591 | T | TAAGAAGT others(311): Show |
4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.673+10990_673+1099 others(322): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | ||||||
| chr5:180922591 | T | TAAGAAGT others(310): Show |
2 | a0002c0002t0001g0030 a0002c0002t0001g0057 |
2 | HG02897.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.673+10990_673+1099 others(321): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | ||||||
| chr5:180922591 | T | TAAGAAGT others(311): Show |
38 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(35): Show |
45 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(42): Show |
intron_variant | MODIFIER | c.673+10990_673+1099 others(322): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180922591 | ||||||
| chr5:180922618 | G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+11004G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922618 | |||||||
| chr5:180922654 | A | C | 1 | a0002c0002t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.673+11040A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922654 | |||||||
| chr5:180922778 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.673+11164C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922778 | |||||||
| chr5:180922832 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.673+11218T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180922832 | |||||||
| chr5:180923052 | A | T | 5 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(2): Show |
5 | HG01243.hp2 HG02451.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.673+11438A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923052 | |||||||
| chr5:180923084 | C | T | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+11470C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923084 | |||||||
| chr5:180923131 | C | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+11517C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923131 | |||||||
| chr5:180923167 | A | G | 117 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(114): Show |
141 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(138): Show |
intron_variant | MODIFIER | c.673+11553A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923167 | |||||||
| chr5:180923423 | A | G | 1 | a0002c0002t0001g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.673+11809A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923423 | |||||||
| chr5:180923485 | T | G | 1 | a0002c0002t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.673+11871T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923485 | |||||||
| chr5:180923705 | T | C | 1 | a0001c0001t0001g0089 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.673+12091T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923705 | |||||||
| chr5:180923779 | C | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+12165C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923779 | |||||||
| chr5:180923975 | G | A | 1 | a0011c0026t0001g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.673+12361G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180923975 | |||||||
| chr5:180924514 | C | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+12900C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180924514 | |||||||
| chr5:180924666 | C | G | 1 | a0004c0004t0001g0151 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.673+13052C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180924666 | |||||||
| chr5:180925753 | T | C | 5 | a0002c0002t0001g0027 a0002c0005t0001g0135 a0002c0005t0001g0136 others(2): Show |
5 | HG00280.hp1 HG01192.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+14139T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180925753 | |||||||
| chr5:180925879 | T | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+14265T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180925879 | |||||||
| chr5:180926005 | CA | C | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+14398delA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180926005 | ||||||
| chr5:180926206 | C | G | 1 | a0003c0006t0001g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.673+14592C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926206 | |||||||
| chr5:180926220 | G | T | 1 | a0001c0001t0001g0112 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.673+14606G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926220 | |||||||
| chr5:180926318 | C | T | 15 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(12): Show |
22 | HG00544.hp2 HG01167.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.673+14704C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926318 | |||||||
| chr5:180926553 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.673+14939A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926553 | |||||||
| chr5:180926677 | T | G | 40 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(37): Show |
47 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(44): Show |
intron_variant | MODIFIER | c.673+15063T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926677 | |||||||
| chr5:180926976 | G | T | 6 | a0002c0007t0001g0040 a0005c0012t0001g0039 a0005c0012t0001g0041 others(3): Show |
6 | HG02615.hp1 HG02922.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.673+15362G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180926976 | |||||||
| chr5:180927003 | C | T | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+15389C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927003 | |||||||
| chr5:180927034 | C | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+15420C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927034 | |||||||
| chr5:180927303 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.673+15689C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927303 | |||||||
| chr5:180927320 | C | T | 1 | a0005c0012t0001g0041 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.673+15706C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927320 | |||||||
| chr5:180927570 | G | C | 2 | a0002c0005t0001g0060 a0002c0005t0001g0061 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.673+15956G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927570 | |||||||
| chr5:180927664 | C | T | 1 | a0002c0002t0001g0027 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.673+16050C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927664 | |||||||
| chr5:180927720 | G | T | 1 | a0002c0002t0001g0031 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.673+16106G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927720 | |||||||
| chr5:180927858 | T | C | 1 | a0002c0002t0001g0024 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.673+16244T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927858 | |||||||
| chr5:180927874 | T | C | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+16260T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927874 | |||||||
| chr5:180927910 | C | A | 1 | a0001c0001t0001g0099 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.673+16296C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180927910 | |||||||
| chr5:180928495 | C | A | 1 | a0002c0002t0001g0048 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.673+16881C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928495 | |||||||
| chr5:180928527 | A | G | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+16913A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928527 | |||||||
| chr5:180928541 | C | A | 5 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0050 others(2): Show |
5 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.673+16927C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928541 | |||||||
| chr5:180928655 | G | A | 1 | a0001c0001t0001g0129 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.673+17041G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928655 | |||||||
| chr5:180928741 | A | T | 1 | a0001c0001t0001g0107 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.673+17127A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928741 | |||||||
| chr5:180928905 | C | T | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0003c0003t0001g0001 others(12): Show |
23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.673+17291C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180928905 | |||||||
| chr5:180929028 | A | G | 46 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(43): Show |
53 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.673+17414A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929028 | |||||||
| chr5:180929227 | G | C | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.673+17613G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929227 | |||||||
| chr5:180929293 | C | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.673+17679C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929293 | |||||||
| chr5:180929314 | C | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.673+17700C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929314 | |||||||
| chr5:180929471 | A | G | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.673+17857A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929471 | |||||||
| chr5:180929550 | AATAG | A | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.673+17942_673+1794 others(8): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180929550 | ||||||
| chr5:180929560 | C | A | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0003c0003t0001g0001 others(12): Show |
23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.673+17946C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929560 | |||||||
| chr5:180929603 | T | C | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-17909T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929603 | |||||||
| chr5:180929648 | C | A | 1 | a0002c0005t0001g0085 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.674-17864C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929648 | |||||||
| chr5:180929684 | C | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-17828C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929684 | |||||||
| chr5:180929736 | C | T | 1 | a0005c0009t0001g0036 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.674-17776C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929736 | |||||||
| chr5:180929764 | G | A | 3 | a0001c0001t0001g0018 a0001c0001t0001g0116 a0001c0001t0001g0125 |
4 | HG01071.hp2 HG01255.hp2 HG01934.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-17748G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929764 | |||||||
| chr5:180929835 | C | A | 1 | a0001c0001t0001g0128 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.674-17677C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180929835 | |||||||
| chr5:180929947 | CT | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-17563delT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180929947 | ||||||
| chr5:180930002 | A | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-17510A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930002 | |||||||
| chr5:180930108 | G | A | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-17404G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930108 | |||||||
| chr5:180930118 | C | T | 1 | a0006c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.674-17394C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930118 | |||||||
| chr5:180930164 | C | T | 1 | a0001c0001t0001g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.674-17348C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930164 | |||||||
| chr5:180930179 | G | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-17333G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930179 | |||||||
| chr5:180930244 | C | T | 46 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(43): Show |
53 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(50): Show |
intron_variant | MODIFIER | c.674-17268C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930244 | |||||||
| chr5:180930325 | T | C | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-17187T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930325 | |||||||
| chr5:180930401 | A | G | 2 | a0003c0006t0001g0145 a0003c0006t0001g0146 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.674-17111A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930401 | |||||||
| chr5:180930409 | A | T | 1 | a0001c0001t0001g0019 | 2 | HG02027.hp1 NA18943.hp2 |
intron_variant | MODIFIER | c.674-17103A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930409 | |||||||
| chr5:180930457 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.674-17055C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930457 | |||||||
| chr5:180930607 | C | G | 1 | a0004c0004t0001g0143 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.674-16905C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930607 | |||||||
| chr5:180930710 | A | G | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-16802A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930710 | |||||||
| chr5:180930884 | G | A | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-16628G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930884 | |||||||
| chr5:180930923 | G | T | 1 | a0001c0001t0001g0127 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.674-16589G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180930923 | |||||||
| chr5:180931005 | A | T | 1 | a0001c0001t0001g0113 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.674-16507A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931005 | |||||||
| chr5:180931260 | T | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-16252T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931260 | |||||||
| chr5:180931432 | G | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-16080G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931432 | |||||||
| chr5:180931438 | C | T | 1 | a0002c0005t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674-16074C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931438 | |||||||
| chr5:180931626 | A | G | 1 | a0003c0006t0001g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.674-15886A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931626 | |||||||
| chr5:180931635 | G | A | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-15877G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931635 | |||||||
| chr5:180931990 | T | C | 1 | a0011c0026t0001g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.674-15522T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180931990 | |||||||
| chr5:180932083 | T | A | 155 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(152): Show |
187 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(184): Show |
intron_variant | MODIFIER | c.674-15429T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932083 | |||||||
| chr5:180932258 | T | C | 18 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0020 others(15): Show |
21 | HG00140.hp2 HG00438.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.674-15254T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932258 | |||||||
| chr5:180932440 | G | A | 5 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0050 others(2): Show |
5 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-15072G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932440 | |||||||
| chr5:180932448 | G | A | 47 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.674-15064G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932448 | |||||||
| chr5:180932460 | C | T | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0003c0003t0001g0001 others(12): Show |
23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.674-15052C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932460 | |||||||
| chr5:180932480 | G | A | 3 | a0002c0002t0001g0010 a0002c0002t0001g0033 a0002c0005t0001g0085 |
4 | HG01167.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-15032G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932480 | |||||||
| chr5:180932515 | T | G | 1 | a0004c0004t0001g0151 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.674-14997T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932515 | |||||||
| chr5:180932571 | G | C | 1 | a0013c0016t0001g0064 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.674-14941G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932571 | |||||||
| chr5:180932591 | C | T | 1 | a0001c0001t0002g0063 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.674-14921C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932591 | |||||||
| chr5:180932733 | A | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-14779A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180932733 | |||||||
| chr5:180933005 | CA | C | 80 | a0001c0001t0001g0096 a0002c0002t0001g0003 a0002c0002t0001g0007 others(77): Show |
99 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(96): Show |
intron_variant | MODIFIER | c.674-14494delA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180933005 | ||||||
| chr5:180933005 | CAA | C | 11 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0002c0005t0001g0058 others(8): Show |
12 | HG01243.hp2 HG01884.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.674-14495_674-1449 others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180933005 | ||||||
| chr5:180933103 | G | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-14409G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933103 | |||||||
| chr5:180933106 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.674-14406G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933106 | |||||||
| chr5:180933107 | G | C | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-14405G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933107 | |||||||
| chr5:180933127 | A | G | 36 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(33): Show |
43 | HG00544.hp2 HG01167.hp1 HG01243.hp1 others(40): Show |
intron_variant | MODIFIER | c.674-14385A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933127 | |||||||
| chr5:180933437 | C | G | 1 | a0002c0002t0001g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.674-14075C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933437 | |||||||
| chr5:180933751 | C | T | 1 | a0001c0001t0001g0095 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.674-13761C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933751 | |||||||
| chr5:180933880 | G | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-13632G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180933880 | |||||||
| chr5:180933979 | G | GA | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-13524dupA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180933979 | ||||||
| chr5:180934037 | C | G | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-13475C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934037 | |||||||
| chr5:180934240 | C | A | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-13272C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934240 | |||||||
| chr5:180934248 | G | C | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-13264G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934248 | |||||||
| chr5:180934266 | A | T | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-13246A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934266 | |||||||
| chr5:180934272 | G | A | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-13240G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934272 | |||||||
| chr5:180934516 | C | T | 1 | a0003c0003t0001g0069 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.674-12996C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934516 | |||||||
| chr5:180934665 | C | G | 47 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.674-12847C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934665 | |||||||
| chr5:180934801 | C | T | 2 | a0002c0005t0001g0060 a0002c0005t0001g0061 |
2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.674-12711C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934801 | |||||||
| chr5:180934813 | T | C | 47 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.674-12699T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934813 | |||||||
| chr5:180934838 | G | A | 18 | a0003c0006t0001g0021 a0003c0006t0001g0149 a0003c0006t0001g0156 others(15): Show |
23 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.674-12674G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934838 | |||||||
| chr5:180934887 | A | G | 1 | a0002c0002t0001g0008 | 2 | HG03688.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.674-12625A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180934887 | |||||||
| chr5:180934946 | G | GGTGA | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-12564_674-1256 others(8): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180934946 | ||||||
| chr5:180935131 | T | C | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-12381T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935131 | |||||||
| chr5:180935264 | G | T | 2 | a0001c0001t0001g0082 a0001c0001t0001g0106 |
2 | NA18952.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.674-12248G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935264 | |||||||
| chr5:180935269 | G | A | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-12243G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935269 | |||||||
| chr5:180935499 | C | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-12013C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935499 | |||||||
| chr5:180935614 | C | T | 47 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.674-11898C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935614 | |||||||
| chr5:180935647 | G | A | 5 | a0004c0004t0001g0002 a0004c0004t0001g0152 a0004c0004t0001g0153 others(2): Show |
8 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.674-11865G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935647 | |||||||
| chr5:180935775 | C | T | 1 | a0001c0001t0001g0077 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.674-11737C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180935775 | |||||||
| chr5:180935919 | C | CT | 6 | a0001c0001t0001g0089 a0001c0001t0001g0094 a0001c0001t0001g0104 others(3): Show |
6 | HG01192.hp2 HG01952.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.674-11580dupT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180935919 | ||||||
| chr5:180936042 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-11470G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936042 | |||||||
| chr5:180936043 | G | T | 1 | a0001c0001t0001g0074 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.674-11469G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936043 | |||||||
| chr5:180936093 | G | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-11419G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936093 | |||||||
| chr5:180936161 | G | T | 11 | a0002c0007t0001g0040 a0002c0007t0001g0042 a0002c0007t0001g0044 others(8): Show |
11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-11351G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936161 | |||||||
| chr5:180936220 | A | C | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0003c0003t0001g0001 others(12): Show |
23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.674-11292A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936220 | |||||||
| chr5:180936514 | T | C | 1 | a0001c0001t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.674-10998T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936514 | |||||||
| chr5:180936573 | G | T | 1 | a0011c0026t0001g0076 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.674-10939G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936573 | |||||||
| chr5:180936610 | T | C | 3 | a0005c0009t0001g0034 a0005c0009t0001g0035 a0005c0009t0001g0036 |
3 | HG02622.hp2 HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.674-10902T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936610 | |||||||
| chr5:180936668 | G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-10844G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180936668 | |||||||
| chr5:180937002 | C | T | 11 | a0002c0007t0001g0040 a0002c0007t0001g0042 a0002c0007t0001g0044 others(8): Show |
11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-10510C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180937002 | |||||||
| chr5:180937072 | C | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-10440C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180937072 | |||||||
| chr5:180937157 | G | A | 5 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0050 others(2): Show |
5 | HG02145.hp2 HG02922.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-10355G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180937157 | |||||||
| chr5:180937164 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.674-10348G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180937164 | |||||||
| chr5:180937888 | G | A | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-9624G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180937888 | |||||||
| chr5:180937942 | T | TA | 154 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0013 others(151): Show |
186 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.674-9559dupA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180937942 | ||||||
| chr5:180938103 | A | G | 90 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0002c0002t0001g0003 others(87): Show |
110 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(107): Show |
intron_variant | MODIFIER | c.674-9409A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938103 | |||||||
| chr5:180938159 | T | C | 69 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0002c0002t0001g0003 others(66): Show |
84 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.674-9353T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938159 | |||||||
| chr5:180938313 | T | C | 53 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(50): Show |
60 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.674-9199T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938313 | |||||||
| chr5:180938314 | G | A | 1 | a0002c0005t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674-9198G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938314 | |||||||
| chr5:180938488 | A | G | 5 | a0002c0002t0001g0027 a0002c0005t0001g0135 a0002c0005t0001g0136 others(2): Show |
5 | HG00280.hp1 HG01192.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.674-9024A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938488 | |||||||
| chr5:180938515 | T | TCTTCCTT others(1): Show |
3 | a0002c0005t0001g0060 a0002c0005t0001g0061 a0006c0017t0001g0052 |
3 | HG01243.hp2 HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.674-8981_674-8974d others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180938515 | ||||||
| chr5:180938535 | CCTTT | C | 4 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0003c0003t0001g0072 others(1): Show |
4 | HG01884.hp1 HG02145.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-8968_674-8965d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180938535 | ||||||
| chr5:180938539 | T | C | 8 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0009 others(5): Show |
12 | HG00544.hp2 HG02027.hp2 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.674-8973T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938539 | |||||||
| chr5:180938541 | TTTC | T | 11 | a0003c0003t0001g0001 a0003c0003t0001g0006 a0003c0003t0001g0012 others(8): Show |
19 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(16): Show |
intron_variant | MODIFIER | c.674-8968_674-8966d others(5): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180938541 | ||||||
| chr5:180938543 | T | C | 1 | a0002c0005t0001g0058 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.674-8969T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938543 | |||||||
| chr5:180938544 | CT | C | 39 | a0002c0002t0001g0007 a0002c0002t0001g0010 a0002c0002t0001g0024 others(36): Show |
42 | HG00280.hp1 HG01167.hp1 HG01192.hp1 others(39): Show |
intron_variant | MODIFIER | c.674-8954delT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180938544 | ||||||
| chr5:180938545 | T | TTTC | 7 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0009 others(4): Show |
11 | HG00544.hp2 HG02027.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-8965_674-8964i others(5): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180938545 | ||||||
| chr5:180938578 | G | A | 47 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(44): Show |
54 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.674-8934G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938578 | |||||||
| chr5:180938591 | C | G | 53 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(50): Show |
60 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(57): Show |
intron_variant | MODIFIER | c.674-8921C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938591 | |||||||
| chr5:180938727 | G | A | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-8785G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938727 | |||||||
| chr5:180938817 | T | C | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-8695T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938817 | |||||||
| chr5:180938890 | G | T | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-8622G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180938890 | |||||||
| chr5:180939298 | G | C | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-8214G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180939298 | |||||||
| chr5:180939860 | A | AT | 4 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0003c0006t0001g0145 others(1): Show |
4 | HG02572.hp2 HG02886.hp2 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.674-7644dupT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180939860 | ||||||
| chr5:180939869 | A | T | 1 | a0005c0021t0001g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.674-7643A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180939869 | |||||||
| chr5:180939970 | C | T | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-7542C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180939970 | |||||||
| chr5:180940215 | A | G | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-7297A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940215 | |||||||
| chr5:180940231 | C | T | 3 | a0002c0007t0001g0040 a0008c0019t0001g0046 a0008c0025t0001g0045 |
3 | HG02280.hp1 HG02809.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.674-7281C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940231 | |||||||
| chr5:180940308 | C | A | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-7204C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940308 | |||||||
| chr5:180940478 | C | T | 1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-7034C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940478 | |||||||
| chr5:180940576 | A | C | 1 | a0001c0001t0001g0093 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.674-6936A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940576 | |||||||
| chr5:180940787 | G | A | 1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-6725G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940787 | |||||||
| chr5:180940895 | C | A | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-6617C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940895 | |||||||
| chr5:180940906 | A | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-6606A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940906 | |||||||
| chr5:180940933 | A | C | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-6579A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940933 | |||||||
| chr5:180940948 | C | G | 1 | a0001c0001t0001g0020 | 2 | HG01109.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.674-6564C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180940948 | |||||||
| chr5:180941086 | AAGGG | A | 39 | a0002c0002t0001g0007 a0002c0002t0001g0009 a0002c0002t0001g0010 others(36): Show |
43 | HG00280.hp1 HG01167.hp1 HG01192.hp1 others(40): Show |
intron_variant | MODIFIER | c.674-6414_674-6411d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941086 | ||||||
| chr5:180941098 | G | A | 14 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0023 others(11): Show |
17 | HG00544.hp2 HG01243.hp2 HG01952.hp2 others(14): Show |
intron_variant | MODIFIER | c.674-6414G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180941098 | |||||||
| chr5:180941102 | A | AAGGG | 3 | a0002c0005t0001g0060 a0002c0005t0001g0061 a0008c0025t0001g0045 |
3 | HG02451.hp2 HG02809.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.674-6407_674-6406i others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941102 | ||||||
| chr5:180941106 | A | G | 11 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0023 others(8): Show |
14 | HG00544.hp2 HG01243.hp2 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.674-6406A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180941106 | |||||||
| chr5:180941110 | G | A | 15 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0023 others(12): Show |
18 | HG00544.hp2 HG01243.hp2 HG01952.hp2 others(15): Show |
intron_variant | MODIFIER | c.674-6402G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180941110 | |||||||
| chr5:180941110 | G | GAGGA | 7 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0086 others(4): Show |
9 | HG00280.hp2 HG01109.hp2 HG01123.hp2 others(6): Show |
intron_variant | MODIFIER | c.674-6361_674-6358d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | ||||||
| chr5:180941110 | G | GAGGAAGG others(1): Show |
24 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0065 others(21): Show |
35 | HG00621.hp1 HG00621.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.674-6365_674-6358d others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | ||||||
| chr5:180941110 | G | GAGGAAGG others(5): Show |
43 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0017 others(40): Show |
49 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.674-6369_674-6358d others(14): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | ||||||
| chr5:180941110 | G | GAGGAAGG others(9): Show |
7 | a0001c0001t0001g0077 a0001c0001t0001g0084 a0001c0001t0001g0104 others(4): Show |
7 | HG01255.hp1 HG02155.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.674-6373_674-6358d others(18): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | ||||||
| chr5:180941110 | GAGGA | G | 8 | a0002c0002t0001g0028 a0002c0007t0001g0042 a0002c0007t0001g0044 others(5): Show |
9 | HG00140.hp1 HG02615.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.674-6361_674-6358d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | ||||||
| chr5:180941110 | GAGGAAGG others(1): Show |
G | 6 | a0001c0001t0001g0019 a0001c0001t0001g0118 a0002c0002t0001g0048 others(3): Show |
7 | HG02027.hp1 HG02040.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.674-6365_674-6358d others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941110 | ||||||
| chr5:180941461 | C | A | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.674-6051C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180941461 | |||||||
| chr5:180941784 | A | G | 2 | a0002c0007t0001g0042 a0002c0007t0001g0044 |
2 | HG02723.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.674-5728A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180941784 | |||||||
| chr5:180941895 | T | TGCCCACT others(105): Show |
1 | a0006c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.674-5598_674-5597i others(114): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | ||||||
| chr5:180941895 | T | TGCCCACT others(111): Show |
1 | a0009c0018t0001g0047 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.674-5598_674-5597i others(120): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | ||||||
| chr5:180941895 | T | TGCCCACT others(116): Show |
3 | a0002c0002t0001g0023 a0002c0002t0001g0024 a0009c0022t0001g0053 |
3 | HG03041.hp2 HG03139.hp1 NA18942.hp2 |
intron_variant | MODIFIER | c.674-5598_674-5597i others(125): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | ||||||
| chr5:180941895 | T | TGCCCACT others(117): Show |
1 | a0002c0005t0001g0137 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.674-5598_674-5597i others(126): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | ||||||
| chr5:180941895 | T | TGCCCACT others(117): Show |
35 | a0002c0002t0001g0003 a0002c0002t0001g0008 a0002c0002t0001g0009 others(32): Show |
41 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.674-5598_674-5597i others(126): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | ||||||
| chr5:180941895 | T | TGCCCACT others(118): Show |
12 | a0002c0002t0001g0007 a0002c0002t0001g0048 a0002c0002t0001g0050 others(9): Show |
13 | HG02145.hp2 HG02280.hp1 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.674-5598_674-5597i others(127): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | ||||||
| chr5:180941895 | T | TGCCCACT others(119): Show |
1 | a0002c0024t0001g0062 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.674-5598_674-5597i others(128): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180941895 | ||||||
| chr5:180942129 | T | C | 1 | a0002c0002t0001g0007 | 2 | HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.674-5383T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942129 | |||||||
| chr5:180942282 | G | T | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-5230G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942282 | |||||||
| chr5:180942317 | C | G | 11 | a0002c0007t0001g0040 a0002c0007t0001g0042 a0002c0007t0001g0044 others(8): Show |
11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-5195C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942317 | |||||||
| chr5:180942360 | C | T | 69 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0002c0002t0001g0003 others(66): Show |
84 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.674-5152C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942360 | |||||||
| chr5:180942367 | C | T | 11 | a0002c0007t0001g0040 a0002c0007t0001g0042 a0002c0007t0001g0044 others(8): Show |
11 | HG02615.hp1 HG02622.hp2 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.674-5145C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942367 | |||||||
| chr5:180942759 | A | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0083 |
3 | NA18966.hp2 NA19010.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.674-4753A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942759 | |||||||
| chr5:180942779 | A | T | 54 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(51): Show |
61 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(58): Show |
intron_variant | MODIFIER | c.674-4733A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180942779 | |||||||
| chr5:180943130 | C | CT | 87 | a0001c0001t0001g0013 a0001c0001t0001g0015 a0001c0001t0001g0016 others(84): Show |
108 | HG00140.hp2 HG00438.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.674-4360dupT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180943130 | ||||||
| chr5:180943181 | C | G | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-4331C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943181 | |||||||
| chr5:180943230 | G | T | 2 | a0003c0006t0001g0145 a0003c0006t0001g0146 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.674-4282G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943230 | |||||||
| chr5:180943323 | C | T | 1 | a0005c0021t0001g0029 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.674-4189C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943323 | |||||||
| chr5:180943419 | C | T | 25 | a0001c0001t0001g0015 a0001c0001t0001g0018 a0001c0001t0001g0019 others(22): Show |
29 | HG00140.hp2 HG00438.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.674-4093C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943419 | |||||||
| chr5:180943499 | G | A | 18 | a0003c0006t0001g0021 a0003c0006t0001g0149 a0003c0006t0001g0156 others(15): Show |
23 | HG00140.hp1 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.674-4013G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943499 | |||||||
| chr5:180943503 | A | G | 1 | a0001c0001t0001g0083 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.674-4009A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943503 | |||||||
| chr5:180943599 | C | A | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-3913C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943599 | |||||||
| chr5:180943812 | A | G | 2 | a0002c0002t0001g0007 a0005c0021t0001g0029 |
3 | HG01884.hp2 HG03195.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.674-3700A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180943812 | |||||||
| chr5:180944194 | GAA | G | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-3316_674-3315d others(4): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180944194 | ||||||
| chr5:180944349 | C | T | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-3163C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944349 | |||||||
| chr5:180944504 | ACTAGAGG others(5): Show |
A | 3 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 |
3 | HG01243.hp1 HG01952.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.674-3007_674-2996d others(14): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944504 | |||||||
| chr5:180944569 | T | C | 51 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(48): Show |
57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.674-2943T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944569 | |||||||
| chr5:180944763 | T | A | 2 | a0003c0006t0001g0145 a0003c0006t0001g0146 |
2 | HG02572.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.674-2749T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944763 | |||||||
| chr5:180944860 | T | C | 1 | a0008c0019t0001g0046 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.674-2652T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944860 | |||||||
| chr5:180944958 | A | G | 1 | a0002c0005t0001g0138 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.674-2554A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180944958 | |||||||
| chr5:180945082 | T | C | 5 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(2): Show |
5 | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.674-2430T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945082 | |||||||
| chr5:180945237 | T | C | 51 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(48): Show |
57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.674-2275T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945237 | |||||||
| chr5:180945334 | A | G | 66 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0002c0002t0001g0003 others(63): Show |
80 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.674-2178A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945334 | |||||||
| chr5:180945437 | A | T | 1 | a0003c0003t0001g0012 | 2 | HG03688.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.674-2075A>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945437 | |||||||
| chr5:180945456 | CA | C | 44 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(41): Show |
50 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.674-2053delA | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180945456 | ||||||
| chr5:180945473 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.674-2039A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945473 | |||||||
| chr5:180945531 | G | A | 1 | a0007c0008t0001g0011 | 2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.674-1981G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945531 | |||||||
| chr5:180945713 | C | T | 1 | a0001c0001t0001g0132 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.674-1799C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945713 | |||||||
| chr5:180945838 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.674-1674T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180945838 | |||||||
| chr5:180945987 | T | TAATA | 2 | a0003c0003t0001g0071 a0003c0006t0001g0147 |
2 | HG02622.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.674-1497_674-1494d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180945987 | ||||||
| chr5:180945987 | TAATA | T | 2 | a0001c0001t0001g0108 a0003c0003t0001g0069 |
2 | HG02602.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.674-1497_674-1494d others(6): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180945987 | ||||||
| chr5:180945987 | TAATAAAT others(1): Show |
T | 50 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(47): Show |
56 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(53): Show |
intron_variant | MODIFIER | c.674-1501_674-1494d others(10): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180945987 | ||||||
| chr5:180945987 | TAATAAAT others(5): Show |
T | 1 | a0002c0002t0001g0050 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.674-1505_674-1494d others(14): Show |
BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr5 | 180945987 | ||||||
| chr5:180946093 | T | C | 1 | a0002c0007t0001g0040 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.674-1419T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180946093 | |||||||
| chr5:180946205 | C | A | 9 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(6): Show |
9 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.674-1307C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180946205 | |||||||
| chr5:180946581 | G | C | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0003c0003t0001g0001 others(12): Show |
23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.674-931G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180946581 | |||||||
| chr5:180946862 | G | A | 49 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(46): Show |
55 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.674-650G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180946862 | |||||||
| chr5:180947019 | T | C | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-493T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180947019 | |||||||
| chr5:180947139 | T | A | 4 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.674-373T>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180947139 | |||||||
| chr5:180947379 | A | C | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.674-133A>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180947379 | |||||||
| chr5:180947387 | G | A | 51 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(48): Show |
57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.674-125G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 3/7 | chr5 | 180947387 | |||||||
| chr5:180947898 | A | G | 51 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(48): Show |
57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.787+273A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/7 | chr5 | 180947898 | |||||||
| chr5:180947919 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.787+294A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/7 | chr5 | 180947919 | |||||||
| chr5:180948095 | T | C | 53 | a0001c0001t0001g0084 a0001c0001t0001g0090 a0002c0002t0001g0003 others(50): Show |
59 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(56): Show |
intron_variant | MODIFIER | c.788-260T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/7 | chr5 | 180948095 | |||||||
| chr5:180948208 | A | G | 44 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(41): Show |
50 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(47): Show |
intron_variant | MODIFIER | c.788-147A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/7 | chr5 | 180948208 | |||||||
| chr5:180948341 | T | C | 1 | a0002c0005t0001g0061 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.788-14T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 4/7 | chr5 | 180948341 | |||||||
| chr5:180948469 | G | A | 7 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.808+94G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948469 | |||||||
| chr5:180948499 | A | G | 7 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(4): Show |
7 | HG01243.hp2 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.808+124A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948499 | |||||||
| chr5:180948512 | G | A | 8 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(5): Show |
8 | HG01243.hp2 HG02257.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.808+137G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948512 | |||||||
| chr5:180948643 | A | G | 52 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(49): Show |
58 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(55): Show |
intron_variant | MODIFIER | c.808+268A>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948643 | |||||||
| chr5:180948672 | C | G | 66 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0002c0002t0001g0003 others(63): Show |
80 | HG00280.hp1 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.809-248C>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948672 | |||||||
| chr5:180948682 | G | GT | 15 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0003c0003t0001g0001 others(12): Show |
23 | HG00438.hp2 HG00621.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.809-237dupT | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr5 | 180948682 | ||||||
| chr5:180948790 | T | C | 49 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(46): Show |
55 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(52): Show |
intron_variant | MODIFIER | c.809-130T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948790 | |||||||
| chr5:180948821 | T | C | 5 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(2): Show |
5 | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-99T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948821 | |||||||
| chr5:180948877 | G | A | 4 | a0002c0002t0001g0048 a0002c0002t0001g0049 a0002c0002t0001g0050 others(1): Show |
4 | HG02145.hp2 HG02965.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.809-43G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 5/7 | chr5 | 180948877 | |||||||
| chr5:180949083 | G | T | 9 | a0002c0002t0001g0024 a0002c0002t0001g0025 a0002c0002t0001g0026 others(6): Show |
9 | HG01243.hp1 HG01891.hp1 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.835+137G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949083 | |||||||
| chr5:180949115 | T | G | 1 | a0006c0017t0001g0052 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.836-124T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949115 | |||||||
| chr5:180949116 | T | C | 51 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(48): Show |
57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.836-123T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949116 | |||||||
| chr5:180949121 | G | A | 51 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(48): Show |
57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.836-118G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949121 | |||||||
| chr5:180949133 | G | T | 5 | a0002c0005t0001g0058 a0002c0005t0001g0060 a0002c0005t0001g0061 others(2): Show |
5 | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.836-106G>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949133 | |||||||
| chr5:180949208 | T | G | 51 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(48): Show |
57 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(54): Show |
intron_variant | MODIFIER | c.836-31T>G | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949208 | |||||||
| chr5:180949223 | G | C | 55 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(52): Show |
62 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(59): Show |
intron_variant | MODIFIER | c.836-16G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 6/7 | chr5 | 180949223 | |||||||
| chr5:180949273 | C | T | 2 | a0008c0019t0001g0046 a0008c0025t0001g0045 |
2 | HG02280.hp1 HG02809.hp2 |
splice_region_variant&intron_variant | LOW | c.862+8C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949273 | |||||||
| chr5:180949343 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.862+78C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949343 | |||||||
| chr5:180949475 | G | A | 1 | a0006c0013t0001g0037 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.862+210G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949475 | |||||||
| chr5:180949482 | C | T | 1 | a0003c0006t0001g0147 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.862+217C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949482 | |||||||
| chr5:180949489 | C | CG | 39 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(36): Show |
45 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.862+231dupG | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr5 | 180949489 | ||||||
| chr5:180949711 | C | T | 34 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(31): Show |
40 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(37): Show |
intron_variant | MODIFIER | c.863-193C>T | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949711 | |||||||
| chr5:180949719 | T | C | 5 | a0002c0005t0001g0058 a0002c0024t0001g0062 a0008c0019t0001g0046 others(2): Show |
5 | HG02257.hp2 HG02280.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.863-185T>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949719 | |||||||
| chr5:180949766 | G | A | 3 | a0004c0004t0001g0148 a0004c0004t0001g0154 a0004c0004t0002g0150 |
3 | HG03490.hp2 HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.863-138G>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949766 | |||||||
| chr5:180949804 | C | A | 34 | a0002c0002t0001g0003 a0002c0002t0001g0007 a0002c0002t0001g0008 others(31): Show |
42 | HG00280.hp1 HG00544.hp2 HG01167.hp1 others(39): Show |
intron_variant | MODIFIER | c.863-100C>A | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949804 | |||||||
| chr5:180949860 | G | C | 46 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0134 others(43): Show |
57 | HG00280.hp1 HG00438.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.863-44G>C | BTNL8 | ENSG00000113303.12 | transcript | ENST00000340184.9 | protein_coding | 7/7 | chr5 | 180949860 |