Item | Value |
---|---|
geneid | 113878 |
ensemblid | ENSG00000091073.20 |
hgncid | 15973 |
symbol | DTX2 |
name | deltex E3 ubiquitin ligase 2 |
refseq_nuc | NM_001102594.3 |
refseq_prot | NP_001096064.1 |
ensembl_nuc | ENST00000430490.7 |
ensembl_prot | ENSP00000411986.2 |
mane_status | MANE Select |
chr | chr7 |
start | 76461709 |
end | 76505991 |
strand | + |
ver | v1.2 |
region | chr7:76461709-76505991 |
region5000 | chr7:76456709-76510991 |
regionname0 | DTX2_chr7_76461709_76505991 |
regionname5000 | DTX2_chr7_76456709_76510991 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 622 | 146 | 40 | 24 | 60 | 5 | 17 | 36 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0002 | 0/0 | 622 | 65 | 12 | 20 | 24 | 2 | 7 | 10 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0003 | 0/1 | 622 | 38 | 14 | 13 | 1 | 2 | 7 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0004 | 0/0 | 352 | 10 | 2 | 2 | 5 | 0 | 1 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(347): Show |
chr7 | 76456709 | 76510991 |
a0005 | 0/0 | 622 | 10 | 8 | 2 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0006 | 0/0 | 622 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0007 | 0/0 | 622 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0008 | 1/0 | 622 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0009 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0010 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0011 | 0/0 | 622 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0012 | 0/0 | 622 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
a0013 | 0/0 | 622 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | MAMAP others(617): Show |
chr7 | 76456709 | 76510991 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 1866 | 111 | 18 | 19 | 54 | 4 | 16 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0001c0003 | 0/0 | 1866 | 31 | 20 | 4 | 5 | 1 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0001c0013 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0001c0018 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0001c0023 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0001c0031 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0002c0002 | 0/0 | 1866 | 44 | 3 | 17 | 16 | 2 | 6 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0002c0007 | 0/0 | 1866 | 9 | 0 | 2 | 7 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0002c0008 | 0/0 | 1866 | 5 | 5 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0002c0011 | 0/0 | 1866 | 2 | 2 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0002c0017 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0002c0020 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0002c0028 | 0/0 | 1866 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0002c0029 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0002c0032 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0003c0004 | 0/1 | 1866 | 25 | 5 | 11 | 1 | 2 | 5 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0003c0005 | 0/0 | 1866 | 13 | 9 | 2 | 0 | 0 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0004c0009 | 0/0 | 1867 | 5 | 0 | 1 | 3 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1862): Show |
chr7 | 76456709 | 76510991 | ||
a0004c0014 | 0/0 | 1867 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1862): Show |
chr7 | 76456709 | 76510991 | ||
a0004c0025 | 0/0 | 1867 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1862): Show |
chr7 | 76456709 | 76510991 | ||
a0004c0026 | 0/0 | 1867 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1862): Show |
chr7 | 76456709 | 76510991 | ||
a0004c0027 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1862): Show |
chr7 | 76456709 | 76510991 | ||
a0004c0033 | 0/0 | 1867 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1862): Show |
chr7 | 76456709 | 76510991 | ||
a0005c0006 | 0/0 | 1866 | 9 | 8 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0005c0024 | 0/0 | 1866 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0006c0010 | 0/0 | 1866 | 3 | 0 | 0 | 0 | 1 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0007c0012 | 0/0 | 1866 | 2 | 1 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0008c0021 | 1/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0009c0019 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0010c0016 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0011c0030 | 0/0 | 1866 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0012c0022 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 | ||
a0013c0015 | 0/0 | 1866 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | ATGGC others(1861): Show |
chr7 | 76456709 | 76510991 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2641 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0001c0001t0002 | 0/0 | 2641 | 109 | 18 | 18 | 54 | 4 | 15 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0001c0001t0010 | 0/0 | 2641 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0001c0003t0001 | 0/0 | 2641 | 31 | 20 | 4 | 5 | 1 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0001c0013t0001 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0001c0018t0011 | 0/0 | 2641 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0001c0023t0006 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0001c0031t0001 | 0/0 | 2641 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0002t0001 | 0/0 | 2641 | 41 | 3 | 15 | 16 | 1 | 6 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0002t0005 | 0/0 | 2641 | 2 | 0 | 1 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0002t0007 | 0/0 | 2641 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0007t0001 | 0/0 | 2641 | 9 | 0 | 2 | 7 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0008t0001 | 0/0 | 2641 | 2 | 2 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0008t0004 | 0/0 | 2641 | 3 | 3 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0011t0003 | 0/0 | 2641 | 2 | 2 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0017t0001 | 0/0 | 2641 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0020t0009 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0028t0001 | 0/0 | 2641 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0029t0001 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0002c0032t0001 | 0/0 | 2641 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0003c0004t0001 | 0/1 | 2641 | 25 | 5 | 11 | 1 | 2 | 5 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0003c0005t0001 | 0/0 | 2641 | 13 | 9 | 2 | 0 | 0 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0004c0009t0002 | 0/0 | 2642 | 4 | 0 | 1 | 3 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2637): Show |
chr7 | 76456709 | 76510991 |
a0004c0009t0008 | 0/0 | 2642 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2637): Show |
chr7 | 76456709 | 76510991 |
a0004c0014t0001 | 0/0 | 2642 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2637): Show |
chr7 | 76456709 | 76510991 |
a0004c0025t0001 | 0/0 | 2642 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2637): Show |
chr7 | 76456709 | 76510991 |
a0004c0026t0001 | 0/0 | 2642 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2637): Show |
chr7 | 76456709 | 76510991 |
a0004c0027t0001 | 0/0 | 2642 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2637): Show |
chr7 | 76456709 | 76510991 |
a0004c0033t0001 | 0/0 | 2642 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2637): Show |
chr7 | 76456709 | 76510991 |
a0005c0006t0001 | 0/0 | 2641 | 9 | 8 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0005c0024t0001 | 0/0 | 2641 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0006c0010t0002 | 0/0 | 2641 | 3 | 0 | 0 | 0 | 1 | 2 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0007c0012t0001 | 0/0 | 2641 | 2 | 1 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0008c0021t0001 | 1/0 | 2641 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0009c0019t0001 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0010c0016t0001 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0011c0030t0003 | 0/0 | 2641 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0012c0022t0002 | 0/0 | 2641 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
a0013c0015t0001 | 0/0 | 2641 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | GAGTT others(2636): Show |
chr7 | 76456709 | 76510991 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0001t0010g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0003t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0013t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0018t0011g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0023t0006g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0001c0031t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0005g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0005g0274 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0002t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0007t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0007t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0007t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0007t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0007t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0007t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0007t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0007t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0007t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0008t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0008t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0008t0004g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0008t0004g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0008t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0011t0003g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0011t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0017t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0020t0009g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0028t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0029t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0002c0032t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0232 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0004t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0003c0005t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0004c0009t0002g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0004c0009t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0004c0009t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0004c0009t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0004c0009t0008g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0004c0014t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0004c0025t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0004c0026t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0004c0027t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0004c0033t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0005c0006t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0005c0006t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0005c0006t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0005c0006t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0005c0006t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0005c0006t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0005c0006t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0005c0006t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0005c0006t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0005c0024t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0006c0010t0002g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0006c0010t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0006c0010t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0007c0012t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0007c0012t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0008c0021t0001g0079 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0009c0019t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0010c0016t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0011c0030t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0012c0022t0002g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
a0013c0015t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0021 | EUR | GBR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00140 | hp2 | a0003 | c0004 | t0001 | g0240 | EUR | GBR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00280 | hp2 | a0002 | c0002 | t0001 | g0205 | EUR | FIN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00323 | hp2 | a0001 | c0003 | t0001 | g0135 | EUR | FIN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00408 | hp1 | a0001 | c0003 | t0001 | g0148 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0216 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00544 | hp1 | a0001 | c0031 | t0001 | g0273 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0210 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00558 | hp2 | a0002 | c0007 | t0001 | g0271 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00597 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00609 | hp2 | a0002 | c0007 | t0001 | g0276 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0163 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00621 | hp2 | a0004 | c0009 | t0002 | g0172 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00639 | hp1 | a0007 | c0012 | t0001 | g0245 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00639 | hp2 | a0003 | c0005 | t0001 | g0065 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00673 | hp2 | a0002 | c0002 | t0001 | g0187 | EAS | CHS | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00733 | hp1 | a0002 | c0032 | t0001 | g0256 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00735 | hp1 | a0003 | c0004 | t0001 | g0250 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00735 | hp2 | a0002 | c0002 | t0005 | g0006 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0098 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0025 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0126 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01071 | hp2 | a0002 | c0002 | t0001 | g0127 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01081 | hp1 | a0003 | c0004 | t0001 | g0241 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01081 | hp2 | a0002 | c0002 | t0001 | g0228 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01099 | hp1 | a0003 | c0004 | t0001 | g0243 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01099 | hp2 | a0002 | c0002 | t0001 | g0198 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01109 | hp1 | a0005 | c0006 | t0001 | g0124 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01109 | hp2 | a0003 | c0004 | t0001 | g0254 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01167 | hp2 | a0003 | c0004 | t0001 | g0236 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0097 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01168 | hp2 | a0003 | c0004 | t0001 | g0242 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01175 | hp1 | a0003 | c0004 | t0001 | g0251 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01175 | hp2 | a0001 | c0003 | t0001 | g0158 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01192 | hp1 | a0003 | c0005 | t0001 | g0064 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01243 | hp1 | a0005 | c0024 | t0001 | g0159 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01243 | hp2 | a0004 | c0025 | t0001 | g0143 | AMR | PUR | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0010 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01256 | hp2 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01258 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01261 | hp1 | a0003 | c0004 | t0001 | g0255 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0220 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01346 | hp1 | a0001 | c0018 | t0011 | g0099 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01358 | hp1 | a0002 | c0002 | t0001 | g0219 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01358 | hp2 | a0003 | c0004 | t0001 | g0253 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01496 | hp2 | a0002 | c0007 | t0001 | g0259 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01884 | hp1 | a0005 | c0006 | t0001 | g0121 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01884 | hp2 | a0002 | c0008 | t0004 | g0134 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01891 | hp1 | a0001 | c0003 | t0001 | g0154 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01928 | hp1 | a0002 | c0002 | t0001 | g0208 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01928 | hp2 | a0002 | c0002 | t0001 | g0199 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0056 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01934 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01952 | hp1 | a0001 | c0003 | t0001 | g0128 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01952 | hp2 | a0002 | c0002 | t0001 | g0215 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0186 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0131 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01993 | hp2 | a0003 | c0004 | t0001 | g0244 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02015 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0231 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02055 | hp1 | a0004 | c0033 | t0001 | g0234 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02055 | hp2 | a0009 | c0019 | t0001 | g0108 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02056 | hp2 | a0002 | c0028 | t0001 | g0258 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0183 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02071 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0217 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02080 | hp2 | a0004 | c0009 | t0002 | g0164 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02083 | hp1 | a0002 | c0007 | t0001 | g0185 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02129 | hp1 | a0002 | c0007 | t0001 | g0272 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02135 | hp2 | a0003 | c0004 | t0001 | g0257 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02148 | hp1 | a0004 | c0009 | t0002 | g0095 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02148 | hp2 | a0002 | c0002 | t0001 | g0204 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CDX | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0055 | EAS | CDX | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02165 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CDX | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02165 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CDX | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02257 | hp2 | a0001 | c0003 | t0001 | g0152 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02258 | hp1 | a0003 | c0004 | t0001 | g0248 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02258 | hp2 | a0005 | c0006 | t0001 | g0120 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02273 | hp1 | a0001 | c0003 | t0001 | g0130 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02273 | hp2 | a0002 | c0002 | t0001 | g0196 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02293 | hp1 | a0002 | c0007 | t0001 | g0260 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02293 | hp2 | a0002 | c0002 | t0007 | g0203 | AMR | PEL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0111 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02451 | hp2 | a0001 | c0023 | t0006 | g0074 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02523 | hp2 | a0004 | c0026 | t0001 | g0269 | EAS | KHV | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02622 | hp1 | a0002 | c0002 | t0001 | g0224 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0137 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02630 | hp2 | a0002 | c0002 | t0001 | g0211 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0146 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0160 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02683 | hp2 | a0003 | c0005 | t0001 | g0077 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02698 | hp1 | a0001 | c0001 | t0010 | g0085 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0214 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02717 | hp1 | a0002 | c0008 | t0004 | g0133 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02723 | hp2 | a0001 | c0003 | t0001 | g0222 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0096 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02818 | hp1 | a0001 | c0003 | t0001 | g0136 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02818 | hp2 | a0003 | c0005 | t0001 | g0067 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02886 | hp1 | a0001 | c0003 | t0001 | g0142 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02886 | hp2 | a0003 | c0005 | t0001 | g0071 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02896 | hp2 | a0003 | c0005 | t0001 | g0014 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02897 | hp1 | a0002 | c0020 | t0009 | g0011 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02897 | hp2 | a0003 | c0005 | t0001 | g0015 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02922 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02922 | hp2 | a0005 | c0006 | t0001 | g0117 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0266 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02965 | hp2 | a0005 | c0006 | t0001 | g0119 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0114 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0194 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0150 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0112 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03130 | hp1 | a0010 | c0016 | t0001 | g0227 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03130 | hp2 | a0001 | c0003 | t0001 | g0267 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03139 | hp1 | a0003 | c0004 | t0001 | g0238 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03139 | hp2 | a0001 | c0003 | t0001 | g0145 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03209 | hp2 | a0005 | c0006 | t0001 | g0118 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03225 | hp1 | a0002 | c0029 | t0001 | g0005 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0116 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03239 | hp2 | a0003 | c0005 | t0001 | g0076 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0138 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03486 | hp1 | a0002 | c0011 | t0003 | g0265 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0221 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03490 | hp1 | a0006 | c0010 | t0002 | g0009 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03490 | hp2 | a0003 | c0004 | t0001 | g0262 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03492 | hp2 | a0006 | c0010 | t0002 | g0086 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03516 | hp1 | a0003 | c0005 | t0001 | g0069 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03516 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | ESN | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0140 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03540 | hp2 | a0011 | c0030 | t0003 | g0263 | AFR | GWD | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03579 | hp1 | a0007 | c0012 | t0001 | g0233 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03579 | hp2 | a0002 | c0008 | t0001 | g0229 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0094 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0213 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0192 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03704 | hp2 | a0003 | c0004 | t0001 | g0247 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0107 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03710 | hp2 | a0012 | c0022 | t0002 | g0093 | SAS | PJL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0181 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03831 | hp2 | a0002 | c0002 | t0001 | g0195 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03927 | hp1 | a0003 | c0004 | t0001 | g0246 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03927 | hp2 | a0004 | c0009 | t0008 | g0060 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0100 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03942 | hp2 | a0013 | c0015 | t0001 | g0191 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG04115 | hp1 | a0002 | c0002 | t0001 | g0125 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0105 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0104 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG04184 | hp2 | a0002 | c0002 | t0001 | g0226 | SAS | BEB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG04199 | hp1 | a0003 | c0004 | t0001 | g0252 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG04199 | hp2 | a0002 | c0017 | t0001 | g0188 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0023 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0091 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0031 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0155 | SAS | STU | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18522 | hp1 | a0003 | c0005 | t0001 | g0075 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18522 | hp2 | a0005 | c0006 | t0001 | g0123 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CHB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0218 | EAS | CHB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18906 | hp1 | a0003 | c0005 | t0001 | g0066 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18906 | hp2 | a0003 | c0004 | t0001 | g0239 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18942 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0034 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18947 | hp1 | a0002 | c0007 | t0001 | g0275 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18952 | hp2 | a0001 | c0003 | t0001 | g0149 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18959 | hp1 | a0001 | c0001 | t0002 | g0090 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18960 | hp2 | a0004 | c0014 | t0001 | g0212 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0101 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0012 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0201 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18983 | hp1 | a0002 | c0002 | t0001 | g0206 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18983 | hp2 | a0002 | c0007 | t0001 | g0270 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18984 | hp2 | a0001 | c0003 | t0001 | g0144 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18986 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0190 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0202 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19043 | hp1 | a0002 | c0011 | t0003 | g0264 | AFR | LWK | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0156 | AFR | LWK | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19060 | hp2 | a0002 | c0002 | t0001 | g0209 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19068 | hp1 | a0004 | c0009 | t0002 | g0162 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19068 | hp2 | a0001 | c0003 | t0001 | g0147 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19074 | hp1 | a0002 | c0007 | t0001 | g0268 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19074 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19240 | hp1 | a0005 | c0006 | t0001 | g0115 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA19240 | hp2 | a0002 | c0008 | t0004 | g0132 | AFR | YRI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0161 | AFR | ASW | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA20129 | hp2 | a0005 | c0006 | t0001 | g0122 | AFR | ASW | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA20752 | hp1 | a0003 | c0004 | t0001 | g0237 | EUR | TSI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA20752 | hp2 | a0002 | c0002 | t0005 | g0274 | EUR | TSI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA20805 | hp1 | a0006 | c0010 | t0002 | g0087 | EUR | TSI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0017 | EUR | TSI | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA20905 | hp1 | a0003 | c0004 | t0001 | g0189 | SAS | GIH | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0030 | SAS | GIH | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01123 | hp1 | a0003 | c0004 | t0001 | g0235 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0225 | AMR | CLM | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02109 | hp1 | a0004 | c0027 | t0001 | g0139 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02109 | hp2 | a0002 | c0008 | t0001 | g0230 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02486 | hp1 | a0003 | c0004 | t0001 | g0249 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0084 | AFR | ACB | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03471 | hp1 | a0001 | c0013 | t0001 | g0193 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG03471 | hp2 | a0003 | c0005 | t0001 | g0068 | AFR | MSL | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG06807 | hp1 | a0003 | c0004 | t0001 | g0261 | AFR | USA | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
HG06807 | hp2 | a0003 | c0005 | t0001 | g0070 | AFR | USA | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA20300 | hp1 | a0001 | c0001 | t0002 | g0062 | AFR | USA | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA20300 | hp2 | a0001 | c0003 | t0001 | g0153 | AFR | USA | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA21309 | hp1 | a0001 | c0003 | t0001 | g0157 | AFR | LWK | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0106 | AFR | LWK | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
homoSapiens | chm13v2 | a0003 | c0004 | t0001 | g0232 | REF | REF | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
homoSapiens | grch38p0 | a0008 | c0021 | t0001 | g0079 | REF | REF | DTX2_chr7_76456709_76510991 | DTX2 | chr7 | 76456709 | 76510991 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:76482621 | G | A | 1 | a0006 | 3 | HG03490.hp1 HG03492.hp2 NA20805.hp1 |
missense_variant | MODERATE | c.382G>A | p.Val128Ile | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 764/2641 | 382/1869 | 128/622 | chr7 | 76482621 | |||
chr7:76482880 | A | AC | 1 | a0004 | 10 | HG00621.hp2 HG01243.hp2 HG02055.hp1 others(7): Show |
frameshift_variant | HIGH | c.643dupC | p.Arg215fs | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1026/2641 | 644/1869 | 215/622 | INFO_REALIGN_3_PRIME | chr7 | 76482880 | ||
chr7:76483042 | G | A | 1 | a0013 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.803G>A | p.Gly268Asp | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1185/2641 | 803/1869 | 268/622 | chr7 | 76483042 | |||
chr7:76483129 | C | A | 1 | a0010 | 1 | HG03130.hp1 | missense_variant | MODERATE | c.890C>A | p.Ser297Tyr | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1272/2641 | 890/1869 | 297/622 | chr7 | 76483129 | |||
chr7:76497420 | C | T | 1 | a0005 | 10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
missense_variant | MODERATE | c.1093C>T | p.Arg365Cys | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/11 | 1475/2641 | 1093/1869 | 365/622 | chr7 | 76497420 | |||
chr7:76497421 | G | A | 1 | a0007 | 2 | HG00639.hp1 HG03579.hp1 |
missense_variant | MODERATE | c.1094G>A | p.Arg365His | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/11 | 1476/2641 | 1094/1869 | 365/622 | chr7 | 76497421 | |||
chr7:76500441 | G | A | 9 | a0002 a0003 a0004 others(6): Show |
122 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(119): Show |
missense_variant&splice_region_variant | MODERATE | c.1151G>A | p.Gly384Glu | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/11 | 1533/2641 | 1151/1869 | 384/622 | chr7 | 76500441 | |||
chr7:76502328 | A | G | 9 | a0001 a0002 a0004 others(6): Show |
236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
missense_variant | MODERATE | c.1261A>G | p.Thr421Ala | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/11 | 1643/2641 | 1261/1869 | 421/622 | chr7 | 76502328 | |||
chr7:76502332 | C | T | 1 | a0009 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1265C>T | p.Ala422Val | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/11 | 1647/2641 | 1265/1869 | 422/622 | chr7 | 76502332 | |||
chr7:76502433 | G | A | 1 | a0012 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.1366G>A | p.Ala456Thr | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/11 | 1748/2641 | 1366/1869 | 456/622 | chr7 | 76502433 | |||
chr7:76505598 | G | C | 1 | a0011 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.1866G>C | p.Gln622His | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 2248/2641 | 1866/1869 | 622/622 | chr7 | 76505598 | |||
chr7:76505989 | A | G | 1 | a0002 | 1 | HG02897.hp1 | splice_region_variant | LOW | c.*388A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | chr7 | 76505989 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:76482518 | G | A | 6 | a0001c0013 a0002c0002 a0002c0008 others(3): Show |
53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
synonymous_variant | LOW | c.279G>A | p.Arg93Arg | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 661/2641 | 279/1869 | 93/622 | chr7 | 76482518 | |||
chr7:76482605 | T | C | 1 | a0002c0017 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.366T>C | p.Thr122Thr | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 748/2641 | 366/1869 | 122/622 | chr7 | 76482605 | |||
chr7:76482677 | C | G | 3 | a0003c0004 a0004c0033 a0007c0012 |
27 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
synonymous_variant | LOW | c.438C>G | p.Ala146Ala | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 820/2641 | 438/1869 | 146/622 | chr7 | 76482677 | |||
chr7:76482743 | C | T | 23 | a0001c0003 a0001c0013 a0001c0031 others(20): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
synonymous_variant | LOW | c.504C>T | p.Phe168Phe | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 886/2641 | 504/1869 | 168/622 | chr7 | 76482743 | |||
chr7:76482782 | G | A | 2 | a0001c0013 a0001c0018 |
2 | HG01346.hp1 HG03471.hp1 |
synonymous_variant | LOW | c.543G>A | p.Pro181Pro | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 925/2641 | 543/1869 | 181/622 | chr7 | 76482782 | |||
chr7:76482806 | G | A | 2 | a0005c0006 a0005c0024 |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
synonymous_variant | LOW | c.567G>A | p.Pro189Pro | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 949/2641 | 567/1869 | 189/622 | chr7 | 76482806 | |||
chr7:76482902 | C | T | 1 | a0002c0032 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.663C>T | p.Leu221Leu | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1045/2641 | 663/1869 | 221/622 | chr7 | 76482902 | |||
chr7:76482932 | A | C | 1 | a0002c0032 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.693A>C | p.Pro231Pro | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1075/2641 | 693/1869 | 231/622 | chr7 | 76482932 | |||
chr7:76483013 | G | A | 1 | a0002c0028 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.774G>A | p.Ala258Ala | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/11 | 1156/2641 | 774/1869 | 258/622 | chr7 | 76483013 | |||
chr7:76492192 | C | T | 5 | a0001c0013 a0002c0002 a0004c0014 others(2): Show |
48 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(45): Show |
synonymous_variant | LOW | c.948C>T | p.Ser316Ser | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/11 | 1330/2641 | 948/1869 | 316/622 | chr7 | 76492192 | |||
chr7:76502333 | G | A | 5 | a0001c0001 a0001c0018 a0004c0009 others(2): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
synonymous_variant | LOW | c.1266G>A | p.Ala422Ala | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/11 | 1648/2641 | 1266/1869 | 422/622 | chr7 | 76502333 | |||
chr7:76502378 | A | G | 23 | a0001c0001 a0001c0013 a0001c0018 others(20): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
synonymous_variant | LOW | c.1311A>G | p.Leu437Leu | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/11 | 1693/2641 | 1311/1869 | 437/622 | chr7 | 76502378 | |||
chr7:76503488 | C | G | 3 | a0001c0023 a0002c0011 a0011c0030 |
4 | HG02451.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
synonymous_variant | LOW | c.1452C>G | p.Pro484Pro | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/11 | 1834/2641 | 1452/1869 | 484/622 | chr7 | 76503488 | |||
chr7:76503551 | C | T | 1 | a0005c0024 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1515C>T | p.Thr505Thr | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/11 | 1897/2641 | 1515/1869 | 505/622 | chr7 | 76503551 | |||
chr7:76503581 | T | C | 8 | a0001c0001 a0001c0018 a0001c0023 others(5): Show |
125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
synonymous_variant | LOW | c.1545T>C | p.Gly515Gly | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/11 | 1927/2641 | 1545/1869 | 515/622 | chr7 | 76503581 | |||
chr7:76505412 | C | T | 2 | a0005c0006 a0005c0024 |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
synonymous_variant | LOW | c.1680C>T | p.Leu560Leu | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 2062/2641 | 1680/1869 | 560/622 | chr7 | 76505412 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:76463617 | A | G | 1 | a0002c0008t0004 | 3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
5_prime_UTR_variant | MODIFIER | c.-182A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/11 | 16893 | chr7 | 76463617 | ||||||
chr7:76480450 | G | A | 1 | a0001c0023t0006 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-60G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/11 | 60 | chr7 | 76480450 | ||||||
chr7:76480466 | G | A | 1 | a0002c0002t0007 | 1 | HG02293.hp2 | 5_prime_UTR_variant | MODIFIER | c.-44G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/11 | 44 | chr7 | 76480466 | ||||||
chr7:76505612 | C | G | 1 | a0001c0018t0011 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*11C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 11 | chr7 | 76505612 | ||||||
chr7:76505735 | C | G | 1 | a0002c0002t0005 | 2 | HG00735.hp2 NA20752.hp2 |
3_prime_UTR_variant | MODIFIER | c.*134C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 134 | chr7 | 76505735 | ||||||
chr7:76505735 | C | T | 1 | a0001c0001t0010 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*134C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 134 | chr7 | 76505735 | ||||||
chr7:76505817 | G | A | 7 | a0001c0001t0002 a0001c0001t0010 a0001c0018t0011 others(4): Show |
120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
3_prime_UTR_variant | MODIFIER | c.*216G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 216 | chr7 | 76505817 | ||||||
chr7:76505846 | G | A | 1 | a0004c0009t0008 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*245G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 245 | chr7 | 76505846 | ||||||
chr7:76505922 | G | A | 3 | a0001c0023t0006 a0002c0011t0003 a0011c0030t0003 |
4 | HG02451.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*321G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 11/11 | 321 | chr7 | 76505922 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:76462005 | G | T | 92 | a0001c0003t0001g0221 a0001c0003t0001g0222 a0001c0003t0001g0266 others(89): Show |
93 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.-255+169G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462005 | |||||||
chr7:76462045 | C | A | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-255+209C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462045 | |||||||
chr7:76462317 | C | T | 1 | a0001c0001t0002g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-255+481C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462317 | |||||||
chr7:76462599 | A | G | 2 | a0002c0007t0001g0275 a0002c0007t0001g0276 |
2 | HG00609.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.-255+763A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462599 | |||||||
chr7:76462814 | C | T | 25 | a0001c0001t0002g0003 a0001c0001t0002g0161 a0001c0001t0002g0165 others(22): Show |
26 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.-254-731C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462814 | |||||||
chr7:76462926 | G | T | 1 | a0001c0001t0002g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-254-619G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76462926 | |||||||
chr7:76463044 | G | C | 1 | a0002c0002t0005g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-254-501G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463044 | |||||||
chr7:76463062 | G | A | 1 | a0002c0007t0001g0185 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-254-483G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463062 | |||||||
chr7:76463089 | TAAA | T | 138 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(135): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-254-451_-254-449d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 76463089 | ||||||
chr7:76463101 | CT | C | 8 | a0001c0001t0002g0007 a0001c0001t0002g0008 a0001c0001t0002g0010 others(5): Show |
8 | HG00673.hp2 HG01256.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.-254-430delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr7 | 76463101 | ||||||
chr7:76463152 | C | G | 1 | a0002c0002t0005g0274 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-254-393C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463152 | |||||||
chr7:76463192 | A | G | 8 | a0001c0031t0001g0273 a0002c0007t0001g0268 a0002c0007t0001g0270 others(5): Show |
8 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(5): Show |
intron_variant | MODIFIER | c.-254-353A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463192 | |||||||
chr7:76463206 | A | G | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-254-339A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463206 | |||||||
chr7:76463210 | G | A | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-254-335G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463210 | |||||||
chr7:76463309 | A | G | 1 | a0005c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-254-236A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463309 | |||||||
chr7:76463401 | C | G | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-254-144C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 1/10 | chr7 | 76463401 | |||||||
chr7:76463747 | A | G | 6 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(3): Show |
6 | HG00735.hp2 HG02451.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+38A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76463747 | |||||||
chr7:76463779 | G | C | 1 | a0003c0004t0001g0189 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-90+70G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76463779 | |||||||
chr7:76463838 | C | G | 2 | a0001c0003t0001g0158 a0003c0004t0001g0262 |
2 | HG01175.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.-90+129C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76463838 | |||||||
chr7:76463984 | T | C | 1 | a0002c0002t0001g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.-90+275T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76463984 | |||||||
chr7:76464017 | G | A | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-90+308G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464017 | |||||||
chr7:76464152 | G | T | 1 | a0001c0003t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-90+443G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464152 | |||||||
chr7:76464222 | G | A | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+513G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464222 | |||||||
chr7:76464245 | A | G | 142 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(139): Show |
143 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.-90+536A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464245 | |||||||
chr7:76464263 | C | T | 2 | a0001c0001t0002g0109 a0001c0001t0002g0110 |
2 | HG02970.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-90+554C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464263 | |||||||
chr7:76464264 | G | A | 11 | a0001c0003t0001g0116 a0005c0006t0001g0115 a0005c0006t0001g0117 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+555G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464264 | |||||||
chr7:76464316 | T | G | 3 | a0002c0011t0003g0264 a0002c0011t0003g0265 a0011c0030t0003g0263 |
3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+607T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464316 | |||||||
chr7:76464394 | G | A | 1 | a0001c0001t0002g0012 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-90+685G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464394 | |||||||
chr7:76464420 | CT | C | 49 | a0001c0003t0001g0221 a0001c0003t0001g0222 a0001c0013t0001g0193 others(46): Show |
50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90+712delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464420 | |||||||
chr7:76464421 | T | C | 109 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(106): Show |
109 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.-90+712T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464421 | |||||||
chr7:76464698 | C | T | 127 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(124): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-90+989C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464698 | |||||||
chr7:76464715 | T | A | 5 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(2): Show |
5 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90+1006T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464715 | |||||||
chr7:76464759 | C | T | 1 | a0002c0002t0001g0231 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-90+1050C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464759 | |||||||
chr7:76464777 | TTACA | T | 16 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(13): Show |
16 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.-90+1074_-90+1077d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76464777 | ||||||
chr7:76464833 | C | T | 1 | a0003c0004t0001g0261 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-90+1124C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464833 | |||||||
chr7:76464859 | A | G | 2 | a0002c0008t0001g0229 a0002c0008t0001g0230 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-90+1150A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464859 | |||||||
chr7:76464867 | A | G | 4 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+1158A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464867 | |||||||
chr7:76464971 | T | C | 236 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(233): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-90+1262T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76464971 | |||||||
chr7:76465038 | A | C | 13 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(10): Show |
13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-90+1329A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465038 | |||||||
chr7:76465044 | T | G | 5 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(2): Show |
5 | HG02451.hp1 HG02897.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90+1335T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465044 | |||||||
chr7:76465136 | A | G | 17 | a0001c0001t0002g0078 a0001c0001t0002g0111 a0001c0001t0002g0112 others(14): Show |
17 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.-90+1427A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465136 | |||||||
chr7:76465224 | G | A | 4 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(1): Show |
4 | HG00597.hp2 HG01952.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+1515G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465224 | |||||||
chr7:76465227 | A | G | 144 | a0001c0001t0002g0107 a0001c0001t0002g0111 a0001c0001t0002g0112 others(141): Show |
145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.-90+1518A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465227 | |||||||
chr7:76465462 | A | G | 262 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(259): Show |
266 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(263): Show |
intron_variant | MODIFIER | c.-90+1753A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465462 | |||||||
chr7:76465471 | C | T | 205 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(202): Show |
209 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(206): Show |
intron_variant | MODIFIER | c.-90+1762C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465471 | |||||||
chr7:76465501 | C | T | 1 | a0003c0004t0001g0257 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-90+1792C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465501 | |||||||
chr7:76465661 | A | G | 11 | a0001c0001t0002g0106 a0001c0001t0002g0111 a0001c0001t0002g0112 others(8): Show |
11 | HG01081.hp2 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90+1952A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465661 | |||||||
chr7:76465673 | C | T | 109 | a0001c0003t0001g0116 a0001c0003t0001g0157 a0001c0003t0001g0221 others(106): Show |
110 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.-90+1964C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465673 | |||||||
chr7:76465712 | C | G | 27 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(24): Show |
27 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.-90+2003C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465712 | |||||||
chr7:76465769 | C | T | 2 | a0002c0032t0001g0256 a0003c0005t0001g0075 |
2 | HG00733.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-90+2060C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465769 | |||||||
chr7:76465860 | C | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-90+2151C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465860 | |||||||
chr7:76465886 | G | T | 1 | a0001c0001t0002g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-90+2177G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465886 | |||||||
chr7:76465984 | C | T | 1 | a0001c0003t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-90+2275C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465984 | |||||||
chr7:76465991 | C | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-90+2282C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76465991 | |||||||
chr7:76466019 | C | T | 11 | a0001c0003t0001g0116 a0005c0006t0001g0115 a0005c0006t0001g0117 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+2310C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466019 | |||||||
chr7:76466268 | G | A | 11 | a0001c0003t0001g0116 a0005c0006t0001g0115 a0005c0006t0001g0117 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+2559G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466268 | |||||||
chr7:76466351 | C | T | 6 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(3): Show |
6 | HG02071.hp1 HG02451.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-90+2642C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466351 | |||||||
chr7:76466413 | C | CT | 138 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(135): Show |
139 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-90+2714dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76466413 | ||||||
chr7:76466592 | CT | C | 48 | a0001c0001t0002g0012 a0001c0003t0001g0128 a0001c0003t0001g0129 others(45): Show |
48 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-90+2895delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76466592 | ||||||
chr7:76466592 | CTT | C | 9 | a0001c0003t0001g0136 a0001c0003t0001g0137 a0001c0003t0001g0138 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-90+2894_-90+2895d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76466592 | ||||||
chr7:76466631 | G | A | 2 | a0001c0001t0002g0183 a0002c0020t0009g0011 |
2 | HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+2922G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466631 | |||||||
chr7:76466660 | C | T | 1 | a0001c0023t0006g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-90+2951C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466660 | |||||||
chr7:76466678 | A | G | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-90+2969A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466678 | |||||||
chr7:76466690 | C | A | 1 | a0002c0002t0001g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-90+2981C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466690 | |||||||
chr7:76466713 | C | T | 1 | a0001c0001t0002g0105 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-90+3004C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466713 | |||||||
chr7:76466722 | C | T | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-90+3013C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466722 | |||||||
chr7:76466743 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-90+3034C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466743 | |||||||
chr7:76466786 | C | T | 11 | a0001c0003t0001g0116 a0005c0006t0001g0115 a0005c0006t0001g0117 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+3077C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466786 | |||||||
chr7:76466787 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-90+3078G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466787 | |||||||
chr7:76466836 | G | T | 11 | a0001c0003t0001g0116 a0005c0006t0001g0115 a0005c0006t0001g0117 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+3127G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466836 | |||||||
chr7:76466844 | T | C | 3 | a0001c0001t0002g0183 a0001c0003t0001g0158 a0002c0020t0009g0011 |
3 | HG01175.hp2 HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+3135T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466844 | |||||||
chr7:76466877 | T | C | 3 | a0001c0001t0002g0183 a0001c0003t0001g0158 a0002c0020t0009g0011 |
3 | HG01175.hp2 HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+3168T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466877 | |||||||
chr7:76466888 | G | A | 2 | a0001c0001t0002g0183 a0002c0020t0009g0011 |
2 | HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+3179G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466888 | |||||||
chr7:76466929 | A | G | 2 | a0001c0001t0002g0183 a0002c0020t0009g0011 |
2 | HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+3220A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466929 | |||||||
chr7:76466945 | A | G | 1 | a0010c0016t0001g0227 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-90+3236A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466945 | |||||||
chr7:76466964 | A | G | 2 | a0001c0001t0002g0183 a0002c0020t0009g0011 |
2 | HG02071.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-90+3255A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466964 | |||||||
chr7:76466980 | C | T | 1 | a0003c0004t0001g0255 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-90+3271C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466980 | |||||||
chr7:76466981 | G | A | 1 | a0002c0002t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-90+3272G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76466981 | |||||||
chr7:76467097 | C | T | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-90+3388C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467097 | |||||||
chr7:76467106 | C | G | 2 | a0002c0008t0001g0229 a0002c0008t0001g0230 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-90+3397C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467106 | |||||||
chr7:76467116 | C | G | 31 | a0001c0001t0002g0072 a0001c0001t0002g0073 a0001c0001t0002g0183 others(28): Show |
31 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.-90+3407C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467116 | |||||||
chr7:76467143 | C | G | 1 | a0001c0003t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-90+3434C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467143 | |||||||
chr7:76467145 | C | T | 2 | a0002c0008t0001g0229 a0002c0008t0001g0230 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-90+3436C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467145 | |||||||
chr7:76467189 | A | G | 139 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(136): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-90+3480A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467189 | |||||||
chr7:76467229 | A | G | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-90+3520A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467229 | |||||||
chr7:76467241 | T | A | 141 | a0001c0001t0002g0183 a0001c0003t0001g0116 a0001c0003t0001g0128 others(138): Show |
142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.-90+3532T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467241 | |||||||
chr7:76467243 | G | A | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-90+3534G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467243 | |||||||
chr7:76467376 | G | A | 1 | a0002c0008t0004g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-90+3667G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467376 | |||||||
chr7:76467384 | G | A | 128 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(125): Show |
129 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(126): Show |
intron_variant | MODIFIER | c.-90+3675G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467384 | |||||||
chr7:76467447 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-90+3738C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467447 | |||||||
chr7:76467733 | A | C | 6 | a0001c0001t0002g0016 a0001c0001t0002g0017 a0001c0001t0002g0018 others(3): Show |
6 | HG00140.hp1 HG00741.hp1 HG01106.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+4024A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467733 | |||||||
chr7:76467746 | G | C | 11 | a0001c0003t0001g0116 a0005c0006t0001g0115 a0005c0006t0001g0117 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+4037G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467746 | |||||||
chr7:76467750 | C | T | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-90+4041C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467750 | |||||||
chr7:76467799 | G | A | 89 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(86): Show |
92 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(89): Show |
intron_variant | MODIFIER | c.-90+4090G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467799 | |||||||
chr7:76467897 | C | T | 139 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(136): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-90+4188C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467897 | |||||||
chr7:76467904 | C | A | 1 | a0001c0003t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-90+4195C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76467904 | |||||||
chr7:76468028 | T | C | 1 | a0011c0030t0003g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-90+4319T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468028 | |||||||
chr7:76468140 | G | A | 1 | a0001c0001t0010g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-90+4431G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468140 | |||||||
chr7:76468178 | G | A | 12 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90+4469G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468178 | |||||||
chr7:76468438 | GCCC | G | 99 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(96): Show |
102 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.-90+4730_-90+4732d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468438 | |||||||
chr7:76468447 | C | CT | 6 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0002c0011t0003g0264 others(3): Show |
6 | HG00733.hp1 HG01891.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+4738_-90+4739i others(3): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | |||||||
chr7:76468447 | CA | C | 15 | a0001c0003t0001g0221 a0001c0003t0001g0222 a0001c0003t0001g0266 others(12): Show |
15 | HG00735.hp2 HG01123.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-90+4739delA | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | |||||||
chr7:76468447 | CAT | C | 36 | a0002c0002t0001g0004 a0002c0002t0001g0126 a0002c0002t0001g0127 others(33): Show |
37 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(34): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4740d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | |||||||
chr7:76468447 | CATTT | C | 11 | a0001c0001t0002g0061 a0001c0001t0002g0062 a0001c0001t0002g0063 others(8): Show |
11 | HG01192.hp2 HG01993.hp1 HG02683.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4742d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | |||||||
chr7:76468447 | CATTTT | C | 82 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(79): Show |
85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4743d others(7): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | |||||||
chr7:76468447 | CATTTTT | C | 5 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0024 others(2): Show |
5 | HG01167.hp1 HG02080.hp2 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4744d others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | |||||||
chr7:76468447 | CATTTTTT | C | 11 | a0001c0003t0001g0116 a0005c0006t0001g0115 a0005c0006t0001g0117 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4745d others(9): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | |||||||
chr7:76468447 | CATTTTTT others(5): Show |
C | 56 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(53): Show |
56 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4750d others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | |||||||
chr7:76468447 | CATTTTTT others(6): Show |
C | 13 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(10): Show |
13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-90+4739_-90+4751d others(15): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468447 | |||||||
chr7:76468448 | A | AT | 8 | a0001c0001t0002g0089 a0001c0001t0002g0091 a0001c0001t0002g0096 others(5): Show |
8 | HG00741.hp2 HG01106.hp1 HG02148.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+4767dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468448 | ||||||
chr7:76468448 | A | T | 9 | a0001c0001t0002g0080 a0001c0001t0002g0083 a0001c0001t0002g0084 others(6): Show |
9 | HG00733.hp1 HG01891.hp2 HG02486.hp2 others(6): Show |
intron_variant | MODIFIER | c.-90+4739A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468448 | |||||||
chr7:76468561 | A | T | 7 | a0005c0006t0001g0115 a0005c0006t0001g0119 a0005c0006t0001g0120 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90+4852A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468561 | |||||||
chr7:76468578 | C | T | 4 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+4869C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468578 | |||||||
chr7:76468677 | C | T | 58 | a0001c0003t0001g0221 a0001c0003t0001g0222 a0001c0003t0001g0266 others(55): Show |
59 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-90+4968C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468677 | |||||||
chr7:76468758 | A | ATT | 8 | a0001c0003t0001g0138 a0001c0003t0001g0140 a0001c0003t0001g0141 others(5): Show |
8 | HG01243.hp2 HG02109.hp1 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.-90+5070_-90+5071d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTT | 32 | a0001c0003t0001g0221 a0001c0003t0001g0222 a0002c0002t0001g0004 others(29): Show |
33 | HG00280.hp2 HG00558.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.-90+5068_-90+5071d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTT | 19 | a0002c0002t0001g0125 a0002c0002t0001g0187 a0002c0002t0001g0190 others(16): Show |
19 | HG00423.hp1 HG00673.hp2 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.-90+5067_-90+5071d others(7): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0265 others(2): Show |
5 | HG02965.hp1 HG02965.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90+5065_-90+5071d others(9): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(1): Show |
14 | a0001c0001t0002g0111 a0001c0003t0001g0116 a0002c0007t0001g0259 others(11): Show |
14 | HG00558.hp2 HG01109.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-90+5064_-90+5071d others(10): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(2): Show |
10 | a0001c0001t0002g0112 a0001c0001t0002g0113 a0001c0001t0002g0114 others(7): Show |
10 | HG00544.hp1 HG00609.hp2 HG00733.hp1 others(7): Show |
intron_variant | MODIFIER | c.-90+5063_-90+5071d others(11): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(3): Show |
13 | a0003c0004t0001g0235 a0003c0004t0001g0236 a0003c0004t0001g0237 others(10): Show |
13 | HG00140.hp2 HG00639.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.-90+5062_-90+5071d others(12): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(4): Show |
15 | a0003c0004t0001g0189 a0003c0004t0001g0246 a0003c0004t0001g0247 others(12): Show |
15 | HG00735.hp1 HG01175.hp1 HG01261.hp1 others(12): Show |
intron_variant | MODIFIER | c.-90+5061_-90+5071d others(13): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(5): Show |
1 | a0003c0004t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-90+5060_-90+5071d others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(12): Show |
1 | a0001c0003t0001g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-90+5053_-90+5071d others(21): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(13): Show |
3 | a0001c0003t0001g0144 a0001c0003t0001g0145 a0001c0003t0001g0146 |
3 | HG02647.hp1 HG03139.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.-90+5052_-90+5071d others(22): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(14): Show |
11 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(8): Show |
11 | HG00408.hp1 HG00597.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.-90+5051_-90+5071d others(23): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(15): Show |
1 | a0001c0003t0001g0152 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-90+5050_-90+5071d others(24): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(19): Show |
1 | a0001c0003t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-90+5071_-90+5072i others(28): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | A | ATTTTTTT others(20): Show |
1 | a0001c0003t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-90+5071_-90+5072i others(29): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468758 | AT | A | 77 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(74): Show |
80 | HG00280.hp1 HG00323.hp1 HG00408.hp2 others(77): Show |
intron_variant | MODIFIER | c.-90+5071delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468758 | ||||||
chr7:76468797 | CTG | C | 4 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+5090_-90+5091d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76468797 | ||||||
chr7:76468800 | T | C | 4 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+5091T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468800 | |||||||
chr7:76468825 | C | T | 3 | a0001c0001t0002g0019 a0001c0001t0002g0020 a0001c0001t0002g0021 |
3 | HG00140.hp1 HG01346.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.-90+5116C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468825 | |||||||
chr7:76468832 | G | A | 27 | a0003c0004t0001g0189 a0003c0004t0001g0235 a0003c0004t0001g0236 others(24): Show |
27 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-90+5123G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76468832 | |||||||
chr7:76469017 | A | G | 132 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(129): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.-90+5308A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469017 | |||||||
chr7:76469051 | T | C | 143 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(140): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.-90+5342T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469051 | |||||||
chr7:76469133 | T | C | 143 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(140): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.-90+5424T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469133 | |||||||
chr7:76469166 | A | G | 3 | a0002c0011t0003g0264 a0002c0011t0003g0265 a0011c0030t0003g0263 |
3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-90+5457A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469166 | |||||||
chr7:76469221 | A | G | 4 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+5512A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469221 | |||||||
chr7:76469330 | C | T | 143 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(140): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.-90+5621C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469330 | |||||||
chr7:76469359 | G | GAT | 61 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(58): Show |
61 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.-90+5651_-90+5652d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76469359 | ||||||
chr7:76469360 | A | AT | 7 | a0001c0001t0002g0018 a0001c0001t0002g0107 a0001c0001t0002g0180 others(4): Show |
7 | HG00741.hp1 HG01361.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.-90+5671dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76469360 | ||||||
chr7:76469360 | A | ATAT | 5 | a0001c0003t0001g0142 a0002c0011t0003g0264 a0003c0004t0001g0257 others(2): Show |
5 | HG01243.hp2 HG02135.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+5652_-90+5653i others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76469360 | ||||||
chr7:76469360 | A | ATTT | 11 | a0001c0003t0001g0116 a0005c0006t0001g0115 a0005c0006t0001g0117 others(8): Show |
11 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90+5669_-90+5671d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76469360 | ||||||
chr7:76469361 | T | TA | 49 | a0001c0003t0001g0221 a0001c0003t0001g0222 a0001c0003t0001g0266 others(46): Show |
50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90+5652_-90+5653i others(3): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469361 | |||||||
chr7:76469362 | T | A | 12 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.-90+5653T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469362 | |||||||
chr7:76469381 | A | T | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-90+5672A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469381 | |||||||
chr7:76469394 | CTT | C | 138 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(135): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-90+5700_-90+5701d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76469394 | ||||||
chr7:76469415 | C | T | 1 | a0001c0001t0002g0178 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-90+5706C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469415 | |||||||
chr7:76469416 | G | A | 17 | a0001c0001t0002g0165 a0001c0001t0002g0166 a0001c0001t0002g0181 others(14): Show |
17 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(14): Show |
intron_variant | MODIFIER | c.-90+5707G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469416 | |||||||
chr7:76469425 | T | C | 143 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(140): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.-90+5716T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469425 | |||||||
chr7:76469481 | T | G | 19 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(16): Show |
19 | HG00639.hp2 HG01192.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.-90+5772T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469481 | |||||||
chr7:76469503 | C | T | 1 | a0001c0001t0002g0052 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-90+5794C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469503 | |||||||
chr7:76469507 | C | T | 4 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+5798C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469507 | |||||||
chr7:76469548 | A | G | 1 | a0001c0013t0001g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90+5839A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469548 | |||||||
chr7:76469550 | A | G | 1 | a0001c0013t0001g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90+5841A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469550 | |||||||
chr7:76469552 | T | C | 1 | a0001c0013t0001g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-90+5843T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469552 | |||||||
chr7:76469670 | G | A | 1 | a0001c0001t0010g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-90+5961G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469670 | |||||||
chr7:76469763 | C | T | 3 | a0002c0002t0001g0194 a0002c0002t0001g0211 a0002c0002t0001g0224 |
3 | HG02622.hp1 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.-90+6054C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469763 | |||||||
chr7:76469766 | C | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-90+6057C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469766 | |||||||
chr7:76469856 | T | G | 1 | a0003c0004t0001g0189 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-90+6147T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469856 | |||||||
chr7:76469908 | A | T | 53 | a0001c0003t0001g0221 a0001c0003t0001g0222 a0001c0013t0001g0193 others(50): Show |
54 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.-90+6199A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469908 | |||||||
chr7:76469937 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-90+6228A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76469937 | |||||||
chr7:76470121 | A | C | 4 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0113 others(1): Show |
4 | HG02451.hp1 HG02970.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+6412A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470121 | |||||||
chr7:76470159 | G | A | 139 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(136): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-90+6450G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470159 | |||||||
chr7:76470243 | T | C | 139 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(136): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-90+6534T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470243 | |||||||
chr7:76470308 | A | G | 4 | a0003c0005t0001g0014 a0003c0005t0001g0015 a0003c0005t0001g0067 others(1): Show |
4 | HG02818.hp2 HG02886.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+6599A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470308 | |||||||
chr7:76470409 | G | A | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.-90+6700G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470409 | |||||||
chr7:76470661 | T | G | 27 | a0003c0004t0001g0189 a0003c0004t0001g0235 a0003c0004t0001g0236 others(24): Show |
27 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-90+6952T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470661 | |||||||
chr7:76470713 | G | A | 1 | a0002c0002t0001g0197 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-90+7004G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470713 | |||||||
chr7:76470878 | G | C | 49 | a0001c0003t0001g0221 a0001c0003t0001g0222 a0001c0013t0001g0193 others(46): Show |
50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-90+7169G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470878 | |||||||
chr7:76470907 | T | C | 30 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(27): Show |
30 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.-90+7198T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76470907 | |||||||
chr7:76471154 | T | G | 76 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(73): Show |
77 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(74): Show |
intron_variant | MODIFIER | c.-90+7445T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471154 | |||||||
chr7:76471156 | C | CT | 72 | a0001c0001t0002g0012 a0001c0001t0002g0058 a0001c0001t0002g0059 others(69): Show |
73 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.-90+7470dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76471156 | ||||||
chr7:76471156 | C | CTT | 33 | a0002c0002t0001g0125 a0002c0002t0001g0190 a0002c0002t0001g0195 others(30): Show |
33 | HG00140.hp2 HG00558.hp1 HG00733.hp1 others(30): Show |
intron_variant | MODIFIER | c.-90+7469_-90+7470d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76471156 | ||||||
chr7:76471156 | C | CTTT | 6 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0003c0004t0001g0252 others(3): Show |
6 | HG00639.hp1 HG01109.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.-90+7468_-90+7470d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76471156 | ||||||
chr7:76471156 | CT | C | 10 | a0001c0001t0002g0022 a0001c0001t0002g0025 a0001c0001t0002g0080 others(7): Show |
10 | HG01070.hp1 HG01167.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.-90+7470delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76471156 | ||||||
chr7:76471156 | CTTT | C | 25 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(22): Show |
25 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.-90+7468_-90+7470d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76471156 | ||||||
chr7:76471184 | C | T | 1 | a0001c0003t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-90+7475C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471184 | |||||||
chr7:76471200 | C | T | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+7491C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471200 | |||||||
chr7:76471209 | T | G | 1 | a0001c0001t0002g0106 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-90+7500T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471209 | |||||||
chr7:76471218 | G | A | 1 | a0001c0001t0002g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-90+7509G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471218 | |||||||
chr7:76471287 | T | A | 134 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(131): Show |
135 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.-90+7578T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471287 | |||||||
chr7:76471322 | C | T | 136 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(133): Show |
137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.-90+7613C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471322 | |||||||
chr7:76471350 | A | G | 1 | a0002c0002t0001g0228 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-90+7641A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471350 | |||||||
chr7:76471352 | A | G | 8 | a0002c0002t0001g0187 a0002c0002t0001g0192 a0002c0002t0001g0209 others(5): Show |
8 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(5): Show |
intron_variant | MODIFIER | c.-90+7643A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471352 | |||||||
chr7:76471363 | A | G | 1 | a0002c0002t0001g0228 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-90+7654A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471363 | |||||||
chr7:76471434 | T | A | 4 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(1): Show |
4 | HG00597.hp2 HG01952.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-90+7725T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471434 | |||||||
chr7:76471452 | C | T | 28 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(25): Show |
28 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.-90+7743C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471452 | |||||||
chr7:76471540 | T | G | 24 | a0001c0001t0002g0106 a0001c0003t0001g0266 a0001c0003t0001g0267 others(21): Show |
24 | HG01081.hp2 HG01109.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.-90+7831T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471540 | |||||||
chr7:76471622 | G | A | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+7913G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471622 | |||||||
chr7:76471726 | G | A | 1 | a0002c0002t0005g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-90+8017G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471726 | |||||||
chr7:76471822 | C | T | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90+8113C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76471822 | |||||||
chr7:76472035 | C | T | 139 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(136): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-90+8326C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472035 | |||||||
chr7:76472122 | GGTTT | G | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-8295_-89-8292d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76472122 | ||||||
chr7:76472156 | G | T | 15 | a0001c0023t0006g0074 a0003c0005t0001g0014 a0003c0005t0001g0015 others(12): Show |
15 | HG00639.hp2 HG01192.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-89-8265G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472156 | |||||||
chr7:76472171 | C | T | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-8250C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472171 | |||||||
chr7:76472210 | A | G | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-8211A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472210 | |||||||
chr7:76472225 | C | G | 2 | a0001c0001t0002g0161 a0001c0001t0002g0177 |
2 | HG00733.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-89-8196C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472225 | |||||||
chr7:76472236 | G | T | 29 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(26): Show |
29 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-89-8185G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472236 | |||||||
chr7:76472323 | A | C | 134 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0050 others(131): Show |
136 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-89-8098A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472323 | |||||||
chr7:76472382 | G | A | 238 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(235): Show |
242 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.-89-8039G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472382 | |||||||
chr7:76472412 | C | T | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-8009C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472412 | |||||||
chr7:76472436 | C | A | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-7985C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472436 | |||||||
chr7:76472447 | T | C | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-7974T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472447 | |||||||
chr7:76472482 | A | G | 44 | a0002c0002t0001g0004 a0002c0002t0001g0125 a0002c0002t0001g0126 others(41): Show |
45 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.-89-7939A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472482 | |||||||
chr7:76472602 | A | G | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-89-7819A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472602 | |||||||
chr7:76472750 | T | A | 1 | a0001c0001t0002g0167 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.-89-7671T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472750 | |||||||
chr7:76472887 | G | A | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-7534G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472887 | |||||||
chr7:76472892 | A | C | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-7529A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472892 | |||||||
chr7:76472903 | A | G | 129 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(126): Show |
130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-89-7518A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472903 | |||||||
chr7:76472996 | C | T | 1 | a0001c0003t0001g0131 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.-89-7425C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76472996 | |||||||
chr7:76473162 | T | C | 1 | a0001c0001t0002g0026 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-89-7259T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473162 | |||||||
chr7:76473400 | T | C | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-7021T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473400 | |||||||
chr7:76473574 | A | G | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-6847A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473574 | |||||||
chr7:76473607 | C | T | 27 | a0003c0004t0001g0189 a0003c0004t0001g0235 a0003c0004t0001g0236 others(24): Show |
27 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-89-6814C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473607 | |||||||
chr7:76473826 | A | G | 2 | a0003c0005t0001g0065 a0003c0005t0001g0066 |
2 | HG00639.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-89-6595A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473826 | |||||||
chr7:76473898 | G | A | 129 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(126): Show |
130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-89-6523G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473898 | |||||||
chr7:76473919 | CT | C | 127 | a0001c0001t0002g0010 a0001c0001t0002g0181 a0001c0003t0001g0116 others(124): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.-89-6483delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76473919 | ||||||
chr7:76473959 | T | C | 1 | a0009c0019t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-89-6462T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76473959 | |||||||
chr7:76474082 | C | T | 13 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(10): Show |
13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-6339C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474082 | |||||||
chr7:76474141 | A | G | 1 | a0001c0003t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-89-6280A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474141 | |||||||
chr7:76474146 | C | G | 1 | a0001c0003t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-89-6275C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474146 | |||||||
chr7:76474148 | C | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-6273C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474148 | |||||||
chr7:76474163 | C | T | 6 | a0001c0001t0002g0024 a0001c0001t0002g0047 a0001c0001t0002g0048 others(3): Show |
6 | HG01496.hp1 HG01934.hp2 NA18947.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-6258C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474163 | |||||||
chr7:76474181 | T | TTTTTTC | 24 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(21): Show |
24 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.-89-6217_-89-6212d others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76474181 | ||||||
chr7:76474181 | TTTTTTCT others(5): Show |
T | 56 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(53): Show |
56 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.-89-6223_-89-6212d others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76474181 | ||||||
chr7:76474223 | CT | C | 116 | a0001c0001t0002g0007 a0001c0001t0002g0022 a0001c0001t0002g0025 others(113): Show |
117 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-89-6185delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76474223 | ||||||
chr7:76474223 | CTT | C | 27 | a0003c0004t0001g0189 a0003c0004t0001g0235 a0003c0004t0001g0236 others(24): Show |
27 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-89-6186_-89-6185d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76474223 | ||||||
chr7:76474278 | C | T | 2 | a0002c0002t0001g0186 a0002c0002t0001g0215 |
2 | HG01952.hp2 HG01975.hp1 |
intron_variant | MODIFIER | c.-89-6143C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474278 | |||||||
chr7:76474279 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0002g0103 |
2 | HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.-89-6142G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474279 | |||||||
chr7:76474507 | G | C | 139 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(136): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-89-5914G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474507 | |||||||
chr7:76474514 | A | G | 49 | a0001c0003t0001g0116 a0001c0003t0001g0221 a0001c0003t0001g0222 others(46): Show |
50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-89-5907A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474514 | |||||||
chr7:76474515 | G | T | 60 | a0001c0003t0001g0116 a0001c0003t0001g0156 a0001c0003t0001g0221 others(57): Show |
61 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.-89-5906G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474515 | |||||||
chr7:76474563 | C | G | 5 | a0001c0003t0001g0116 a0001c0003t0001g0140 a0001c0003t0001g0141 others(2): Show |
5 | HG02723.hp2 HG02922.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.-89-5858C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474563 | |||||||
chr7:76474864 | G | T | 50 | a0001c0003t0001g0116 a0001c0003t0001g0158 a0001c0003t0001g0221 others(47): Show |
51 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(48): Show |
intron_variant | MODIFIER | c.-89-5557G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474864 | |||||||
chr7:76474906 | C | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-5515C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76474906 | |||||||
chr7:76475069 | G | T | 12 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.-89-5352G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475069 | |||||||
chr7:76475097 | A | T | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-89-5324A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475097 | |||||||
chr7:76475183 | T | A | 14 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(11): Show |
14 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.-89-5238T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475183 | |||||||
chr7:76475226 | A | G | 270 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(267): Show |
274 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(271): Show |
intron_variant | MODIFIER | c.-89-5195A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475226 | |||||||
chr7:76475226 | A | T | 1 | a0001c0001t0002g0059 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-89-5195A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475226 | |||||||
chr7:76475243 | G | A | 9 | a0001c0003t0001g0136 a0001c0003t0001g0137 a0001c0003t0001g0138 others(6): Show |
9 | HG01243.hp2 HG02109.hp1 HG02630.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-5178G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475243 | |||||||
chr7:76475259 | C | T | 1 | a0002c0011t0003g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-89-5162C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475259 | |||||||
chr7:76475271 | A | G | 49 | a0001c0003t0001g0116 a0001c0003t0001g0221 a0001c0003t0001g0222 others(46): Show |
50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.-89-5150A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475271 | |||||||
chr7:76475456 | G | A | 129 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(126): Show |
130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.-89-4965G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475456 | |||||||
chr7:76475510 | A | T | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-4911A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475510 | |||||||
chr7:76475513 | C | G | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-4908C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475513 | |||||||
chr7:76475515 | C | A | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-4906C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475515 | |||||||
chr7:76475515 | C | T | 1 | a0001c0001t0002g0046 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.-89-4906C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475515 | |||||||
chr7:76475519 | T | A | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-4902T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475519 | |||||||
chr7:76475553 | G | C | 1 | a0001c0023t0006g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-89-4868G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475553 | |||||||
chr7:76475574 | C | T | 14 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(11): Show |
14 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.-89-4847C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76475574 | |||||||
chr7:76475701 | GA | G | 100 | a0001c0003t0001g0116 a0001c0003t0001g0221 a0001c0003t0001g0222 others(97): Show |
101 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.-89-4712delA | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76475701 | ||||||
chr7:76475701 | GAA | G | 29 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(26): Show |
29 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.-89-4713_-89-4712d others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76475701 | ||||||
chr7:76476000 | A | G | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-89-4421A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476000 | |||||||
chr7:76476017 | G | A | 51 | a0001c0003t0001g0116 a0001c0003t0001g0221 a0001c0003t0001g0222 others(48): Show |
52 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(49): Show |
intron_variant | MODIFIER | c.-89-4404G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476017 | |||||||
chr7:76476021 | C | T | 138 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(135): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.-89-4400C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476021 | |||||||
chr7:76476095 | T | G | 27 | a0003c0004t0001g0189 a0003c0004t0001g0235 a0003c0004t0001g0236 others(24): Show |
27 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-89-4326T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476095 | |||||||
chr7:76476156 | T | C | 1 | a0004c0009t0002g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-89-4265T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476156 | |||||||
chr7:76476186 | A | G | 1 | a0001c0003t0001g0136 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-89-4235A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476186 | |||||||
chr7:76476227 | G | C | 139 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(136): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-89-4194G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476227 | |||||||
chr7:76476402 | T | C | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-4019T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476402 | |||||||
chr7:76476540 | T | C | 5 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0011t0003g0264 others(2): Show |
5 | HG02965.hp1 HG03130.hp2 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-89-3881T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476540 | |||||||
chr7:76476748 | T | A | 1 | a0001c0023t0006g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-89-3673T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476748 | |||||||
chr7:76476771 | C | T | 1 | a0004c0009t0002g0164 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-89-3650C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476771 | |||||||
chr7:76476871 | T | C | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-3550T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476871 | |||||||
chr7:76476872 | G | A | 130 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(127): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.-89-3549G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476872 | |||||||
chr7:76476895 | G | A | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-3526G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76476895 | |||||||
chr7:76477041 | G | A | 2 | a0001c0003t0001g0146 a0001c0003t0001g0154 |
2 | HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-89-3380G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477041 | |||||||
chr7:76477157 | C | CGCCCGCC others(1): Show |
87 | a0001c0003t0001g0116 a0001c0003t0001g0221 a0001c0003t0001g0222 others(84): Show |
88 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.-89-3257_-89-3256i others(10): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477157 | ||||||
chr7:76477189 | C | T | 13 | a0003c0004t0001g0242 a0003c0004t0001g0243 a0003c0004t0001g0251 others(10): Show |
13 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-3232C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477189 | |||||||
chr7:76477194 | C | T | 2 | a0005c0006t0001g0117 a0005c0006t0001g0118 |
2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-89-3227C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477194 | |||||||
chr7:76477195 | A | G | 13 | a0003c0004t0001g0242 a0003c0004t0001g0243 a0003c0004t0001g0251 others(10): Show |
13 | HG01099.hp1 HG01109.hp1 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-3226A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477195 | |||||||
chr7:76477231 | G | A | 3 | a0001c0003t0001g0146 a0001c0003t0001g0154 a0001c0003t0001g0158 |
3 | HG01175.hp2 HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-89-3190G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477231 | |||||||
chr7:76477235 | C | T | 136 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(133): Show |
137 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(134): Show |
intron_variant | MODIFIER | c.-89-3186C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477235 | |||||||
chr7:76477244 | C | T | 137 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(134): Show |
138 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.-89-3177C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477244 | |||||||
chr7:76477273 | G | A | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-3148G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477273 | |||||||
chr7:76477378 | T | G | 63 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(60): Show |
63 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(60): Show |
intron_variant | MODIFIER | c.-89-3043T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477378 | |||||||
chr7:76477499 | T | C | 13 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(10): Show |
13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-2922T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477499 | |||||||
chr7:76477537 | A | C | 3 | a0001c0001t0002g0012 a0001c0001t0002g0101 a0001c0003t0001g0158 |
3 | HG01175.hp2 NA18961.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.-89-2884A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477537 | |||||||
chr7:76477602 | A | G | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-89-2819A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477602 | |||||||
chr7:76477666 | C | A | 139 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(136): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.-89-2755C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477666 | |||||||
chr7:76477728 | A | G | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-2693A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477728 | |||||||
chr7:76477800 | C | CTAAA | 16 | a0001c0001t0002g0002 a0001c0001t0002g0008 a0001c0001t0002g0016 others(13): Show |
17 | HG00280.hp1 HG00323.hp1 HG00673.hp1 others(14): Show |
intron_variant | MODIFIER | c.-89-2583_-89-2580d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | ||||||
chr7:76477800 | C | CTAAATAA others(1): Show |
3 | a0001c0001t0002g0012 a0001c0001t0002g0090 a0001c0001t0002g0168 |
3 | NA18959.hp1 NA18959.hp2 NA18967.hp2 |
intron_variant | MODIFIER | c.-89-2587_-89-2580d others(10): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | ||||||
chr7:76477800 | CTAAA | C | 9 | a0001c0001t0002g0184 a0001c0003t0001g0128 a0001c0003t0001g0138 others(6): Show |
9 | HG01358.hp1 HG01884.hp2 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-89-2583_-89-2580d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | ||||||
chr7:76477800 | CTAAATAA others(1): Show |
C | 116 | a0001c0001t0002g0110 a0001c0003t0001g0116 a0001c0003t0001g0129 others(113): Show |
117 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.-89-2587_-89-2580d others(10): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | ||||||
chr7:76477800 | CTAAATAA others(5): Show |
C | 8 | a0001c0001t0002g0175 a0001c0001t0002g0176 a0001c0003t0001g0266 others(5): Show |
8 | HG02165.hp1 HG02897.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-2591_-89-2580d others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | ||||||
chr7:76477800 | CTAAATAA others(9): Show |
C | 13 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(10): Show |
13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-2595_-89-2580d others(18): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76477800 | ||||||
chr7:76477991 | C | T | 1 | a0001c0013t0001g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-89-2430C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76477991 | |||||||
chr7:76478093 | G | A | 7 | a0005c0006t0001g0115 a0005c0006t0001g0119 a0005c0006t0001g0120 others(4): Show |
7 | HG01109.hp1 HG01884.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-89-2328G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478093 | |||||||
chr7:76478229 | G | A | 48 | a0001c0013t0001g0193 a0002c0002t0001g0004 a0002c0002t0001g0125 others(45): Show |
49 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-89-2192G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478229 | |||||||
chr7:76478231 | A | G | 58 | a0001c0013t0001g0193 a0002c0002t0001g0004 a0002c0002t0001g0125 others(55): Show |
59 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-89-2190A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478231 | |||||||
chr7:76478414 | A | AT | 28 | a0001c0001t0002g0045 a0001c0001t0002g0098 a0001c0001t0002g0100 others(25): Show |
28 | HG00597.hp1 HG00741.hp2 HG01109.hp1 others(25): Show |
intron_variant | MODIFIER | c.-89-1988dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76478414 | ||||||
chr7:76478414 | AT | A | 8 | a0001c0001t0002g0090 a0001c0001t0002g0167 a0001c0003t0001g0116 others(5): Show |
8 | HG01884.hp2 HG02717.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.-89-1988delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76478414 | ||||||
chr7:76478457 | C | T | 6 | a0001c0001t0002g0105 a0001c0003t0001g0266 a0001c0003t0001g0267 others(3): Show |
6 | HG01192.hp1 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-1964C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478457 | |||||||
chr7:76478514 | G | T | 3 | a0003c0004t0001g0241 a0003c0004t0001g0250 a0003c0004t0001g0254 |
3 | HG00735.hp1 HG01081.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.-89-1907G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478514 | |||||||
chr7:76478568 | G | A | 1 | a0002c0002t0001g0199 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.-89-1853G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478568 | |||||||
chr7:76478613 | A | G | 49 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0026 others(46): Show |
49 | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(46): Show |
intron_variant | MODIFIER | c.-89-1808A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478613 | |||||||
chr7:76478658 | C | T | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-89-1763C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478658 | |||||||
chr7:76478662 | C | G | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-89-1759C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478662 | |||||||
chr7:76478662 | C | T | 1 | a0001c0001t0002g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-89-1759C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478662 | |||||||
chr7:76478687 | G | A | 236 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(233): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.-89-1734G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478687 | |||||||
chr7:76478746 | G | A | 78 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(75): Show |
81 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.-89-1675G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478746 | |||||||
chr7:76478829 | C | A | 3 | a0002c0011t0003g0264 a0002c0011t0003g0265 a0011c0030t0003g0263 |
3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-89-1592C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478829 | |||||||
chr7:76478957 | T | C | 2 | a0001c0001t0002g0081 a0001c0001t0002g0082 |
2 | HG02647.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.-89-1464T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478957 | |||||||
chr7:76478963 | A | G | 83 | a0001c0001t0002g0105 a0001c0003t0001g0266 a0001c0003t0001g0267 others(80): Show |
84 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.-89-1458A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478963 | |||||||
chr7:76478993 | C | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-1428C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76478993 | |||||||
chr7:76479036 | A | G | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-1385A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479036 | |||||||
chr7:76479039 | C | G | 27 | a0003c0004t0001g0189 a0003c0004t0001g0235 a0003c0004t0001g0236 others(24): Show |
27 | HG00140.hp2 HG00639.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-89-1382C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479039 | |||||||
chr7:76479104 | C | T | 1 | a0001c0001t0002g0021 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-89-1317C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479104 | |||||||
chr7:76479251 | A | T | 91 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(88): Show |
91 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-89-1170A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479251 | |||||||
chr7:76479262 | G | A | 6 | a0001c0001t0002g0027 a0001c0001t0002g0053 a0001c0001t0002g0054 others(3): Show |
6 | HG02109.hp2 HG02257.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-1159G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479262 | |||||||
chr7:76479288 | C | T | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-89-1133C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479288 | |||||||
chr7:76479316 | G | A | 11 | a0001c0001t0002g0033 a0001c0001t0002g0034 a0001c0001t0002g0035 others(8): Show |
11 | HG02056.hp1 HG02129.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.-89-1105G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479316 | |||||||
chr7:76479395 | A | G | 145 | a0001c0001t0010g0085 a0001c0003t0001g0116 a0001c0003t0001g0128 others(142): Show |
146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.-89-1026A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479395 | |||||||
chr7:76479508 | A | T | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-913A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479508 | |||||||
chr7:76479529 | G | A | 135 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(132): Show |
136 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.-89-892G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479529 | |||||||
chr7:76479610 | T | A | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-811T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479610 | |||||||
chr7:76479641 | C | T | 1 | a0002c0002t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-89-780C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479641 | |||||||
chr7:76479710 | G | A | 123 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(120): Show |
124 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.-89-711G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479710 | |||||||
chr7:76479839 | A | T | 1 | a0001c0001t0010g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-89-582A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479839 | |||||||
chr7:76479873 | G | T | 8 | a0005c0006t0001g0115 a0005c0006t0001g0119 a0005c0006t0001g0120 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.-89-548G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479873 | |||||||
chr7:76479907 | G | A | 12 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.-89-514G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479907 | |||||||
chr7:76479915 | G | A | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-89-506G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479915 | |||||||
chr7:76479924 | G | A | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-89-497G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479924 | |||||||
chr7:76479964 | G | C | 1 | a0002c0008t0004g0133 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-89-457G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76479964 | |||||||
chr7:76480034 | C | T | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-387C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480034 | |||||||
chr7:76480077 | G | A | 61 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(58): Show |
61 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.-89-344G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480077 | |||||||
chr7:76480079 | C | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-89-342C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480079 | |||||||
chr7:76480099 | G | A | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-322G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480099 | |||||||
chr7:76480103 | C | G | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-318C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480103 | |||||||
chr7:76480195 | C | T | 1 | a0005c0006t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-89-226C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480195 | |||||||
chr7:76480227 | A | C | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.-89-194A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480227 | |||||||
chr7:76480228 | C | A | 1 | a0001c0001t0002g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-89-193C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480228 | |||||||
chr7:76480273 | G | C | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.-89-148G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480273 | |||||||
chr7:76480301 | T | C | 13 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(10): Show |
13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.-89-120T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480301 | |||||||
chr7:76480305 | C | CA | 6 | a0001c0003t0001g0266 a0001c0003t0001g0267 a0002c0002t0001g0226 others(3): Show |
6 | HG02056.hp2 HG02965.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.-89-101dupA | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr7 | 76480305 | ||||||
chr7:76480327 | G | C | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.-89-94G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480327 | |||||||
chr7:76480342 | G | A | 1 | a0010c0016t0001g0227 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-89-79G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480342 | |||||||
chr7:76480396 | C | A | 3 | a0002c0002t0001g0125 a0002c0002t0001g0126 a0002c0002t0001g0127 |
3 | HG01070.hp2 HG01071.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.-89-25C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480396 | |||||||
chr7:76480399 | C | G | 1 | a0002c0011t0003g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-89-22C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 2/10 | chr7 | 76480399 | |||||||
chr7:76480812 | T | C | 2 | a0005c0006t0001g0117 a0005c0006t0001g0118 |
2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.268+35T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76480812 | |||||||
chr7:76480917 | G | A | 34 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(31): Show |
34 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.268+140G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76480917 | |||||||
chr7:76481018 | C | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.268+241C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481018 | |||||||
chr7:76481109 | G | A | 4 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(1): Show |
4 | HG00597.hp2 HG01952.hp1 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.268+332G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481109 | |||||||
chr7:76481111 | G | A | 9 | a0003c0005t0001g0064 a0003c0005t0001g0065 a0003c0005t0001g0066 others(6): Show |
9 | HG00639.hp2 HG01192.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.268+334G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481111 | |||||||
chr7:76481155 | C | T | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.268+378C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481155 | |||||||
chr7:76481181 | G | A | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.268+404G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481181 | |||||||
chr7:76481189 | CT | C | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.268+427delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 76481189 | ||||||
chr7:76481232 | A | G | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.268+455A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481232 | |||||||
chr7:76481251 | G | A | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.268+474G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481251 | |||||||
chr7:76481376 | G | A | 1 | a0013c0015t0001g0191 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.268+599G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481376 | |||||||
chr7:76481385 | C | G | 1 | a0001c0023t0006g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.268+608C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481385 | |||||||
chr7:76481706 | G | T | 49 | a0001c0013t0001g0193 a0002c0002t0001g0004 a0002c0002t0001g0125 others(46): Show |
50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.269-802G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481706 | |||||||
chr7:76481806 | T | G | 1 | a0001c0001t0002g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.269-702T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481806 | |||||||
chr7:76481835 | GT | G | 127 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(124): Show |
128 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(125): Show |
intron_variant | MODIFIER | c.269-662delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 76481835 | ||||||
chr7:76481848 | GTGTT | G | 141 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(138): Show |
142 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.269-642_269-639del others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr7 | 76481848 | ||||||
chr7:76481922 | T | A | 12 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.269-586T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481922 | |||||||
chr7:76481923 | C | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-585C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481923 | |||||||
chr7:76481925 | T | A | 12 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.269-583T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481925 | |||||||
chr7:76481953 | C | T | 1 | a0001c0001t0002g0012 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.269-555C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481953 | |||||||
chr7:76481954 | T | C | 1 | a0001c0001t0002g0012 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.269-554T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481954 | |||||||
chr7:76481955 | C | A | 1 | a0001c0001t0002g0012 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.269-553C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481955 | |||||||
chr7:76481956 | C | T | 13 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(10): Show |
13 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(10): Show |
intron_variant | MODIFIER | c.269-552C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481956 | |||||||
chr7:76481957 | G | A | 2 | a0001c0001t0002g0104 a0001c0003t0001g0136 |
2 | HG02818.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.269-551G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481957 | |||||||
chr7:76481979 | C | T | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.269-529C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481979 | |||||||
chr7:76481980 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0177 |
2 | HG00733.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.269-528G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481980 | |||||||
chr7:76481980 | G | C | 1 | a0005c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.269-528G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76481980 | |||||||
chr7:76482094 | A | G | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.269-414A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76482094 | |||||||
chr7:76482215 | C | G | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.269-293C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76482215 | |||||||
chr7:76482274 | C | T | 1 | a0002c0011t0003g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.269-234C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 3/10 | chr7 | 76482274 | |||||||
chr7:76483152 | C | T | 1 | a0001c0023t0006g0074 | 1 | HG02451.hp2 | splice_region_variant&intron_variant | LOW | c.908+5C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483152 | |||||||
chr7:76483163 | G | A | 2 | a0002c0008t0001g0229 a0002c0008t0001g0230 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.908+16G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483163 | |||||||
chr7:76483166 | G | A | 1 | a0003c0005t0001g0075 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.908+19G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483166 | |||||||
chr7:76483170 | G | A | 61 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(58): Show |
61 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(58): Show |
intron_variant | MODIFIER | c.908+23G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483170 | |||||||
chr7:76483258 | C | T | 1 | a0002c0002t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.908+111C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483258 | |||||||
chr7:76483300 | C | T | 2 | a0001c0001t0002g0043 a0001c0001t0002g0044 |
2 | HG00408.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.908+153C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483300 | |||||||
chr7:76483307 | A | G | 1 | a0011c0030t0003g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.908+160A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483307 | |||||||
chr7:76483345 | C | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+198C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483345 | |||||||
chr7:76483346 | G | A | 1 | a0011c0030t0003g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.908+199G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483346 | |||||||
chr7:76483385 | T | C | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.908+238T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483385 | |||||||
chr7:76483584 | C | T | 1 | a0001c0001t0002g0016 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.908+437C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483584 | |||||||
chr7:76483638 | T | C | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.908+491T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483638 | |||||||
chr7:76483969 | A | G | 2 | a0001c0001t0002g0038 a0001c0001t0002g0045 |
2 | NA18999.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.908+822A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76483969 | |||||||
chr7:76484013 | C | T | 3 | a0002c0002t0001g0194 a0002c0002t0001g0211 a0002c0002t0001g0224 |
3 | HG02622.hp1 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.908+866C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484013 | |||||||
chr7:76484014 | A | G | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.908+867A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484014 | |||||||
chr7:76484022 | A | G | 6 | a0001c0003t0001g0137 a0001c0013t0001g0193 a0002c0002t0001g0228 others(3): Show |
6 | HG01081.hp2 HG01884.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.908+875A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484022 | |||||||
chr7:76484046 | C | T | 130 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(127): Show |
131 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.908+899C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484046 | |||||||
chr7:76484217 | G | T | 1 | a0001c0001t0002g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.908+1070G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484217 | |||||||
chr7:76484333 | G | A | 144 | a0001c0001t0002g0003 a0001c0001t0002g0161 a0001c0001t0002g0165 others(141): Show |
146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.908+1186G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484333 | |||||||
chr7:76484378 | AC | A | 52 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0028 others(49): Show |
53 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.908+1238delC | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76484378 | ||||||
chr7:76484550 | C | T | 5 | a0001c0001t0002g0013 a0002c0002t0001g0004 a0002c0008t0004g0132 others(2): Show |
6 | HG01256.hp2 HG01258.hp1 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.908+1403C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484550 | |||||||
chr7:76484551 | G | A | 17 | a0001c0001t0002g0003 a0001c0001t0002g0161 a0001c0001t0002g0167 others(14): Show |
18 | HG00544.hp2 HG00597.hp1 HG00733.hp2 others(15): Show |
intron_variant | MODIFIER | c.908+1404G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484551 | |||||||
chr7:76484579 | G | T | 1 | a0001c0001t0002g0179 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.908+1432G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484579 | |||||||
chr7:76484581 | C | T | 3 | a0003c0004t0001g0235 a0003c0004t0001g0240 a0003c0004t0001g0261 |
3 | HG00140.hp2 HG01123.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.908+1434C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484581 | |||||||
chr7:76484582 | A | G | 156 | a0001c0001t0001g0088 a0001c0001t0002g0003 a0001c0001t0002g0025 others(153): Show |
158 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.908+1435A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484582 | |||||||
chr7:76484659 | G | A | 39 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(36): Show |
41 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.908+1512G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484659 | |||||||
chr7:76484685 | G | A | 3 | a0001c0003t0001g0135 a0001c0003t0001g0144 a0001c0003t0001g0149 |
3 | HG00323.hp2 NA18952.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.908+1538G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484685 | |||||||
chr7:76484719 | C | T | 1 | a0001c0001t0002g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.908+1572C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484719 | |||||||
chr7:76484720 | G | T | 93 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0007 others(90): Show |
95 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(92): Show |
intron_variant | MODIFIER | c.908+1573G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484720 | |||||||
chr7:76484812 | G | A | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.908+1665G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484812 | |||||||
chr7:76484857 | T | G | 157 | a0001c0001t0002g0003 a0001c0001t0002g0102 a0001c0001t0002g0161 others(154): Show |
159 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.908+1710T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484857 | |||||||
chr7:76484879 | C | T | 27 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(24): Show |
27 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.908+1732C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76484879 | |||||||
chr7:76484904 | C | CT | 31 | a0001c0001t0002g0003 a0001c0001t0002g0161 a0001c0001t0002g0165 others(28): Show |
32 | HG00544.hp2 HG00597.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.908+1759dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76484904 | ||||||
chr7:76485079 | C | A | 1 | a0002c0002t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.908+1932C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485079 | |||||||
chr7:76485235 | A | G | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.908+2088A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485235 | |||||||
chr7:76485253 | A | G | 163 | a0001c0001t0002g0003 a0001c0001t0002g0161 a0001c0001t0002g0165 others(160): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.908+2106A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485253 | |||||||
chr7:76485262 | G | A | 1 | a0002c0007t0001g0260 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.908+2115G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485262 | |||||||
chr7:76485267 | G | T | 33 | a0001c0001t0002g0003 a0001c0001t0002g0161 a0001c0001t0002g0165 others(30): Show |
34 | HG00544.hp2 HG00597.hp1 HG00733.hp2 others(31): Show |
intron_variant | MODIFIER | c.908+2120G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485267 | |||||||
chr7:76485270 | A | G | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.908+2123A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485270 | |||||||
chr7:76485280 | G | A | 1 | a0001c0001t0002g0101 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.908+2133G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485280 | |||||||
chr7:76485311 | T | C | 165 | a0001c0001t0002g0003 a0001c0001t0002g0058 a0001c0001t0002g0161 others(162): Show |
167 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.908+2164T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485311 | |||||||
chr7:76485450 | G | T | 139 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(136): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.908+2303G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485450 | |||||||
chr7:76485462 | G | T | 139 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(136): Show |
140 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.908+2315G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485462 | |||||||
chr7:76485555 | A | T | 140 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.908+2408A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485555 | |||||||
chr7:76485565 | C | T | 5 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0090 others(2): Show |
5 | NA18959.hp1 NA18961.hp1 NA18967.hp2 others(2): Show |
intron_variant | MODIFIER | c.908+2418C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485565 | |||||||
chr7:76485612 | T | G | 1 | a0001c0001t0002g0180 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.908+2465T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485612 | |||||||
chr7:76485625 | A | C | 1 | a0005c0006t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.908+2478A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485625 | |||||||
chr7:76485772 | A | C | 1 | a0007c0012t0001g0233 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.908+2625A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485772 | |||||||
chr7:76485816 | G | A | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.908+2669G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485816 | |||||||
chr7:76485920 | G | A | 1 | a0002c0002t0001g0196 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.908+2773G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76485920 | |||||||
chr7:76486163 | C | T | 133 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(130): Show |
134 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.908+3016C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486163 | |||||||
chr7:76486197 | C | T | 1 | a0001c0001t0002g0179 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.908+3050C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486197 | |||||||
chr7:76486232 | C | T | 138 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(135): Show |
139 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.908+3085C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486232 | |||||||
chr7:76486452 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.908+3305C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486452 | |||||||
chr7:76486516 | G | A | 1 | a0002c0011t0003g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.908+3369G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486516 | |||||||
chr7:76486518 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0002g0103 |
2 | HG01258.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.908+3371C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486518 | |||||||
chr7:76486557 | G | C | 1 | a0001c0001t0002g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.908+3410G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486557 | |||||||
chr7:76486558 | G | A | 1 | a0001c0018t0011g0099 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.908+3411G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486558 | |||||||
chr7:76486559 | G | A | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.908+3412G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486559 | |||||||
chr7:76486658 | A | G | 2 | a0001c0001t0002g0058 a0002c0017t0001g0188 |
2 | HG02738.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.908+3511A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486658 | |||||||
chr7:76486688 | T | C | 3 | a0002c0011t0003g0264 a0002c0011t0003g0265 a0011c0030t0003g0263 |
3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.908+3541T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486688 | |||||||
chr7:76486700 | G | C | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.908+3553G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486700 | |||||||
chr7:76486712 | C | T | 1 | a0001c0001t0002g0045 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.908+3565C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486712 | |||||||
chr7:76486733 | A | G | 1 | a0005c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.908+3586A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486733 | |||||||
chr7:76486754 | G | A | 1 | a0001c0001t0002g0033 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.908+3607G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486754 | |||||||
chr7:76486805 | G | A | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.908+3658G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486805 | |||||||
chr7:76486810 | A | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.908+3663A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486810 | |||||||
chr7:76486814 | C | A | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.908+3667C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486814 | |||||||
chr7:76486846 | G | GGCGGCGG others(8): Show |
1 | a0002c0011t0003g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.908+3701_908+3702i others(17): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | ||||||
chr7:76486846 | G | GGCGGCGG others(14): Show |
1 | a0011c0030t0003g0263 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.908+3701_908+3702i others(23): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | ||||||
chr7:76486846 | G | GGCGGCGG others(17): Show |
1 | a0002c0011t0003g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.908+3701_908+3702i others(26): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | ||||||
chr7:76486846 | G | GGCGGCGG others(20): Show |
2 | a0005c0006t0001g0117 a0005c0006t0001g0118 |
2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.908+3701_908+3702i others(29): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | ||||||
chr7:76486846 | G | GGCGGCGG others(23): Show |
7 | a0005c0006t0001g0119 a0005c0006t0001g0120 a0005c0006t0001g0121 others(4): Show |
7 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+3701_908+3702i others(32): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | ||||||
chr7:76486846 | G | GGCT | 4 | a0001c0001t0001g0088 a0001c0001t0002g0041 a0001c0001t0002g0103 others(1): Show |
4 | HG00609.hp1 HG01258.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+3738_908+3740d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | ||||||
chr7:76486846 | GGCTGCT | G | 49 | a0001c0013t0001g0193 a0002c0002t0001g0004 a0002c0002t0001g0125 others(46): Show |
50 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(47): Show |
intron_variant | MODIFIER | c.908+3735_908+3740d others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | ||||||
chr7:76486846 | GGCTGCTG others(23): Show |
G | 1 | a0002c0002t0001g0199 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.908+3711_908+3740d others(32): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486846 | ||||||
chr7:76486849 | T | G | 92 | a0001c0001t0002g0058 a0001c0003t0001g0116 a0001c0003t0001g0128 others(89): Show |
92 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.908+3702T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486849 | |||||||
chr7:76486858 | T | G | 1 | a0005c0006t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.908+3711T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486858 | |||||||
chr7:76486861 | T | G | 1 | a0005c0006t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.908+3714T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486861 | |||||||
chr7:76486883 | G | T | 1 | a0005c0006t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.908+3736G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486883 | |||||||
chr7:76486884 | C | CTGCTGCT others(44): Show |
1 | a0003c0005t0001g0069 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.908+3740_908+3741i others(53): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(41): Show |
1 | a0003c0005t0001g0064 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.908+3740_908+3741i others(50): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(35): Show |
1 | a0009c0019t0001g0108 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.908+3740_908+3741i others(44): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(32): Show |
3 | a0003c0005t0001g0068 a0003c0005t0001g0070 a0003c0005t0001g0076 |
3 | HG03239.hp2 HG03471.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.908+3740_908+3741i others(41): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(29): Show |
2 | a0003c0004t0001g0248 a0003c0005t0001g0077 |
2 | HG02258.hp1 HG02683.hp2 |
intron_variant | MODIFIER | c.908+3740_908+3741i others(38): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(26): Show |
4 | a0003c0004t0001g0238 a0003c0004t0001g0246 a0003c0004t0001g0249 others(1): Show |
4 | HG00639.hp2 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(35): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(23): Show |
12 | a0003c0004t0001g0236 a0003c0004t0001g0239 a0003c0004t0001g0240 others(9): Show |
12 | HG00140.hp2 HG00639.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(32): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(20): Show |
9 | a0002c0002t0001g0209 a0003c0004t0001g0189 a0003c0004t0001g0235 others(6): Show |
9 | HG00735.hp1 HG01109.hp2 HG01123.hp1 others(6): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(29): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(17): Show |
2 | a0003c0004t0001g0241 a0003c0004t0001g0255 |
2 | HG01081.hp1 HG01261.hp1 |
intron_variant | MODIFIER | c.908+3740_908+3741i others(26): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(14): Show |
2 | a0003c0005t0001g0014 a0003c0005t0001g0015 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.908+3740_908+3741i others(23): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(8): Show |
4 | a0001c0001t0002g0058 a0001c0003t0001g0138 a0003c0005t0001g0071 others(1): Show |
4 | HG02109.hp1 HG02738.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(17): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(5): Show |
11 | a0001c0003t0001g0136 a0001c0003t0001g0137 a0001c0003t0001g0140 others(8): Show |
11 | HG01243.hp2 HG02056.hp2 HG02083.hp1 others(8): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTGCT others(2): Show |
14 | a0001c0003t0001g0158 a0001c0003t0001g0266 a0001c0003t0001g0267 others(11): Show |
14 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(11): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(11): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTGCTTT | 5 | a0001c0003t0001g0146 a0001c0003t0001g0154 a0002c0020t0009g0011 others(2): Show |
5 | HG01891.hp1 HG02647.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.908+3740_908+3741i others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | CTTT | 33 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(30): Show |
33 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.908+3738_908+3739i others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76486884 | ||||||
chr7:76486884 | C | T | 1 | a0005c0006t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.908+3737C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486884 | |||||||
chr7:76486894 | C | T | 1 | a0001c0001t0002g0026 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.908+3747C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76486894 | |||||||
chr7:76487119 | G | A | 3 | a0002c0011t0003g0264 a0002c0011t0003g0265 a0011c0030t0003g0263 |
3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.908+3972G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487119 | |||||||
chr7:76487189 | C | G | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.908+4042C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487189 | |||||||
chr7:76487213 | G | A | 2 | a0001c0001t0002g0161 a0001c0001t0002g0177 |
2 | HG00733.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.908+4066G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487213 | |||||||
chr7:76487234 | T | A | 3 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 |
3 | HG02165.hp2 NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.908+4087T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487234 | |||||||
chr7:76487258 | A | G | 1 | a0002c0011t0003g0264 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.908+4111A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487258 | |||||||
chr7:76487438 | C | T | 2 | a0001c0003t0001g0145 a0001c0003t0001g0151 |
2 | HG03139.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.908+4291C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487438 | |||||||
chr7:76487443 | G | A | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.908+4296G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487443 | |||||||
chr7:76487571 | C | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.908+4424C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487571 | |||||||
chr7:76487607 | G | T | 1 | a0002c0002t0001g0186 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.908+4460G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487607 | |||||||
chr7:76487718 | C | T | 28 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(25): Show |
28 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.909-4435C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487718 | |||||||
chr7:76487740 | G | A | 8 | a0005c0006t0001g0115 a0005c0006t0001g0119 a0005c0006t0001g0120 others(5): Show |
8 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(5): Show |
intron_variant | MODIFIER | c.909-4413G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487740 | |||||||
chr7:76487757 | C | T | 18 | a0001c0001t0002g0039 a0001c0001t0002g0040 a0001c0001t0002g0041 others(15): Show |
18 | HG00544.hp1 HG00558.hp2 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.909-4396C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487757 | |||||||
chr7:76487921 | G | A | 54 | a0001c0003t0001g0146 a0001c0003t0001g0154 a0001c0003t0001g0158 others(51): Show |
55 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(52): Show |
intron_variant | MODIFIER | c.909-4232G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487921 | |||||||
chr7:76487930 | G | A | 6 | a0001c0001t0002g0002 a0001c0001t0002g0007 a0001c0001t0002g0028 others(3): Show |
7 | HG00280.hp1 HG00323.hp1 HG00423.hp2 others(4): Show |
intron_variant | MODIFIER | c.909-4223G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487930 | |||||||
chr7:76487960 | C | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-4193C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487960 | |||||||
chr7:76487975 | C | T | 103 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-4178C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76487975 | |||||||
chr7:76488056 | T | C | 103 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-4097T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488056 | |||||||
chr7:76488125 | A | T | 103 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-4028A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488125 | |||||||
chr7:76488153 | C | T | 103 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-4000C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488153 | |||||||
chr7:76488171 | T | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-3982T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488171 | |||||||
chr7:76488176 | G | A | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-3977G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488176 | |||||||
chr7:76488186 | C | T | 103 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-3967C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488186 | |||||||
chr7:76488198 | G | T | 1 | a0002c0002t0001g0210 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.909-3955G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488198 | |||||||
chr7:76488283 | G | A | 52 | a0001c0013t0001g0193 a0002c0002t0001g0004 a0002c0002t0001g0125 others(49): Show |
53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-3870G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488283 | |||||||
chr7:76488427 | T | C | 2 | a0002c0008t0001g0229 a0002c0008t0001g0230 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.909-3726T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488427 | |||||||
chr7:76488434 | T | C | 156 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(153): Show |
157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-3719T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488434 | |||||||
chr7:76488501 | C | T | 52 | a0001c0013t0001g0193 a0002c0002t0001g0004 a0002c0002t0001g0125 others(49): Show |
53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-3652C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488501 | |||||||
chr7:76488550 | T | C | 103 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-3603T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488550 | |||||||
chr7:76488559 | A | T | 34 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(31): Show |
34 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.909-3594A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488559 | |||||||
chr7:76488661 | C | T | 1 | a0002c0002t0001g0196 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.909-3492C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488661 | |||||||
chr7:76488662 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.909-3491G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488662 | |||||||
chr7:76488741 | T | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-3412T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488741 | |||||||
chr7:76488756 | C | T | 1 | a0002c0017t0001g0188 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.909-3397C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488756 | |||||||
chr7:76488760 | G | A | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.909-3393G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488760 | |||||||
chr7:76488782 | G | C | 1 | a0002c0002t0001g0209 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.909-3371G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488782 | |||||||
chr7:76488789 | A | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-3364A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488789 | |||||||
chr7:76488820 | C | T | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-3333C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488820 | |||||||
chr7:76488893 | G | A | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.909-3260G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488893 | |||||||
chr7:76488894 | A | AG | 52 | a0001c0013t0001g0193 a0002c0002t0001g0004 a0002c0002t0001g0125 others(49): Show |
53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-3258dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76488894 | ||||||
chr7:76488895 | GA | G | 8 | a0001c0001t0002g0073 a0001c0003t0001g0146 a0002c0011t0003g0264 others(5): Show |
8 | HG02056.hp1 HG02523.hp2 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.909-3245delA | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76488895 | ||||||
chr7:76488913 | G | A | 1 | a0001c0013t0001g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.909-3240G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488913 | |||||||
chr7:76488950 | A | T | 104 | a0001c0001t0002g0100 a0001c0003t0001g0116 a0001c0003t0001g0128 others(101): Show |
104 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.909-3203A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76488950 | |||||||
chr7:76489026 | T | A | 90 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(87): Show |
90 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(87): Show |
intron_variant | MODIFIER | c.909-3127T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489026 | |||||||
chr7:76489157 | A | G | 1 | a0001c0001t0002g0049 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.909-2996A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489157 | |||||||
chr7:76489251 | C | T | 1 | a0005c0006t0001g0117 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.909-2902C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489251 | |||||||
chr7:76489288 | C | A | 39 | a0002c0008t0001g0229 a0002c0008t0001g0230 a0003c0004t0001g0189 others(36): Show |
39 | HG00140.hp2 HG00639.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.909-2865C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489288 | |||||||
chr7:76489290 | A | C | 6 | a0001c0003t0001g0146 a0001c0003t0001g0154 a0001c0003t0001g0158 others(3): Show |
6 | HG00639.hp1 HG00733.hp1 HG01175.hp2 others(3): Show |
intron_variant | MODIFIER | c.909-2863A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489290 | |||||||
chr7:76489469 | A | G | 103 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-2684A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489469 | |||||||
chr7:76489518 | G | A | 52 | a0001c0013t0001g0193 a0002c0002t0001g0004 a0002c0002t0001g0125 others(49): Show |
53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-2635G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489518 | |||||||
chr7:76489553 | G | C | 33 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(30): Show |
33 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.909-2600G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489553 | |||||||
chr7:76489624 | C | T | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-2529C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489624 | |||||||
chr7:76489640 | G | T | 102 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(99): Show |
102 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.909-2513G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489640 | |||||||
chr7:76489667 | A | T | 75 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(72): Show |
75 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.909-2486A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489667 | |||||||
chr7:76489875 | A | C | 52 | a0001c0013t0001g0193 a0002c0002t0001g0004 a0002c0002t0001g0125 others(49): Show |
53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-2278A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489875 | |||||||
chr7:76489896 | A | C | 103 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-2257A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489896 | |||||||
chr7:76489899 | A | AC | 4 | a0001c0001t0002g0097 a0001c0001t0002g0098 a0002c0002t0001g0190 others(1): Show |
4 | HG00741.hp2 HG01123.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.909-2254_909-2253i others(3): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489899 | |||||||
chr7:76489899 | A | C | 52 | a0001c0001t0002g0038 a0001c0001t0002g0045 a0001c0013t0001g0193 others(49): Show |
53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-2254A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489899 | |||||||
chr7:76489902 | C | T | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.909-2251C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76489902 | |||||||
chr7:76490056 | G | C | 1 | a0001c0023t0006g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.909-2097G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490056 | |||||||
chr7:76490068 | C | A | 2 | a0002c0002t0001g0126 a0002c0002t0001g0127 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.909-2085C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490068 | |||||||
chr7:76490109 | C | T | 70 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(67): Show |
70 | HG00140.hp2 HG00544.hp1 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.909-2044C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490109 | |||||||
chr7:76490115 | C | T | 1 | a0001c0003t0001g0148 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.909-2038C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490115 | |||||||
chr7:76490142 | A | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-2011A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490142 | |||||||
chr7:76490182 | T | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-1971T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490182 | |||||||
chr7:76490257 | T | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-1896T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490257 | |||||||
chr7:76490334 | C | G | 52 | a0001c0013t0001g0193 a0001c0023t0006g0074 a0002c0002t0001g0004 others(49): Show |
53 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(50): Show |
intron_variant | MODIFIER | c.909-1819C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490334 | |||||||
chr7:76490334 | C | T | 103 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-1819C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490334 | |||||||
chr7:76490385 | T | C | 103 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(100): Show |
103 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.909-1768T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490385 | |||||||
chr7:76490408 | A | G | 3 | a0001c0001t0002g0105 a0001c0001t0002g0107 a0002c0002t0001g0004 |
4 | HG01256.hp2 HG01258.hp1 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.909-1745A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490408 | |||||||
chr7:76490620 | A | G | 53 | a0001c0001t0002g0104 a0001c0013t0001g0193 a0002c0002t0001g0004 others(50): Show |
54 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
intron_variant | MODIFIER | c.909-1533A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490620 | |||||||
chr7:76490810 | C | T | 4 | a0003c0004t0001g0238 a0003c0004t0001g0239 a0003c0004t0001g0248 others(1): Show |
4 | HG02258.hp1 HG02486.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.909-1343C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490810 | |||||||
chr7:76490884 | G | A | 3 | a0001c0001t0002g0008 a0001c0001t0002g0012 a0001c0001t0002g0101 |
3 | NA18961.hp1 NA18967.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.909-1269G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76490884 | |||||||
chr7:76490995 | C | CTTT | 9 | a0002c0002t0001g0126 a0002c0002t0001g0186 a0002c0002t0001g0204 others(6): Show |
9 | HG00558.hp1 HG01070.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.909-1141_909-1139d others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76490995 | ||||||
chr7:76490995 | C | CTTTT | 85 | a0001c0013t0001g0193 a0001c0031t0001g0273 a0002c0002t0001g0004 others(82): Show |
86 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.909-1142_909-1139d others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76490995 | ||||||
chr7:76490995 | C | CTTTTT | 47 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(44): Show |
47 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.909-1143_909-1139d others(7): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76490995 | ||||||
chr7:76490995 | C | CTTTTTT | 11 | a0001c0003t0001g0136 a0001c0003t0001g0147 a0001c0003t0001g0151 others(8): Show |
11 | HG01109.hp1 HG01175.hp2 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.909-1144_909-1139d others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76490995 | ||||||
chr7:76491053 | G | A | 33 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(30): Show |
33 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.909-1100G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491053 | |||||||
chr7:76491060 | A | G | 2 | a0001c0001t0002g0030 a0001c0001t0002g0031 |
2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.909-1093A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491060 | |||||||
chr7:76491187 | A | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-966A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491187 | |||||||
chr7:76491188 | G | A | 5 | a0003c0005t0001g0014 a0003c0005t0001g0015 a0003c0005t0001g0067 others(2): Show |
5 | HG02818.hp2 HG02886.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.909-965G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491188 | |||||||
chr7:76491296 | A | AT | 9 | a0001c0001t0002g0016 a0001c0001t0002g0036 a0001c0001t0002g0046 others(6): Show |
9 | HG00733.hp2 HG01106.hp2 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.909-841dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76491296 | ||||||
chr7:76491296 | AT | A | 67 | a0001c0003t0001g0221 a0001c0003t0001g0267 a0001c0013t0001g0193 others(64): Show |
68 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(65): Show |
intron_variant | MODIFIER | c.909-841delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76491296 | ||||||
chr7:76491317 | C | T | 2 | a0001c0001t0002g0170 a0001c0001t0002g0173 |
2 | HG02040.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.909-836C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491317 | |||||||
chr7:76491411 | A | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-742A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491411 | |||||||
chr7:76491535 | G | A | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-618G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491535 | |||||||
chr7:76491615 | A | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.909-538A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491615 | |||||||
chr7:76491624 | C | CT | 56 | a0001c0013t0001g0193 a0002c0002t0001g0004 a0002c0002t0001g0125 others(53): Show |
57 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(54): Show |
intron_variant | MODIFIER | c.909-520dupT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76491624 | ||||||
chr7:76491686 | TTA | T | 6 | a0001c0003t0001g0266 a0002c0002t0001g0192 a0002c0002t0001g0201 others(3): Show |
6 | HG00639.hp2 HG02523.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.909-465_909-464del others(2): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76491686 | ||||||
chr7:76491687 | TA | T | 132 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(129): Show |
133 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.909-465delA | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491687 | |||||||
chr7:76491688 | A | T | 17 | a0001c0003t0001g0146 a0002c0002t0001g0213 a0002c0002t0007g0203 others(14): Show |
17 | HG01109.hp1 HG01175.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.909-465A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491688 | |||||||
chr7:76491715 | ACT | A | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.909-435_909-434del others(2): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr7 | 76491715 | ||||||
chr7:76491837 | C | A | 1 | a0001c0001t0002g0167 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.909-316C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491837 | |||||||
chr7:76491896 | AACTCCTG others(41): Show |
A | 1 | a0005c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.909-256_909-209del others(48): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76491896 | |||||||
chr7:76492052 | A | G | 156 | a0001c0001t0002g0171 a0001c0003t0001g0116 a0001c0003t0001g0128 others(153): Show |
157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.909-101A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76492052 | |||||||
chr7:76492101 | C | G | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.909-52C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76492101 | |||||||
chr7:76492102 | G | A | 1 | a0004c0009t0002g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.909-51G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 4/10 | chr7 | 76492102 | |||||||
chr7:76492265 | A | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1009+12A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492265 | |||||||
chr7:76492269 | C | T | 1 | a0001c0001t0002g0035 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1009+16C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492269 | |||||||
chr7:76492295 | C | CG | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1009+44dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76492295 | ||||||
chr7:76492361 | A | G | 34 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(31): Show |
34 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.1009+108A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492361 | |||||||
chr7:76492403 | G | A | 120 | a0001c0013t0001g0193 a0001c0031t0001g0273 a0002c0002t0001g0004 others(117): Show |
121 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(118): Show |
intron_variant | MODIFIER | c.1009+150G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492403 | |||||||
chr7:76492422 | A | G | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1009+169A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492422 | |||||||
chr7:76492450 | C | T | 42 | a0001c0031t0001g0273 a0002c0029t0001g0005 a0003c0004t0001g0189 others(39): Show |
42 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1009+197C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492450 | |||||||
chr7:76492463 | A | ACGGTGGG others(4): Show |
11 | a0002c0007t0001g0185 a0002c0007t0001g0259 a0002c0007t0001g0260 others(8): Show |
11 | HG00558.hp2 HG00609.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.1009+214_1009+224d others(13): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76492463 | ||||||
chr7:76492502 | A | G | 1 | a0001c0001t0002g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1009+249A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492502 | |||||||
chr7:76492939 | C | T | 1 | a0002c0002t0001g0218 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1009+686C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492939 | |||||||
chr7:76492940 | T | C | 1 | a0002c0002t0001g0218 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1009+687T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76492940 | |||||||
chr7:76493121 | CGCCATGT others(8): Show |
C | 1 | a0002c0002t0001g0204 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1009+869_1009+883d others(17): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493121 | |||||||
chr7:76493122 | G | C | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1009+869G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493122 | |||||||
chr7:76493170 | C | T | 1 | a0001c0001t0002g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1009+917C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493170 | |||||||
chr7:76493203 | G | A | 144 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(141): Show |
145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1009+950G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493203 | |||||||
chr7:76493218 | C | T | 1 | a0002c0002t0001g0198 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1009+965C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493218 | |||||||
chr7:76493222 | G | C | 1 | a0005c0006t0001g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1009+969G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493222 | |||||||
chr7:76493224 | C | A | 1 | a0005c0006t0001g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1009+971C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493224 | |||||||
chr7:76493225 | A | T | 1 | a0005c0006t0001g0120 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1009+972A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493225 | |||||||
chr7:76493247 | A | T | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1009+994A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493247 | |||||||
chr7:76493321 | G | A | 143 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(140): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1009+1068G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493321 | |||||||
chr7:76493322 | G | A | 1 | a0004c0026t0001g0269 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1009+1069G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493322 | |||||||
chr7:76493608 | G | A | 1 | a0005c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1009+1355G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493608 | |||||||
chr7:76493649 | A | G | 144 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(141): Show |
145 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.1009+1396A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493649 | |||||||
chr7:76493756 | G | T | 8 | a0002c0002t0001g0186 a0002c0002t0001g0198 a0002c0002t0001g0199 others(5): Show |
8 | HG01099.hp2 HG01928.hp1 HG01928.hp2 others(5): Show |
intron_variant | MODIFIER | c.1009+1503G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493756 | |||||||
chr7:76493860 | C | G | 154 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(151): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1009+1607C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493860 | |||||||
chr7:76493948 | T | C | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1009+1695T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76493948 | |||||||
chr7:76493969 | A | AGAATTTA others(7): Show |
1 | a0002c0007t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1009+1717_1009+173 others(18): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76493969 | ||||||
chr7:76494005 | T | G | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1009+1752T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494005 | |||||||
chr7:76494074 | G | T | 12 | a0002c0007t0001g0185 a0002c0007t0001g0259 a0002c0007t0001g0260 others(9): Show |
12 | HG00558.hp2 HG00609.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1009+1821G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494074 | |||||||
chr7:76494142 | AGAGCAGT others(4): Show |
A | 1 | a0002c0002t0001g0198 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1009+1891_1009+190 others(15): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76494142 | ||||||
chr7:76494146 | C | T | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1009+1893C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494146 | |||||||
chr7:76494213 | A | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1009+1960A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494213 | |||||||
chr7:76494276 | T | C | 2 | a0002c0002t0005g0006 a0002c0002t0005g0274 |
2 | HG00735.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1009+2023T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494276 | |||||||
chr7:76494327 | C | T | 145 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(142): Show |
146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1009+2074C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494327 | |||||||
chr7:76494537 | A | G | 156 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(153): Show |
157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1009+2284A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494537 | |||||||
chr7:76494579 | C | T | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1009+2326C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494579 | |||||||
chr7:76494762 | A | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1009+2509A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494762 | |||||||
chr7:76494885 | C | T | 1 | a0001c0001t0002g0058 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1010-2452C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494885 | |||||||
chr7:76494930 | G | A | 1 | a0002c0008t0001g0230 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1010-2407G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494930 | |||||||
chr7:76494941 | C | T | 145 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(142): Show |
146 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.1010-2396C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494941 | |||||||
chr7:76494955 | C | A | 1 | a0002c0007t0001g0185 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1010-2382C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76494955 | |||||||
chr7:76495246 | G | A | 1 | a0002c0002t0001g0195 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1010-2091G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495246 | |||||||
chr7:76495368 | T | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-1969T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495368 | |||||||
chr7:76495665 | G | T | 1 | a0003c0004t0001g0244 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1010-1672G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495665 | |||||||
chr7:76495678 | G | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1010-1659G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495678 | |||||||
chr7:76495798 | A | G | 1 | a0001c0001t0002g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1010-1539A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495798 | |||||||
chr7:76495842 | T | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-1495T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495842 | |||||||
chr7:76495847 | C | G | 1 | a0001c0001t0002g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1010-1490C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495847 | |||||||
chr7:76495906 | G | A | 1 | a0003c0005t0001g0076 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1010-1431G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495906 | |||||||
chr7:76495931 | A | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-1406A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495931 | |||||||
chr7:76495959 | T | C | 153 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(150): Show |
154 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1010-1378T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495959 | |||||||
chr7:76495959 | T | G | 2 | a0002c0002t0001g0126 a0002c0002t0001g0127 |
2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.1010-1378T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495959 | |||||||
chr7:76495963 | C | T | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-1374C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495963 | |||||||
chr7:76495969 | T | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-1368T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495969 | |||||||
chr7:76495983 | C | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-1354C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76495983 | |||||||
chr7:76496011 | C | T | 151 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(148): Show |
152 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1010-1326C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496011 | |||||||
chr7:76496048 | G | A | 1 | a0002c0007t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1010-1289G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496048 | |||||||
chr7:76496112 | G | C | 1 | a0004c0014t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-1225G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496112 | |||||||
chr7:76496113 | C | G | 1 | a0004c0014t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-1224C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496113 | |||||||
chr7:76496114 | T | C | 1 | a0004c0014t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-1223T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496114 | |||||||
chr7:76496132 | G | GC | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-1205_1010-120 others(5): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496132 | |||||||
chr7:76496160 | C | T | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-1177C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496160 | |||||||
chr7:76496221 | G | A | 2 | a0002c0011t0003g0264 a0011c0030t0003g0263 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1010-1116G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496221 | |||||||
chr7:76496293 | C | T | 1 | a0003c0005t0001g0075 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1010-1044C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496293 | |||||||
chr7:76496339 | T | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-998T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496339 | |||||||
chr7:76496415 | A | C | 1 | a0004c0014t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-922A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496415 | |||||||
chr7:76496415 | A | G | 154 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(151): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1010-922A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496415 | |||||||
chr7:76496433 | A | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1010-904A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496433 | |||||||
chr7:76496485 | C | T | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1010-852C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496485 | |||||||
chr7:76496498 | G | GGAGCTGG others(6): Show |
1 | a0001c0001t0002g0024 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1010-837_1010-825d others(15): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76496498 | ||||||
chr7:76496530 | A | AG | 3 | a0001c0003t0001g0147 a0001c0003t0001g0158 a0002c0002t0001g0198 |
3 | HG01099.hp2 HG01175.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.1010-804dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr7 | 76496530 | ||||||
chr7:76496565 | C | A | 1 | a0005c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1010-772C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496565 | |||||||
chr7:76496565 | C | T | 149 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(146): Show |
150 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.1010-772C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496565 | |||||||
chr7:76496664 | G | A | 42 | a0001c0031t0001g0273 a0003c0004t0001g0189 a0003c0004t0001g0235 others(39): Show |
42 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1010-673G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496664 | |||||||
chr7:76496692 | C | T | 1 | a0002c0002t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1010-645C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496692 | |||||||
chr7:76496743 | G | A | 1 | a0001c0001t0002g0161 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1010-594G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496743 | |||||||
chr7:76496802 | A | T | 1 | a0002c0002t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1010-535A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496802 | |||||||
chr7:76496825 | C | T | 3 | a0002c0011t0003g0264 a0002c0011t0003g0265 a0011c0030t0003g0263 |
3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1010-512C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496825 | |||||||
chr7:76496909 | A | C | 1 | a0004c0026t0001g0269 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1010-428A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496909 | |||||||
chr7:76496909 | A | G | 153 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(150): Show |
154 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1010-428A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496909 | |||||||
chr7:76496910 | C | G | 1 | a0004c0014t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-427C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496910 | |||||||
chr7:76496981 | T | A | 1 | a0004c0014t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-356T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496981 | |||||||
chr7:76496982 | G | T | 1 | a0004c0014t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-355G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496982 | |||||||
chr7:76496984 | A | G | 1 | a0004c0014t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1010-353A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76496984 | |||||||
chr7:76497042 | G | A | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1010-295G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76497042 | |||||||
chr7:76497184 | C | T | 2 | a0001c0001t0002g0094 a0001c0001t0002g0096 |
2 | HG02738.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1010-153C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76497184 | |||||||
chr7:76497260 | G | A | 1 | a0001c0001t0002g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1010-77G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76497260 | |||||||
chr7:76497284 | G | T | 1 | a0001c0023t0006g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1010-53G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 5/10 | chr7 | 76497284 | |||||||
chr7:76497524 | C | T | 120 | a0001c0013t0001g0193 a0001c0031t0001g0273 a0002c0002t0001g0004 others(117): Show |
121 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.1150+47C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497524 | |||||||
chr7:76497540 | T | C | 163 | a0001c0001t0002g0003 a0001c0001t0002g0167 a0001c0001t0002g0171 others(160): Show |
165 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.1150+63T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497540 | |||||||
chr7:76497583 | C | T | 1 | a0001c0023t0006g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1150+106C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497583 | |||||||
chr7:76497612 | C | A | 1 | a0005c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1150+135C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497612 | |||||||
chr7:76497642 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1150+165C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497642 | |||||||
chr7:76497664 | C | T | 1 | a0002c0002t0001g0190 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1150+187C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497664 | |||||||
chr7:76497707 | A | G | 1 | a0001c0023t0006g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1150+230A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497707 | |||||||
chr7:76497750 | A | G | 2 | a0001c0003t0001g0157 a0002c0008t0001g0229 |
2 | HG03579.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1150+273A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497750 | |||||||
chr7:76497754 | G | T | 153 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(150): Show |
154 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.1150+277G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497754 | |||||||
chr7:76497755 | T | A | 1 | a0005c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1150+278T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497755 | |||||||
chr7:76497788 | C | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1150+311C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497788 | |||||||
chr7:76497837 | C | T | 12 | a0002c0007t0001g0185 a0002c0007t0001g0259 a0002c0007t0001g0260 others(9): Show |
12 | HG00558.hp2 HG00609.hp2 HG01496.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150+360C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497837 | |||||||
chr7:76497849 | GGCCCAGG others(6): Show |
G | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150+390_1150+402d others(15): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76497849 | ||||||
chr7:76497932 | G | A | 1 | a0003c0004t0001g0189 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1150+455G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76497932 | |||||||
chr7:76498056 | C | A | 1 | a0001c0003t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1150+579C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498056 | |||||||
chr7:76498058 | A | G | 1 | a0001c0003t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1150+581A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498058 | |||||||
chr7:76498060 | C | T | 37 | a0001c0031t0001g0273 a0003c0004t0001g0189 a0003c0004t0001g0235 others(34): Show |
37 | HG00544.hp1 HG00639.hp1 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.1150+583C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498060 | |||||||
chr7:76498072 | C | T | 140 | a0001c0001t0002g0110 a0001c0001t0002g0166 a0001c0003t0001g0116 others(137): Show |
141 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.1150+595C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498072 | |||||||
chr7:76498120 | C | T | 5 | a0001c0001t0002g0027 a0002c0002t0001g0194 a0002c0002t0001g0211 others(2): Show |
5 | HG02622.hp1 HG02622.hp2 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150+643C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498120 | |||||||
chr7:76498136 | T | TG | 3 | a0001c0001t0002g0048 a0002c0002t0001g0187 a0002c0002t0001g0226 |
3 | HG00673.hp2 HG04184.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1150+661dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498136 | ||||||
chr7:76498142 | C | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150+665C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498142 | |||||||
chr7:76498191 | T | C | 23 | a0001c0001t0002g0090 a0001c0003t0001g0128 a0001c0003t0001g0129 others(20): Show |
23 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(20): Show |
intron_variant | MODIFIER | c.1150+714T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498191 | |||||||
chr7:76498236 | C | T | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1150+759C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498236 | |||||||
chr7:76498260 | G | A | 1 | a0010c0016t0001g0227 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1150+783G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498260 | |||||||
chr7:76498270 | C | T | 2 | a0001c0003t0001g0222 a0001c0023t0006g0074 |
2 | HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1150+793C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498270 | |||||||
chr7:76498291 | G | A | 1 | a0005c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1150+814G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498291 | |||||||
chr7:76498337 | G | A | 1 | a0001c0003t0001g0142 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1150+860G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498337 | |||||||
chr7:76498366 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1150+889G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498366 | |||||||
chr7:76498389 | C | A | 1 | a0001c0001t0002g0055 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1150+912C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498389 | |||||||
chr7:76498537 | C | T | 159 | a0001c0001t0002g0022 a0001c0001t0002g0023 a0001c0001t0002g0109 others(156): Show |
160 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.1150+1060C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498537 | |||||||
chr7:76498569 | G | C | 1 | a0002c0008t0004g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1150+1092G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498569 | |||||||
chr7:76498570 | C | CG | 7 | a0001c0001t0002g0023 a0001c0001t0002g0039 a0001c0001t0002g0181 others(4): Show |
7 | HG00673.hp2 HG02056.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150+1098dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498570 | ||||||
chr7:76498570 | C | G | 1 | a0002c0008t0004g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1150+1093C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498570 | |||||||
chr7:76498616 | G | A | 28 | a0001c0031t0001g0273 a0003c0004t0001g0189 a0003c0004t0001g0235 others(25): Show |
28 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(25): Show |
intron_variant | MODIFIER | c.1150+1139G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498616 | |||||||
chr7:76498625 | G | A | 1 | a0002c0002t0001g0223 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1150+1148G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498625 | |||||||
chr7:76498716 | C | T | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1150+1239C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498716 | |||||||
chr7:76498727 | TG | T | 154 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(151): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1150+1255delG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498727 | ||||||
chr7:76498738 | G | A | 1 | a0003c0005t0001g0067 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1150+1261G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498738 | |||||||
chr7:76498768 | A | C | 42 | a0001c0031t0001g0273 a0003c0004t0001g0189 a0003c0004t0001g0235 others(39): Show |
42 | HG00140.hp2 HG00544.hp1 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.1150+1291A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498768 | |||||||
chr7:76498788 | C | CTGGGATG others(17): Show |
1 | a0005c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1150+1313_1150+131 others(28): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498788 | ||||||
chr7:76498788 | CTGTA | C | 123 | a0001c0003t0001g0116 a0001c0003t0001g0136 a0001c0003t0001g0137 others(120): Show |
124 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(121): Show |
intron_variant | MODIFIER | c.1150+1314_1150+131 others(8): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498788 | ||||||
chr7:76498789 | T | TGGGTGTG others(5): Show |
4 | a0005c0006t0001g0120 a0005c0006t0001g0121 a0005c0006t0001g0122 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+1313_1150+131 others(16): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498789 | ||||||
chr7:76498791 | T | G | 27 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(24): Show |
27 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1150+1314T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498791 | |||||||
chr7:76498792 | A | G | 28 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(25): Show |
28 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(25): Show |
intron_variant | MODIFIER | c.1150+1315A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498792 | |||||||
chr7:76498794 | G | GGGGGTGT others(4): Show |
4 | a0005c0006t0001g0120 a0005c0006t0001g0121 a0005c0006t0001g0122 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150+1319_1150+132 others(15): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498794 | ||||||
chr7:76498794 | G | GGGTGTGT others(3): Show |
1 | a0002c0002t0001g0228 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1150+1324_1150+133 others(14): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498794 | ||||||
chr7:76498794 | G | GGGTGTGT others(21): Show |
2 | a0002c0007t0001g0259 a0002c0028t0001g0258 |
2 | HG01496.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1150+1336_1150+133 others(32): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498794 | ||||||
chr7:76498794 | G | GGGTGTGT others(20): Show |
71 | a0001c0003t0001g0116 a0001c0003t0001g0136 a0001c0003t0001g0137 others(68): Show |
72 | HG00280.hp2 HG00423.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1150+1336_1150+133 others(31): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498794 | ||||||
chr7:76498794 | G | GTGTGGAG others(16): Show |
27 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(24): Show |
27 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1150+1317_1150+131 others(27): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498794 | |||||||
chr7:76498809 | T | TGGGGGTG others(21): Show |
2 | a0001c0031t0001g0273 a0002c0017t0001g0188 |
2 | HG00544.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.1150+1336_1150+133 others(32): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498809 | ||||||
chr7:76498810 | G | GGGGGTGT others(45): Show |
3 | a0002c0011t0003g0264 a0002c0011t0003g0265 a0011c0030t0003g0263 |
3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1150+1336_1150+133 others(56): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498810 | ||||||
chr7:76498810 | G | GGGGGTGT others(70): Show |
1 | a0002c0002t0001g0206 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1150+1336_1150+133 others(81): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498810 | ||||||
chr7:76498811 | GGGTGTGT others(17): Show |
G | 1 | a0001c0001t0002g0097 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1150+1337_1150+136 others(28): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76498811 | ||||||
chr7:76498817 | G | A | 2 | a0002c0008t0001g0229 a0002c0008t0001g0230 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1150+1340G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498817 | |||||||
chr7:76498820 | G | A | 2 | a0002c0008t0001g0229 a0002c0008t0001g0230 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1150+1343G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498820 | |||||||
chr7:76498828 | A | G | 114 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(111): Show |
115 | HG00280.hp2 HG00323.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1150+1351A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498828 | |||||||
chr7:76498835 | A | G | 2 | a0002c0008t0001g0229 a0002c0008t0001g0230 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1150+1358A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498835 | |||||||
chr7:76498845 | G | A | 1 | a0001c0001t0002g0097 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1150+1368G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498845 | |||||||
chr7:76498859 | G | T | 1 | a0002c0007t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1150+1382G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498859 | |||||||
chr7:76498860 | A | G | 1 | a0002c0007t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1150+1383A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498860 | |||||||
chr7:76498861 | G | A | 1 | a0002c0007t0001g0268 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1150+1384G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498861 | |||||||
chr7:76498871 | G | A | 1 | a0003c0005t0001g0077 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1150+1394G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498871 | |||||||
chr7:76498871 | G | T | 1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1150+1394G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498871 | |||||||
chr7:76498889 | G | C | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1150+1412G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498889 | |||||||
chr7:76498917 | GT | G | 154 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(151): Show |
155 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(152): Show |
intron_variant | MODIFIER | c.1150+1441delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498917 | |||||||
chr7:76498918 | T | G | 1 | a0001c0003t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1150+1441T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498918 | |||||||
chr7:76498919 | G | T | 1 | a0001c0003t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1150+1442G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498919 | |||||||
chr7:76498969 | G | T | 12 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.1151-1472G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76498969 | |||||||
chr7:76499011 | A | AGT | 143 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(140): Show |
144 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.1151-1426_1151-142 others(6): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499011 | ||||||
chr7:76499017 | G | T | 9 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(6): Show |
9 | HG01243.hp1 HG01884.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1151-1424G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499017 | |||||||
chr7:76499020 | T | G | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1151-1421T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499020 | |||||||
chr7:76499026 | A | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1151-1415A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499026 | |||||||
chr7:76499030 | G | A | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1151-1411G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499030 | |||||||
chr7:76499041 | T | A | 1 | a0002c0007t0001g0185 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1151-1400T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499041 | |||||||
chr7:76499055 | T | G | 1 | a0002c0002t0001g0187 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1151-1386T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499055 | |||||||
chr7:76499097 | G | T | 1 | a0005c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1151-1344G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499097 | |||||||
chr7:76499117 | C | G | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1151-1324C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499117 | |||||||
chr7:76499154 | T | TGGGTGTG others(2948): Show |
1 | a0002c0002t0005g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1151-1286_1151-128 others(2959): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3039): Show |
1 | a0001c0001t0002g0181 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1151-1273_1151-127 others(3050): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3044): Show |
1 | a0005c0006t0001g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1151-1273_1151-127 others(3055): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2970): Show |
1 | a0001c0003t0001g0147 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1151-1273_1151-127 others(2981): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2942): Show |
1 | a0003c0004t0001g0242 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1151-1273_1151-127 others(2953): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2931): Show |
1 | a0003c0004t0001g0249 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1151-1273_1151-127 others(2942): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3033): Show |
1 | a0001c0001t0002g0034 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3044): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3032): Show |
1 | a0001c0001t0002g0033 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3043): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3030): Show |
1 | a0001c0001t0002g0017 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3041): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3034): Show |
1 | a0004c0009t0002g0164 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3112): Show |
1 | a0001c0001t0002g0091 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3123): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3106): Show |
1 | a0001c0001t0002g0096 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3117): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3034): Show |
1 | a0004c0009t0008g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3032): Show |
1 | a0001c0023t0006g0074 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3043): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3104): Show |
1 | a0001c0001t0002g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3115): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3024): Show |
1 | a0001c0001t0002g0165 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3035): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3033): Show |
1 | a0001c0001t0002g0019 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3044): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3032): Show |
1 | a0001c0001t0002g0160 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3043): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3030): Show |
2 | a0001c0001t0002g0161 a0001c0001t0002g0177 |
2 | HG00733.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3041): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3008): Show |
1 | a0001c0001t0002g0046 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3019): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3115): Show |
1 | a0001c0001t0002g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3126): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3108): Show |
1 | a0001c0001t0002g0081 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3119): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3087): Show |
1 | a0001c0001t0002g0113 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3098): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3086): Show |
3 | a0001c0001t0002g0111 a0001c0001t0002g0112 a0001c0001t0002g0114 |
3 | HG02451.hp1 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3097): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3086): Show |
1 | a0001c0001t0002g0080 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3097): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3083): Show |
1 | a0001c0001t0002g0083 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3094): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3034): Show |
1 | a0001c0001t0002g0184 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3111): Show |
1 | a0001c0001t0002g0010 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3122): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3107): Show |
1 | a0001c0001t0002g0101 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3118): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3109): Show |
1 | a0001c0001t0002g0008 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3120): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3108): Show |
2 | a0001c0001t0002g0012 a0001c0001t0002g0092 |
2 | NA18967.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3119): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3112): Show |
2 | a0001c0001t0002g0105 a0001c0001t0002g0107 |
2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3123): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3108): Show |
1 | a0001c0001t0002g0097 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3119): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3111): Show |
7 | a0001c0001t0001g0088 a0001c0001t0002g0089 a0001c0001t0002g0102 others(4): Show |
7 | HG01071.hp1 HG01106.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3122): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3109): Show |
1 | a0001c0001t0002g0100 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3120): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3110): Show |
1 | a0012c0022t0002g0093 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3121): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3016): Show |
3 | a0001c0001t0002g0055 a0001c0001t0002g0072 a0001c0001t0002g0073 |
3 | HG02056.hp1 HG02155.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3027): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3035): Show |
1 | a0001c0001t0002g0063 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3046): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3035): Show |
1 | a0001c0001t0002g0050 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3046): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3034): Show |
2 | a0001c0001t0002g0031 a0001c0001t0002g0175 |
2 | HG04228.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3035): Show |
1 | a0001c0001t0002g0169 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3046): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3033): Show |
44 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(41): Show |
47 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(44): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3044): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3032): Show |
1 | a0001c0001t0002g0036 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3043): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3030): Show |
1 | a0001c0001t0002g0061 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3041): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3004): Show |
1 | a0001c0001t0002g0052 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3015): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3032): Show |
2 | a0001c0001t0002g0110 a0001c0001t0002g0167 |
2 | HG02970.hp1 NA18961.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3043): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3060): Show |
3 | a0006c0010t0002g0009 a0006c0010t0002g0086 a0006c0010t0002g0087 |
3 | HG03490.hp1 HG03492.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3071): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3039): Show |
1 | a0001c0001t0002g0178 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3050): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3077): Show |
1 | a0001c0001t0002g0084 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3088): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2830): Show |
1 | a0001c0001t0002g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2841): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2824): Show |
4 | a0001c0001t0002g0040 a0001c0001t0002g0041 a0001c0001t0002g0042 others(1): Show |
4 | HG00609.hp1 HG01934.hp1 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2835): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3104): Show |
1 | a0001c0001t0002g0094 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3115): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3086): Show |
1 | a0001c0001t0002g0090 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3097): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3044): Show |
1 | a0001c0001t0002g0024 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3055): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3034): Show |
1 | a0004c0009t0002g0162 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3106): Show |
1 | a0001c0001t0002g0082 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3117): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3110): Show |
1 | a0001c0018t0011g0099 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3121): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3034): Show |
1 | a0001c0001t0002g0027 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3045): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3033): Show |
3 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0059 |
3 | HG02257.hp1 HG02717.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3044): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3060): Show |
1 | a0002c0007t0001g0259 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3071): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2946): Show |
1 | a0004c0026t0001g0269 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2945): Show |
1 | a0001c0003t0001g0151 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2956): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3022): Show |
1 | a0005c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3033): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2942): Show |
1 | a0001c0003t0001g0157 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2953): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2947): Show |
1 | a0001c0003t0001g0146 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2958): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2946): Show |
1 | a0001c0003t0001g0144 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2947): Show |
1 | a0001c0003t0001g0128 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2958): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2947): Show |
1 | a0001c0003t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2958): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2948): Show |
1 | a0001c0003t0001g0154 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2959): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2947): Show |
1 | a0001c0003t0001g0155 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2958): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2946): Show |
1 | a0001c0003t0001g0158 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2946): Show |
6 | a0001c0003t0001g0129 a0001c0003t0001g0131 a0001c0003t0001g0145 others(3): Show |
6 | HG00597.hp2 HG01975.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2946): Show |
3 | a0001c0003t0001g0116 a0001c0003t0001g0221 a0001c0003t0001g0222 |
3 | HG02723.hp2 HG03225.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2946): Show |
6 | a0001c0003t0001g0136 a0001c0003t0001g0138 a0001c0003t0001g0140 others(3): Show |
6 | HG01243.hp2 HG02109.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2945): Show |
1 | a0001c0003t0001g0130 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2956): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2945): Show |
1 | a0001c0003t0001g0141 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2956): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2946): Show |
1 | a0001c0003t0001g0153 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2957): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2949): Show |
1 | a0001c0003t0001g0266 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2960): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2949): Show |
1 | a0001c0003t0001g0267 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2960): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2926): Show |
1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2937): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2893): Show |
3 | a0002c0011t0003g0264 a0002c0011t0003g0265 a0011c0030t0003g0263 |
3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2904): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2925): Show |
1 | a0004c0033t0001g0234 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2936): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2924): Show |
4 | a0003c0004t0001g0238 a0003c0004t0001g0248 a0007c0012t0001g0233 others(1): Show |
4 | HG00639.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2935): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2905): Show |
1 | a0003c0005t0001g0077 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2916): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2904): Show |
13 | a0003c0005t0001g0014 a0003c0005t0001g0015 a0003c0005t0001g0064 others(10): Show |
13 | HG00639.hp2 HG01192.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2915): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3190): Show |
2 | a0002c0008t0004g0132 a0002c0008t0004g0133 |
2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3201): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2943): Show |
1 | a0001c0031t0001g0273 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2954): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2945): Show |
1 | a0002c0007t0001g0275 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2956): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2942): Show |
8 | a0002c0007t0001g0185 a0002c0007t0001g0260 a0002c0007t0001g0268 others(5): Show |
8 | HG00558.hp2 HG00609.hp2 HG02083.hp1 others(5): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2953): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2942): Show |
1 | a0002c0028t0001g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2953): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3192): Show |
1 | a0002c0008t0004g0134 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3203): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2938): Show |
1 | a0003c0004t0001g0252 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2949): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2941): Show |
13 | a0003c0004t0001g0189 a0003c0004t0001g0236 a0003c0004t0001g0240 others(10): Show |
13 | HG00140.hp2 HG01099.hp1 HG01167.hp2 others(10): Show |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2952): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2939): Show |
1 | a0003c0004t0001g0237 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2950): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2840): Show |
1 | a0003c0004t0001g0235 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2851): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3021): Show |
1 | a0005c0006t0001g0121 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3032): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3022): Show |
2 | a0005c0006t0001g0120 a0005c0006t0001g0122 |
2 | HG02258.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3033): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3019): Show |
1 | a0005c0006t0001g0119 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3030): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3022): Show |
2 | a0005c0006t0001g0117 a0005c0006t0001g0123 |
2 | HG02922.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(3033): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3023): Show |
1 | a0005c0006t0001g0115 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3034): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2943): Show |
1 | a0001c0003t0001g0135 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2954): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2940): Show |
1 | a0001c0003t0001g0148 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2951): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2940): Show |
1 | a0001c0003t0001g0156 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2951): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3080): Show |
1 | a0002c0032t0001g0256 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(3091): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2958): Show |
1 | a0003c0004t0001g0239 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2969): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(2942): Show |
1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2953): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGAGG others(3029): Show |
1 | a0005c0006t0001g0118 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1151-1276_1151-127 others(3040): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2955): Show |
1 | a0002c0002t0001g0187 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2966): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2955): Show |
1 | a0002c0002t0001g0192 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2966): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2952): Show |
1 | a0002c0002t0001g0207 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2963): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2955): Show |
1 | a0002c0002t0001g0226 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2966): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2952): Show |
1 | a0002c0002t0001g0208 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2963): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2952): Show |
1 | a0002c0002t0001g0205 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2963): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2950): Show |
1 | a0002c0002t0001g0214 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2950): Show |
1 | a0002c0002t0001g0231 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2956): Show |
1 | a0002c0002t0001g0198 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2967): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2953): Show |
1 | a0002c0002t0001g0216 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2964): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2951): Show |
5 | a0002c0002t0001g0186 a0002c0002t0001g0199 a0002c0002t0001g0204 others(2): Show |
5 | HG01928.hp2 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-1283_1151-128 others(2962): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2951): Show |
17 | a0002c0002t0001g0125 a0002c0002t0001g0126 a0002c0002t0001g0127 others(14): Show |
17 | HG00558.hp1 HG01070.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1151-1283_1151-128 others(2962): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2951): Show |
1 | a0001c0013t0001g0193 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2962): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2950): Show |
4 | a0002c0002t0001g0004 a0002c0002t0001g0219 a0002c0002t0001g0220 others(1): Show |
5 | HG01123.hp2 HG01256.hp2 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2950): Show |
1 | a0002c0002t0001g0197 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2934): Show |
1 | a0002c0002t0001g0163 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2945): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(3434): Show |
1 | a0013c0015t0001g0191 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(3445): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2950): Show |
1 | a0002c0002t0001g0202 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2950): Show |
1 | a0002c0002t0001g0223 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2961): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2935): Show |
2 | a0002c0008t0001g0229 a0002c0008t0001g0230 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1151-1283_1151-128 others(2946): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2948): Show |
3 | a0002c0002t0001g0194 a0002c0002t0001g0211 a0002c0002t0001g0224 |
3 | HG02622.hp1 HG02630.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1151-1283_1151-128 others(2959): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499154 | T | TGTGGGGT others(2988): Show |
1 | a0004c0014t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1151-1283_1151-128 others(2999): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499154 | ||||||
chr7:76499158 | G | GAGGTGTG others(2921): Show |
1 | a0003c0004t0001g0254 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1151-1265_1151-126 others(2932): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499158 | ||||||
chr7:76499158 | G | GAGGTGTG others(2920): Show |
2 | a0003c0004t0001g0241 a0003c0004t0001g0250 |
2 | HG00735.hp1 HG01081.hp1 |
intron_variant | MODIFIER | c.1151-1265_1151-126 others(2931): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr7 | 76499158 | ||||||
chr7:76499190 | G | T | 2 | a0003c0004t0001g0237 a0003c0004t0001g0247 |
2 | HG03704.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1151-1251G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499190 | |||||||
chr7:76499231 | A | G | 1 | a0003c0004t0001g0262 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1151-1210A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499231 | |||||||
chr7:76499273 | C | T | 1 | a0002c0028t0001g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1151-1168C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499273 | |||||||
chr7:76499276 | G | C | 1 | a0002c0028t0001g0258 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1151-1165G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499276 | |||||||
chr7:76499277 | T | G | 2 | a0002c0028t0001g0258 a0004c0027t0001g0139 |
2 | HG02056.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1151-1164T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499277 | |||||||
chr7:76499286 | A | G | 3 | a0002c0011t0003g0264 a0002c0011t0003g0265 a0011c0030t0003g0263 |
3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1151-1155A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499286 | |||||||
chr7:76499349 | C | T | 3 | a0001c0001t0002g0169 a0001c0001t0002g0182 a0002c0029t0001g0005 |
3 | HG03225.hp1 NA18967.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1151-1092C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499349 | |||||||
chr7:76499354 | C | T | 4 | a0001c0001t0002g0027 a0001c0001t0002g0053 a0001c0001t0002g0054 others(1): Show |
4 | HG02257.hp1 HG02622.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.1151-1087C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499354 | |||||||
chr7:76499368 | A | G | 155 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(152): Show |
156 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.1151-1073A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499368 | |||||||
chr7:76499488 | C | T | 1 | a0001c0003t0001g0137 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1151-953C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499488 | |||||||
chr7:76499600 | C | G | 72 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(69): Show |
72 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(69): Show |
intron_variant | MODIFIER | c.1151-841C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499600 | |||||||
chr7:76499663 | A | G | 3 | a0002c0011t0003g0264 a0002c0011t0003g0265 a0011c0030t0003g0263 |
3 | HG03486.hp1 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1151-778A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499663 | |||||||
chr7:76499693 | G | A | 1 | a0001c0001t0002g0037 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1151-748G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499693 | |||||||
chr7:76499697 | C | T | 1 | a0001c0001t0002g0044 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1151-744C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499697 | |||||||
chr7:76499800 | A | G | 45 | a0001c0001t0002g0028 a0001c0001t0002g0033 a0001c0001t0002g0183 others(42): Show |
45 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1151-641A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499800 | |||||||
chr7:76499801 | C | T | 45 | a0001c0001t0002g0028 a0001c0001t0002g0033 a0001c0001t0002g0183 others(42): Show |
45 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
intron_variant | MODIFIER | c.1151-640C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499801 | |||||||
chr7:76499931 | G | C | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1151-510G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499931 | |||||||
chr7:76499985 | C | G | 49 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(46): Show |
49 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(46): Show |
intron_variant | MODIFIER | c.1151-456C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76499985 | |||||||
chr7:76500047 | G | C | 156 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(153): Show |
157 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1151-394G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500047 | |||||||
chr7:76500080 | G | A | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1151-361G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500080 | |||||||
chr7:76500202 | A | G | 3 | a0001c0001t0002g0044 a0001c0001t0002g0109 a0001c0001t0002g0110 |
3 | HG02970.hp1 HG03453.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1151-239A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500202 | |||||||
chr7:76500222 | G | A | 78 | a0001c0003t0001g0128 a0001c0003t0001g0129 a0001c0003t0001g0130 others(75): Show |
78 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.1151-219G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500222 | |||||||
chr7:76500249 | G | A | 1 | a0002c0002t0001g0231 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1151-192G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500249 | |||||||
chr7:76500368 | C | G | 158 | a0001c0001t0002g0169 a0001c0001t0002g0182 a0001c0003t0001g0116 others(155): Show |
159 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.1151-73C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500368 | |||||||
chr7:76500414 | C | T | 1 | a0001c0001t0002g0098 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1151-27C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 6/10 | chr7 | 76500414 | |||||||
chr7:76500546 | C | T | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230+26C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500546 | |||||||
chr7:76500597 | T | G | 1 | a0001c0001t0002g0112 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1230+77T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500597 | |||||||
chr7:76500613 | T | G | 12 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.1230+93T>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500613 | |||||||
chr7:76500642 | G | C | 42 | a0003c0004t0001g0189 a0003c0004t0001g0235 a0003c0004t0001g0236 others(39): Show |
42 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1230+122G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500642 | |||||||
chr7:76500674 | C | T | 2 | a0001c0001t0002g0105 a0001c0001t0002g0107 |
2 | HG03710.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1230+154C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500674 | |||||||
chr7:76500686 | A | G | 2 | a0002c0020t0009g0011 a0002c0032t0001g0256 |
2 | HG00733.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1230+166A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500686 | |||||||
chr7:76500695 | G | A | 3 | a0001c0001t0002g0169 a0001c0001t0002g0182 a0002c0020t0009g0011 |
3 | HG02897.hp1 NA18967.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.1230+175G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500695 | |||||||
chr7:76500793 | A | G | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1230+273A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500793 | |||||||
chr7:76500933 | A | T | 1 | a0003c0005t0001g0015 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1230+413A>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500933 | |||||||
chr7:76500971 | T | A | 42 | a0003c0004t0001g0189 a0003c0004t0001g0235 a0003c0004t0001g0236 others(39): Show |
42 | HG00140.hp2 HG00639.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.1230+451T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500971 | |||||||
chr7:76500993 | A | C | 1 | a0001c0001t0002g0173 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1230+473A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76500993 | |||||||
chr7:76501018 | C | T | 1 | a0003c0005t0001g0015 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1230+498C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501018 | |||||||
chr7:76501019 | T | C | 1 | a0003c0005t0001g0015 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1230+499T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501019 | |||||||
chr7:76501151 | A | G | 1 | a0002c0002t0001g0187 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1230+631A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501151 | |||||||
chr7:76501157 | T | TG | 3 | a0002c0002t0001g0198 a0002c0007t0001g0259 a0004c0009t0002g0172 |
3 | HG00621.hp2 HG01099.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1230+640dupG | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 76501157 | ||||||
chr7:76501340 | C | T | 1 | a0002c0002t0001g0216 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1230+820C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501340 | |||||||
chr7:76501515 | G | C | 118 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1231-783G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501515 | |||||||
chr7:76501529 | C | G | 3 | a0002c0002t0001g0200 a0002c0002t0001g0201 a0002c0002t0001g0202 |
3 | HG02165.hp2 NA18971.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1231-769C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501529 | |||||||
chr7:76501581 | C | T | 2 | a0002c0011t0003g0264 a0011c0030t0003g0263 |
2 | HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1231-717C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501581 | |||||||
chr7:76501649 | A | C | 122 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(119): Show |
125 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.1231-649A>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501649 | |||||||
chr7:76501661 | G | A | 118 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1231-637G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501661 | |||||||
chr7:76501737 | G | T | 2 | a0001c0003t0001g0266 a0001c0003t0001g0267 |
2 | HG02965.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.1231-561G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501737 | |||||||
chr7:76501744 | C | T | 118 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1231-554C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501744 | |||||||
chr7:76501814 | G | A | 10 | a0005c0006t0001g0115 a0005c0006t0001g0117 a0005c0006t0001g0118 others(7): Show |
10 | HG01109.hp1 HG01243.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1231-484G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501814 | |||||||
chr7:76501850 | C | G | 1 | a0001c0001t0002g0046 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.1231-448C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501850 | |||||||
chr7:76501852 | C | T | 117 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(114): Show |
120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1231-446C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501852 | |||||||
chr7:76501888 | CT | C | 82 | a0001c0001t0002g0001 a0001c0001t0002g0002 a0001c0001t0002g0003 others(79): Show |
85 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(82): Show |
intron_variant | MODIFIER | c.1231-394delT | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 76501888 | ||||||
chr7:76501897 | T | C | 1 | a0002c0011t0003g0265 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1231-401T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501897 | |||||||
chr7:76501929 | C | T | 1 | a0001c0003t0001g0267 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1231-369C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76501929 | |||||||
chr7:76502011 | C | G | 118 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1231-287C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76502011 | |||||||
chr7:76502019 | T | A | 1 | a0004c0014t0001g0212 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1231-279T>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76502019 | |||||||
chr7:76502136 | T | C | 199 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(196): Show |
203 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.1231-162T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76502136 | |||||||
chr7:76502200 | TC | T | 15 | a0003c0005t0001g0014 a0003c0005t0001g0015 a0003c0005t0001g0064 others(12): Show |
15 | HG00639.hp2 HG01192.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1231-96delC | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | INFO_REALIGN_3_PRIME | chr7 | 76502200 | ||||||
chr7:76502269 | G | A | 118 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1231-29G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 7/10 | chr7 | 76502269 | |||||||
chr7:76502472 | C | A | 1 | a0004c0027t0001g0139 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1389+16C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502472 | |||||||
chr7:76502495 | C | G | 118 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1389+39C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502495 | |||||||
chr7:76502526 | C | T | 3 | a0001c0003t0001g0146 a0001c0003t0001g0154 a0001c0003t0001g0158 |
3 | HG01175.hp2 HG01891.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.1389+70C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502526 | |||||||
chr7:76502538 | G | A | 2 | a0001c0001t0002g0109 a0002c0002t0001g0218 |
2 | HG03453.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1389+82G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502538 | |||||||
chr7:76502592 | G | A | 2 | a0001c0013t0001g0193 a0010c0016t0001g0227 |
2 | HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1389+136G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502592 | |||||||
chr7:76502657 | C | G | 36 | a0001c0001t0001g0088 a0001c0001t0002g0008 a0001c0001t0002g0010 others(33): Show |
36 | HG00741.hp2 HG01071.hp1 HG01106.hp1 others(33): Show |
intron_variant | MODIFIER | c.1389+201C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502657 | |||||||
chr7:76502756 | C | A | 2 | a0002c0008t0001g0229 a0002c0008t0001g0230 |
2 | HG02109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1389+300C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502756 | |||||||
chr7:76502760 | C | T | 12 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(9): Show |
12 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(9): Show |
intron_variant | MODIFIER | c.1389+304C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502760 | |||||||
chr7:76502816 | G | A | 1 | a0003c0004t0001g0235 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1389+360G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502816 | |||||||
chr7:76502952 | G | A | 1 | a0002c0002t0001g0194 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1390-474G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502952 | |||||||
chr7:76502953 | C | A | 118 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1390-473C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76502953 | |||||||
chr7:76503060 | G | A | 71 | a0001c0013t0001g0193 a0001c0023t0006g0074 a0001c0031t0001g0273 others(68): Show |
72 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1390-366G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503060 | |||||||
chr7:76503080 | A | G | 118 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1390-346A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503080 | |||||||
chr7:76503094 | G | A | 1 | a0005c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1390-332G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503094 | |||||||
chr7:76503156 | C | A | 118 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1390-270C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503156 | |||||||
chr7:76503291 | G | A | 7 | a0003c0005t0001g0064 a0003c0005t0001g0065 a0003c0005t0001g0066 others(4): Show |
7 | HG00639.hp2 HG01192.hp1 HG01243.hp2 others(4): Show |
intron_variant | MODIFIER | c.1390-135G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503291 | |||||||
chr7:76503359 | C | T | 1 | a0005c0024t0001g0159 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1390-67C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503359 | |||||||
chr7:76503360 | G | A | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1390-66G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503360 | |||||||
chr7:76503374 | T | C | 2 | a0003c0005t0001g0014 a0003c0005t0001g0015 |
2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1390-52T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503374 | |||||||
chr7:76503421 | G | C | 1 | a0004c0009t0002g0164 | 1 | HG02080.hp2 | splice_region_variant&intron_variant | LOW | c.1390-5G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 8/10 | chr7 | 76503421 | |||||||
chr7:76503645 | A | G | 169 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(166): Show |
173 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.1551+58A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503645 | |||||||
chr7:76503724 | A | G | 24 | a0001c0001t0001g0088 a0001c0001t0002g0091 a0001c0001t0002g0094 others(21): Show |
24 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(21): Show |
intron_variant | MODIFIER | c.1551+137A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503724 | |||||||
chr7:76503737 | C | T | 27 | a0001c0001t0001g0088 a0001c0001t0002g0091 a0001c0001t0002g0094 others(24): Show |
27 | HG00423.hp1 HG00558.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.1551+150C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503737 | |||||||
chr7:76503757 | C | T | 74 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(71): Show |
74 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(71): Show |
intron_variant | MODIFIER | c.1551+170C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503757 | |||||||
chr7:76503781 | G | T | 3 | a0001c0023t0006g0074 a0002c0011t0003g0264 a0011c0030t0003g0263 |
3 | HG02451.hp2 HG03540.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1551+194G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503781 | |||||||
chr7:76503814 | T | C | 15 | a0001c0001t0001g0088 a0001c0001t0002g0091 a0001c0001t0002g0094 others(12): Show |
15 | HG00741.hp2 HG01168.hp1 HG01258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1551+227T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503814 | |||||||
chr7:76503818 | G | A | 7 | a0001c0001t0002g0080 a0001c0001t0002g0083 a0001c0001t0002g0084 others(4): Show |
7 | HG01891.hp2 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1551+231G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503818 | |||||||
chr7:76503923 | C | T | 9 | a0001c0031t0001g0273 a0002c0007t0001g0268 a0002c0007t0001g0270 others(6): Show |
9 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.1551+336C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503923 | |||||||
chr7:76503944 | G | A | 29 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(26): Show |
29 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(26): Show |
intron_variant | MODIFIER | c.1551+357G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76503944 | |||||||
chr7:76504036 | C | T | 61 | a0001c0013t0001g0193 a0001c0031t0001g0273 a0002c0002t0001g0004 others(58): Show |
62 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.1552-320C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504036 | |||||||
chr7:76504040 | C | T | 1 | a0002c0020t0009g0011 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1552-316C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504040 | |||||||
chr7:76504081 | G | A | 1 | a0001c0001t0002g0022 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1552-275G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504081 | |||||||
chr7:76504092 | G | T | 16 | a0001c0031t0001g0273 a0002c0007t0001g0185 a0002c0007t0001g0259 others(13): Show |
16 | HG00544.hp1 HG00558.hp2 HG00609.hp2 others(13): Show |
intron_variant | MODIFIER | c.1552-264G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504092 | |||||||
chr7:76504110 | C | CAG | 129 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(126): Show |
132 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1552-246_1552-245i others(4): Show |
DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504110 | |||||||
chr7:76504312 | C | T | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1552-44C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504312 | |||||||
chr7:76504321 | G | A | 1 | a0003c0005t0001g0064 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1552-35G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 9/10 | chr7 | 76504321 | |||||||
chr7:76504461 | C | A | 3 | a0002c0008t0004g0132 a0002c0008t0004g0133 a0002c0008t0004g0134 |
3 | HG01884.hp2 HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1641+16C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504461 | |||||||
chr7:76504466 | G | C | 269 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(266): Show |
273 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.1641+21G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504466 | |||||||
chr7:76504493 | G | A | 1 | a0002c0029t0001g0005 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1641+48G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504493 | |||||||
chr7:76504534 | G | A | 1 | a0002c0002t0001g0215 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.1641+89G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504534 | |||||||
chr7:76504558 | C | T | 1 | a0002c0002t0005g0006 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1641+113C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504558 | |||||||
chr7:76504584 | A | G | 31 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(28): Show |
31 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1641+139A>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504584 | |||||||
chr7:76504685 | T | C | 2 | a0005c0006t0001g0117 a0005c0006t0001g0118 |
2 | HG02922.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1641+240T>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504685 | |||||||
chr7:76504718 | G | A | 4 | a0001c0023t0006g0074 a0002c0011t0003g0264 a0002c0011t0003g0265 others(1): Show |
4 | HG02451.hp2 HG03486.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1641+273G>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504718 | |||||||
chr7:76504886 | G | T | 71 | a0001c0013t0001g0193 a0001c0023t0006g0074 a0001c0031t0001g0273 others(68): Show |
72 | HG00280.hp2 HG00423.hp1 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.1641+441G>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504886 | |||||||
chr7:76504919 | C | T | 117 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(114): Show |
120 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.1642-455C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76504919 | |||||||
chr7:76505081 | C | T | 32 | a0001c0003t0001g0116 a0001c0003t0001g0128 a0001c0003t0001g0129 others(29): Show |
32 | HG00323.hp2 HG00408.hp1 HG00597.hp2 others(29): Show |
intron_variant | MODIFIER | c.1642-293C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76505081 | |||||||
chr7:76505116 | C | A | 118 | a0001c0001t0001g0088 a0001c0001t0002g0001 a0001c0001t0002g0002 others(115): Show |
121 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.1642-258C>A | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76505116 | |||||||
chr7:76505167 | G | C | 4 | a0005c0006t0001g0120 a0005c0006t0001g0121 a0005c0006t0001g0122 others(1): Show |
4 | HG01884.hp1 HG02258.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1642-207G>C | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76505167 | |||||||
chr7:76505264 | C | T | 2 | a0002c0007t0001g0275 a0002c0007t0001g0276 |
2 | HG00609.hp2 NA18947.hp1 |
intron_variant | MODIFIER | c.1642-110C>T | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76505264 | |||||||
chr7:76505356 | C | G | 3 | a0001c0001t0002g0010 a0001c0001t0002g0089 a0001c0001t0002g0102 |
3 | HG01071.hp1 HG01106.hp1 HG01256.hp1 |
intron_variant | MODIFIER | c.1642-18C>G | DTX2 | ENSG00000091073.20 | transcript | ENST00000430490.7 | protein_coding | 10/10 | chr7 | 76505356 |