Item | Value |
---|---|
geneid | 558 |
ensemblid | ENSG00000167601.12 |
hgncid | 905 |
symbol | AXL |
name | AXL receptor tyrosine kinase |
refseq_nuc | NM_021913.5 |
refseq_prot | NP_068713.2 |
ensembl_nuc | ENST00000301178.9 |
ensembl_prot | ENSP00000301178.3 |
mane_status | MANE Select |
chr | chr19 |
start | 41219223 |
end | 41261766 |
strand | + |
ver | v1.2 |
region | chr19:41219223-41261766 |
region5000 | chr19:41214223-41266766 |
regionname0 | AXL_chr19_41219223_41261766 |
regionname5000 | AXL_chr19_41214223_41266766 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 894 | 304 | 90 | 60 | 108 | 10 | 34 | 78 | AXL_chr19_41214223_41266766 | AXL | MAWRC others(889): Show |
chr19 | 41214223 | 41266766 |
a0002 | 0/0 | 894 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | AXL_chr19_41214223_41266766 | AXL | MAWRC others(889): Show |
chr19 | 41214223 | 41266766 |
a0003 | 0/0 | 894 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | MAWRC others(889): Show |
chr19 | 41214223 | 41266766 |
a0004 | 0/0 | 894 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | MAWRC others(889): Show |
chr19 | 41214223 | 41266766 |
a0005 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | MAWRC others(889): Show |
chr19 | 41214223 | 41266766 |
a0006 | 0/0 | 894 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | MAWRC others(889): Show |
chr19 | 41214223 | 41266766 |
a0007 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | MAWRC others(889): Show |
chr19 | 41214223 | 41266766 |
a0008 | 0/0 | 894 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | MAWRC others(889): Show |
chr19 | 41214223 | 41266766 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2682 | 293 | 80 | 60 | 107 | 10 | 34 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0001c0002 | 0/0 | 2682 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0001c0003 | 0/0 | 2682 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0001c0007 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0001c0011 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0001c0013 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0002c0004 | 0/0 | 2682 | 3 | 0 | 0 | 3 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0002c0010 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0003c0008 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0004c0012 | 0/0 | 2682 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0005c0009 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0006c0014 | 0/0 | 2682 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0007c0005 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 | ||
a0008c0006 | 0/0 | 2682 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | ATGGC others(2677): Show |
chr19 | 41214223 | 41266766 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4717 | 30 | 1 | 7 | 19 | 1 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0002 | 0/0 | 4711 | 28 | 5 | 7 | 14 | 1 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4706): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0003 | 0/0 | 4711 | 20 | 3 | 1 | 15 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4706): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0004 | 0/0 | 4706 | 20 | 11 | 0 | 8 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4701): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0005 | 0/0 | 4718 | 16 | 0 | 4 | 6 | 1 | 5 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4713): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0006 | 0/1 | 4717 | 17 | 3 | 2 | 6 | 1 | 4 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0007 | 0/0 | 4718 | 13 | 0 | 4 | 6 | 1 | 2 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4713): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0008 | 0/0 | 4706 | 12 | 7 | 0 | 4 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4701): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0009 | 0/0 | 4724 | 7 | 5 | 2 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4719): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0010 | 0/0 | 4721 | 8 | 0 | 3 | 1 | 0 | 4 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4716): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0011 | 0/0 | 4723 | 7 | 2 | 2 | 2 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4718): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0012 | 0/0 | 4724 | 8 | 0 | 2 | 2 | 0 | 4 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4719): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0013 | 0/0 | 4712 | 6 | 1 | 1 | 4 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4707): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0014 | 0/0 | 4717 | 5 | 1 | 2 | 1 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0015 | 0/0 | 4712 | 5 | 1 | 0 | 3 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4707): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0016 | 0/0 | 4719 | 5 | 0 | 1 | 3 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4714): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0017 | 0/0 | 4725 | 5 | 2 | 0 | 1 | 0 | 2 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4720): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0018 | 0/0 | 4726 | 5 | 4 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4721): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0019 | 0/0 | 4727 | 5 | 2 | 2 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4722): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0020 | 0/0 | 4717 | 5 | 1 | 3 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0021 | 0/0 | 4706 | 4 | 0 | 4 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4701): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0022 | 0/0 | 4722 | 4 | 0 | 3 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4717): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0023 | 0/0 | 4723 | 2 | 1 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4718): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0024 | 0/0 | 4719 | 4 | 1 | 3 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4714): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0025 | 0/0 | 4726 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4721): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0026 | 0/0 | 4718 | 3 | 0 | 0 | 3 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4713): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0027 | 0/0 | 4721 | 3 | 1 | 1 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4716): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0028 | 0/0 | 4722 | 3 | 1 | 0 | 1 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4717): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0029 | 0/0 | 4725 | 2 | 1 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4720): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0030 | 0/0 | 4727 | 3 | 2 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4722): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0031 | 0/0 | 4730 | 3 | 2 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4725): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0032 | 0/0 | 4706 | 3 | 3 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4701): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0033 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4725): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0034 | 0/0 | 4737 | 2 | 1 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4732): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0035 | 0/0 | 4717 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0036 | 0/0 | 4740 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4735): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0037 | 0/0 | 4702 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4697): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0038 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4700): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0039 | 0/0 | 4707 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4702): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0040 | 0/0 | 4717 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0041 | 0/0 | 4717 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0042 | 0/0 | 4728 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4723): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0043 | 0/0 | 4733 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4728): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0045 | 0/0 | 4718 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4713): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0046 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0047 | 0/0 | 4702 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4697): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0048 | 0/0 | 4702 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4697): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0049 | 0/0 | 4705 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4700): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0050 | 0/0 | 4707 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4702): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0051 | 0/0 | 4711 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4706): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0052 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4718): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0053 | 0/0 | 4731 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4726): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0054 | 0/0 | 4732 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4727): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0055 | 0/0 | 4733 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4728): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0056 | 0/0 | 4736 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4731): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0057 | 0/0 | 4737 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4732): Show |
chr19 | 41214223 | 41266766 |
a0001c0001t0058 | 0/0 | 4739 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4734): Show |
chr19 | 41214223 | 41266766 |
a0001c0002t0009 | 0/0 | 4724 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4719): Show |
chr19 | 41214223 | 41266766 |
a0001c0002t0023 | 0/0 | 4723 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4718): Show |
chr19 | 41214223 | 41266766 |
a0001c0002t0029 | 0/0 | 4725 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4720): Show |
chr19 | 41214223 | 41266766 |
a0001c0003t0009 | 0/0 | 4724 | 4 | 4 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4719): Show |
chr19 | 41214223 | 41266766 |
a0001c0007t0001 | 0/0 | 4717 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0001c0011t0011 | 0/0 | 4723 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4718): Show |
chr19 | 41214223 | 41266766 |
a0001c0013t0044 | 0/0 | 4735 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4730): Show |
chr19 | 41214223 | 41266766 |
a0002c0004t0005 | 0/0 | 4718 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4713): Show |
chr19 | 41214223 | 41266766 |
a0002c0004t0007 | 0/0 | 4718 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4713): Show |
chr19 | 41214223 | 41266766 |
a0002c0010t0005 | 0/0 | 4718 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4713): Show |
chr19 | 41214223 | 41266766 |
a0003c0008t0014 | 0/0 | 4717 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0004c0012t0007 | 0/0 | 4718 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4713): Show |
chr19 | 41214223 | 41266766 |
a0005c0009t0033 | 0/0 | 4730 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4725): Show |
chr19 | 41214223 | 41266766 |
a0006c0014t0001 | 0/0 | 4717 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0007c0005t0006 | 0/0 | 4717 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4712): Show |
chr19 | 41214223 | 41266766 |
a0008c0006t0015 | 0/0 | 4712 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | GAGAA others(4707): Show |
chr19 | 41214223 | 41266766 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0005 | 1/0 | 3 | 0 | 1 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0002 | 0/0 | 4 | 0 | 0 | 3 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0202 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0004g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0005g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0246 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0006g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0001 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0007g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0008g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0009g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0010g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0011g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0012g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0013g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0014g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0014g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0014g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0014g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0014g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0015g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0015g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0015g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0015g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0015g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0016g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0016g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0016g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0016g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0016g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0017g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0017g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0017g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0017g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0017g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0018g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0018g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0018g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0018g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0018g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0019g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0019g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0019g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0019g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0019g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0020g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0020g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0020g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0020g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0020g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0021g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0021g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0021g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0021g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0022g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0022g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0022g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0022g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0023g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0023g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0024g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0024g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0024g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0024g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0025g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0025g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0025g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0025g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0026g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0026g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0026g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0027g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0027g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0027g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0028g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0028g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0028g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0029g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0029g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0030g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0030g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0030g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0031g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0031g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0031g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0032g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0032g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0032g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0033g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0034g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0034g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0035g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0035g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0036g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0036g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0037g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0038g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0039g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0040g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0041g0073 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0042g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0043g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0045g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0046g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0047g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0048g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0049g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0050g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0051g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0052g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0053g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0054g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0055g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0056g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0057g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0001t0058g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0002t0009g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0002t0023g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0002t0023g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0002t0029g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0003t0009g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0003t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0003t0009g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0007t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0011t0011g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0001c0013t0044g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0002c0004t0005g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0002c0004t0005g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0002c0004t0007g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0002c0010t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0003c0008t0014g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0004c0012t0007g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0005c0009t0033g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0006c0014t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0007c0005t0006g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
a0008c0006t0015g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0217 | EUR | GBR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00099 | hp2 | a0001 | c0001 | t0005 | g0085 | EUR | GBR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0195 | EUR | FIN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00280 | hp2 | a0001 | c0001 | t0003 | g0002 | EUR | FIN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0202 | EUR | FIN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00323 | hp2 | a0001 | c0001 | t0007 | g0087 | EUR | FIN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00423 | hp1 | a0001 | c0001 | t0015 | g0179 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00423 | hp2 | a0001 | c0001 | t0015 | g0182 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00558 | hp1 | a0001 | c0001 | t0003 | g0033 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0049 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00639 | hp1 | a0001 | c0001 | t0012 | g0248 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0086 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00642 | hp1 | a0001 | c0001 | t0014 | g0048 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00642 | hp2 | a0001 | c0001 | t0058 | g0013 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00733 | hp1 | a0001 | c0001 | t0007 | g0075 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00735 | hp1 | a0001 | c0001 | t0020 | g0191 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00735 | hp2 | a0001 | c0001 | t0013 | g0062 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00738 | hp1 | a0001 | c0001 | t0034 | g0107 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG00738 | hp2 | a0001 | c0001 | t0057 | g0013 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01070 | hp2 | a0001 | c0001 | t0010 | g0011 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01071 | hp1 | a0001 | c0001 | t0010 | g0011 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01071 | hp2 | a0001 | c0001 | t0023 | g0028 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01074 | hp1 | a0001 | c0001 | t0005 | g0218 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01074 | hp2 | a0001 | c0001 | t0011 | g0132 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01081 | hp1 | a0001 | c0001 | t0030 | g0253 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01081 | hp2 | a0001 | c0001 | t0022 | g0094 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01099 | hp1 | a0001 | c0001 | t0027 | g0250 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01109 | hp1 | a0001 | c0001 | t0024 | g0194 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01109 | hp2 | a0001 | c0001 | t0024 | g0006 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01167 | hp2 | a0001 | c0001 | t0021 | g0042 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01168 | hp1 | a0001 | c0001 | t0006 | g0171 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01168 | hp2 | a0001 | c0001 | t0010 | g0119 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01169 | hp1 | a0001 | c0001 | t0022 | g0117 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01169 | hp2 | a0001 | c0001 | t0021 | g0044 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01175 | hp1 | a0001 | c0001 | t0005 | g0130 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0123 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01192 | hp2 | a0001 | c0001 | t0022 | g0093 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01243 | hp1 | a0001 | c0001 | t0019 | g0105 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01243 | hp2 | a0001 | c0001 | t0019 | g0106 | AMR | PUR | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01256 | hp1 | a0001 | c0001 | t0011 | g0216 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0081 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01257 | hp1 | a0001 | c0001 | t0024 | g0200 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0237 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01346 | hp1 | a0001 | c0001 | t0007 | g0053 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01346 | hp2 | a0001 | c0001 | t0020 | g0271 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0219 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01361 | hp1 | a0001 | c0001 | t0021 | g0274 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0001 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01433 | hp2 | a0004 | c0012 | t0007 | g0092 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01496 | hp1 | a0001 | c0001 | t0012 | g0152 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01496 | hp2 | a0001 | c0001 | t0045 | g0074 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01515 | hp1 | a0001 | c0001 | t0016 | g0126 | EUR | IBS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01515 | hp2 | a0001 | c0001 | t0014 | g0065 | EUR | IBS | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01884 | hp1 | a0005 | c0009 | t0033 | g0273 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01884 | hp2 | a0001 | c0001 | t0030 | g0214 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01891 | hp1 | a0001 | c0001 | t0009 | g0280 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0131 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01928 | hp1 | a0001 | c0001 | t0021 | g0043 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01928 | hp2 | a0001 | c0001 | t0006 | g0184 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0146 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01952 | hp2 | a0001 | c0001 | t0016 | g0041 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01981 | hp2 | a0001 | c0001 | t0020 | g0198 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0230 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02027 | hp2 | a0001 | c0001 | t0013 | g0068 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02040 | hp1 | a0001 | c0001 | t0027 | g0201 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02040 | hp2 | a0001 | c0001 | t0007 | g0010 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0260 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02055 | hp2 | a0001 | c0002 | t0009 | g0277 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02056 | hp1 | a0001 | c0001 | t0005 | g0249 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02071 | hp1 | a0001 | c0001 | t0011 | g0251 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02071 | hp2 | a0001 | c0001 | t0016 | g0077 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0001 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02083 | hp1 | a0001 | c0001 | t0012 | g0027 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02083 | hp2 | a0001 | c0001 | t0003 | g0050 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02129 | hp1 | a0001 | c0001 | t0035 | g0183 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02129 | hp2 | a0001 | c0001 | t0015 | g0281 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02135 | hp1 | a0001 | c0001 | t0016 | g0001 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02135 | hp2 | a0001 | c0001 | t0010 | g0091 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02145 | hp1 | a0001 | c0003 | t0009 | g0019 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02145 | hp2 | a0001 | c0001 | t0019 | g0111 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02155 | hp1 | a0001 | c0001 | t0050 | g0252 | EAS | CDX | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02155 | hp2 | a0001 | c0001 | t0026 | g0243 | EAS | CDX | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0144 | EAS | CDX | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CDX | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02257 | hp1 | a0001 | c0001 | t0025 | g0166 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02257 | hp2 | a0001 | c0001 | t0004 | g0156 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02258 | hp1 | a0001 | c0001 | t0018 | g0112 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02258 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02273 | hp1 | a0001 | c0001 | t0009 | g0030 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02273 | hp2 | a0001 | c0001 | t0009 | g0070 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0110 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02280 | hp2 | a0001 | c0001 | t0055 | g0151 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02293 | hp1 | a0001 | c0001 | t0014 | g0047 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0229 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02451 | hp2 | a0001 | c0001 | t0006 | g0155 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02523 | hp2 | a0001 | c0001 | t0014 | g0064 | EAS | KHV | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0207 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02572 | hp2 | a0001 | c0001 | t0011 | g0212 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02615 | hp1 | a0001 | c0001 | t0031 | g0150 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0167 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02622 | hp1 | a0001 | c0002 | t0029 | g0228 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02622 | hp2 | a0001 | c0001 | t0019 | g0114 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02630 | hp1 | a0001 | c0001 | t0032 | g0283 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02630 | hp2 | a0001 | c0001 | t0030 | g0206 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0220 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02683 | hp1 | a0001 | c0001 | t0038 | g0076 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02683 | hp2 | a0001 | c0001 | t0049 | g0185 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02698 | hp1 | a0001 | c0001 | t0010 | g0089 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02698 | hp2 | a0001 | c0001 | t0010 | g0124 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02723 | hp1 | a0001 | c0001 | t0008 | g0017 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02723 | hp2 | a0006 | c0014 | t0001 | g0135 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02735 | hp1 | a0001 | c0001 | t0005 | g0244 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02735 | hp2 | a0001 | c0001 | t0017 | g0059 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02738 | hp1 | a0001 | c0001 | t0005 | g0170 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02738 | hp2 | a0001 | c0001 | t0015 | g0169 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02809 | hp1 | a0001 | c0002 | t0023 | g0279 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02809 | hp2 | a0001 | c0001 | t0034 | g0034 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02818 | hp1 | a0001 | c0003 | t0009 | g0018 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02818 | hp2 | a0001 | c0001 | t0011 | g0205 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02886 | hp1 | a0001 | c0001 | t0008 | g0165 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02886 | hp2 | a0001 | c0001 | t0042 | g0015 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02895 | hp1 | a0001 | c0001 | t0028 | g0204 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02896 | hp1 | a0001 | c0001 | t0032 | g0158 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02896 | hp2 | a0001 | c0001 | t0037 | g0031 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02897 | hp2 | a0001 | c0001 | t0032 | g0159 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02922 | hp1 | a0001 | c0013 | t0044 | g0063 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0004 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02965 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02965 | hp2 | a0001 | c0001 | t0025 | g0225 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02970 | hp1 | a0001 | c0001 | t0018 | g0113 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0148 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02976 | hp2 | a0001 | c0001 | t0036 | g0210 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03017 | hp1 | a0001 | c0001 | t0012 | g0226 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03017 | hp2 | a0001 | c0001 | t0005 | g0001 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03041 | hp1 | a0001 | c0001 | t0054 | g0154 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0236 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0140 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03098 | hp2 | a0001 | c0001 | t0013 | g0137 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03130 | hp1 | a0001 | c0001 | t0027 | g0163 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03130 | hp2 | a0001 | c0001 | t0036 | g0211 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03139 | hp1 | a0001 | c0001 | t0047 | g0272 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03139 | hp2 | a0001 | c0001 | t0056 | g0224 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0138 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03195 | hp2 | a0001 | c0001 | t0043 | g0015 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03225 | hp1 | a0001 | c0001 | t0048 | g0109 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0147 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03239 | hp1 | a0001 | c0001 | t0010 | g0120 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0199 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03486 | hp1 | a0001 | c0001 | t0004 | g0157 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03486 | hp2 | a0001 | c0001 | t0046 | g0103 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03490 | hp1 | a0001 | c0001 | t0012 | g0186 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0096 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03491 | hp1 | a0001 | c0001 | t0031 | g0227 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03491 | hp2 | a0001 | c0001 | t0005 | g0270 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03492 | hp1 | a0001 | c0001 | t0012 | g0187 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0269 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03516 | hp1 | a0001 | c0002 | t0023 | g0278 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03516 | hp2 | a0001 | c0003 | t0009 | g0007 | AFR | ESN | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03540 | hp1 | a0001 | c0003 | t0009 | g0007 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | GWD | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03579 | hp1 | a0001 | c0001 | t0008 | g0004 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03579 | hp2 | a0001 | c0001 | t0017 | g0100 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03669 | hp1 | a0001 | c0001 | t0029 | g0188 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03669 | hp2 | a0001 | c0001 | t0012 | g0196 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0261 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03710 | hp2 | a0001 | c0001 | t0020 | g0267 | SAS | PJL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03834 | hp1 | a0001 | c0001 | t0017 | g0026 | SAS | BEB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03834 | hp2 | a0001 | c0001 | t0019 | g0029 | SAS | BEB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03942 | hp1 | a0001 | c0001 | t0011 | g0265 | SAS | BEB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03942 | hp2 | a0001 | c0001 | t0006 | g0173 | SAS | BEB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04115 | hp1 | a0001 | c0001 | t0007 | g0023 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0180 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04199 | hp1 | a0001 | c0001 | t0022 | g0095 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04199 | hp2 | a0001 | c0001 | t0028 | g0197 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04204 | hp1 | a0001 | c0001 | t0008 | g0024 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0122 | SAS | STU | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18522 | hp1 | a0001 | c0001 | t0009 | g0139 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0008 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18906 | hp1 | a0001 | c0001 | t0025 | g0162 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18906 | hp2 | a0001 | c0001 | t0017 | g0098 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18942 | hp1 | a0001 | c0001 | t0006 | g0160 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18943 | hp1 | a0001 | c0001 | t0039 | g0009 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18943 | hp2 | a0001 | c0001 | t0035 | g0241 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18944 | hp2 | a0001 | c0001 | t0008 | g0009 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18946 | hp2 | a0001 | c0001 | t0013 | g0104 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18947 | hp1 | a0001 | c0001 | t0004 | g0266 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18950 | hp1 | a0001 | c0001 | t0007 | g0001 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18950 | hp2 | a0001 | c0001 | t0051 | g0174 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18952 | hp1 | a0001 | c0001 | t0004 | g0276 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18952 | hp2 | a0001 | c0001 | t0003 | g0052 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18957 | hp1 | a0001 | c0001 | t0018 | g0038 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18957 | hp2 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18959 | hp1 | a0002 | c0010 | t0005 | g0118 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0045 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18962 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18968 | hp1 | a0002 | c0004 | t0007 | g0101 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18968 | hp2 | a0001 | c0001 | t0028 | g0233 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18970 | hp2 | a0001 | c0001 | t0008 | g0021 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18971 | hp1 | a0002 | c0004 | t0005 | g0221 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18971 | hp2 | a0007 | c0005 | t0006 | g0234 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18975 | hp1 | a0001 | c0001 | t0011 | g0254 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18975 | hp2 | a0001 | c0001 | t0007 | g0090 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18977 | hp1 | a0001 | c0001 | t0004 | g0231 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18977 | hp2 | a0001 | c0001 | t0003 | g0275 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18981 | hp1 | a0008 | c0006 | t0015 | g0242 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18981 | hp2 | a0001 | c0001 | t0006 | g0263 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18982 | hp1 | a0001 | c0001 | t0006 | g0036 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18984 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18984 | hp2 | a0001 | c0001 | t0026 | g0256 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18986 | hp2 | a0001 | c0001 | t0004 | g0232 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18989 | hp1 | a0001 | c0001 | t0005 | g0203 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0282 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18990 | hp2 | a0002 | c0004 | t0005 | g0222 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18995 | hp2 | a0001 | c0001 | t0016 | g0054 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18997 | hp1 | a0001 | c0001 | t0013 | g0051 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18997 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19007 | hp2 | a0001 | c0001 | t0006 | g0176 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19010 | hp1 | a0001 | c0001 | t0026 | g0240 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19012 | hp1 | a0001 | c0001 | t0006 | g0177 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19030 | hp1 | a0001 | c0001 | t0053 | g0006 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0149 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19043 | hp1 | a0001 | c0011 | t0011 | g0255 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19043 | hp2 | a0001 | c0001 | t0052 | g0262 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19060 | hp2 | a0001 | c0007 | t0001 | g0001 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19067 | hp1 | a0001 | c0001 | t0004 | g0014 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19068 | hp1 | a0001 | c0001 | t0007 | g0055 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0245 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19079 | hp1 | a0001 | c0001 | t0013 | g0002 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19079 | hp2 | a0001 | c0001 | t0008 | g0039 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19081 | hp1 | a0001 | c0001 | t0040 | g0066 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19082 | hp1 | a0001 | c0001 | t0017 | g0037 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19084 | hp1 | a0001 | c0001 | t0007 | g0057 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19085 | hp2 | a0001 | c0001 | t0003 | g0116 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19088 | hp1 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0258 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19091 | hp1 | a0001 | c0001 | t0012 | g0193 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0115 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA19240 | hp2 | a0001 | c0001 | t0018 | g0020 | AFR | YRI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20129 | hp1 | a0001 | c0001 | t0023 | g0099 | AFR | ASW | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20129 | hp2 | a0001 | c0001 | t0014 | g0097 | AFR | ASW | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20752 | hp1 | a0001 | c0001 | t0041 | g0073 | EUR | TSI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0061 | EUR | TSI | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0268 | SAS | GIH | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20905 | hp2 | a0001 | c0001 | t0010 | g0079 | SAS | GIH | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0215 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG01123 | hp2 | a0003 | c0008 | t0014 | g0046 | AMR | CLM | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02486 | hp1 | a0001 | c0001 | t0031 | g0006 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02486 | hp2 | a0001 | c0001 | t0033 | g0121 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02559 | hp1 | a0001 | c0001 | t0020 | g0190 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG02559 | hp2 | a0001 | c0001 | t0024 | g0134 | AFR | ACB | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03471 | hp1 | a0001 | c0001 | t0029 | g0153 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | MSL | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | USA | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0259 | AFR | USA | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0125 | AFR | USA | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA20300 | hp2 | a0001 | c0001 | t0015 | g0161 | AFR | USA | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA21309 | hp1 | a0001 | c0001 | t0018 | g0209 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
NA21309 | hp2 | a0001 | c0001 | t0025 | g0168 | AFR | LWK | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
homoSapiens | chm13v2 | a0001 | c0001 | t0006 | g0246 | REF | REF | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | AXL_chr19_41214223_41266766 | AXL | chr19 | 41214223 | 41266766 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41219445 | C | T | 1 | a0006 | 1 | HG02723.hp2 | missense_variant | MODERATE | c.53C>T | p.Ala18Val | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/20 | 223/4717 | 53/2685 | 18/894 | chr19 | 41219445 | |||
chr19:41220693 | G | A | 1 | a0007 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.143G>A | p.Arg48Gln | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 2/20 | 313/4717 | 143/2685 | 48/894 | chr19 | 41220693 | |||
chr19:41221919 | T | C | 1 | a0008 | 1 | NA18981.hp1 | missense_variant | MODERATE | c.449T>C | p.Val150Ala | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/20 | 619/4717 | 449/2685 | 150/894 | chr19 | 41221919 | |||
chr19:41238005 | C | T | 1 | a0004 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.845C>T | p.Pro282Leu | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/20 | 1015/4717 | 845/2685 | 282/894 | chr19 | 41238005 | |||
chr19:41242913 | G | T | 1 | a0002 | 4 | NA18959.hp1 NA18968.hp1 NA18971.hp1 others(1): Show |
missense_variant | MODERATE | c.1343G>T | p.Trp448Leu | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/20 | 1513/4717 | 1343/2685 | 448/894 | chr19 | 41242913 | |||
chr19:41253609 | C | T | 1 | a0004 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.1937C>T | p.Thr646Ile | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/20 | 2107/4717 | 1937/2685 | 646/894 | chr19 | 41253609 | |||
chr19:41257584 | G | A | 1 | a0003 | 1 | HG01123.hp2 | missense_variant | MODERATE | c.2288G>A | p.Arg763His | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/20 | 2458/4717 | 2288/2685 | 763/894 | chr19 | 41257584 | |||
chr19:41259633 | A | C | 1 | a0005 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.2414A>C | p.Asn805Thr | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 2584/4717 | 2414/2685 | 805/894 | chr19 | 41259633 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41221905 | C | T | 1 | a0001c0013 | 1 | HG02922.hp1 | synonymous_variant | LOW | c.435C>T | p.Pro145Pro | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/20 | 605/4717 | 435/2685 | 145/894 | chr19 | 41221905 | |||
chr19:41238024 | C | T | 1 | a0001c0011 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.864C>T | p.Ser288Ser | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/20 | 1034/4717 | 864/2685 | 288/894 | chr19 | 41238024 | |||
chr19:41238144 | G | A | 1 | a0001c0007 | 1 | NA19060.hp2 | synonymous_variant | LOW | c.984G>A | p.Thr328Thr | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/20 | 1154/4717 | 984/2685 | 328/894 | chr19 | 41238144 | |||
chr19:41242986 | C | T | 1 | a0002c0010 | 1 | NA18959.hp1 | synonymous_variant | LOW | c.1416C>T | p.Val472Val | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/20 | 1586/4717 | 1416/2685 | 472/894 | chr19 | 41242986 | |||
chr19:41259670 | C | T | 1 | a0001c0003 | 4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
synonymous_variant | LOW | c.2451C>T | p.Asp817Asp | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 2621/4717 | 2451/2685 | 817/894 | chr19 | 41259670 | |||
chr19:41259712 | T | C | 1 | a0001c0002 | 4 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.2493T>C | p.Pro831Pro | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 2663/4717 | 2493/2685 | 831/894 | chr19 | 41259712 | |||
chr19:41259847 | C | T | 1 | a0001c0011 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.2628C>T | p.Pro876Pro | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 2798/4717 | 2628/2685 | 876/894 | chr19 | 41259847 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41219353 | C | T | 1 | a0001c0001t0032 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-40C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/20 | chr19 | 41219353 | |||||||
chr19:41219366 | A | G | 37 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(34): Show |
156 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(153): Show |
5_prime_UTR_variant | MODIFIER | c.-27A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/20 | 27 | chr19 | 41219366 | ||||||
chr19:41259953 | C | T | 1 | a0001c0001t0046 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*49C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 49 | chr19 | 41259953 | ||||||
chr19:41259975 | C | A | 2 | a0001c0001t0037 a0001c0001t0047 |
2 | HG02896.hp2 HG03139.hp1 |
3_prime_UTR_variant | MODIFIER | c.*71C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 71 | chr19 | 41259975 | ||||||
chr19:41259992 | C | T | 1 | a0001c0001t0045 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*88C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 88 | chr19 | 41259992 | ||||||
chr19:41260272 | T | C | 1 | a0001c0001t0032 | 3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*368T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 368 | chr19 | 41260272 | ||||||
chr19:41260298 | C | CT | 8 | a0001c0001t0005 a0001c0001t0007 a0001c0001t0026 others(5): Show |
38 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*425dupT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTT | 2 | a0001c0001t0016 a0001c0001t0024 |
9 | HG01109.hp1 HG01109.hp2 HG01257.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*424_*425dupTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTT | 2 | a0001c0001t0010 a0001c0001t0027 |
11 | HG01070.hp2 HG01071.hp1 HG01099.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*422_*425dupTTTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTT | 2 | a0001c0001t0022 a0001c0001t0028 |
7 | HG01081.hp2 HG01169.hp1 HG01192.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*421_*425dupTTTTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTT | 5 | a0001c0001t0011 a0001c0001t0023 a0001c0001t0052 others(2): Show |
13 | HG01071.hp2 HG01074.hp2 HG01256.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*420_*425dupTTTTTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT | 4 | a0001c0001t0009 a0001c0001t0012 a0001c0002t0009 others(1): Show |
20 | HG00639.hp1 HG01496.hp1 HG01891.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*419_*425dupTTTTTT others(1): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(1): Show |
3 | a0001c0001t0017 a0001c0001t0029 a0001c0002t0029 |
8 | HG02622.hp1 HG02735.hp2 HG03471.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*418_*425dupTTTTTT others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(2): Show |
2 | a0001c0001t0018 a0001c0001t0025 |
9 | HG02257.hp1 HG02258.hp1 HG02965.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*417_*425dupTTTTTT others(3): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(3): Show |
2 | a0001c0001t0019 a0001c0001t0030 |
8 | HG01081.hp1 HG01243.hp1 HG01243.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*416_*425dupTTTTTT others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(4): Show |
1 | a0001c0001t0042 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*415_*425dupTTTTTT others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(6): Show |
3 | a0001c0001t0031 a0001c0001t0033 a0005c0009t0033 |
5 | HG01884.hp1 HG02486.hp1 HG02486.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*413_*425dupTTTTTT others(7): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0053 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*412_*425dupTTTTTT others(8): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(8): Show |
1 | a0001c0001t0054 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*411_*425dupTTTTTT others(9): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(9): Show |
2 | a0001c0001t0043 a0001c0001t0055 |
2 | HG02280.hp2 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*410_*425dupTTTTTT others(10): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(11): Show |
1 | a0001c0013t0044 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*408_*425dupTTTTTT others(12): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(12): Show |
1 | a0001c0001t0056 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*407_*425dupTTTTTT others(13): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(13): Show |
2 | a0001c0001t0034 a0001c0001t0057 |
3 | HG00738.hp1 HG00738.hp2 HG02809.hp2 |
3_prime_UTR_variant | MODIFIER | c.*406_*425dupTTTTTT others(14): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(15): Show |
1 | a0001c0001t0058 | 1 | HG00642.hp2 | 3_prime_UTR_variant | MODIFIER | c.*404_*425dupTTTTTT others(16): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | C | CTTTTTTT others(16): Show |
1 | a0001c0001t0036 | 2 | HG02976.hp2 HG03130.hp2 |
3_prime_UTR_variant | MODIFIER | c.*403_*425dupTTTTTT others(17): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 426 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | CTTTTT | C | 3 | a0001c0001t0013 a0001c0001t0015 a0008c0006t0015 |
12 | HG00423.hp1 HG00423.hp2 HG00735.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*421_*425delTTTTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 421 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | CTTTTTT | C | 3 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0051 |
49 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*420_*425delTTTTTT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 420 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0039 a0001c0001t0050 |
2 | HG02155.hp1 NA18943.hp1 |
3_prime_UTR_variant | MODIFIER | c.*416_*425delTTTTTT others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 416 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | CTTTTTTT others(4): Show |
C | 4 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0021 others(1): Show |
39 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*415_*425delTTTTTT others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 415 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0038 a0001c0001t0049 |
2 | HG02683.hp1 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*414_*425delTTTTTT others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 414 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260298 | CTTTTTTT others(8): Show |
C | 3 | a0001c0001t0037 a0001c0001t0047 a0001c0001t0048 |
3 | HG02896.hp2 HG03139.hp1 HG03225.hp1 |
3_prime_UTR_variant | MODIFIER | c.*411_*425delTTTTTT others(9): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 411 | INFO_REALIGN_3_PRIME | chr19 | 41260298 | |||||
chr19:41260380 | C | T | 1 | a0001c0001t0041 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*476C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 476 | chr19 | 41260380 | ||||||
chr19:41260473 | G | A | 1 | a0001c0001t0021 | 4 | HG01167.hp2 HG01169.hp2 HG01361.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*569G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 569 | chr19 | 41260473 | ||||||
chr19:41260853 | T | C | 1 | a0001c0001t0047 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*949T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 949 | chr19 | 41260853 | ||||||
chr19:41260890 | G | A | 1 | a0001c0001t0040 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*986G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 986 | chr19 | 41260890 | ||||||
chr19:41261043 | A | G | 1 | a0001c0001t0051 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1139A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1139 | chr19 | 41261043 | ||||||
chr19:41261073 | G | C | 3 | a0001c0001t0014 a0001c0001t0020 a0003c0008t0014 |
11 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1169G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1169 | chr19 | 41261073 | ||||||
chr19:41261077 | C | T | 1 | a0001c0001t0052 | 1 | NA19043.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1173C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1173 | chr19 | 41261077 | ||||||
chr19:41261085 | C | T | 2 | a0001c0001t0056 a0001c0013t0044 |
2 | HG02922.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1181C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1181 | chr19 | 41261085 | ||||||
chr19:41261138 | G | A | 1 | a0001c0001t0037 | 1 | HG02896.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1234G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1234 | chr19 | 41261138 | ||||||
chr19:41261390 | C | T | 7 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0021 others(4): Show |
45 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*1486C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 20/20 | 1486 | chr19 | 41261390 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:41219505 | G | A | 5 | a0001c0001t0008g0017 a0001c0001t0018g0020 a0001c0003t0009g0007 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+28G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219505 | |||||||
chr19:41219625 | GAC | G | 5 | a0001c0001t0008g0017 a0001c0001t0018g0020 a0001c0003t0009g0007 others(2): Show |
6 | HG02145.hp1 HG02723.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.85+152_85+153delCA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | 41219625 | ||||||
chr19:41219846 | C | T | 1 | a0001c0001t0032g0283 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.85+369C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219846 | |||||||
chr19:41219847 | A | G | 165 | a0001c0001t0001g0016 a0001c0001t0001g0145 a0001c0001t0002g0003 others(162): Show |
170 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.85+370A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219847 | |||||||
chr19:41219849 | T | C | 163 | a0001c0001t0001g0145 a0001c0001t0002g0003 a0001c0001t0002g0012 others(160): Show |
167 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.85+372T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219849 | |||||||
chr19:41219852 | G | C | 1 | a0001c0001t0005g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.85+375G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219852 | |||||||
chr19:41219885 | G | C | 161 | a0001c0001t0001g0145 a0001c0001t0002g0003 a0001c0001t0002g0012 others(158): Show |
165 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(162): Show |
intron_variant | MODIFIER | c.85+408G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219885 | |||||||
chr19:41219931 | C | A | 1 | a0001c0001t0004g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.85+454C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219931 | |||||||
chr19:41219933 | C | A | 1 | a0001c0001t0047g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.85+456C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41219933 | |||||||
chr19:41220027 | C | A | 3 | a0001c0001t0002g0133 a0001c0001t0011g0132 a0001c0001t0024g0134 |
3 | HG01074.hp2 HG01358.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.85+550C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220027 | |||||||
chr19:41220068 | GTCTC | G | 10 | a0001c0001t0002g0264 a0001c0001t0004g0266 a0001c0001t0005g0270 others(7): Show |
10 | HG00597.hp2 HG01346.hp2 HG03491.hp2 others(7): Show |
intron_variant | MODIFIER | c.86-558_86-555delCT others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | 41220068 | ||||||
chr19:41220093 | C | G | 1 | a0001c0001t0009g0030 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.86-543C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220093 | |||||||
chr19:41220124 | C | G | 4 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0129 others(1): Show |
4 | HG01070.hp1 HG01361.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.86-512C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220124 | |||||||
chr19:41220228 | GCCACCAC others(15): Show |
G | 59 | a0001c0001t0002g0003 a0001c0001t0002g0133 a0001c0001t0002g0235 others(56): Show |
63 | HG00597.hp1 HG00621.hp2 HG00639.hp1 others(60): Show |
intron_variant | MODIFIER | c.86-391_86-370delCC others(20): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | 41220228 | ||||||
chr19:41220242 | CTCCCCCC others(11): Show |
C | 1 | a0006c0014t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.86-392_86-375delCC others(16): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | INFO_REALIGN_3_PRIME | chr19 | 41220242 | ||||||
chr19:41220262 | A | C | 84 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0189 others(81): Show |
84 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.86-374A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220262 | |||||||
chr19:41220448 | T | C | 3 | a0001c0001t0042g0015 a0001c0001t0043g0015 a0005c0009t0033g0273 |
3 | HG01884.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.86-188T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220448 | |||||||
chr19:41220548 | C | T | 3 | a0001c0001t0002g0223 a0002c0004t0005g0221 a0002c0004t0005g0222 |
3 | NA18964.hp2 NA18971.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.86-88C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220548 | |||||||
chr19:41220549 | G | A | 6 | a0001c0001t0003g0110 a0001c0001t0003g0115 a0001c0001t0018g0112 others(3): Show |
6 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.86-87G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220549 | |||||||
chr19:41220573 | T | C | 1 | a0006c0014t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.86-63T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 1/19 | chr19 | 41220573 | |||||||
chr19:41221074 | C | T | 2 | a0001c0001t0006g0125 a0001c0001t0048g0109 |
2 | HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.309-72C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 2/19 | chr19 | 41221074 | |||||||
chr19:41221131 | C | T | 1 | a0001c0001t0001g0108 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.309-15C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 2/19 | chr19 | 41221131 | |||||||
chr19:41221292 | C | T | 40 | a0001c0001t0002g0215 a0001c0001t0002g0217 a0001c0001t0002g0264 others(37): Show |
40 | HG00099.hp1 HG00597.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.409+46C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221292 | |||||||
chr19:41221326 | GGGTCAA | G | 40 | a0001c0001t0002g0215 a0001c0001t0002g0217 a0001c0001t0002g0264 others(37): Show |
40 | HG00099.hp1 HG00597.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.409+87_409+92delGG others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | INFO_REALIGN_3_PRIME | chr19 | 41221326 | ||||||
chr19:41221552 | G | A | 1 | a0001c0001t0037g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.409+306G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221552 | |||||||
chr19:41221563 | G | T | 1 | a0001c0001t0020g0271 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.409+317G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221563 | |||||||
chr19:41221587 | C | A | 11 | a0001c0001t0003g0110 a0001c0001t0003g0115 a0001c0001t0003g0167 others(8): Show |
11 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.410-293C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221587 | |||||||
chr19:41221724 | T | C | 11 | a0001c0001t0003g0110 a0001c0001t0003g0115 a0001c0001t0003g0167 others(8): Show |
11 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.410-156T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221724 | |||||||
chr19:41221864 | C | T | 1 | a0001c0001t0002g0213 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.410-16C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 3/19 | chr19 | 41221864 | |||||||
chr19:41222202 | T | C | 1 | a0001c0001t0001g0032 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.586+146T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222202 | |||||||
chr19:41222269 | T | G | 2 | a0001c0001t0003g0033 a0001c0001t0003g0116 |
2 | HG00558.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.586+213T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222269 | |||||||
chr19:41222306 | G | GTC | 10 | a0001c0001t0002g0264 a0001c0001t0004g0266 a0001c0001t0005g0270 others(7): Show |
10 | HG00597.hp2 HG01346.hp2 HG02129.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+260_586+261dup others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41222306 | ||||||
chr19:41222330 | C | T | 3 | a0001c0001t0003g0167 a0001c0001t0006g0125 a0001c0001t0048g0109 |
3 | HG02615.hp2 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.586+274C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222330 | |||||||
chr19:41222483 | C | T | 1 | a0001c0001t0004g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.586+427C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222483 | |||||||
chr19:41222530 | C | T | 3 | a0001c0001t0019g0105 a0001c0001t0019g0106 a0001c0001t0034g0107 |
3 | HG00738.hp1 HG01243.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.586+474C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222530 | |||||||
chr19:41222548 | G | T | 1 | a0001c0001t0013g0104 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.586+492G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222548 | |||||||
chr19:41222550 | G | C | 15 | a0001c0001t0008g0004 a0001c0001t0008g0008 a0001c0001t0008g0017 others(12): Show |
19 | HG02145.hp1 HG02258.hp2 HG02723.hp1 others(16): Show |
intron_variant | MODIFIER | c.586+494G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222550 | |||||||
chr19:41222634 | T | C | 41 | a0001c0001t0002g0215 a0001c0001t0002g0217 a0001c0001t0002g0264 others(38): Show |
41 | HG00099.hp1 HG00597.hp2 HG01074.hp1 others(38): Show |
intron_variant | MODIFIER | c.586+578T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222634 | |||||||
chr19:41222688 | C | T | 1 | a0006c0014t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.586+632C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222688 | |||||||
chr19:41222722 | C | T | 1 | a0001c0001t0006g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.586+666C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222722 | |||||||
chr19:41222740 | A | C | 1 | a0001c0001t0002g0259 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.586+684A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222740 | |||||||
chr19:41222798 | C | T | 20 | a0001c0001t0004g0207 a0001c0001t0004g0208 a0001c0001t0004g0266 others(17): Show |
20 | HG01346.hp2 HG02129.hp2 HG02572.hp1 others(17): Show |
intron_variant | MODIFIER | c.586+742C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222798 | |||||||
chr19:41222855 | G | A | 8 | a0001c0001t0008g0004 a0001c0001t0008g0008 a0001c0001t0009g0138 others(5): Show |
11 | HG02258.hp2 HG02809.hp2 HG02922.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+799G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222855 | |||||||
chr19:41222860 | T | C | 178 | a0001c0001t0001g0035 a0001c0001t0002g0003 a0001c0001t0002g0012 others(175): Show |
186 | HG00099.hp1 HG00280.hp1 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.586+804T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222860 | |||||||
chr19:41222884 | C | A | 5 | a0001c0001t0001g0035 a0001c0001t0002g0012 a0001c0001t0002g0141 others(2): Show |
6 | NA18944.hp1 NA18986.hp1 NA19009.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+828C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222884 | |||||||
chr19:41222910 | GA | G | 93 | a0001c0001t0001g0035 a0001c0001t0001g0102 a0001c0001t0002g0003 others(90): Show |
97 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.586+869delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41222910 | ||||||
chr19:41222960 | C | A | 2 | a0001c0001t0012g0226 a0001c0001t0031g0227 |
2 | HG03017.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.586+904C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41222960 | |||||||
chr19:41223032 | C | T | 1 | a0002c0004t0007g0101 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.586+976C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223032 | |||||||
chr19:41223164 | GGGCATCT others(3): Show |
G | 3 | a0001c0001t0042g0015 a0001c0001t0043g0015 a0005c0009t0033g0273 |
3 | HG01884.hp1 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.586+1110_586+1119d others(12): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41223164 | ||||||
chr19:41223269 | T | G | 1 | a0001c0001t0013g0104 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.586+1213T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223269 | |||||||
chr19:41223486 | C | T | 4 | a0001c0001t0004g0164 a0001c0001t0025g0162 a0001c0001t0027g0163 others(1): Show |
4 | HG02486.hp2 HG03130.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.586+1430C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223486 | |||||||
chr19:41223600 | T | C | 118 | a0001c0001t0001g0016 a0001c0001t0001g0032 a0001c0001t0001g0035 others(115): Show |
126 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.586+1544T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223600 | |||||||
chr19:41223606 | G | A | 1 | a0001c0001t0007g0123 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.586+1550G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223606 | |||||||
chr19:41223808 | G | C | 3 | a0001c0001t0001g0061 a0001c0001t0013g0062 a0001c0001t0015g0169 |
3 | HG00735.hp2 HG02738.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.586+1752G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223808 | |||||||
chr19:41223902 | C | T | 1 | a0001c0001t0001g0060 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.586+1846C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41223902 | |||||||
chr19:41223969 | G | GGT | 6 | a0001c0001t0005g0199 a0001c0001t0005g0270 a0001c0001t0006g0125 others(3): Show |
6 | HG03225.hp1 HG03239.hp2 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+1933_586+1934d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41223969 | ||||||
chr19:41223969 | G | GGTGT | 6 | a0001c0001t0011g0205 a0001c0001t0011g0212 a0001c0001t0025g0225 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.586+1931_586+1934d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41223969 | ||||||
chr19:41223969 | GGT | G | 63 | a0001c0001t0002g0215 a0001c0001t0003g0115 a0001c0001t0004g0131 others(60): Show |
67 | HG00642.hp2 HG00735.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.586+1933_586+1934d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41223969 | ||||||
chr19:41224046 | T | C | 1 | a0001c0001t0007g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.586+1990T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224046 | |||||||
chr19:41224066 | G | A | 1 | a0001c0001t0047g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.586+2010G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224066 | |||||||
chr19:41224108 | G | A | 10 | a0001c0001t0003g0115 a0001c0001t0009g0280 a0001c0001t0018g0112 others(7): Show |
10 | HG01891.hp1 HG02055.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+2052G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224108 | |||||||
chr19:41224114 | T | C | 2 | a0001c0001t0010g0119 a0001c0001t0022g0117 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.586+2058T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224114 | |||||||
chr19:41224707 | G | T | 1 | a0001c0001t0019g0029 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.586+2651G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224707 | |||||||
chr19:41224734 | G | A | 1 | a0001c0001t0011g0216 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.586+2678G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224734 | |||||||
chr19:41224753 | G | T | 2 | a0001c0001t0008g0009 a0001c0001t0039g0009 |
2 | NA18943.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.586+2697G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224753 | |||||||
chr19:41224788 | C | CTG | 57 | a0001c0001t0001g0096 a0001c0001t0002g0189 a0001c0001t0002g0223 others(54): Show |
58 | HG00735.hp1 HG00738.hp1 HG01070.hp2 others(55): Show |
intron_variant | MODIFIER | c.586+2752_586+2753d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41224788 | ||||||
chr19:41224788 | C | CTGTG | 4 | a0001c0001t0017g0098 a0001c0001t0017g0100 a0001c0001t0023g0099 others(1): Show |
4 | HG02896.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+2750_586+2753d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41224788 | ||||||
chr19:41224788 | CTG | C | 9 | a0001c0001t0006g0125 a0001c0001t0018g0112 a0001c0001t0018g0113 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+2752_586+2753d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41224788 | ||||||
chr19:41224888 | G | A | 1 | a0001c0001t0046g0103 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.586+2832G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41224888 | |||||||
chr19:41225002 | T | G | 19 | a0001c0001t0004g0131 a0001c0001t0004g0136 a0001c0001t0004g0147 others(16): Show |
22 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.586+2946T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225002 | |||||||
chr19:41225067 | G | A | 19 | a0001c0001t0004g0131 a0001c0001t0004g0136 a0001c0001t0004g0147 others(16): Show |
22 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(19): Show |
intron_variant | MODIFIER | c.586+3011G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225067 | |||||||
chr19:41225080 | T | C | 9 | a0001c0001t0006g0125 a0001c0001t0018g0112 a0001c0001t0018g0113 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+3024T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225080 | |||||||
chr19:41225270 | A | G | 10 | a0001c0001t0001g0129 a0001c0001t0014g0064 a0001c0001t0014g0065 others(7): Show |
10 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+3214A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225270 | |||||||
chr19:41225700 | G | A | 1 | a0005c0009t0033g0273 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.586+3644G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225700 | |||||||
chr19:41225844 | T | G | 70 | a0001c0001t0001g0067 a0001c0001t0002g0192 a0001c0001t0002g0217 others(67): Show |
72 | HG00099.hp1 HG00323.hp1 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.586+3788T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225844 | |||||||
chr19:41225961 | G | A | 1 | a0004c0012t0007g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.586+3905G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225961 | |||||||
chr19:41225971 | G | A | 9 | a0001c0001t0006g0125 a0001c0001t0018g0112 a0001c0001t0018g0113 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.586+3915G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41225971 | |||||||
chr19:41226011 | G | T | 2 | a0001c0001t0015g0161 a0001c0011t0011g0255 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.586+3955G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226011 | |||||||
chr19:41226067 | G | A | 1 | a0001c0001t0004g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.586+4011G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226067 | |||||||
chr19:41226097 | A | G | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.586+4041A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226097 | |||||||
chr19:41226123 | G | A | 1 | a0001c0001t0055g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.586+4067G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226123 | |||||||
chr19:41226191 | G | T | 2 | a0001c0001t0005g0270 a0001c0001t0006g0269 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.586+4135G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226191 | |||||||
chr19:41226463 | T | C | 1 | a0001c0001t0006g0263 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.586+4407T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226463 | |||||||
chr19:41226474 | G | T | 1 | a0001c0002t0023g0278 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.586+4418G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226474 | |||||||
chr19:41226518 | T | C | 172 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(169): Show |
185 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.587-4449T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226518 | |||||||
chr19:41226585 | C | T | 1 | a0001c0001t0026g0243 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.587-4382C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226585 | |||||||
chr19:41226705 | C | G | 18 | a0001c0001t0001g0129 a0001c0001t0014g0064 a0001c0001t0014g0065 others(15): Show |
18 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.587-4262C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226705 | |||||||
chr19:41226783 | G | T | 10 | a0001c0001t0001g0129 a0001c0001t0014g0064 a0001c0001t0014g0065 others(7): Show |
10 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.587-4184G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226783 | |||||||
chr19:41226822 | C | G | 159 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0002g0003 others(156): Show |
171 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(168): Show |
intron_variant | MODIFIER | c.587-4145C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226822 | |||||||
chr19:41226826 | T | A | 2 | a0001c0001t0003g0033 a0001c0001t0003g0116 |
2 | HG00558.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.587-4141T>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41226826 | |||||||
chr19:41227240 | G | C | 166 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(163): Show |
177 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(174): Show |
intron_variant | MODIFIER | c.587-3727G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227240 | |||||||
chr19:41227450 | A | G | 17 | a0001c0001t0001g0129 a0001c0001t0014g0064 a0001c0001t0014g0065 others(14): Show |
17 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.587-3517A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227450 | |||||||
chr19:41227454 | G | A | 1 | a0001c0001t0007g0053 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.587-3513G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227454 | |||||||
chr19:41227462 | G | A | 1 | a0001c0001t0033g0121 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.587-3505G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227462 | |||||||
chr19:41227488 | C | CT | 23 | a0001c0001t0001g0035 a0001c0001t0001g0129 a0001c0001t0005g0203 others(20): Show |
23 | HG00735.hp1 HG01192.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.587-3463dupT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41227488 | ||||||
chr19:41227488 | CT | C | 76 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(73): Show |
84 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(81): Show |
intron_variant | MODIFIER | c.587-3463delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41227488 | ||||||
chr19:41227548 | C | T | 3 | a0001c0001t0001g0058 a0001c0001t0001g0145 a0001c0001t0005g0249 |
3 | HG02056.hp1 NA18942.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.587-3419C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227548 | |||||||
chr19:41227725 | G | A | 1 | a0001c0001t0005g0218 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.587-3242G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227725 | |||||||
chr19:41227911 | G | A | 1 | a0001c0001t0002g0235 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.587-3056G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227911 | |||||||
chr19:41227918 | G | A | 1 | a0001c0001t0041g0073 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.587-3049G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227918 | |||||||
chr19:41227923 | G | A | 1 | a0001c0001t0018g0209 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.587-3044G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41227923 | |||||||
chr19:41228110 | G | A | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-2857G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228110 | |||||||
chr19:41228146 | G | A | 3 | a0001c0001t0012g0152 a0001c0001t0056g0224 a0001c0013t0044g0063 |
3 | HG01496.hp1 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.587-2821G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228146 | |||||||
chr19:41228154 | C | T | 170 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(167): Show |
182 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.587-2813C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228154 | |||||||
chr19:41228190 | T | C | 1 | a0001c0001t0004g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.587-2777T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228190 | |||||||
chr19:41228585 | C | G | 106 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(103): Show |
115 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.587-2382C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228585 | |||||||
chr19:41228586 | G | A | 3 | a0001c0001t0005g0170 a0001c0001t0005g0244 a0001c0001t0007g0122 |
3 | HG02735.hp1 HG02738.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.587-2381G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228586 | |||||||
chr19:41228632 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.587-2335G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228632 | |||||||
chr19:41228655 | T | C | 176 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(173): Show |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.587-2312T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228655 | |||||||
chr19:41228675 | C | T | 3 | a0001c0001t0013g0137 a0001c0001t0025g0166 a0001c0001t0031g0150 |
3 | HG02257.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.587-2292C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228675 | |||||||
chr19:41228761 | C | T | 145 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(142): Show |
156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.587-2206C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228761 | |||||||
chr19:41228940 | G | T | 174 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(171): Show |
186 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(183): Show |
intron_variant | MODIFIER | c.587-2027G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41228940 | |||||||
chr19:41228947 | CT | C | 8 | a0001c0001t0014g0064 a0001c0001t0014g0065 a0001c0001t0014g0097 others(5): Show |
8 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-2016delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41228947 | ||||||
chr19:41228953 | TTTC | T | 8 | a0001c0001t0014g0064 a0001c0001t0014g0065 a0001c0001t0014g0097 others(5): Show |
8 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-2011_587-2009d others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41228953 | ||||||
chr19:41228956 | C | CT | 117 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(114): Show |
129 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.587-2001dupT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41228956 | ||||||
chr19:41228956 | C | CTT | 43 | a0001c0001t0003g0275 a0001c0001t0004g0260 a0001c0001t0005g0172 others(40): Show |
43 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(40): Show |
intron_variant | MODIFIER | c.587-2002_587-2001d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41228956 | ||||||
chr19:41229010 | C | T | 1 | a0001c0001t0048g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.587-1957C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229010 | |||||||
chr19:41229053 | T | G | 176 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(173): Show |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.587-1914T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229053 | |||||||
chr19:41229210 | T | C | 176 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(173): Show |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.587-1757T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229210 | |||||||
chr19:41229239 | G | A | 8 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-1728G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229239 | |||||||
chr19:41229305 | C | T | 1 | a0001c0001t0007g0090 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.587-1662C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229305 | |||||||
chr19:41229347 | T | C | 1 | a0001c0001t0005g0249 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.587-1620T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229347 | |||||||
chr19:41229412 | G | T | 1 | a0001c0001t0004g0202 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.587-1555G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229412 | |||||||
chr19:41229466 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.587-1501C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229466 | |||||||
chr19:41229531 | C | T | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.587-1436C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229531 | |||||||
chr19:41229553 | C | G | 8 | a0001c0001t0006g0155 a0001c0001t0011g0205 a0001c0001t0011g0212 others(5): Show |
8 | HG01884.hp1 HG02451.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.587-1414C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229553 | |||||||
chr19:41229751 | A | T | 11 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(8): Show |
12 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.587-1216A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229751 | |||||||
chr19:41229769 | C | T | 1 | a0001c0001t0001g0129 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.587-1198C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229769 | |||||||
chr19:41229887 | G | A | 1 | a0004c0012t0007g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-1080G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229887 | |||||||
chr19:41229937 | A | G | 6 | a0001c0001t0009g0138 a0001c0001t0009g0139 a0001c0001t0009g0140 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.587-1030A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229937 | |||||||
chr19:41229983 | G | A | 1 | a0001c0001t0020g0267 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.587-984G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41229983 | |||||||
chr19:41230100 | G | C | 1 | a0001c0001t0006g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.587-867G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230100 | |||||||
chr19:41230114 | TGTGTGTG others(7): Show |
T | 1 | a0004c0012t0007g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-845_587-832del others(14): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41230114 | ||||||
chr19:41230136 | T | G | 1 | a0004c0012t0007g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-831T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230136 | |||||||
chr19:41230137 | G | C | 1 | a0004c0012t0007g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-830G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230137 | |||||||
chr19:41230142 | G | A | 1 | a0001c0001t0003g0050 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.587-825G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230142 | |||||||
chr19:41230145 | G | C | 1 | a0004c0012t0007g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-822G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230145 | |||||||
chr19:41230147 | G | GTCTGTTT others(3): Show |
1 | a0001c0001t0013g0104 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.587-813_587-812ins others(10): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41230147 | ||||||
chr19:41230149 | C | CTGTT | 133 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(130): Show |
145 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.587-816_587-813dup others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41230149 | ||||||
chr19:41230149 | C | T | 1 | a0004c0012t0007g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.587-818C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230149 | |||||||
chr19:41230153 | TTC | T | 6 | a0001c0001t0011g0205 a0001c0001t0011g0212 a0001c0001t0025g0225 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-812_587-811del others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41230153 | ||||||
chr19:41230159 | G | T | 6 | a0001c0001t0011g0205 a0001c0001t0011g0212 a0001c0001t0025g0225 others(3): Show |
6 | HG02572.hp2 HG02630.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.587-808G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230159 | |||||||
chr19:41230257 | A | C | 1 | a0001c0001t0003g0022 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.587-710A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230257 | |||||||
chr19:41230264 | G | A | 13 | a0001c0001t0004g0131 a0001c0001t0004g0136 a0001c0001t0004g0147 others(10): Show |
13 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.587-703G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230264 | |||||||
chr19:41230321 | A | ATG | 14 | a0001c0001t0004g0131 a0001c0001t0004g0136 a0001c0001t0004g0147 others(11): Show |
14 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.587-630_587-629dup others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | INFO_REALIGN_3_PRIME | chr19 | 41230321 | ||||||
chr19:41230485 | T | G | 15 | a0001c0001t0004g0131 a0001c0001t0004g0136 a0001c0001t0004g0147 others(12): Show |
15 | HG01891.hp2 HG02257.hp1 HG02257.hp2 others(12): Show |
intron_variant | MODIFIER | c.587-482T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230485 | |||||||
chr19:41230517 | T | C | 48 | a0001c0001t0003g0275 a0001c0001t0004g0131 a0001c0001t0004g0136 others(45): Show |
48 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.587-450T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230517 | |||||||
chr19:41230548 | G | C | 48 | a0001c0001t0003g0275 a0001c0001t0004g0131 a0001c0001t0004g0136 others(45): Show |
48 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(45): Show |
intron_variant | MODIFIER | c.587-419G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230548 | |||||||
chr19:41230592 | G | T | 1 | a0001c0001t0010g0089 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.587-375G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230592 | |||||||
chr19:41230756 | G | A | 18 | a0001c0001t0001g0016 a0001c0001t0002g0146 a0001c0001t0002g0235 others(15): Show |
22 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(19): Show |
intron_variant | MODIFIER | c.587-211G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230756 | |||||||
chr19:41230828 | A | C | 1 | a0001c0001t0006g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.587-139A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230828 | |||||||
chr19:41230911 | C | T | 8 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.587-56C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230911 | |||||||
chr19:41230930 | C | T | 3 | a0001c0001t0024g0006 a0001c0001t0031g0006 a0001c0001t0053g0006 |
3 | HG01109.hp2 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.587-37C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 4/19 | chr19 | 41230930 | |||||||
chr19:41231101 | G | C | 1 | a0001c0001t0055g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.667+54G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 5/19 | chr19 | 41231101 | |||||||
chr19:41231103 | G | T | 1 | a0001c0001t0010g0089 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.667+56G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 5/19 | chr19 | 41231103 | |||||||
chr19:41231112 | G | A | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.667+65G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 5/19 | chr19 | 41231112 | |||||||
chr19:41231112 | G | T | 1 | a0001c0001t0015g0161 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.667+65G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 5/19 | chr19 | 41231112 | |||||||
chr19:41231424 | G | T | 39 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(36): Show |
40 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(37): Show |
intron_variant | MODIFIER | c.783+126G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231424 | |||||||
chr19:41231439 | C | T | 10 | a0001c0001t0001g0096 a0001c0001t0010g0011 a0001c0001t0010g0119 others(7): Show |
11 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+141C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231439 | |||||||
chr19:41231505 | C | T | 10 | a0001c0001t0001g0096 a0001c0001t0010g0011 a0001c0001t0010g0119 others(7): Show |
11 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(8): Show |
intron_variant | MODIFIER | c.783+207C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231505 | |||||||
chr19:41231509 | G | A | 3 | a0001c0001t0007g0075 a0001c0001t0007g0123 a0001c0001t0045g0074 |
3 | HG00733.hp1 HG01175.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.783+211G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231509 | |||||||
chr19:41231538 | T | C | 1 | a0001c0001t0006g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.783+240T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231538 | |||||||
chr19:41231583 | G | T | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+285G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231583 | |||||||
chr19:41231584 | T | G | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+286T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231584 | |||||||
chr19:41231585 | G | A | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+287G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231585 | |||||||
chr19:41231616 | A | T | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+318A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231616 | |||||||
chr19:41231620 | C | A | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+322C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231620 | |||||||
chr19:41231625 | G | A | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+327G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231625 | |||||||
chr19:41231639 | A | C | 1 | a0001c0001t0021g0044 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.783+341A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231639 | |||||||
chr19:41231653 | G | A | 1 | a0001c0001t0048g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.783+355G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231653 | |||||||
chr19:41231655 | G | A | 1 | a0001c0001t0049g0185 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.783+357G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231655 | |||||||
chr19:41231798 | G | A | 8 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+500G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231798 | |||||||
chr19:41231859 | G | A | 1 | a0006c0014t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.783+561G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231859 | |||||||
chr19:41231918 | C | A | 1 | a0002c0010t0005g0118 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.783+620C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231918 | |||||||
chr19:41231926 | CA | C | 144 | a0001c0001t0001g0016 a0001c0001t0001g0128 a0001c0001t0001g0129 others(141): Show |
156 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.783+640delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41231926 | ||||||
chr19:41231939 | G | A | 3 | a0001c0001t0004g0136 a0001c0001t0004g0207 a0001c0001t0004g0208 |
3 | HG02572.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.783+641G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231939 | |||||||
chr19:41231940 | A | C | 3 | a0001c0001t0004g0136 a0001c0001t0004g0207 a0001c0001t0004g0208 |
3 | HG02572.hp1 HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.783+642A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231940 | |||||||
chr19:41231943 | C | CA | 9 | a0001c0001t0014g0064 a0001c0001t0018g0112 a0001c0001t0018g0113 others(6): Show |
9 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.783+647dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41231943 | ||||||
chr19:41231945 | A | AAC | 21 | a0001c0001t0001g0096 a0001c0001t0002g0189 a0001c0001t0006g0125 others(18): Show |
22 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.783+647_783+648ins others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231945 | |||||||
chr19:41231945 | AC | A | 3 | a0001c0001t0003g0052 a0001c0001t0014g0065 a0001c0001t0015g0169 |
3 | HG01515.hp2 HG02738.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.783+648delC | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231945 | |||||||
chr19:41231946 | C | A | 93 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(90): Show |
105 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(102): Show |
intron_variant | MODIFIER | c.783+648C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231946 | |||||||
chr19:41231947 | A | C | 7 | a0001c0001t0002g0239 a0001c0001t0032g0158 a0001c0001t0032g0159 others(4): Show |
8 | HG02145.hp1 HG02630.hp1 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.783+649A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231947 | |||||||
chr19:41231948 | A | C | 4 | a0001c0001t0004g0157 a0001c0001t0008g0004 a0001c0001t0008g0008 others(1): Show |
7 | HG02258.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.783+650A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231948 | |||||||
chr19:41231949 | C | A | 94 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(91): Show |
106 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.783+651C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231949 | |||||||
chr19:41231949 | C | CAA | 33 | a0001c0001t0003g0275 a0001c0001t0009g0030 a0001c0001t0009g0220 others(30): Show |
33 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.783+658_783+659dup others(2): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41231949 | ||||||
chr19:41231949 | C | CAAA | 34 | a0001c0001t0004g0014 a0001c0001t0004g0147 a0001c0001t0004g0148 others(31): Show |
35 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(32): Show |
intron_variant | MODIFIER | c.783+657_783+659dup others(3): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41231949 | ||||||
chr19:41231951 | A | C | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.783+653A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41231951 | |||||||
chr19:41232091 | A | G | 177 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(174): Show |
190 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.783+793A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232091 | |||||||
chr19:41232307 | C | T | 72 | a0001c0001t0003g0275 a0001c0001t0004g0014 a0001c0001t0004g0131 others(69): Show |
73 | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.783+1009C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232307 | |||||||
chr19:41232547 | C | T | 6 | a0001c0001t0009g0138 a0001c0001t0009g0139 a0001c0001t0009g0140 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.783+1249C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232547 | |||||||
chr19:41232619 | G | A | 1 | a0001c0001t0012g0196 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.783+1321G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232619 | |||||||
chr19:41232628 | A | G | 176 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(173): Show |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.783+1330A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232628 | |||||||
chr19:41232811 | C | T | 72 | a0001c0001t0003g0275 a0001c0001t0004g0014 a0001c0001t0004g0131 others(69): Show |
73 | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.783+1513C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232811 | |||||||
chr19:41232948 | C | T | 2 | a0001c0001t0015g0161 a0001c0011t0011g0255 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.783+1650C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41232948 | |||||||
chr19:41233149 | C | T | 11 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(8): Show |
12 | HG02055.hp2 HG02145.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.783+1851C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233149 | |||||||
chr19:41233162 | G | A | 1 | a0001c0001t0027g0250 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.783+1864G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233162 | |||||||
chr19:41233164 | A | G | 1 | a0001c0001t0027g0163 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.783+1866A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233164 | |||||||
chr19:41233275 | G | C | 103 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(100): Show |
115 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.783+1977G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233275 | |||||||
chr19:41233278 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.783+1980C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233278 | |||||||
chr19:41233281 | C | T | 1 | a0001c0001t0005g0199 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.783+1983C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233281 | |||||||
chr19:41233349 | T | C | 176 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(173): Show |
189 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(186): Show |
intron_variant | MODIFIER | c.783+2051T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233349 | |||||||
chr19:41233492 | G | A | 3 | a0001c0001t0032g0158 a0001c0001t0032g0159 a0001c0001t0032g0283 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.783+2194G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233492 | |||||||
chr19:41233629 | G | C | 93 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(90): Show |
104 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.783+2331G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233629 | |||||||
chr19:41233669 | C | T | 6 | a0001c0001t0005g0085 a0001c0001t0005g0086 a0001c0001t0007g0075 others(3): Show |
6 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(3): Show |
intron_variant | MODIFIER | c.783+2371C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233669 | |||||||
chr19:41233706 | C | T | 1 | a0001c0001t0031g0227 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.783+2408C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233706 | |||||||
chr19:41233929 | A | C | 38 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(35): Show |
39 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(36): Show |
intron_variant | MODIFIER | c.783+2631A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41233929 | |||||||
chr19:41234015 | C | T | 1 | a0001c0001t0009g0220 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.783+2717C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234015 | |||||||
chr19:41234097 | C | T | 1 | a0001c0001t0007g0023 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.783+2799C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234097 | |||||||
chr19:41234459 | A | T | 1 | a0001c0001t0007g0057 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.783+3161A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234459 | |||||||
chr19:41234686 | T | G | 2 | a0001c0001t0002g0141 a0001c0001t0002g0142 |
2 | NA18986.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.784-3258T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234686 | |||||||
chr19:41234734 | A | G | 29 | a0001c0001t0001g0096 a0001c0001t0002g0189 a0001c0001t0006g0125 others(26): Show |
30 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(27): Show |
intron_variant | MODIFIER | c.784-3210A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234734 | |||||||
chr19:41234930 | G | T | 1 | a0001c0001t0017g0100 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.784-3014G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234930 | |||||||
chr19:41234973 | G | A | 2 | a0001c0001t0011g0265 a0001c0001t0028g0197 |
2 | HG03942.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.784-2971G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234973 | |||||||
chr19:41234990 | T | C | 177 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(174): Show |
190 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(187): Show |
intron_variant | MODIFIER | c.784-2954T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41234990 | |||||||
chr19:41235113 | G | A | 1 | a0001c0001t0038g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.784-2831G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235113 | |||||||
chr19:41235207 | C | T | 32 | a0001c0001t0003g0275 a0001c0001t0009g0030 a0001c0001t0010g0091 others(29): Show |
32 | HG00738.hp1 HG01071.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.784-2737C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235207 | |||||||
chr19:41235351 | CAAAT | C | 3 | a0001c0001t0009g0139 a0001c0001t0009g0140 a0001c0001t0009g0280 |
3 | HG01891.hp1 HG03098.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.784-2575_784-2572d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235351 | ||||||
chr19:41235369 | A | AATAG | 31 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0056 others(28): Show |
32 | HG01109.hp1 HG01123.hp1 HG01168.hp1 others(29): Show |
intron_variant | MODIFIER | c.784-2535_784-2532d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | ||||||
chr19:41235369 | A | G | 2 | a0001c0001t0001g0010 a0001c0001t0009g0138 |
2 | HG03195.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.784-2575A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235369 | |||||||
chr19:41235369 | AATAG | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0127 a0001c0001t0005g0085 others(24): Show |
27 | HG00099.hp2 HG00639.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.784-2535_784-2532d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | ||||||
chr19:41235369 | AATAGATA others(1): Show |
A | 5 | a0001c0001t0006g0184 a0001c0001t0016g0041 a0001c0001t0025g0162 others(2): Show |
5 | HG01928.hp2 HG01952.hp2 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.784-2539_784-2532d others(10): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | ||||||
chr19:41235369 | AATAGATA others(5): Show |
A | 5 | a0001c0001t0012g0152 a0001c0001t0056g0224 a0001c0003t0009g0007 others(2): Show |
6 | HG01496.hp1 HG02145.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.784-2543_784-2532d others(14): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | ||||||
chr19:41235369 | AATAGATA others(9): Show |
A | 15 | a0001c0001t0004g0157 a0001c0001t0006g0155 a0001c0001t0008g0004 others(12): Show |
18 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(15): Show |
intron_variant | MODIFIER | c.784-2547_784-2532d others(18): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | ||||||
chr19:41235369 | AATAGATA others(13): Show |
A | 100 | a0001c0001t0001g0096 a0001c0001t0002g0189 a0001c0001t0003g0275 others(97): Show |
102 | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(99): Show |
intron_variant | MODIFIER | c.784-2551_784-2532d others(22): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | ||||||
chr19:41235369 | AATAGATA others(17): Show |
A | 60 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(57): Show |
67 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.784-2555_784-2532d others(26): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41235369 | ||||||
chr19:41235385 | G | A | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-2559G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235385 | |||||||
chr19:41235389 | G | A | 14 | a0001c0001t0004g0157 a0001c0001t0006g0155 a0001c0001t0008g0004 others(11): Show |
17 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(14): Show |
intron_variant | MODIFIER | c.784-2555G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235389 | |||||||
chr19:41235393 | G | A | 101 | a0001c0001t0001g0096 a0001c0001t0002g0189 a0001c0001t0003g0275 others(98): Show |
103 | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.784-2551G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235393 | |||||||
chr19:41235397 | G | A | 60 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(57): Show |
67 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.784-2547G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235397 | |||||||
chr19:41235435 | A | G | 1 | a0001c0001t0014g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.784-2509A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235435 | |||||||
chr19:41235461 | A | G | 1 | a0001c0001t0004g0208 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.784-2483A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235461 | |||||||
chr19:41235466 | G | A | 1 | a0001c0001t0006g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784-2478G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235466 | |||||||
chr19:41235635 | T | C | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-2309T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235635 | |||||||
chr19:41235652 | G | A | 1 | a0001c0001t0006g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.784-2292G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235652 | |||||||
chr19:41235899 | A | T | 9 | a0001c0001t0001g0058 a0001c0001t0001g0084 a0001c0001t0001g0145 others(6): Show |
9 | HG02056.hp1 HG02698.hp1 NA18942.hp2 others(6): Show |
intron_variant | MODIFIER | c.784-2045A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235899 | |||||||
chr19:41235963 | G | A | 2 | a0001c0001t0010g0120 a0001c0001t0024g0134 |
2 | HG02559.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.784-1981G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41235963 | |||||||
chr19:41236052 | C | T | 8 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-1892C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236052 | |||||||
chr19:41236067 | A | G | 2 | a0001c0001t0009g0030 a0001c0001t0023g0028 |
2 | HG01071.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.784-1877A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236067 | |||||||
chr19:41236204 | A | C | 1 | a0001c0001t0003g0022 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.784-1740A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236204 | |||||||
chr19:41236206 | G | A | 1 | a0001c0001t0002g0236 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.784-1738G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236206 | |||||||
chr19:41236238 | CAGA | C | 8 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-1701_784-1699d others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236238 | ||||||
chr19:41236331 | T | TA | 75 | a0001c0001t0001g0084 a0001c0001t0003g0072 a0001c0001t0003g0275 others(72): Show |
76 | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(73): Show |
intron_variant | MODIFIER | c.784-1592dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236331 | ||||||
chr19:41236331 | T | TAA | 61 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(58): Show |
68 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.784-1593_784-1592d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236331 | ||||||
chr19:41236331 | T | TAAA | 6 | a0001c0001t0002g0012 a0001c0001t0002g0180 a0001c0001t0002g0213 others(3): Show |
7 | HG02055.hp1 HG02056.hp2 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-1594_784-1592d others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236331 | ||||||
chr19:41236331 | TA | T | 7 | a0001c0001t0001g0128 a0001c0001t0004g0157 a0001c0001t0008g0004 others(4): Show |
10 | HG01070.hp1 HG02258.hp2 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.784-1592delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236331 | ||||||
chr19:41236386 | C | T | 1 | a0001c0001t0006g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784-1558C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236386 | |||||||
chr19:41236403 | G | A | 61 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(58): Show |
68 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.784-1541G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236403 | |||||||
chr19:41236498 | A | G | 1 | a0001c0001t0020g0198 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.784-1446A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236498 | |||||||
chr19:41236627 | G | A | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-1317G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236627 | |||||||
chr19:41236685 | A | G | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-1259A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236685 | |||||||
chr19:41236786 | GA | G | 143 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(140): Show |
151 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.784-1143delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236786 | ||||||
chr19:41236786 | GAA | G | 24 | a0001c0001t0001g0096 a0001c0001t0003g0072 a0001c0001t0004g0157 others(21): Show |
28 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.784-1144_784-1143d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | INFO_REALIGN_3_PRIME | chr19 | 41236786 | ||||||
chr19:41236871 | G | A | 1 | a0001c0001t0046g0103 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.784-1073G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236871 | |||||||
chr19:41236880 | G | T | 1 | a0001c0001t0028g0197 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.784-1064G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41236880 | |||||||
chr19:41237024 | G | A | 46 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(43): Show |
48 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.784-920G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237024 | |||||||
chr19:41237093 | C | T | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.784-851C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237093 | |||||||
chr19:41237112 | G | C | 2 | a0001c0001t0004g0131 a0001c0001t0004g0147 |
2 | HG01891.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.784-832G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237112 | |||||||
chr19:41237115 | C | A | 1 | a0001c0001t0012g0193 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.784-829C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237115 | |||||||
chr19:41237239 | A | G | 1 | a0004c0012t0007g0092 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.784-705A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237239 | |||||||
chr19:41237344 | G | A | 41 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(38): Show |
42 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.784-600G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237344 | |||||||
chr19:41237387 | C | T | 8 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.784-557C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237387 | |||||||
chr19:41237477 | C | T | 2 | a0001c0001t0004g0136 a0001c0001t0004g0208 |
2 | HG03471.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.784-467C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237477 | |||||||
chr19:41237549 | C | A | 50 | a0001c0001t0001g0096 a0001c0001t0003g0275 a0001c0001t0006g0125 others(47): Show |
51 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.784-395C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237549 | |||||||
chr19:41237549 | C | T | 2 | a0001c0001t0015g0161 a0001c0011t0011g0255 |
2 | NA19043.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.784-395C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237549 | |||||||
chr19:41237601 | C | G | 1 | a0001c0001t0006g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.784-343C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237601 | |||||||
chr19:41237671 | C | T | 4 | a0001c0001t0004g0157 a0001c0001t0008g0004 a0001c0001t0008g0008 others(1): Show |
7 | HG02258.hp2 HG02723.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.784-273C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 6/19 | chr19 | 41237671 | |||||||
chr19:41238178 | C | T | 1 | a0005c0009t0033g0273 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.994+24C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/19 | chr19 | 41238178 | |||||||
chr19:41238196 | G | A | 1 | a0001c0001t0008g0017 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.994+42G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/19 | chr19 | 41238196 | |||||||
chr19:41238196 | G | T | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.994+42G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/19 | chr19 | 41238196 | |||||||
chr19:41238324 | T | C | 1 | a0001c0001t0006g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.995-146T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/19 | chr19 | 41238324 | |||||||
chr19:41238450 | C | A | 3 | a0001c0001t0013g0137 a0001c0001t0025g0166 a0001c0001t0031g0150 |
3 | HG02257.hp1 HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.995-20C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 7/19 | chr19 | 41238450 | |||||||
chr19:41238926 | C | T | 65 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(62): Show |
75 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.1135-238C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 8/19 | chr19 | 41238926 | |||||||
chr19:41239104 | G | A | 8 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1135-60G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 8/19 | chr19 | 41239104 | |||||||
chr19:41239376 | C | G | 4 | a0001c0001t0006g0155 a0001c0003t0009g0007 a0001c0003t0009g0018 others(1): Show |
5 | HG02145.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1285+62C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | chr19 | 41239376 | |||||||
chr19:41239468 | C | CCCTCACT others(18): Show |
1 | a0001c0001t0004g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1285+164_1285+188d others(27): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr19 | 41239468 | ||||||
chr19:41239509 | C | T | 66 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(63): Show |
76 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.1286-185C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | chr19 | 41239509 | |||||||
chr19:41239535 | G | A | 45 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(42): Show |
47 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(44): Show |
intron_variant | MODIFIER | c.1286-159G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | chr19 | 41239535 | |||||||
chr19:41239570 | TTCACTCC others(18): Show |
T | 40 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(37): Show |
41 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(38): Show |
intron_variant | MODIFIER | c.1286-111_1286-87de others(26): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | INFO_REALIGN_3_PRIME | chr19 | 41239570 | ||||||
chr19:41239634 | C | T | 1 | a0001c0001t0030g0206 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1286-60C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | chr19 | 41239634 | |||||||
chr19:41239635 | G | A | 4 | a0001c0001t0006g0155 a0001c0003t0009g0007 a0001c0003t0009g0018 others(1): Show |
5 | HG02145.hp1 HG02451.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1286-59G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 9/19 | chr19 | 41239635 | |||||||
chr19:41239806 | C | A | 1 | a0001c0001t0047g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1312+86C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41239806 | |||||||
chr19:41239934 | A | G | 1 | a0001c0001t0006g0195 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1312+214A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41239934 | |||||||
chr19:41239981 | G | C | 1 | a0001c0001t0006g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1312+261G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41239981 | |||||||
chr19:41239999 | C | G | 8 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(5): Show |
8 | HG02055.hp2 HG02145.hp2 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.1312+279C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41239999 | |||||||
chr19:41240025 | C | T | 41 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(38): Show |
42 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.1312+305C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240025 | |||||||
chr19:41240073 | A | C | 1 | a0001c0001t0006g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1312+353A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240073 | |||||||
chr19:41240086 | G | C | 1 | a0001c0001t0015g0281 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1312+366G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240086 | |||||||
chr19:41240095 | A | G | 1 | a0001c0001t0002g0181 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1312+375A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240095 | |||||||
chr19:41240376 | G | GTGGA | 144 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(141): Show |
157 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
intron_variant | MODIFIER | c.1312+679_1312+682d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41240376 | ||||||
chr19:41240630 | C | T | 63 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(60): Show |
70 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.1312+910C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240630 | |||||||
chr19:41240655 | A | G | 3 | a0001c0001t0002g0215 a0001c0001t0025g0168 a0001c0001t0054g0154 |
3 | HG01123.hp1 HG03041.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1312+935A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240655 | |||||||
chr19:41240952 | A | G | 1 | a0001c0001t0002g0238 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.1312+1232A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41240952 | |||||||
chr19:41241414 | C | T | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-1469C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41241414 | |||||||
chr19:41241433 | G | A | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-1450G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41241433 | |||||||
chr19:41241543 | C | CA | 75 | a0001c0001t0001g0016 a0001c0001t0001g0078 a0001c0001t0001g0129 others(72): Show |
85 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.1313-1324dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41241543 | ||||||
chr19:41241543 | CA | C | 6 | a0001c0001t0005g0270 a0001c0001t0047g0272 a0001c0003t0009g0007 others(3): Show |
7 | HG01884.hp1 HG02145.hp1 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1313-1324delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41241543 | ||||||
chr19:41241576 | A | G | 1 | a0001c0001t0007g0087 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1313-1307A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41241576 | |||||||
chr19:41241922 | C | T | 41 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(38): Show |
42 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(39): Show |
intron_variant | MODIFIER | c.1313-961C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41241922 | |||||||
chr19:41241990 | AT | A | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1313-892delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41241990 | |||||||
chr19:41242103 | C | A | 1 | a0001c0001t0004g0231 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1313-780C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242103 | |||||||
chr19:41242186 | T | C | 42 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(39): Show |
46 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(43): Show |
intron_variant | MODIFIER | c.1313-697T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242186 | |||||||
chr19:41242248 | A | G | 113 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(110): Show |
125 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1313-635A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242248 | |||||||
chr19:41242282 | G | A | 1 | a0001c0001t0004g0156 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1313-601G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242282 | |||||||
chr19:41242315 | C | CT | 10 | a0001c0001t0001g0056 a0001c0001t0001g0084 a0001c0001t0001g0102 others(7): Show |
10 | HG01071.hp2 HG01934.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1313-542dupT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | ||||||
chr19:41242315 | CT | C | 48 | a0001c0001t0001g0080 a0001c0001t0002g0215 a0001c0001t0004g0131 others(45): Show |
48 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(45): Show |
intron_variant | MODIFIER | c.1313-542delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | ||||||
chr19:41242315 | CTT | C | 24 | a0001c0001t0001g0096 a0001c0001t0004g0136 a0001c0001t0004g0157 others(21): Show |
28 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.1313-543_1313-542d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | ||||||
chr19:41242315 | CTTT | C | 8 | a0001c0001t0003g0025 a0001c0001t0004g0260 a0001c0001t0006g0155 others(5): Show |
8 | HG01884.hp1 HG02055.hp1 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.1313-544_1313-542d others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | ||||||
chr19:41242315 | CTTTT | C | 78 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(75): Show |
86 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1313-545_1313-542d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | ||||||
chr19:41242315 | CTTTTT | C | 8 | a0001c0001t0002g0144 a0001c0001t0002g0223 a0001c0001t0003g0072 others(5): Show |
9 | HG01169.hp2 HG02145.hp1 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.1313-546_1313-542d others(7): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | INFO_REALIGN_3_PRIME | chr19 | 41242315 | ||||||
chr19:41242392 | C | T | 1 | a0001c0001t0011g0216 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1313-491C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242392 | |||||||
chr19:41242479 | C | A | 1 | a0001c0001t0011g0216 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1313-404C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242479 | |||||||
chr19:41242498 | A | G | 1 | a0001c0001t0004g0202 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1313-385A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242498 | |||||||
chr19:41242848 | T | C | 148 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(145): Show |
161 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1313-35T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 10/19 | chr19 | 41242848 | |||||||
chr19:41243140 | C | T | 4 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 others(1): Show |
5 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.1445+125C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/19 | chr19 | 41243140 | |||||||
chr19:41243143 | G | T | 44 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(41): Show |
48 | HG00323.hp1 HG00423.hp2 HG01167.hp2 others(45): Show |
intron_variant | MODIFIER | c.1445+128G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/19 | chr19 | 41243143 | |||||||
chr19:41243422 | A | G | 1 | a0001c0001t0006g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1446-194A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/19 | chr19 | 41243422 | |||||||
chr19:41243607 | C | T | 1 | a0001c0001t0002g0235 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1446-9C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 11/19 | chr19 | 41243607 | |||||||
chr19:41243941 | C | T | 2 | a0001c0001t0001g0128 a0001c0001t0019g0105 |
2 | HG01070.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.1537+234C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41243941 | |||||||
chr19:41244398 | C | T | 1 | a0001c0001t0012g0193 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1537+691C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244398 | |||||||
chr19:41244451 | A | T | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1537+744A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244451 | |||||||
chr19:41244492 | T | G | 5 | a0001c0001t0034g0034 a0001c0001t0036g0210 a0001c0001t0036g0211 others(2): Show |
5 | HG00642.hp2 HG00738.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1537+785T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244492 | |||||||
chr19:41244582 | T | C | 5 | a0001c0001t0006g0125 a0001c0003t0009g0007 a0001c0003t0009g0018 others(2): Show |
6 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537+875T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244582 | |||||||
chr19:41244596 | C | T | 1 | a0001c0001t0010g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1537+889C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244596 | |||||||
chr19:41244645 | A | G | 12 | a0001c0001t0014g0064 a0001c0001t0014g0065 a0001c0001t0014g0097 others(9): Show |
12 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.1537+938A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244645 | |||||||
chr19:41244790 | C | T | 1 | a0001c0001t0048g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1537+1083C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244790 | |||||||
chr19:41244852 | A | G | 1 | a0001c0001t0027g0201 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1537+1145A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41244852 | |||||||
chr19:41244934 | AT | A | 124 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(121): Show |
136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1537+1243delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41244934 | ||||||
chr19:41245007 | T | C | 20 | a0001c0001t0004g0014 a0001c0001t0004g0164 a0001c0001t0004g0230 others(17): Show |
21 | HG00423.hp2 HG01167.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.1537+1300T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245007 | |||||||
chr19:41245275 | G | A | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537+1568G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245275 | |||||||
chr19:41245339 | C | A | 1 | a0001c0003t0009g0018 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1537+1632C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245339 | |||||||
chr19:41245450 | G | A | 1 | a0001c0001t0031g0227 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1537+1743G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245450 | |||||||
chr19:41245504 | C | T | 10 | a0001c0001t0011g0205 a0001c0001t0011g0212 a0001c0001t0018g0112 others(7): Show |
10 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1537+1797C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245504 | |||||||
chr19:41245534 | C | G | 1 | a0001c0001t0023g0099 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1537+1827C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245534 | |||||||
chr19:41245615 | G | A | 12 | a0001c0001t0014g0064 a0001c0001t0014g0065 a0001c0001t0014g0097 others(9): Show |
12 | HG00735.hp1 HG01346.hp2 HG01515.hp2 others(9): Show |
intron_variant | MODIFIER | c.1537+1908G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245615 | |||||||
chr19:41245639 | G | A | 5 | a0001c0001t0006g0125 a0001c0003t0009g0007 a0001c0003t0009g0018 others(2): Show |
6 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1537+1932G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245639 | |||||||
chr19:41245674 | A | C | 1 | a0001c0001t0047g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1537+1967A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245674 | |||||||
chr19:41245713 | C | CA | 6 | a0001c0001t0005g0203 a0001c0001t0015g0161 a0001c0001t0022g0093 others(3): Show |
6 | HG01192.hp2 HG04199.hp2 NA18981.hp1 others(3): Show |
intron_variant | MODIFIER | c.1537+2026dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41245713 | ||||||
chr19:41245713 | CA | C | 30 | a0001c0001t0001g0061 a0001c0001t0001g0083 a0001c0001t0001g0128 others(27): Show |
31 | HG00735.hp1 HG01070.hp1 HG01169.hp1 others(28): Show |
intron_variant | MODIFIER | c.1537+2026delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41245713 | ||||||
chr19:41245793 | T | C | 4 | a0001c0001t0011g0251 a0001c0001t0011g0254 a0001c0001t0028g0233 others(1): Show |
4 | HG02071.hp1 HG02155.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537+2086T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245793 | |||||||
chr19:41245810 | G | C | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1537+2103G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245810 | |||||||
chr19:41245866 | T | C | 1 | a0001c0001t0047g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1537+2159T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245866 | |||||||
chr19:41245876 | G | C | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1537+2169G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41245876 | |||||||
chr19:41246222 | C | A | 57 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(54): Show |
64 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(61): Show |
intron_variant | MODIFIER | c.1538-2292C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246222 | |||||||
chr19:41246315 | T | G | 1 | a0001c0001t0011g0251 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1538-2199T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246315 | |||||||
chr19:41246429 | A | G | 1 | a0001c0001t0047g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1538-2085A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246429 | |||||||
chr19:41246444 | C | CA | 34 | a0001c0001t0003g0275 a0001c0001t0009g0030 a0001c0001t0009g0220 others(31): Show |
34 | HG00642.hp1 HG00735.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.1538-2056dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41246444 | ||||||
chr19:41246483 | T | G | 1 | a0006c0014t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1538-2031T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246483 | |||||||
chr19:41246489 | G | GC | 123 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(120): Show |
135 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(132): Show |
intron_variant | MODIFIER | c.1538-2023dupC | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41246489 | ||||||
chr19:41246540 | T | A | 1 | a0001c0001t0056g0224 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1538-1974T>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246540 | |||||||
chr19:41246569 | G | A | 1 | a0001c0001t0003g0033 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1538-1945G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246569 | |||||||
chr19:41246589 | C | T | 1 | a0001c0001t0013g0051 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1538-1925C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246589 | |||||||
chr19:41246598 | C | T | 1 | a0001c0001t0047g0272 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1538-1916C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246598 | |||||||
chr19:41246611 | A | G | 1 | a0001c0001t0006g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1538-1903A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246611 | |||||||
chr19:41246615 | T | C | 1 | a0001c0001t0020g0191 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1538-1899T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246615 | |||||||
chr19:41246730 | A | C | 124 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(121): Show |
136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1538-1784A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246730 | |||||||
chr19:41246826 | T | A | 146 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1688T>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246826 | |||||||
chr19:41246827 | G | T | 146 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1687G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246827 | |||||||
chr19:41246828 | A | T | 146 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1686A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246828 | |||||||
chr19:41246831 | C | A | 146 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1683C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246831 | |||||||
chr19:41246833 | C | G | 146 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1681C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246833 | |||||||
chr19:41246834 | T | C | 146 | a0001c0001t0001g0016 a0001c0001t0001g0096 a0001c0001t0001g0129 others(143): Show |
159 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1538-1680T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41246834 | |||||||
chr19:41247010 | T | TCAA | 124 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(121): Show |
136 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1538-1499_1538-149 others(7): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41247010 | ||||||
chr19:41247036 | T | G | 1 | a0001c0001t0006g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1538-1478T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247036 | |||||||
chr19:41247325 | C | A | 4 | a0001c0001t0017g0098 a0001c0001t0017g0100 a0001c0001t0023g0099 others(1): Show |
4 | HG02896.hp2 HG03579.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.1538-1189C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247325 | |||||||
chr19:41247358 | A | T | 2 | a0001c0001t0002g0192 a0001c0001t0002g0217 |
2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1538-1156A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247358 | |||||||
chr19:41247375 | T | A | 1 | a0001c0001t0052g0262 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1538-1139T>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247375 | |||||||
chr19:41247460 | G | A | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1538-1054G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247460 | |||||||
chr19:41247474 | G | T | 3 | a0001c0001t0024g0006 a0001c0001t0031g0006 a0001c0001t0053g0006 |
3 | HG01109.hp2 HG02486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1538-1040G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247474 | |||||||
chr19:41247729 | G | A | 58 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(55): Show |
65 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.1538-785G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247729 | |||||||
chr19:41247773 | C | T | 1 | a0001c0001t0046g0103 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1538-741C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247773 | |||||||
chr19:41247794 | A | G | 4 | a0001c0002t0009g0277 a0001c0002t0023g0278 a0001c0002t0023g0279 others(1): Show |
4 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1538-720A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247794 | |||||||
chr19:41247842 | C | T | 1 | a0001c0001t0027g0163 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1538-672C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247842 | |||||||
chr19:41247877 | A | G | 122 | a0001c0001t0001g0016 a0001c0001t0001g0129 a0001c0001t0002g0003 others(119): Show |
134 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
intron_variant | MODIFIER | c.1538-637A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247877 | |||||||
chr19:41247879 | C | T | 1 | a0001c0001t0010g0091 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1538-635C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247879 | |||||||
chr19:41247895 | T | TTTTTA | 7 | a0001c0001t0017g0037 a0001c0001t0017g0098 a0001c0001t0018g0038 others(4): Show |
7 | HG01109.hp2 HG02486.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.1538-579_1538-575d others(7): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41247895 | ||||||
chr19:41247895 | TTTTTA | T | 84 | a0001c0001t0001g0096 a0001c0001t0002g0189 a0001c0001t0003g0050 others(81): Show |
89 | HG00323.hp1 HG00423.hp2 HG00642.hp1 others(86): Show |
intron_variant | MODIFIER | c.1538-579_1538-575d others(7): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41247895 | ||||||
chr19:41247895 | TTTTTATT others(3): Show |
T | 63 | a0001c0001t0001g0016 a0001c0001t0001g0084 a0001c0001t0001g0127 others(60): Show |
71 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(68): Show |
intron_variant | MODIFIER | c.1538-584_1538-575d others(12): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | INFO_REALIGN_3_PRIME | chr19 | 41247895 | ||||||
chr19:41247945 | C | T | 5 | a0001c0001t0006g0125 a0001c0003t0009g0007 a0001c0003t0009g0018 others(2): Show |
6 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1538-569C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41247945 | |||||||
chr19:41248204 | G | A | 3 | a0001c0001t0001g0058 a0001c0001t0001g0145 a0001c0001t0005g0249 |
3 | HG02056.hp1 NA18942.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1538-310G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41248204 | |||||||
chr19:41248285 | C | T | 1 | a0001c0001t0005g0219 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1538-229C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41248285 | |||||||
chr19:41248312 | G | T | 118 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(115): Show |
130 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.1538-202G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41248312 | |||||||
chr19:41248321 | T | C | 2 | a0001c0001t0018g0112 a0001c0001t0019g0111 |
2 | HG02145.hp2 HG02258.hp1 |
intron_variant | MODIFIER | c.1538-193T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 12/19 | chr19 | 41248321 | |||||||
chr19:41248632 | C | T | 2 | a0001c0001t0002g0192 a0001c0001t0002g0217 |
2 | HG00099.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.1633+23C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 13/19 | chr19 | 41248632 | |||||||
chr19:41248882 | G | A | 1 | a0001c0001t0014g0048 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1711+62G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41248882 | |||||||
chr19:41249272 | C | G | 1 | a0001c0001t0006g0155 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1711+452C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249272 | |||||||
chr19:41249333 | T | G | 56 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(53): Show |
63 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.1711+513T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249333 | |||||||
chr19:41249353 | A | G | 1 | a0001c0001t0004g0131 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1711+533A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249353 | |||||||
chr19:41249383 | C | T | 4 | a0001c0002t0009g0277 a0001c0002t0023g0278 a0001c0002t0023g0279 others(1): Show |
4 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1711+563C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249383 | |||||||
chr19:41249452 | C | T | 39 | a0001c0001t0001g0016 a0001c0001t0002g0012 a0001c0001t0002g0133 others(36): Show |
44 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.1711+632C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249452 | |||||||
chr19:41249481 | C | T | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1711+661C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249481 | |||||||
chr19:41249482 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1711+662G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249482 | |||||||
chr19:41249485 | G | A | 15 | a0001c0001t0014g0047 a0001c0001t0014g0048 a0001c0001t0014g0064 others(12): Show |
15 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1711+665G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249485 | |||||||
chr19:41249520 | C | A | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1711+700C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249520 | |||||||
chr19:41249523 | A | G | 1 | a0001c0001t0037g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1711+703A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249523 | |||||||
chr19:41249587 | C | G | 5 | a0001c0001t0006g0125 a0001c0003t0009g0007 a0001c0003t0009g0018 others(2): Show |
6 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1711+767C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249587 | |||||||
chr19:41249705 | G | A | 1 | a0001c0001t0048g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1711+885G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249705 | |||||||
chr19:41249710 | C | T | 1 | a0006c0014t0001g0135 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1711+890C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249710 | |||||||
chr19:41249892 | G | A | 1 | a0001c0001t0006g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1711+1072G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249892 | |||||||
chr19:41249933 | G | A | 3 | a0001c0001t0032g0158 a0001c0001t0032g0159 a0001c0001t0032g0283 |
3 | HG02630.hp1 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1711+1113G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41249933 | |||||||
chr19:41250044 | C | T | 8 | a0001c0001t0001g0081 a0001c0001t0001g0082 a0001c0001t0005g0199 others(5): Show |
8 | HG00280.hp1 HG01099.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.1711+1224C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250044 | |||||||
chr19:41250099 | A | G | 1 | a0001c0001t0006g0160 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1711+1279A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250099 | |||||||
chr19:41250133 | T | G | 116 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(113): Show |
128 | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.1711+1313T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250133 | |||||||
chr19:41250180 | T | C | 15 | a0001c0001t0014g0047 a0001c0001t0014g0048 a0001c0001t0014g0064 others(12): Show |
15 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1711+1360T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250180 | |||||||
chr19:41250183 | A | G | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1711+1363A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250183 | |||||||
chr19:41250382 | A | ACCCACTC others(32): Show |
1 | a0001c0001t0010g0091 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1711+1563_1711+160 others(43): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41250382 | ||||||
chr19:41250598 | A | G | 55 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(52): Show |
62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1712-1753A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250598 | |||||||
chr19:41250658 | G | T | 15 | a0001c0001t0014g0047 a0001c0001t0014g0048 a0001c0001t0014g0064 others(12): Show |
15 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1712-1693G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250658 | |||||||
chr19:41250836 | T | C | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1712-1515T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250836 | |||||||
chr19:41250886 | G | T | 1 | a0001c0001t0052g0262 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1712-1465G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41250886 | |||||||
chr19:41251001 | G | T | 15 | a0001c0001t0014g0047 a0001c0001t0014g0048 a0001c0001t0014g0064 others(12): Show |
15 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(12): Show |
intron_variant | MODIFIER | c.1712-1350G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251001 | |||||||
chr19:41251151 | A | T | 1 | a0001c0001t0020g0271 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1712-1200A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251151 | |||||||
chr19:41251354 | G | C | 1 | a0001c0001t0015g0161 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1712-997G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251354 | |||||||
chr19:41251418 | T | G | 2 | a0001c0001t0001g0067 a0001c0001t0005g0175 |
2 | NA18990.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1712-933T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251418 | |||||||
chr19:41251470 | G | A | 10 | a0001c0001t0001g0010 a0001c0001t0001g0032 a0001c0001t0001g0083 others(7): Show |
10 | HG02040.hp2 HG02129.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.1712-881G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251470 | |||||||
chr19:41251519 | G | A | 14 | a0001c0001t0002g0012 a0001c0001t0002g0141 a0001c0001t0002g0142 others(11): Show |
15 | HG00597.hp1 HG00621.hp2 HG02083.hp2 others(12): Show |
intron_variant | MODIFIER | c.1712-832G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251519 | |||||||
chr19:41251539 | G | A | 55 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(52): Show |
62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1712-812G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251539 | |||||||
chr19:41251562 | C | CA | 7 | a0001c0001t0006g0177 a0001c0001t0026g0240 a0001c0001t0026g0243 others(4): Show |
7 | HG02155.hp2 HG02896.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1712-773dupA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41251562 | ||||||
chr19:41251698 | C | T | 55 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(52): Show |
62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1712-653C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251698 | |||||||
chr19:41251746 | A | G | 1 | a0001c0001t0008g0040 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1712-605A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251746 | |||||||
chr19:41251802 | A | G | 11 | a0001c0001t0014g0047 a0001c0001t0014g0048 a0001c0001t0014g0064 others(8): Show |
11 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1712-549A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251802 | |||||||
chr19:41251938 | C | A | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1712-413C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41251938 | |||||||
chr19:41252045 | G | A | 1 | a0005c0009t0033g0273 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1712-306G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41252045 | |||||||
chr19:41252111 | TA | T | 50 | a0001c0001t0001g0083 a0001c0001t0004g0014 a0001c0001t0004g0131 others(47): Show |
54 | HG00323.hp1 HG00642.hp1 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.1712-223delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41252111 | ||||||
chr19:41252111 | TAA | T | 6 | a0001c0001t0004g0208 a0001c0001t0008g0040 a0001c0002t0009g0277 others(3): Show |
6 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.1712-224_1712-223d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41252111 | ||||||
chr19:41252128 | A | T | 1 | a0001c0001t0048g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1712-223A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41252128 | |||||||
chr19:41252139 | ATT | A | 19 | a0001c0001t0006g0155 a0001c0001t0014g0047 a0001c0001t0014g0048 others(16): Show |
19 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.1712-209_1712-208d others(4): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41252139 | ||||||
chr19:41252142 | T | A | 55 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(52): Show |
62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.1712-209T>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41252142 | |||||||
chr19:41252144 | A | T | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1712-207A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | chr19 | 41252144 | |||||||
chr19:41252256 | GTGA | G | 4 | a0001c0001t0006g0155 a0001c0001t0037g0031 a0001c0001t0047g0272 others(1): Show |
4 | HG02451.hp2 HG02896.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1712-71_1712-69del others(3): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 14/19 | INFO_REALIGN_3_PRIME | chr19 | 41252256 | ||||||
chr19:41252975 | G | C | 6 | a0001c0001t0009g0138 a0001c0001t0009g0139 a0001c0001t0009g0140 others(3): Show |
6 | HG00639.hp1 HG01891.hp1 HG03098.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.1926+8G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41252975 | |||||||
chr19:41253186 | G | T | 4 | a0001c0001t0011g0251 a0001c0001t0011g0254 a0001c0001t0028g0233 others(1): Show |
4 | HG02071.hp1 HG02155.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.1926+219G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41253186 | |||||||
chr19:41253234 | G | A | 2 | a0001c0001t0001g0035 a0001c0001t0001g0078 |
2 | NA18944.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.1926+267G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41253234 | |||||||
chr19:41253348 | G | A | 1 | a0001c0001t0004g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1927-251G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41253348 | |||||||
chr19:41253505 | C | T | 1 | a0001c0001t0006g0125 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1927-94C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41253505 | |||||||
chr19:41253569 | C | T | 11 | a0001c0001t0014g0047 a0001c0001t0014g0048 a0001c0001t0014g0064 others(8): Show |
11 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.1927-30C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 16/19 | chr19 | 41253569 | |||||||
chr19:41253726 | A | AC | 93 | a0001c0001t0001g0001 a0001c0001t0001g0010 a0001c0001t0001g0035 others(90): Show |
99 | HG00639.hp1 HG01099.hp1 HG01099.hp2 others(96): Show |
intron_variant | MODIFIER | c.2036+30dupC | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41253726 | ||||||
chr19:41253726 | AC | A | 13 | a0001c0001t0001g0058 a0001c0001t0001g0080 a0001c0001t0001g0102 others(10): Show |
13 | HG00323.hp1 HG01074.hp2 HG02040.hp1 others(10): Show |
intron_variant | MODIFIER | c.2036+30delC | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41253726 | ||||||
chr19:41253726 | ACCC | A | 73 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(70): Show |
80 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2036+28_2036+30del others(3): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41253726 | ||||||
chr19:41253732 | C | T | 73 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(70): Show |
80 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2036+24C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41253732 | |||||||
chr19:41253736 | C | A | 1 | a0001c0001t0038g0076 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2036+28C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41253736 | |||||||
chr19:41253972 | G | T | 2 | a0001c0001t0017g0026 a0001c0001t0029g0188 |
2 | HG03669.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.2036+264G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41253972 | |||||||
chr19:41254128 | T | C | 77 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(74): Show |
85 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.2036+420T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254128 | |||||||
chr19:41254376 | CA | C | 18 | a0001c0001t0006g0125 a0001c0001t0012g0226 a0001c0001t0014g0047 others(15): Show |
19 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(16): Show |
intron_variant | MODIFIER | c.2036+685delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41254376 | ||||||
chr19:41254390 | A | G | 4 | a0001c0001t0001g0061 a0001c0001t0001g0129 a0001c0001t0037g0031 others(1): Show |
4 | HG02896.hp2 HG03139.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2036+682A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254390 | |||||||
chr19:41254391 | AAAG | A | 53 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(50): Show |
59 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(56): Show |
intron_variant | MODIFIER | c.2036+686_2036+688d others(5): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41254391 | ||||||
chr19:41254551 | A | T | 1 | a0001c0001t0015g0161 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2036+843A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254551 | |||||||
chr19:41254710 | G | A | 1 | a0001c0001t0005g0130 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.2036+1002G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254710 | |||||||
chr19:41254913 | A | G | 2 | a0001c0001t0003g0110 a0001c0001t0003g0167 |
2 | HG02280.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.2036+1205A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254913 | |||||||
chr19:41254992 | C | A | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2036+1284C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41254992 | |||||||
chr19:41255008 | A | G | 11 | a0001c0001t0014g0047 a0001c0001t0014g0048 a0001c0001t0014g0064 others(8): Show |
11 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.2036+1300A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255008 | |||||||
chr19:41255348 | CTTCT | C | 73 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(70): Show |
80 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2037-1097_2037-109 others(8): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41255348 | ||||||
chr19:41255355 | C | T | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-1097C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255355 | |||||||
chr19:41255356 | T | C | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-1096T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255356 | |||||||
chr19:41255362 | T | C | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-1090T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255362 | |||||||
chr19:41255364 | C | T | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-1088C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255364 | |||||||
chr19:41255368 | T | C | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-1084T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255368 | |||||||
chr19:41255368 | T | TTC | 73 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(70): Show |
80 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.2037-1076_2037-107 others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41255368 | ||||||
chr19:41255591 | C | T | 1 | a0001c0001t0015g0161 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2037-861C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255591 | |||||||
chr19:41255625 | G | C | 1 | a0001c0001t0048g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2037-827G>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255625 | |||||||
chr19:41255745 | T | G | 2 | a0001c0001t0037g0031 a0001c0001t0047g0272 |
2 | HG02896.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.2037-707T>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255745 | |||||||
chr19:41255804 | G | A | 4 | a0001c0001t0011g0251 a0001c0001t0011g0254 a0001c0001t0028g0233 others(1): Show |
4 | HG02071.hp1 HG02155.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.2037-648G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255804 | |||||||
chr19:41255849 | A | T | 1 | a0001c0001t0034g0034 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2037-603A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255849 | |||||||
chr19:41255964 | C | T | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-488C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41255964 | |||||||
chr19:41256080 | G | GGTGT | 54 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(51): Show |
61 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.2037-354_2037-351d others(6): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41256080 | ||||||
chr19:41256080 | G | GGTGTGT | 4 | a0001c0001t0014g0047 a0001c0001t0014g0048 a0001c0001t0037g0031 others(1): Show |
4 | HG00642.hp1 HG01123.hp2 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.2037-356_2037-351d others(8): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41256080 | ||||||
chr19:41256080 | G | GGTGTGTG others(1): Show |
5 | a0001c0001t0006g0125 a0001c0001t0047g0272 a0001c0003t0009g0007 others(2): Show |
6 | HG02145.hp1 HG02818.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.2037-358_2037-351d others(10): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41256080 | ||||||
chr19:41256080 | G | GGTGTGTG others(3): Show |
12 | a0001c0001t0014g0064 a0001c0001t0014g0097 a0001c0001t0020g0190 others(9): Show |
12 | HG00735.hp1 HG01346.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.2037-360_2037-351d others(12): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41256080 | ||||||
chr19:41256080 | G | GGTGTGTG others(5): Show |
2 | a0001c0001t0014g0065 a0001c0011t0011g0255 |
2 | HG01515.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2037-362_2037-351d others(14): Show |
AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | INFO_REALIGN_3_PRIME | chr19 | 41256080 | ||||||
chr19:41256095 | G | T | 11 | a0001c0001t0010g0011 a0001c0001t0010g0119 a0001c0001t0010g0120 others(8): Show |
12 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(9): Show |
intron_variant | MODIFIER | c.2037-357G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41256095 | |||||||
chr19:41256137 | C | T | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2037-315C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41256137 | |||||||
chr19:41256245 | G | A | 3 | a0001c0001t0037g0031 a0001c0001t0047g0272 a0001c0001t0048g0109 |
3 | HG02896.hp2 HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2037-207G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41256245 | |||||||
chr19:41256404 | T | C | 1 | a0001c0001t0004g0260 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2037-48T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 17/19 | chr19 | 41256404 | |||||||
chr19:41256620 | A | G | 55 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(52): Show |
62 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.2196+9A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41256620 | |||||||
chr19:41256765 | T | C | 62 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(59): Show |
69 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.2196+154T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41256765 | |||||||
chr19:41256794 | TA | T | 62 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(59): Show |
69 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.2196+184delA | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41256794 | |||||||
chr19:41256961 | A | T | 36 | a0001c0001t0004g0014 a0001c0001t0004g0131 a0001c0001t0004g0136 others(33): Show |
40 | HG00323.hp1 HG01167.hp2 HG01169.hp2 others(37): Show |
intron_variant | MODIFIER | c.2196+350A>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41256961 | |||||||
chr19:41257023 | T | C | 1 | a0001c0001t0006g0160 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2196+412T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41257023 | |||||||
chr19:41257075 | G | A | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2197-418G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41257075 | |||||||
chr19:41257334 | G | A | 1 | a0001c0001t0005g0218 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.2197-159G>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 18/19 | chr19 | 41257334 | |||||||
chr19:41257726 | A | G | 3 | a0001c0003t0009g0007 a0001c0003t0009g0018 a0001c0003t0009g0019 |
4 | HG02145.hp1 HG02818.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.2333+97A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41257726 | |||||||
chr19:41257886 | A | C | 1 | a0001c0003t0009g0019 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2333+257A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41257886 | |||||||
chr19:41257889 | C | G | 1 | a0001c0001t0048g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2333+260C>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41257889 | |||||||
chr19:41257993 | C | T | 3 | a0001c0001t0012g0186 a0001c0001t0012g0187 a0001c0001t0012g0226 |
3 | HG03017.hp1 HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2333+364C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41257993 | |||||||
chr19:41258068 | C | A | 5 | a0001c0001t0018g0112 a0001c0001t0018g0113 a0001c0001t0019g0111 others(2): Show |
5 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.2333+439C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258068 | |||||||
chr19:41258099 | G | T | 3 | a0001c0001t0014g0047 a0001c0001t0014g0048 a0003c0008t0014g0046 |
3 | HG00642.hp1 HG01123.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.2333+470G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258099 | |||||||
chr19:41258221 | C | T | 1 | a0001c0001t0022g0095 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2333+592C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258221 | |||||||
chr19:41258353 | T | C | 2 | a0001c0001t0017g0100 a0001c0001t0023g0099 |
2 | HG03579.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.2333+724T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258353 | |||||||
chr19:41258378 | AT | A | 54 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(51): Show |
61 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(58): Show |
intron_variant | MODIFIER | c.2333+751delT | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | INFO_REALIGN_3_PRIME | chr19 | 41258378 | ||||||
chr19:41258519 | A | G | 4 | a0001c0001t0002g0215 a0001c0001t0012g0152 a0001c0001t0042g0015 others(1): Show |
4 | HG01123.hp1 HG01496.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2333+890A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258519 | |||||||
chr19:41258540 | A | G | 1 | a0001c0001t0002g0133 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2333+911A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258540 | |||||||
chr19:41258663 | G | T | 12 | a0001c0001t0006g0125 a0001c0001t0014g0047 a0001c0001t0014g0048 others(9): Show |
12 | HG00642.hp1 HG00735.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.2334-890G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258663 | |||||||
chr19:41258823 | C | A | 2 | a0001c0001t0006g0176 a0001c0001t0006g0178 |
2 | NA18997.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.2334-730C>A | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258823 | |||||||
chr19:41258840 | G | T | 2 | a0001c0001t0032g0158 a0001c0001t0032g0159 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2334-713G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258840 | |||||||
chr19:41258853 | A | G | 39 | a0001c0001t0001g0016 a0001c0001t0002g0012 a0001c0001t0002g0133 others(36): Show |
44 | HG00280.hp2 HG00423.hp1 HG00423.hp2 others(41): Show |
intron_variant | MODIFIER | c.2334-700A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258853 | |||||||
chr19:41258869 | A | G | 4 | a0001c0002t0009g0277 a0001c0002t0023g0278 a0001c0002t0023g0279 others(1): Show |
4 | HG02055.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2334-684A>G | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41258869 | |||||||
chr19:41259241 | G | T | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2334-312G>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259241 | |||||||
chr19:41259324 | T | C | 67 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(64): Show |
74 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(71): Show |
intron_variant | MODIFIER | c.2334-229T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259324 | |||||||
chr19:41259339 | C | T | 1 | a0001c0011t0011g0255 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2334-214C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259339 | |||||||
chr19:41259356 | C | T | 4 | a0001c0001t0010g0011 a0001c0001t0014g0048 a0001c0001t0022g0093 others(1): Show |
5 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
intron_variant | MODIFIER | c.2334-197C>T | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259356 | |||||||
chr19:41259409 | T | C | 1 | a0002c0004t0005g0221 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.2334-144T>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259409 | |||||||
chr19:41259502 | A | C | 56 | a0001c0001t0001g0016 a0001c0001t0002g0003 a0001c0001t0002g0012 others(53): Show |
63 | HG00099.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.2334-51A>C | AXL | ENSG00000167601.12 | transcript | ENST00000301178.9 | protein_coding | 19/19 | chr19 | 41259502 |