Item | Value |
---|---|
geneid | 55112 |
ensemblid | ENSG00000126870.16 |
hgncid | 21862 |
symbol | DYNC2I1 |
name | dynein 2 intermediate chain 1 |
refseq_nuc | NM_018051.5 |
refseq_prot | NP_060521.4 |
ensembl_nuc | ENST00000407559.8 |
ensembl_prot | ENSP00000384290.3 |
mane_status | MANE Select |
chr | chr7 |
start | 158856558 |
end | 158946189 |
strand | + |
ver | v1.2 |
region | chr7:158856558-158946189 |
region5000 | chr7:158851558-158951189 |
regionname0 | DYNC2I1_chr7_158856558_158946189 |
regionname5000 | DYNC2I1_chr7_158851558_158951189 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1066 | 121 | 17 | 20 | 72 | 1 | 11 | 52 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0002 | 1/0 | 1066 | 99 | 16 | 24 | 44 | 3 | 11 | 31 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0003 | 0/0 | 1065 | 31 | 5 | 8 | 8 | 4 | 6 | 5 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1060): Show |
chr7 | 158851558 | 158951189 |
a0004 | 0/0 | 1066 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0005 | 0/0 | 1066 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0006 | 0/0 | 1066 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0007 | 0/0 | 1066 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0008 | 0/0 | 1066 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0009 | 0/0 | 1066 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0010 | 0/0 | 1066 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0011 | 0/0 | 1066 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0012 | 0/0 | 1066 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0013 | 0/0 | 203 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(198): Show |
chr7 | 158851558 | 158951189 |
a0014 | 0/0 | 1066 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0015 | 0/0 | 1066 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0016 | 0/0 | 1066 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
a0017 | 0/1 | 1066 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | MEPGK others(1061): Show |
chr7 | 158851558 | 158951189 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3198 | 117 | 15 | 20 | 70 | 1 | 11 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0001c0013 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0001c0020 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0001c0021 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0001c0022 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0002c0002 | 0/0 | 3198 | 95 | 15 | 23 | 43 | 3 | 11 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0002c0005 | 1/0 | 3198 | 2 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0002c0016 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0002c0018 | 0/0 | 3198 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0003c0003 | 0/0 | 3195 | 24 | 1 | 7 | 8 | 2 | 6 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3190): Show |
chr7 | 158851558 | 158951189 | ||
a0003c0010 | 0/0 | 3195 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3190): Show |
chr7 | 158851558 | 158951189 | ||
a0003c0011 | 0/0 | 3195 | 2 | 0 | 0 | 0 | 2 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3190): Show |
chr7 | 158851558 | 158951189 | ||
a0003c0027 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3190): Show |
chr7 | 158851558 | 158951189 | ||
a0003c0028 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3190): Show |
chr7 | 158851558 | 158951189 | ||
a0003c0029 | 0/0 | 3195 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3190): Show |
chr7 | 158851558 | 158951189 | ||
a0004c0004 | 0/0 | 3198 | 6 | 6 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0005c0008 | 0/0 | 3198 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0006c0006 | 0/0 | 3198 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0007c0009 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0008c0007 | 0/0 | 3198 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0009c0024 | 0/0 | 3198 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0010c0023 | 0/0 | 3198 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0011c0012 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0012c0015 | 0/0 | 3198 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0013c0014 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0014c0019 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0015c0017 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0016c0026 | 0/0 | 3198 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 | ||
a0017c0025 | 0/1 | 3198 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | ATGGA others(3193): Show |
chr7 | 158851558 | 158951189 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3789 | 6 | 1 | 4 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0001t0002 | 0/0 | 3789 | 76 | 7 | 16 | 45 | 0 | 8 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0001t0003 | 0/0 | 3789 | 21 | 0 | 0 | 20 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0001t0005 | 0/0 | 3789 | 5 | 0 | 0 | 3 | 1 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0001t0006 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0001t0009 | 0/0 | 3789 | 3 | 3 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0001t0012 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0001t0013 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0001t0019 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0013t0002 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0020t0003 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0021t0008 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0001c0022t0018 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0002c0002t0001 | 0/0 | 3789 | 91 | 14 | 23 | 42 | 3 | 9 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0002c0002t0014 | 0/0 | 3789 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0002c0002t0016 | 0/0 | 3789 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0002c0002t0017 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0002c0002t0021 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0002c0005t0010 | 1/0 | 3789 | 2 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0002c0016t0001 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0002c0018t0015 | 0/0 | 3789 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0003c0003t0004 | 0/0 | 3786 | 19 | 1 | 7 | 3 | 2 | 6 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3781): Show |
chr7 | 158851558 | 158951189 |
a0003c0003t0007 | 0/0 | 3786 | 5 | 0 | 0 | 5 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3781): Show |
chr7 | 158851558 | 158951189 |
a0003c0010t0011 | 0/0 | 3786 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3781): Show |
chr7 | 158851558 | 158951189 |
a0003c0011t0004 | 0/0 | 3786 | 2 | 0 | 0 | 0 | 2 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3781): Show |
chr7 | 158851558 | 158951189 |
a0003c0027t0022 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3781): Show |
chr7 | 158851558 | 158951189 |
a0003c0028t0023 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3781): Show |
chr7 | 158851558 | 158951189 |
a0003c0029t0004 | 0/0 | 3786 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3781): Show |
chr7 | 158851558 | 158951189 |
a0004c0004t0001 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0004c0004t0002 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0004c0004t0006 | 0/0 | 3789 | 3 | 3 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0005c0008t0003 | 0/0 | 3789 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0006c0006t0002 | 0/0 | 3789 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0007c0009t0003 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0007c0009t0020 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0008c0007t0008 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0009c0024t0002 | 0/0 | 3789 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0010c0023t0001 | 0/0 | 3789 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0011c0012t0001 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0012c0015t0001 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0013c0014t0001 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0014c0019t0001 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0015c0017t0001 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0016c0026t0001 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
a0017c0025t0001 | 0/1 | 3789 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | GGGAG others(3784): Show |
chr7 | 158851558 | 158951189 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0005g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0005g0142 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0006g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0006g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0009g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0009g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0009g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0012g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0012g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0013g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0001t0019g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0013t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0020t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0021t0008g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0001c0022t0018g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0014g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0016g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0017g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0002t0021g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0005t0010g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0005t0010g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0016t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0002c0018t0015g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0243 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0245 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0004g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0007g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0007g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0007g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0007g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0003t0007g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0010t0011g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0010t0011g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0011t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0011t0004g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0027t0022g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0028t0023g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0003c0029t0004g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0004c0004t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0004c0004t0002g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0004c0004t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0004c0004t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0004c0004t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0004c0004t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0005c0008t0003g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0005c0008t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0006c0006t0002g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0006c0006t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0007c0009t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0007c0009t0020g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0008c0007t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0008c0007t0008g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0009c0024t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0010c0023t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0011c0012t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0012c0015t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0013c0014t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0014c0019t0001g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0015c0017t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0016c0026t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
a0017c0025t0001g0104 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0009 | c0024 | t0002 | g0155 | EUR | GBR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0063 | EUR | GBR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00140 | hp1 | a0010 | c0023 | t0001 | g0272 | EUR | GBR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00140 | hp2 | a0003 | c0003 | t0004 | g0245 | EUR | GBR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00408 | hp1 | a0003 | c0003 | t0007 | g0240 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0040 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00438 | hp1 | a0002 | c0002 | t0001 | g0061 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00544 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00597 | hp1 | a0002 | c0002 | t0001 | g0031 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00597 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00621 | hp1 | a0001 | c0001 | t0019 | g0235 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0131 | EAS | CHS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0130 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00642 | hp2 | a0002 | c0002 | t0001 | g0055 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00733 | hp1 | a0003 | c0029 | t0004 | g0249 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00733 | hp2 | a0002 | c0002 | t0001 | g0045 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00741 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01070 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0183 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01071 | hp2 | a0003 | c0003 | t0004 | g0238 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01081 | hp2 | a0002 | c0018 | t0015 | g0048 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0085 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01167 | hp1 | a0002 | c0002 | t0001 | g0012 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0110 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01175 | hp1 | a0002 | c0002 | t0001 | g0044 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01175 | hp2 | a0003 | c0003 | t0004 | g0251 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0128 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0062 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0231 | AMR | PUR | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01255 | hp1 | a0003 | c0003 | t0004 | g0243 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01255 | hp2 | a0002 | c0002 | t0001 | g0027 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01257 | hp1 | a0002 | c0002 | t0001 | g0081 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01257 | hp2 | a0005 | c0008 | t0003 | g0223 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01346 | hp1 | a0003 | c0003 | t0004 | g0257 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0089 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01358 | hp1 | a0003 | c0003 | t0004 | g0255 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01358 | hp2 | a0002 | c0002 | t0001 | g0047 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01361 | hp1 | a0002 | c0002 | t0001 | g0023 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01361 | hp2 | a0003 | c0003 | t0004 | g0244 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0160 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01496 | hp2 | a0003 | c0003 | t0004 | g0253 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0075 | EUR | IBS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01516 | hp2 | a0003 | c0011 | t0004 | g0247 | EUR | IBS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01517 | hp1 | a0001 | c0001 | t0005 | g0142 | EUR | IBS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01517 | hp2 | a0003 | c0011 | t0004 | g0250 | EUR | IBS | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0099 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01934 | hp2 | a0006 | c0006 | t0002 | g0118 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0153 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01943 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01975 | hp1 | a0002 | c0002 | t0001 | g0067 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0076 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0191 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02004 | hp2 | a0002 | c0002 | t0001 | g0014 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02015 | hp1 | a0003 | c0003 | t0004 | g0264 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02015 | hp2 | a0001 | c0001 | t0005 | g0161 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02027 | hp1 | a0002 | c0002 | t0001 | g0079 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02027 | hp2 | a0002 | c0002 | t0001 | g0041 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02055 | hp1 | a0001 | c0001 | t0012 | g0218 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02055 | hp2 | a0003 | c0027 | t0022 | g0263 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02071 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02071 | hp2 | a0002 | c0002 | t0001 | g0042 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02080 | hp1 | a0001 | c0001 | t0013 | g0116 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0016 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02083 | hp2 | a0002 | c0002 | t0001 | g0103 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02129 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02155 | hp1 | a0003 | c0003 | t0004 | g0266 | EAS | CDX | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | CDX | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02165 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | CDX | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0148 | EAS | CDX | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02257 | hp2 | a0006 | c0006 | t0002 | g0219 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02258 | hp1 | a0005 | c0008 | t0003 | g0221 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02258 | hp2 | a0004 | c0004 | t0002 | g0137 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02273 | hp1 | a0002 | c0002 | t0001 | g0074 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0198 | AMR | PEL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02280 | hp1 | a0001 | c0001 | t0009 | g0115 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0109 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02451 | hp1 | a0002 | c0002 | t0001 | g0072 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02451 | hp2 | a0002 | c0005 | t0010 | g0100 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0013 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0117 | EAS | KHV | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02615 | hp2 | a0007 | c0009 | t0003 | g0220 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02647 | hp1 | a0002 | c0002 | t0001 | g0111 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02647 | hp2 | a0001 | c0001 | t0009 | g0228 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02683 | hp1 | a0002 | c0002 | t0001 | g0084 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02683 | hp2 | a0001 | c0001 | t0005 | g0139 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02698 | hp2 | a0003 | c0003 | t0004 | g0237 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02717 | hp1 | a0001 | c0021 | t0008 | g0112 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02717 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0227 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0217 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02809 | hp1 | a0008 | c0007 | t0008 | g0114 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02809 | hp2 | a0002 | c0002 | t0021 | g0092 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02818 | hp1 | a0004 | c0004 | t0006 | g0179 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02818 | hp2 | a0008 | c0007 | t0008 | g0113 | AFR | GWD | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02922 | hp1 | a0003 | c0028 | t0023 | g0260 | AFR | ESN | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02922 | hp2 | a0012 | c0015 | t0001 | g0056 | AFR | ESN | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02976 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ESN | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02976 | hp2 | a0003 | c0010 | t0011 | g0261 | AFR | ESN | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03017 | hp2 | a0002 | c0002 | t0014 | g0087 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0032 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03209 | hp2 | a0003 | c0003 | t0004 | g0262 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0233 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0008 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03486 | hp2 | a0004 | c0004 | t0006 | g0178 | AFR | MSL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03491 | hp1 | a0003 | c0003 | t0004 | g0254 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03491 | hp2 | a0003 | c0003 | t0004 | g0256 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0088 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03688 | hp1 | a0002 | c0002 | t0001 | g0093 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0212 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03704 | hp2 | a0002 | c0002 | t0001 | g0068 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0132 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03710 | hp2 | a0002 | c0002 | t0016 | g0034 | SAS | PJL | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03834 | hp2 | a0003 | c0003 | t0004 | g0246 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0184 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0053 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0052 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG04184 | hp1 | a0002 | c0002 | t0001 | g0051 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG04184 | hp2 | a0003 | c0003 | t0004 | g0258 | SAS | BEB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG04204 | hp1 | a0002 | c0002 | t0001 | g0020 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0141 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG04228 | hp2 | a0003 | c0003 | t0004 | g0265 | SAS | STU | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | CHB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18612 | hp2 | a0002 | c0002 | t0001 | g0098 | EAS | CHB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0230 | AFR | YRI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0021 | AFR | YRI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18939 | hp1 | a0002 | c0002 | t0001 | g0105 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18941 | hp1 | a0002 | c0002 | t0001 | g0080 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0124 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18942 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0136 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18943 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18945 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0156 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18951 | hp1 | a0003 | c0003 | t0004 | g0267 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18951 | hp2 | a0002 | c0002 | t0001 | g0033 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18953 | hp1 | a0013 | c0014 | t0001 | g0106 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18953 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18954 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18957 | hp1 | a0001 | c0001 | t0003 | g0216 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18957 | hp2 | a0003 | c0003 | t0007 | g0239 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18959 | hp1 | a0002 | c0002 | t0001 | g0025 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18961 | hp2 | a0002 | c0002 | t0001 | g0050 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18962 | hp1 | a0014 | c0019 | t0001 | g0001 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0186 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18964 | hp2 | a0003 | c0003 | t0007 | g0248 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18965 | hp1 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18965 | hp2 | a0001 | c0013 | t0002 | g0175 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18967 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18969 | hp2 | a0002 | c0002 | t0001 | g0091 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18974 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18974 | hp2 | a0015 | c0017 | t0001 | g0083 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18981 | hp2 | a0002 | c0016 | t0001 | g0018 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18982 | hp1 | a0002 | c0002 | t0001 | g0030 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18985 | hp1 | a0002 | c0002 | t0001 | g0019 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18989 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18989 | hp2 | a0002 | c0002 | t0001 | g0107 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0169 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18990 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18992 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18994 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18999 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19001 | hp2 | a0002 | c0002 | t0001 | g0015 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0129 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19004 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19007 | hp2 | a0002 | c0002 | t0001 | g0001 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19030 | hp1 | a0004 | c0004 | t0002 | g0138 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19030 | hp2 | a0004 | c0004 | t0001 | g0180 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19043 | hp1 | a0002 | c0002 | t0001 | g0071 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19043 | hp2 | a0003 | c0010 | t0011 | g0252 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19055 | hp1 | a0002 | c0002 | t0001 | g0060 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0039 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19060 | hp2 | a0003 | c0003 | t0007 | g0242 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19062 | hp2 | a0002 | c0002 | t0001 | g0094 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19064 | hp1 | a0003 | c0003 | t0007 | g0259 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19064 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0126 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19065 | hp2 | a0002 | c0002 | t0017 | g0029 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19066 | hp1 | a0016 | c0026 | t0001 | g0065 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19068 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0024 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0152 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19070 | hp2 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0226 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19085 | hp1 | a0002 | c0002 | t0001 | g0064 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19087 | hp2 | a0001 | c0001 | t0003 | g0202 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19240 | hp1 | a0007 | c0009 | t0020 | g0222 | AFR | YRI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0007 | AFR | YRI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0146 | AFR | ASW | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA20129 | hp2 | a0001 | c0022 | t0018 | g0229 | AFR | ASW | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA20805 | hp1 | a0003 | c0003 | t0004 | g0241 | EUR | TSI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA20805 | hp2 | a0002 | c0002 | t0001 | g0086 | EUR | TSI | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG01123 | hp2 | a0002 | c0002 | t0001 | g0082 | AMR | CLM | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02109 | hp1 | a0011 | c0012 | t0001 | g0043 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02486 | hp1 | a0002 | c0002 | t0001 | g0101 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0234 | AFR | ACB | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18955 | hp1 | a0001 | c0020 | t0003 | g0210 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | USA | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0077 | AFR | USA | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0078 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
NA21309 | hp2 | a0004 | c0004 | t0006 | g0181 | AFR | LWK | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
homoSapiens | chm13v2 | a0017 | c0025 | t0001 | g0104 | REF | REF | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
homoSapiens | grch38p0 | a0002 | c0005 | t0010 | g0102 | REF | REF | DYNC2I1_chr7_158851558_158951189 | DYNC2I1 | chr7 | 158851558 | 158951189 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:158871383 | TGAA | T | 1 | a0003 | 31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
conservative_inframe_deletion | MODERATE | c.313_315delAAG | p.Lys105del | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/25 | 491/3789 | 313/3201 | 105/1066 | INFO_REALIGN_3_PRIME | chr7 | 158871383 | ||
chr7:158871517 | C | A | 1 | a0011 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.445C>A | p.Arg149Ser | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/25 | 623/3789 | 445/3201 | 149/1066 | chr7 | 158871517 | |||
chr7:158879714 | C | G | 2 | a0005 a0007 |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
missense_variant | MODERATE | c.604C>G | p.Leu202Val | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 782/3789 | 604/3201 | 202/1066 | chr7 | 158879714 | |||
chr7:158879722 | C | A | 1 | a0013 | 1 | NA18953.hp1 | stop_gained | HIGH | c.612C>A | p.Tyr204* | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 790/3789 | 612/3201 | 204/1066 | chr7 | 158879722 | |||
chr7:158879824 | G | T | 1 | a0003 | 2 | HG01516.hp2 HG01517.hp2 |
missense_variant | MODERATE | c.714G>T | p.Glu238Asp | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 892/3789 | 714/3201 | 238/1066 | chr7 | 158879824 | |||
chr7:158879928 | A | G | 9 | a0001 a0003 a0004 others(6): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
missense_variant | MODERATE | c.818A>G | p.Gln273Arg | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 996/3789 | 818/3201 | 273/1066 | chr7 | 158879928 | |||
chr7:158887026 | C | T | 1 | a0009 | 1 | HG00099.hp1 | missense_variant | MODERATE | c.941C>T | p.Ala314Val | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/25 | 1119/3789 | 941/3201 | 314/1066 | chr7 | 158887026 | |||
chr7:158891314 | C | T | 1 | a0007 | 2 | HG02615.hp2 NA19240.hp1 |
missense_variant | MODERATE | c.1040C>T | p.Pro347Leu | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/25 | 1218/3789 | 1040/3201 | 347/1066 | chr7 | 158891314 | |||
chr7:158905989 | A | G | 1 | a0010 | 1 | HG00140.hp1 | missense_variant&splice_region_variant | MODERATE | c.1358A>G | p.Asp453Gly | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/25 | 1536/3789 | 1358/3201 | 453/1066 | chr7 | 158905989 | |||
chr7:158911554 | C | G | 1 | a0008 | 2 | HG02809.hp1 HG02818.hp2 |
missense_variant | MODERATE | c.1465C>G | p.Arg489Gly | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/25 | 1643/3789 | 1465/3201 | 489/1066 | chr7 | 158911554 | |||
chr7:158913079 | G | A | 1 | a0012 | 1 | HG02922.hp2 | missense_variant | MODERATE | c.1685G>A | p.Ser562Asn | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/25 | 1863/3789 | 1685/3201 | 562/1066 | chr7 | 158913079 | |||
chr7:158918774 | C | T | 1 | a0003 | 1 | HG00733.hp1 | missense_variant | MODERATE | c.1826C>T | p.Ala609Val | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/25 | 2004/3789 | 1826/3201 | 609/1066 | chr7 | 158918774 | |||
chr7:158923686 | C | T | 1 | a0003 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.2210C>T | p.Thr737Met | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/25 | 2388/3789 | 2210/3201 | 737/1066 | chr7 | 158923686 | |||
chr7:158926283 | C | T | 1 | a0006 | 2 | HG01934.hp2 HG02257.hp2 |
missense_variant | MODERATE | c.2354C>T | p.Pro785Leu | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 18/25 | 2532/3789 | 2354/3201 | 785/1066 | chr7 | 158926283 | |||
chr7:158926425 | A | G | 2 | a0004 a0006 |
8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
missense_variant | MODERATE | c.2395A>G | p.Ile799Val | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 19/25 | 2573/3789 | 2395/3201 | 799/1066 | chr7 | 158926425 | |||
chr7:158927025 | G | A | 1 | a0014 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.2467G>A | p.Gly823Ser | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/25 | 2645/3789 | 2467/3201 | 823/1066 | chr7 | 158927025 | |||
chr7:158941970 | G | A | 1 | a0016 | 1 | NA19066.hp1 | missense_variant | MODERATE | c.2824G>A | p.Ala942Thr | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/25 | 3002/3789 | 2824/3201 | 942/1066 | chr7 | 158941970 | |||
chr7:158945703 | C | T | 1 | a0015 | 1 | NA18974.hp2 | missense_variant | MODERATE | c.3125C>T | p.Pro1042Leu | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 3303/3789 | 3125/3201 | 1042/1066 | chr7 | 158945703 | |||
chr7:158946187 | A | C | 11 | a0001 a0002 a0003 others(8): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
splice_region_variant | LOW | c.*408A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | chr7 | 158946187 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:158876637 | T | C | 1 | a0001c0013 | 1 | NA18965.hp2 | synonymous_variant | LOW | c.519T>C | p.Asp173Asp | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/25 | 697/3789 | 519/3201 | 173/1066 | chr7 | 158876637 | |||
chr7:158879782 | C | T | 1 | a0016c0026 | 1 | NA19066.hp1 | synonymous_variant | LOW | c.672C>T | p.Asp224Asp | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/25 | 850/3789 | 672/3201 | 224/1066 | chr7 | 158879782 | |||
chr7:158922510 | G | A | 1 | a0001c0020 | 1 | NA18955.hp1 | synonymous_variant | LOW | c.2055G>A | p.Gln685Gln | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/25 | 2233/3789 | 2055/3201 | 685/1066 | chr7 | 158922510 | |||
chr7:158922528 | A | G | 21 | a0001c0001 a0001c0013 a0001c0020 others(18): Show |
240 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(237): Show |
synonymous_variant | LOW | c.2073A>G | p.Lys691Lys | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/25 | 2251/3789 | 2073/3201 | 691/1066 | chr7 | 158922528 | |||
chr7:158926415 | G | A | 3 | a0003c0010 a0004c0004 a0006c0006 |
10 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(7): Show |
synonymous_variant | LOW | c.2385G>A | p.Leu795Leu | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 19/25 | 2563/3789 | 2385/3201 | 795/1066 | chr7 | 158926415 | |||
chr7:158927024 | A | G | 1 | a0014c0019 | 1 | NA18962.hp1 | synonymous_variant | LOW | c.2466A>G | p.Ala822Ala | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/25 | 2644/3789 | 2466/3201 | 822/1066 | chr7 | 158927024 | |||
chr7:158934192 | T | G | 1 | a0002c0016 | 1 | NA18981.hp2 | synonymous_variant | LOW | c.2610T>G | p.Pro870Pro | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 22/25 | 2788/3789 | 2610/3201 | 870/1066 | chr7 | 158934192 | |||
chr7:158941972 | G | C | 1 | a0001c0022 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.2826G>C | p.Ala942Ala | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/25 | 3004/3789 | 2826/3201 | 942/1066 | chr7 | 158941972 | |||
chr7:158942122 | C | T | 3 | a0002c0018 a0003c0011 a0003c0027 |
4 | HG01081.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
synonymous_variant | LOW | c.2976C>T | p.Val992Val | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/25 | 3154/3789 | 2976/3201 | 992/1066 | chr7 | 158942122 | |||
chr7:158945659 | T | C | 1 | a0001c0022 | 1 | NA20129.hp2 | synonymous_variant | LOW | c.3081T>C | p.Ser1027Ser | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 3259/3789 | 3081/3201 | 1027/1066 | chr7 | 158945659 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:158856569 | C | T | 8 | a0001c0001t0012 a0003c0003t0004 a0003c0003t0007 others(5): Show |
33 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(30): Show |
5_prime_UTR_variant | MODIFIER | c.-167C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 167 | chr7 | 158856569 | ||||||
chr7:158856589 | T | C | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(11): Show |
119 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
5_prime_UTR_variant | MODIFIER | c.-147T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 147 | chr7 | 158856589 | ||||||
chr7:158856606 | C | T | 1 | a0003c0003t0007 | 5 | HG00408.hp1 NA18957.hp2 NA18964.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-130C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 130 | chr7 | 158856606 | ||||||
chr7:158856613 | T | C | 14 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0013 others(11): Show |
119 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(116): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-123T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | chr7 | 158856613 | |||||||
chr7:158856643 | C | T | 2 | a0001c0001t0009 a0001c0001t0012 |
5 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-93C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 93 | chr7 | 158856643 | ||||||
chr7:158856654 | C | T | 1 | a0002c0002t0021 | 1 | HG02809.hp2 | 5_prime_UTR_variant | MODIFIER | c.-82C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 82 | chr7 | 158856654 | ||||||
chr7:158856682 | A | G | 25 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(22): Show |
155 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(152): Show |
5_prime_UTR_variant | MODIFIER | c.-54A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 54 | chr7 | 158856682 | ||||||
chr7:158856721 | G | A | 1 | a0001c0001t0013 | 1 | HG02080.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/25 | 15 | chr7 | 158856721 | ||||||
chr7:158945780 | C | T | 1 | a0002c0002t0017 | 1 | NA19065.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 1 | chr7 | 158945780 | ||||||
chr7:158945815 | C | T | 1 | a0007c0009t0020 | 1 | NA19240.hp1 | 3_prime_UTR_variant | MODIFIER | c.*36C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 36 | chr7 | 158945815 | ||||||
chr7:158945832 | T | G | 1 | a0001c0022t0018 | 1 | NA20129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*53T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 53 | chr7 | 158945832 | ||||||
chr7:158945884 | T | C | 1 | a0002c0002t0014 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*105T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 105 | chr7 | 158945884 | ||||||
chr7:158945920 | G | T | 23 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(20): Show |
124 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*141G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 141 | chr7 | 158945920 | ||||||
chr7:158945934 | C | T | 1 | a0002c0002t0016 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*155C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 155 | chr7 | 158945934 | ||||||
chr7:158945943 | G | C | 23 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0012 others(20): Show |
124 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(121): Show |
3_prime_UTR_variant | MODIFIER | c.*164G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 164 | chr7 | 158945943 | ||||||
chr7:158946140 | A | G | 1 | a0001c0001t0012 | 2 | HG02055.hp1 HG02723.hp2 |
3_prime_UTR_variant | MODIFIER | c.*361A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 361 | chr7 | 158946140 | ||||||
chr7:158946158 | T | C | 37 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(34): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
3_prime_UTR_variant | MODIFIER | c.*379T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 379 | chr7 | 158946158 | ||||||
chr7:158946184 | C | G | 1 | a0003c0028t0023 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*405C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 25/25 | 405 | chr7 | 158946184 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:158856911 | A | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+161A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158856911 | |||||||
chr7:158857062 | G | A | 1 | a0002c0002t0001g0002 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.15+312G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857062 | |||||||
chr7:158857095 | G | T | 156 | a0001c0001t0002g0117 a0001c0001t0002g0119 a0001c0001t0002g0120 others(153): Show |
156 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.15+345G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857095 | |||||||
chr7:158857110 | G | T | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+360G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857110 | |||||||
chr7:158857213 | C | T | 1 | a0002c0002t0001g0111 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.15+463C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857213 | |||||||
chr7:158857359 | A | G | 1 | a0002c0002t0001g0110 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.15+609A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857359 | |||||||
chr7:158857432 | A | G | 1 | a0001c0001t0003g0236 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.15+682A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857432 | |||||||
chr7:158857505 | A | G | 1 | a0001c0001t0019g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.15+755A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857505 | |||||||
chr7:158857523 | A | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+773A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857523 | |||||||
chr7:158857534 | G | GT | 16 | a0001c0001t0003g0224 a0001c0001t0003g0225 a0001c0001t0003g0226 others(13): Show |
16 | HG00597.hp2 HG01257.hp2 HG02015.hp1 others(13): Show |
intron_variant | MODIFIER | c.15+789dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857534 | ||||||
chr7:158857534 | G | GTT | 3 | a0001c0001t0009g0227 a0001c0001t0009g0228 a0003c0003t0004g0267 |
3 | HG02647.hp2 HG02723.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.15+788_15+789dupTT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857534 | ||||||
chr7:158857538 | TTG | T | 6 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0002g0232 others(3): Show |
6 | HG01243.hp2 HG02486.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+790_15+791delGT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857538 | ||||||
chr7:158857539 | TG | T | 71 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(68): Show |
71 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.15+790delG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857539 | |||||||
chr7:158857540 | G | GT | 9 | a0001c0001t0001g0269 a0002c0002t0001g0014 a0002c0002t0001g0015 others(6): Show |
9 | HG01981.hp1 HG02004.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+806dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857540 | ||||||
chr7:158857540 | G | T | 84 | a0001c0001t0002g0121 a0001c0001t0002g0128 a0001c0001t0002g0145 others(81): Show |
84 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.15+790G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857540 | |||||||
chr7:158857609 | C | T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+859C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857609 | |||||||
chr7:158857712 | A | G | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+962A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857712 | |||||||
chr7:158857768 | CTTCG | C | 9 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(6): Show |
9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+1020_15+1023del others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857768 | ||||||
chr7:158857773 | T | C | 9 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(6): Show |
9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+1023T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857773 | |||||||
chr7:158857774 | G | A | 9 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(6): Show |
9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+1024G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857774 | |||||||
chr7:158857787 | C | T | 1 | a0001c0001t0002g0198 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.15+1037C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857787 | |||||||
chr7:158857791 | C | CT | 5 | a0002c0002t0001g0105 a0002c0002t0001g0107 a0002c0002t0001g0108 others(2): Show |
5 | HG02280.hp2 NA18939.hp1 NA18953.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+1060dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857791 | ||||||
chr7:158857791 | CT | C | 5 | a0002c0002t0001g0009 a0002c0002t0001g0010 a0002c0002t0001g0011 others(2): Show |
5 | HG01070.hp1 HG01167.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.15+1060delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857791 | ||||||
chr7:158857791 | CTT | C | 9 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(6): Show |
9 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.15+1059_15+1060del others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857791 | ||||||
chr7:158857791 | CTTT | C | 41 | a0001c0001t0002g0193 a0001c0001t0002g0194 a0001c0001t0003g0224 others(38): Show |
41 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.15+1058_15+1060del others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857791 | ||||||
chr7:158857791 | CTTTT | C | 113 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(110): Show |
113 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.15+1057_15+1060del others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158857791 | ||||||
chr7:158857796 | T | C | 1 | a0001c0001t0003g0224 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.15+1046T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857796 | |||||||
chr7:158857853 | C | A | 4 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0008c0007t0008g0113 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+1103C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857853 | |||||||
chr7:158857875 | C | T | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+1125C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158857875 | |||||||
chr7:158858010 | C | T | 2 | a0002c0002t0001g0109 a0002c0002t0001g0111 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.15+1260C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858010 | |||||||
chr7:158858033 | C | T | 4 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0008c0007t0008g0113 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+1283C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858033 | |||||||
chr7:158858155 | C | G | 9 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(6): Show |
9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+1405C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858155 | |||||||
chr7:158858250 | G | A | 123 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(120): Show |
123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.15+1500G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858250 | |||||||
chr7:158858297 | A | G | 4 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0008c0007t0008g0113 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.15+1547A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858297 | |||||||
chr7:158858396 | G | A | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+1646G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858396 | |||||||
chr7:158858465 | A | T | 168 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(165): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.15+1715A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858465 | |||||||
chr7:158858641 | C | T | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.15+1891C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858641 | |||||||
chr7:158858739 | C | G | 3 | a0001c0001t0002g0191 a0001c0001t0005g0190 a0001c0001t0005g0192 |
3 | HG00544.hp2 HG02004.hp1 NA18941.hp2 |
intron_variant | MODIFIER | c.15+1989C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858739 | |||||||
chr7:158858772 | G | C | 1 | a0003c0003t0004g0238 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.15+2022G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858772 | |||||||
chr7:158858784 | C | G | 1 | a0001c0001t0002g0189 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.15+2034C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858784 | |||||||
chr7:158858827 | T | TC | 41 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(38): Show |
41 | HG00408.hp1 HG00423.hp1 HG00423.hp2 others(38): Show |
intron_variant | MODIFIER | c.15+2083dupC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858827 | ||||||
chr7:158858828 | C | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+2078C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858828 | |||||||
chr7:158858850 | TTCCTCTC others(3): Show |
T | 1 | a0001c0001t0002g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.15+2104_15+2113del others(10): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858850 | ||||||
chr7:158858855 | C | CTCCCCTC others(5): Show |
1 | a0002c0002t0001g0063 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.15+2112_15+2123dup others(12): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858855 | ||||||
chr7:158858857 | CCCCTCCC others(10): Show |
C | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.15+2124_15+2140del others(17): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858857 | ||||||
chr7:158858910 | T | C | 1 | a0001c0001t0003g0224 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.15+2160T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858910 | |||||||
chr7:158858922 | T | TC | 11 | a0001c0001t0002g0117 a0001c0001t0002g0132 a0001c0001t0002g0231 others(8): Show |
11 | HG00597.hp2 HG01243.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.15+2178dupC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858922 | ||||||
chr7:158858946 | C | CCCTCCCC others(8): Show |
26 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(23): Show |
26 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.15+2224_15+2238dup others(15): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858946 | ||||||
chr7:158858946 | C | CCCTCCCC others(23): Show |
1 | a0003c0003t0007g0259 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.15+2209_15+2238dup others(30): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858946 | ||||||
chr7:158858946 | CCCTCCCC others(8): Show |
C | 6 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 others(3): Show |
6 | HG02257.hp1 HG02280.hp1 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.15+2224_15+2238del others(15): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858946 | ||||||
chr7:158858979 | T | C | 1 | a0002c0002t0001g0026 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.15+2229T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858979 | |||||||
chr7:158858984 | T | C | 3 | a0001c0001t0003g0202 a0001c0001t0003g0225 a0002c0002t0001g0027 |
3 | HG00597.hp2 HG01255.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.15+2234T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158858984 | |||||||
chr7:158858984 | T | TC | 30 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(27): Show |
30 | HG00597.hp1 HG01169.hp2 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.15+2241dupC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858984 | ||||||
chr7:158858984 | T | TCCCCTTT others(9): Show |
2 | a0003c0003t0004g0267 a0003c0003t0007g0242 |
2 | NA18951.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.15+2238_15+2239ins others(16): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858984 | ||||||
chr7:158858984 | T | TCCCCTTT others(10): Show |
1 | a0003c0003t0007g0239 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.15+2238_15+2239ins others(17): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158858984 | ||||||
chr7:158859040 | A | G | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+2290A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859040 | |||||||
chr7:158859150 | C | G | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.15+2400C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859150 | |||||||
chr7:158859564 | G | C | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+2814G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859564 | |||||||
chr7:158859660 | G | A | 5 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(2): Show |
5 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+2910G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859660 | |||||||
chr7:158859714 | G | A | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+2964G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859714 | |||||||
chr7:158859901 | G | A | 1 | a0002c0002t0001g0033 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.15+3151G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158859901 | |||||||
chr7:158860056 | GT | G | 163 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(160): Show |
163 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.15+3321delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158860056 | ||||||
chr7:158860078 | G | A | 1 | a0001c0001t0002g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.15+3328G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860078 | |||||||
chr7:158860238 | T | A | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+3488T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860238 | |||||||
chr7:158860338 | C | T | 96 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.15+3588C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860338 | |||||||
chr7:158860382 | C | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+3632C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860382 | |||||||
chr7:158860626 | T | C | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15+3876T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860626 | |||||||
chr7:158860726 | A | G | 1 | a0002c0002t0001g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.15+3976A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158860726 | |||||||
chr7:158861034 | G | A | 271 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(268): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.15+4284G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861034 | |||||||
chr7:158861035 | G | T | 1 | a0002c0002t0001g0033 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.15+4285G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861035 | |||||||
chr7:158861235 | T | C | 1 | a0002c0002t0001g0108 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.15+4485T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861235 | |||||||
chr7:158861289 | G | A | 1 | a0002c0002t0001g0033 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.15+4539G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861289 | |||||||
chr7:158861388 | C | T | 8 | a0001c0001t0002g0136 a0001c0001t0002g0185 a0001c0001t0002g0186 others(5): Show |
8 | HG00544.hp2 HG02155.hp2 HG02273.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+4638C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861388 | |||||||
chr7:158861515 | C | A | 1 | a0001c0001t0002g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.15+4765C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861515 | |||||||
chr7:158861706 | G | A | 2 | a0001c0001t0003g0199 a0001c0001t0003g0225 |
2 | HG00597.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.15+4956G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861706 | |||||||
chr7:158861780 | G | A | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.15+5030G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158861780 | |||||||
chr7:158862286 | A | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0182 a0001c0001t0002g0183 others(1): Show |
4 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.15+5536A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862286 | |||||||
chr7:158862303 | CAG | C | 5 | a0001c0001t0019g0235 a0004c0004t0001g0180 a0004c0004t0006g0178 others(2): Show |
5 | HG00621.hp1 HG02818.hp1 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.15+5554_15+5555del others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862303 | |||||||
chr7:158862352 | CATTGATT | C | 9 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(6): Show |
9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.15+5610_15+5616del others(7): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158862352 | ||||||
chr7:158862514 | C | T | 2 | a0007c0009t0003g0220 a0007c0009t0020g0222 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.15+5764C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862514 | |||||||
chr7:158862521 | A | C | 1 | a0001c0001t0019g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.15+5771A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862521 | |||||||
chr7:158862526 | G | C | 8 | a0004c0004t0001g0180 a0004c0004t0002g0137 a0004c0004t0002g0138 others(5): Show |
8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.15+5776G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862526 | |||||||
chr7:158862552 | T | TA | 64 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(61): Show |
64 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(61): Show |
intron_variant | MODIFIER | c.15+5822dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158862552 | ||||||
chr7:158862552 | T | TAA | 95 | a0001c0001t0001g0271 a0001c0001t0002g0003 a0001c0001t0002g0004 others(92): Show |
95 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.15+5821_15+5822dup others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158862552 | ||||||
chr7:158862552 | T | TAAA | 7 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0140 others(4): Show |
7 | HG02056.hp2 HG02683.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.15+5820_15+5822dup others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158862552 | ||||||
chr7:158862552 | TA | T | 6 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0022t0018g0229 others(3): Show |
6 | HG02451.hp2 HG02486.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+5822delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158862552 | ||||||
chr7:158862635 | T | G | 1 | a0011c0012t0001g0043 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.15+5885T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862635 | |||||||
chr7:158862659 | G | A | 1 | a0003c0003t0004g0243 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.15+5909G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862659 | |||||||
chr7:158862667 | C | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.15+5917C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862667 | |||||||
chr7:158862678 | C | T | 1 | a0002c0002t0001g0099 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.15+5928C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862678 | |||||||
chr7:158862764 | A | C | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.15+6014A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862764 | |||||||
chr7:158862843 | T | C | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.15+6093T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862843 | |||||||
chr7:158862955 | G | A | 1 | a0001c0001t0005g0142 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.15+6205G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158862955 | |||||||
chr7:158863013 | A | G | 1 | a0004c0004t0006g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.15+6263A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863013 | |||||||
chr7:158863044 | A | G | 1 | a0002c0002t0001g0098 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.15+6294A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863044 | |||||||
chr7:158863083 | G | A | 1 | a0002c0002t0001g0009 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.15+6333G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863083 | |||||||
chr7:158863131 | G | T | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG01433.hp1 HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.15+6381G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863131 | |||||||
chr7:158863168 | C | T | 96 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.15+6418C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863168 | |||||||
chr7:158863179 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.15+6429G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863179 | |||||||
chr7:158863274 | G | A | 3 | a0002c0002t0001g0044 a0002c0002t0001g0045 a0002c0002t0001g0046 |
3 | HG00733.hp2 HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.15+6524G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863274 | |||||||
chr7:158863285 | C | T | 2 | a0006c0006t0002g0118 a0006c0006t0002g0219 |
2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.15+6535C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863285 | |||||||
chr7:158863293 | C | G | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.15+6543C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863293 | |||||||
chr7:158863294 | A | G | 1 | a0001c0001t0005g0142 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.15+6544A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863294 | |||||||
chr7:158863310 | C | T | 1 | a0002c0002t0001g0097 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.16-6545C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863310 | |||||||
chr7:158863321 | C | T | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.16-6534C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863321 | |||||||
chr7:158863510 | G | C | 1 | a0001c0001t0001g0268 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.16-6345G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863510 | |||||||
chr7:158863527 | T | C | 1 | a0002c0002t0001g0017 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.16-6328T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863527 | |||||||
chr7:158863580 | G | C | 3 | a0002c0002t0001g0002 a0002c0002t0001g0047 a0002c0002t0001g0105 |
3 | HG01358.hp2 NA18939.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.16-6275G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863580 | |||||||
chr7:158863585 | A | AG | 8 | a0001c0001t0002g0129 a0001c0001t0002g0234 a0001c0001t0003g0224 others(5): Show |
8 | HG01255.hp2 HG02486.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.16-6264dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863585 | ||||||
chr7:158863626 | T | TG | 25 | a0001c0001t0001g0270 a0001c0001t0002g0128 a0001c0001t0002g0141 others(22): Show |
25 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.16-6221dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863626 | ||||||
chr7:158863629 | G | C | 2 | a0002c0002t0001g0099 a0002c0018t0015g0048 |
2 | HG01081.hp2 HG01891.hp1 |
intron_variant | MODIFIER | c.16-6226G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863629 | |||||||
chr7:158863643 | G | A | 95 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(92): Show |
95 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(92): Show |
intron_variant | MODIFIER | c.16-6212G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863643 | |||||||
chr7:158863657 | T | TG | 29 | a0001c0001t0001g0006 a0001c0001t0001g0269 a0001c0001t0009g0227 others(26): Show |
29 | HG00423.hp2 HG00597.hp1 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.16-6189dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863657 | ||||||
chr7:158863664 | G | GC | 110 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(107): Show |
110 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.16-6191_16-6190ins others(1): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863664 | |||||||
chr7:158863667 | T | G | 3 | a0001c0021t0008g0112 a0008c0007t0008g0113 a0008c0007t0008g0114 |
3 | HG02717.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.16-6188T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863667 | |||||||
chr7:158863669 | T | TG | 5 | a0001c0001t0003g0203 a0001c0001t0003g0225 a0001c0001t0012g0218 others(2): Show |
5 | HG00597.hp2 HG02055.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-6182dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863669 | ||||||
chr7:158863705 | T | TG | 67 | a0001c0001t0001g0270 a0001c0001t0001g0271 a0001c0001t0002g0121 others(64): Show |
67 | HG00423.hp1 HG00438.hp2 HG00544.hp1 others(64): Show |
intron_variant | MODIFIER | c.16-6142dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863705 | ||||||
chr7:158863713 | G | C | 28 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.16-6142G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863713 | |||||||
chr7:158863785 | C | CG | 88 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(85): Show |
88 | HG00408.hp1 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.16-6063dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863785 | ||||||
chr7:158863785 | C | G | 1 | a0001c0001t0002g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.16-6070C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863785 | |||||||
chr7:158863788 | GGGGGAGC others(110): Show |
G | 1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.16-6043_16-5927del | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863788 | ||||||
chr7:158863847 | CGGGTGTT others(3): Show |
C | 22 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(19): Show |
22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.16-5994_16-5985del others(10): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863847 | ||||||
chr7:158863869 | G | T | 9 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(6): Show |
9 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-5986G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158863869 | |||||||
chr7:158863899 | T | TG | 6 | a0001c0001t0002g0135 a0001c0001t0003g0201 a0001c0001t0003g0205 others(3): Show |
6 | HG00544.hp1 HG02698.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-5951dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863899 | ||||||
chr7:158863935 | T | TG | 7 | a0001c0001t0002g0121 a0001c0001t0002g0165 a0001c0001t0002g0174 others(4): Show |
7 | HG00438.hp2 HG01192.hp2 HG02074.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-5915dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158863935 | ||||||
chr7:158864040 | C | CG | 5 | a0001c0001t0002g0129 a0001c0001t0002g0135 a0001c0001t0002g0197 others(2): Show |
5 | HG01192.hp2 NA19001.hp1 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.16-5811dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158864040 | ||||||
chr7:158864045 | T | G | 1 | a0001c0001t0003g0199 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.16-5810T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864045 | |||||||
chr7:158864088 | T | TG | 7 | a0001c0001t0001g0270 a0001c0001t0003g0202 a0001c0001t0003g0203 others(4): Show |
7 | HG00733.hp1 HG01433.hp1 HG02004.hp2 others(4): Show |
intron_variant | MODIFIER | c.16-5761dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158864088 | ||||||
chr7:158864097 | A | C | 128 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(125): Show |
128 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(125): Show |
intron_variant | MODIFIER | c.16-5758A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864097 | |||||||
chr7:158864118 | T | A | 34 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 others(31): Show |
34 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.16-5737T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864118 | |||||||
chr7:158864120 | T | TG | 38 | a0001c0001t0001g0270 a0001c0001t0002g0121 a0001c0001t0002g0128 others(35): Show |
38 | HG00544.hp1 HG00597.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.16-5726dupG | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158864120 | ||||||
chr7:158864123 | G | T | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.16-5732G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864123 | |||||||
chr7:158864134 | G | A | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.16-5721G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864134 | |||||||
chr7:158864351 | CAT | C | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-5503_16-5502del others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864351 | |||||||
chr7:158864537 | T | C | 181 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(178): Show |
181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.16-5318T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864537 | |||||||
chr7:158864568 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.16-5287G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864568 | |||||||
chr7:158864590 | G | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16-5265G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864590 | |||||||
chr7:158864628 | G | A | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.16-5227G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864628 | |||||||
chr7:158864736 | G | A | 1 | a0001c0001t0002g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.16-5119G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864736 | |||||||
chr7:158864921 | G | A | 1 | a0001c0001t0002g0167 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.16-4934G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158864921 | |||||||
chr7:158865173 | C | T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-4682C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158865173 | |||||||
chr7:158865482 | G | T | 1 | a0001c0001t0002g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.16-4373G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158865482 | |||||||
chr7:158865676 | C | G | 1 | a0001c0001t0009g0228 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.16-4179C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158865676 | |||||||
chr7:158865865 | A | C | 2 | a0002c0002t0017g0029 a0002c0016t0001g0018 |
2 | NA18981.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.16-3990A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158865865 | |||||||
chr7:158866102 | T | TAAC | 159 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(156): Show |
159 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.16-3752_16-3750dup others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158866102 | ||||||
chr7:158866125 | A | G | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.16-3730A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866125 | |||||||
chr7:158866225 | C | T | 4 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0008c0007t0008g0113 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-3630C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866225 | |||||||
chr7:158866329 | T | C | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00408.hp1 HG00733.hp1 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.16-3526T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866329 | |||||||
chr7:158866331 | G | C | 1 | a0003c0003t0004g0245 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.16-3524G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866331 | |||||||
chr7:158866884 | C | CA | 19 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(16): Show |
19 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(16): Show |
intron_variant | MODIFIER | c.16-2957dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158866884 | ||||||
chr7:158866914 | A | C | 6 | a0002c0002t0001g0038 a0002c0002t0001g0074 a0002c0002t0001g0075 others(3): Show |
6 | HG01346.hp2 HG01516.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.16-2941A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866914 | |||||||
chr7:158866963 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-2892A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866963 | |||||||
chr7:158866983 | A | G | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.16-2872A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158866983 | |||||||
chr7:158867018 | G | GT | 26 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(23): Show |
26 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.16-2819dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158867018 | ||||||
chr7:158867018 | G | GTT | 9 | a0001c0001t0003g0203 a0001c0001t0003g0214 a0001c0001t0009g0115 others(6): Show |
9 | HG02055.hp2 HG02056.hp2 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.16-2820_16-2819dup others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158867018 | ||||||
chr7:158867018 | GT | G | 120 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(117): Show |
120 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(117): Show |
intron_variant | MODIFIER | c.16-2819delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158867018 | ||||||
chr7:158867128 | G | C | 1 | a0004c0004t0006g0181 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.16-2727G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867128 | |||||||
chr7:158867193 | G | C | 7 | a0003c0003t0004g0256 a0003c0003t0004g0262 a0003c0003t0004g0264 others(4): Show |
7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-2662G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867193 | |||||||
chr7:158867298 | G | A | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.16-2557G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867298 | |||||||
chr7:158867398 | C | T | 1 | a0002c0002t0001g0041 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.16-2457C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867398 | |||||||
chr7:158867436 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-2419G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867436 | |||||||
chr7:158867650 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.16-2205C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867650 | |||||||
chr7:158867682 | T | C | 1 | a0001c0001t0003g0225 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.16-2173T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867682 | |||||||
chr7:158867729 | G | A | 1 | a0012c0015t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.16-2126G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867729 | |||||||
chr7:158867733 | C | T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-2122C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867733 | |||||||
chr7:158867747 | G | C | 1 | a0001c0001t0002g0135 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.16-2108G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867747 | |||||||
chr7:158867749 | C | T | 1 | a0001c0001t0002g0135 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.16-2106C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867749 | |||||||
chr7:158867750 | T | C | 1 | a0001c0001t0002g0135 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.16-2105T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867750 | |||||||
chr7:158867800 | C | T | 23 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(20): Show |
23 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-2055C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867800 | |||||||
chr7:158867891 | C | T | 7 | a0002c0002t0001g0021 a0002c0002t0001g0058 a0002c0002t0001g0059 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.16-1964C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158867891 | |||||||
chr7:158868059 | G | A | 1 | a0001c0001t0006g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.16-1796G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868059 | |||||||
chr7:158868155 | C | G | 23 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(20): Show |
23 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-1700C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868155 | |||||||
chr7:158868232 | C | T | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.16-1623C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868232 | |||||||
chr7:158868277 | C | G | 1 | a0001c0001t0002g0188 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.16-1578C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868277 | |||||||
chr7:158868286 | G | T | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.16-1569G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868286 | |||||||
chr7:158868407 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.16-1448G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868407 | |||||||
chr7:158868572 | C | T | 1 | a0002c0002t0001g0093 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.16-1283C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868572 | |||||||
chr7:158868613 | G | A | 1 | a0002c0002t0001g0020 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.16-1242G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868613 | |||||||
chr7:158868663 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.16-1192G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868663 | |||||||
chr7:158868682 | G | A | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-1173G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868682 | |||||||
chr7:158868964 | G | C | 1 | a0001c0013t0002g0175 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.16-891G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158868964 | |||||||
chr7:158869005 | A | G | 1 | a0002c0002t0001g0047 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.16-850A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869005 | |||||||
chr7:158869067 | G | A | 158 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(155): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.16-788G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869067 | |||||||
chr7:158869146 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.16-709C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869146 | |||||||
chr7:158869215 | CCCCTCTG others(31): Show |
C | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.16-591_16-554delCC others(36): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158869215 | ||||||
chr7:158869237 | G | A | 3 | a0003c0003t0004g0237 a0003c0003t0004g0253 a0003c0003t0004g0257 |
3 | HG01346.hp1 HG01496.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.16-618G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869237 | |||||||
chr7:158869314 | A | T | 4 | a0004c0004t0002g0137 a0004c0004t0002g0138 a0006c0006t0002g0118 others(1): Show |
4 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-541A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869314 | |||||||
chr7:158869340 | C | T | 2 | a0001c0001t0003g0211 a0001c0013t0002g0175 |
2 | HG02129.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.16-515C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869340 | |||||||
chr7:158869446 | C | T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.16-409C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869446 | |||||||
chr7:158869491 | G | A | 24 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(21): Show |
24 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.16-364G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869491 | |||||||
chr7:158869559 | T | C | 23 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(20): Show |
23 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.16-296T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869559 | |||||||
chr7:158869719 | C | A | 9 | a0002c0002t0001g0016 a0002c0002t0001g0019 a0002c0002t0001g0042 others(6): Show |
9 | HG00438.hp1 HG02027.hp1 HG02071.hp2 others(6): Show |
intron_variant | MODIFIER | c.16-136C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869719 | |||||||
chr7:158869740 | C | T | 4 | a0002c0002t0001g0071 a0002c0002t0001g0072 a0002c0002t0001g0099 others(1): Show |
4 | HG01891.hp1 HG02451.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.16-115C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | chr7 | 158869740 | |||||||
chr7:158869820 | T | TTTTAAAC | 161 | a0001c0001t0001g0006 a0001c0001t0002g0003 a0001c0001t0002g0004 others(158): Show |
161 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.16-34_16-28dupTTTA others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 1/24 | INFO_REALIGN_3_PRIME | chr7 | 158869820 | ||||||
chr7:158869986 | A | G | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.69+78A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158869986 | |||||||
chr7:158869998 | CTT | C | 24 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(21): Show |
24 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.69+92_69+93delTT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr7 | 158869998 | ||||||
chr7:158870007 | T | C | 158 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(155): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.69+99T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870007 | |||||||
chr7:158870149 | A | G | 43 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 others(40): Show |
43 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.69+241A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870149 | |||||||
chr7:158870156 | G | A | 1 | a0002c0002t0001g0108 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.69+248G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870156 | |||||||
chr7:158870199 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(6): Show |
9 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.69+291G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870199 | |||||||
chr7:158870218 | G | C | 1 | a0004c0004t0006g0179 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.69+310G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870218 | |||||||
chr7:158870266 | G | A | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.69+358G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870266 | |||||||
chr7:158870362 | C | CT | 8 | a0004c0004t0001g0180 a0004c0004t0002g0137 a0004c0004t0002g0138 others(5): Show |
8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.69+462dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr7 | 158870362 | ||||||
chr7:158870362 | CTT | C | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.69+461_69+462delTT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr7 | 158870362 | ||||||
chr7:158870402 | G | A | 1 | a0003c0003t0004g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.69+494G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870402 | |||||||
chr7:158870516 | C | CTAATTTT others(1): Show |
91 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
91 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.70-600_70-593dupAA others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | INFO_REALIGN_3_PRIME | chr7 | 158870516 | ||||||
chr7:158870540 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.70-602T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870540 | |||||||
chr7:158870551 | C | G | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.70-591C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870551 | |||||||
chr7:158870713 | T | A | 158 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(155): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.70-429T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870713 | |||||||
chr7:158870741 | G | A | 2 | a0002c0002t0001g0109 a0002c0002t0001g0111 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.70-401G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870741 | |||||||
chr7:158870772 | G | A | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.70-370G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158870772 | |||||||
chr7:158871101 | G | A | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.70-41G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 2/24 | chr7 | 158871101 | |||||||
chr7:158871600 | G | C | 1 | a0011c0012t0001g0043 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.490+38G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871600 | |||||||
chr7:158871772 | G | T | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.490+210G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871772 | |||||||
chr7:158871786 | G | A | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.490+224G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871786 | |||||||
chr7:158871791 | C | T | 1 | a0002c0002t0001g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.490+229C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871791 | |||||||
chr7:158871865 | T | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(1): Show |
4 | HG00140.hp1 HG01433.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.490+303T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871865 | |||||||
chr7:158871917 | T | C | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.490+355T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871917 | |||||||
chr7:158871971 | C | T | 3 | a0003c0003t0004g0264 a0003c0003t0004g0266 a0003c0003t0004g0267 |
3 | HG02015.hp1 HG02155.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.490+409C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158871971 | |||||||
chr7:158872015 | T | C | 2 | a0001c0001t0002g0121 a0001c0001t0005g0161 |
2 | HG02015.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.490+453T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872015 | |||||||
chr7:158872231 | C | T | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.490+669C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872231 | |||||||
chr7:158872315 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.490+753C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872315 | |||||||
chr7:158872425 | G | A | 1 | a0003c0003t0004g0241 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.490+863G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872425 | |||||||
chr7:158872507 | T | C | 161 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(158): Show |
161 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.490+945T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872507 | |||||||
chr7:158872530 | T | G | 37 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(34): Show |
37 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(34): Show |
intron_variant | MODIFIER | c.490+968T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872530 | |||||||
chr7:158872549 | T | C | 1 | a0001c0001t0002g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.490+987T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872549 | |||||||
chr7:158872632 | G | GA | 10 | a0001c0001t0001g0006 a0001c0001t0002g0003 a0001c0001t0002g0170 others(7): Show |
10 | HG01257.hp1 HG01516.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.490+1080dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158872632 | ||||||
chr7:158872635 | A | G | 5 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG00140.hp1 HG01433.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.490+1073A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872635 | |||||||
chr7:158872755 | G | T | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490+1193G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872755 | |||||||
chr7:158872804 | C | G | 3 | a0001c0001t0002g0126 a0001c0001t0002g0133 a0001c0001t0002g0158 |
3 | NA18952.hp2 NA19065.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.490+1242C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872804 | |||||||
chr7:158872915 | C | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.490+1353C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872915 | |||||||
chr7:158872947 | C | T | 1 | a0003c0003t0004g0237 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.490+1385C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158872947 | |||||||
chr7:158873027 | C | T | 1 | a0003c0003t0004g0266 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.490+1465C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873027 | |||||||
chr7:158873044 | G | T | 2 | a0002c0002t0001g0109 a0002c0002t0001g0111 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.490+1482G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873044 | |||||||
chr7:158873057 | G | A | 24 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(21): Show |
24 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.490+1495G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873057 | |||||||
chr7:158873175 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.490+1613A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873175 | |||||||
chr7:158873215 | T | G | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.490+1653T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873215 | |||||||
chr7:158873229 | G | A | 7 | a0002c0002t0001g0021 a0002c0002t0001g0058 a0002c0002t0001g0059 others(4): Show |
7 | HG02109.hp1 HG02451.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.490+1667G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873229 | |||||||
chr7:158873272 | T | C | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.490+1710T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873272 | |||||||
chr7:158873296 | C | T | 37 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0021t0008g0112 others(34): Show |
37 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(34): Show |
intron_variant | MODIFIER | c.490+1734C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873296 | |||||||
chr7:158873379 | C | T | 2 | a0001c0001t0009g0115 a0001c0001t0009g0227 |
2 | HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.490+1817C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873379 | |||||||
chr7:158873389 | T | C | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.490+1827T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873389 | |||||||
chr7:158873405 | G | A | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.490+1843G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873405 | |||||||
chr7:158873818 | G | A | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.490+2256G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873818 | |||||||
chr7:158873943 | C | T | 3 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0014g0087 |
3 | HG03017.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.490+2381C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873943 | |||||||
chr7:158873990 | C | G | 1 | a0001c0001t0002g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.490+2428C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158873990 | |||||||
chr7:158874073 | T | TA | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.490+2519dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158874073 | ||||||
chr7:158874078 | A | G | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.490+2516A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874078 | |||||||
chr7:158874209 | A | AT | 32 | a0001c0001t0002g0169 a0001c0001t0002g0172 a0001c0001t0003g0199 others(29): Show |
32 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(29): Show |
intron_variant | MODIFIER | c.491-2384dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158874209 | ||||||
chr7:158874209 | AT | A | 6 | a0001c0001t0002g0197 a0001c0001t0003g0206 a0002c0002t0001g0010 others(3): Show |
6 | HG02615.hp1 HG02922.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-2384delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158874209 | ||||||
chr7:158874488 | C | T | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.491-2121C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874488 | |||||||
chr7:158874522 | G | A | 3 | a0001c0021t0008g0112 a0008c0007t0008g0113 a0008c0007t0008g0114 |
3 | HG02717.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.491-2087G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874522 | |||||||
chr7:158874732 | C | G | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.491-1877C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874732 | |||||||
chr7:158874746 | C | T | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.491-1863C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874746 | |||||||
chr7:158874784 | C | G | 1 | a0001c0001t0002g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.491-1825C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874784 | |||||||
chr7:158874983 | CCAGTCTC others(3): Show |
C | 1 | a0001c0001t0001g0269 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.491-1625_491-1616d others(12): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158874983 | |||||||
chr7:158875067 | G | C | 1 | a0001c0001t0002g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.491-1542G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875067 | |||||||
chr7:158875091 | C | CT | 64 | a0001c0001t0002g0195 a0001c0001t0003g0200 a0001c0001t0003g0201 others(61): Show |
64 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(61): Show |
intron_variant | MODIFIER | c.491-1498dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158875091 | ||||||
chr7:158875091 | C | CTT | 91 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
91 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.491-1499_491-1498d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158875091 | ||||||
chr7:158875091 | C | CTTT | 5 | a0001c0001t0002g0144 a0001c0001t0002g0176 a0001c0001t0002g0193 others(2): Show |
5 | HG02055.hp1 HG02071.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.491-1500_491-1498d others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158875091 | ||||||
chr7:158875091 | CT | C | 55 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0002c0002t0001g0002 others(52): Show |
55 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.491-1498delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | INFO_REALIGN_3_PRIME | chr7 | 158875091 | ||||||
chr7:158875149 | G | T | 1 | a0001c0001t0002g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.491-1460G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875149 | |||||||
chr7:158875244 | G | A | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.491-1365G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875244 | |||||||
chr7:158875249 | G | C | 175 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(172): Show |
175 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(172): Show |
intron_variant | MODIFIER | c.491-1360G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875249 | |||||||
chr7:158875394 | G | T | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.491-1215G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875394 | |||||||
chr7:158875509 | T | A | 1 | a0001c0001t0002g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.491-1100T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875509 | |||||||
chr7:158875531 | C | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.491-1078C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875531 | |||||||
chr7:158875592 | C | T | 2 | a0001c0001t0002g0135 a0001c0001t0002g0194 |
2 | NA18961.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.491-1017C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875592 | |||||||
chr7:158875593 | G | T | 5 | a0003c0003t0004g0256 a0003c0003t0004g0264 a0003c0003t0004g0265 others(2): Show |
5 | HG02015.hp1 HG02155.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.491-1016G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875593 | |||||||
chr7:158875822 | C | T | 74 | a0001c0001t0002g0117 a0001c0001t0002g0119 a0001c0001t0002g0120 others(71): Show |
74 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.491-787C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875822 | |||||||
chr7:158875833 | G | A | 1 | a0001c0001t0002g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.491-776G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875833 | |||||||
chr7:158875835 | C | T | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.491-774C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875835 | |||||||
chr7:158875854 | G | A | 8 | a0002c0002t0001g0038 a0002c0002t0001g0062 a0002c0002t0001g0074 others(5): Show |
8 | HG01123.hp2 HG01243.hp1 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.491-755G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875854 | |||||||
chr7:158875884 | T | C | 158 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(155): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.491-725T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158875884 | |||||||
chr7:158876096 | T | C | 3 | a0001c0021t0008g0112 a0008c0007t0008g0113 a0008c0007t0008g0114 |
3 | HG02717.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.491-513T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876096 | |||||||
chr7:158876156 | A | G | 1 | a0001c0001t0002g0188 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.491-453A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876156 | |||||||
chr7:158876346 | A | G | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.491-263A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876346 | |||||||
chr7:158876359 | G | A | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.491-250G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876359 | |||||||
chr7:158876398 | T | C | 1 | a0002c0002t0014g0087 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.491-211T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876398 | |||||||
chr7:158876509 | C | T | 1 | a0002c0002t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.491-100C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 3/24 | chr7 | 158876509 | |||||||
chr7:158876756 | T | C | 1 | a0001c0001t0002g0191 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.573+65T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158876756 | |||||||
chr7:158876921 | A | C | 1 | a0002c0002t0001g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.573+230A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158876921 | |||||||
chr7:158876960 | A | C | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.573+269A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158876960 | |||||||
chr7:158877155 | G | C | 2 | a0001c0001t0003g0206 a0001c0001t0003g0216 |
2 | NA18957.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.573+464G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877155 | |||||||
chr7:158877167 | CAGGCACC others(48): Show |
C | 2 | a0001c0001t0002g0145 a0001c0001t0002g0162 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.573+510_573+564del others(55): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158877167 | ||||||
chr7:158877196 | C | CGCGGTGC others(103): Show |
1 | a0001c0001t0002g0141 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.573+558_573+559ins others(110): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158877196 | ||||||
chr7:158877278 | A | C | 7 | a0003c0003t0004g0256 a0003c0003t0004g0262 a0003c0003t0004g0264 others(4): Show |
7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.573+587A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877278 | |||||||
chr7:158877401 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.573+710C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877401 | |||||||
chr7:158877406 | A | G | 1 | a0001c0001t0019g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.573+715A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877406 | |||||||
chr7:158877427 | G | A | 1 | a0002c0002t0001g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.573+736G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877427 | |||||||
chr7:158877552 | T | C | 167 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(164): Show |
167 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(164): Show |
intron_variant | MODIFIER | c.573+861T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877552 | |||||||
chr7:158877577 | C | T | 1 | a0002c0002t0001g0052 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.573+886C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877577 | |||||||
chr7:158877631 | G | T | 1 | a0002c0002t0001g0097 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.573+940G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877631 | |||||||
chr7:158877778 | C | G | 1 | a0001c0001t0002g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.573+1087C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877778 | |||||||
chr7:158877799 | T | C | 4 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0008c0007t0008g0113 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.573+1108T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877799 | |||||||
chr7:158877945 | C | T | 1 | a0002c0002t0001g0051 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.573+1254C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158877945 | |||||||
chr7:158878006 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.573+1315C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878006 | |||||||
chr7:158878112 | GGGGAGGC others(47): Show |
G | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.573+1425_573+1478d others(56): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878112 | ||||||
chr7:158878138 | G | C | 2 | a0001c0001t0005g0190 a0001c0001t0005g0192 |
2 | HG00544.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.573+1447G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878138 | |||||||
chr7:158878175 | G | A | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.573+1484G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878175 | |||||||
chr7:158878185 | A | G | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.573+1494A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878185 | |||||||
chr7:158878197 | C | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.574-1487C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878197 | |||||||
chr7:158878210 | CGGGTGCT others(35): Show |
C | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.574-1467_574-1426d others(44): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878210 | ||||||
chr7:158878293 | C | T | 3 | a0002c0002t0001g0002 a0002c0002t0001g0047 a0002c0002t0001g0105 |
3 | HG01358.hp2 NA18939.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.574-1391C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878293 | |||||||
chr7:158878420 | C | T | 6 | a0002c0002t0001g0026 a0002c0002t0001g0054 a0002c0002t0001g0055 others(3): Show |
6 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.574-1264C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878420 | |||||||
chr7:158878425 | G | A | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.574-1259G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878425 | |||||||
chr7:158878434 | G | A | 1 | a0002c0002t0001g0020 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.574-1250G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878434 | |||||||
chr7:158878436 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.574-1248G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878436 | |||||||
chr7:158878437 | C | T | 72 | a0001c0001t0002g0187 a0002c0002t0001g0002 a0002c0002t0001g0013 others(69): Show |
72 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(69): Show |
intron_variant | MODIFIER | c.574-1247C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878437 | |||||||
chr7:158878471 | GTGCCGGG others(132): Show |
G | 1 | a0002c0002t0001g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.574-1195_574-1057d others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878471 | ||||||
chr7:158878514 | T | A | 217 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(214): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.574-1170T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878514 | |||||||
chr7:158878516 | CCGGGCGC others(35): Show |
C | 8 | a0002c0002t0001g0001 a0002c0002t0001g0035 a0002c0002t0001g0039 others(5): Show |
8 | HG00408.hp2 HG02027.hp2 NA18948.hp2 others(5): Show |
intron_variant | MODIFIER | c.574-1150_574-1109d others(44): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878516 | ||||||
chr7:158878518 | G | A | 136 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(133): Show |
136 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.574-1166G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878518 | |||||||
chr7:158878556 | T | C | 1 | a0001c0001t0002g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.574-1128T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878556 | |||||||
chr7:158878563 | C | T | 3 | a0001c0001t0002g0140 a0001c0001t0002g0151 a0001c0022t0018g0229 |
3 | NA18948.hp1 NA18974.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.574-1121C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878563 | |||||||
chr7:158878602 | G | A | 2 | a0001c0001t0006g0007 a0001c0001t0006g0008 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.574-1082G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878602 | |||||||
chr7:158878618 | T | C | 1 | a0002c0002t0001g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.574-1066T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878618 | |||||||
chr7:158878630 | A | T | 1 | a0002c0002t0001g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.574-1054A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878630 | |||||||
chr7:158878647 | T | A | 1 | a0002c0002t0001g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.574-1037T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878647 | |||||||
chr7:158878648 | C | G | 1 | a0002c0002t0001g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.574-1036C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878648 | |||||||
chr7:158878730 | CTG | C | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.574-951_574-950del others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878730 | ||||||
chr7:158878732 | G | C | 7 | a0003c0003t0004g0256 a0003c0003t0004g0262 a0003c0003t0004g0264 others(4): Show |
7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.574-952G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878732 | |||||||
chr7:158878740 | C | T | 1 | a0004c0004t0001g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-944C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878740 | |||||||
chr7:158878783 | G | A | 1 | a0004c0004t0006g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.574-901G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878783 | |||||||
chr7:158878785 | C | T | 2 | a0002c0002t0001g0010 a0002c0002t0001g0057 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.574-899C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878785 | |||||||
chr7:158878826 | A | G | 23 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(20): Show |
23 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(20): Show |
intron_variant | MODIFIER | c.574-858A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878826 | |||||||
chr7:158878853 | T | TGGCCAGG others(119): Show |
22 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(19): Show |
22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.574-764_574-763ins others(126): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878853 | ||||||
chr7:158878884 | ACCATGTG others(90): Show |
A | 1 | a0008c0007t0008g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.574-749_574-653del others(97): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | INFO_REALIGN_3_PRIME | chr7 | 158878884 | ||||||
chr7:158878941 | G | A | 2 | a0001c0001t0002g0157 a0001c0001t0002g0167 |
2 | NA18969.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.574-743G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878941 | |||||||
chr7:158878976 | C | T | 5 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0021t0008g0112 others(2): Show |
5 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.574-708C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878976 | |||||||
chr7:158878977 | G | C | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.574-707G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878977 | |||||||
chr7:158878988 | G | C | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.574-696G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158878988 | |||||||
chr7:158879050 | C | T | 1 | a0001c0001t0002g0121 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.574-634C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879050 | |||||||
chr7:158879099 | C | T | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.574-585C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879099 | |||||||
chr7:158879442 | A | G | 1 | a0008c0007t0008g0114 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.574-242A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879442 | |||||||
chr7:158879531 | A | G | 2 | a0002c0002t0001g0019 a0002c0002t0001g0094 |
2 | NA18985.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.574-153A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879531 | |||||||
chr7:158879581 | C | T | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.574-103C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879581 | |||||||
chr7:158879582 | G | A | 1 | a0004c0004t0001g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.574-102G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879582 | |||||||
chr7:158879601 | G | A | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.574-83G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879601 | |||||||
chr7:158879610 | C | A | 1 | a0002c0002t0001g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.574-74C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 4/24 | chr7 | 158879610 | |||||||
chr7:158880037 | C | T | 1 | a0012c0015t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.879+48C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880037 | |||||||
chr7:158880057 | C | T | 1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.879+68C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880057 | |||||||
chr7:158880255 | G | A | 1 | a0001c0013t0002g0175 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.879+266G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880255 | |||||||
chr7:158880353 | A | G | 1 | a0004c0004t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.879+364A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880353 | |||||||
chr7:158880570 | A | T | 2 | a0001c0001t0002g0160 a0015c0017t0001g0083 |
2 | HG01433.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.879+581A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880570 | |||||||
chr7:158880913 | A | G | 168 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(165): Show |
168 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.879+924A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158880913 | |||||||
chr7:158881160 | G | A | 2 | a0001c0001t0003g0206 a0001c0001t0003g0216 |
2 | NA18957.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.879+1171G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881160 | |||||||
chr7:158881169 | G | A | 6 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0001c0021t0008g0112 others(3): Show |
6 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.879+1180G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881169 | |||||||
chr7:158881675 | A | C | 1 | a0001c0001t0002g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.879+1686A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881675 | |||||||
chr7:158881733 | A | G | 1 | a0003c0029t0004g0249 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.879+1744A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881733 | |||||||
chr7:158881830 | C | G | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.879+1841C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881830 | |||||||
chr7:158881873 | T | C | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.879+1884T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158881873 | |||||||
chr7:158882066 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.879+2077G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882066 | |||||||
chr7:158882288 | A | C | 1 | a0001c0001t0002g0197 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.880-2276A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882288 | |||||||
chr7:158882400 | A | G | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-2164A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882400 | |||||||
chr7:158882559 | C | T | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.880-2005C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882559 | |||||||
chr7:158882575 | C | G | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.880-1989C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882575 | |||||||
chr7:158882625 | C | G | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-1939C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882625 | |||||||
chr7:158882708 | A | G | 1 | a0002c0002t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.880-1856A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882708 | |||||||
chr7:158882734 | A | G | 40 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(37): Show |
40 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.880-1830A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882734 | |||||||
chr7:158882873 | C | CT | 13 | a0003c0003t0004g0241 a0003c0003t0004g0243 a0003c0003t0004g0244 others(10): Show |
13 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.880-1690dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158882873 | ||||||
chr7:158882875 | C | A | 13 | a0003c0003t0004g0241 a0003c0003t0004g0243 a0003c0003t0004g0244 others(10): Show |
13 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(10): Show |
intron_variant | MODIFIER | c.880-1689C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882875 | |||||||
chr7:158882875 | C | CA | 21 | a0002c0002t0001g0028 a0002c0002t0001g0110 a0003c0003t0004g0237 others(18): Show |
21 | HG00140.hp2 HG01071.hp2 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.880-1673dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158882875 | ||||||
chr7:158882875 | CA | C | 120 | a0001c0001t0001g0006 a0001c0001t0002g0003 a0001c0001t0002g0004 others(117): Show |
120 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.880-1673delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158882875 | ||||||
chr7:158882971 | C | T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.880-1593C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158882971 | |||||||
chr7:158883209 | TTTC | T | 3 | a0001c0001t0013g0116 a0003c0003t0007g0239 a0003c0003t0007g0240 |
3 | HG00408.hp1 HG02080.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.880-1346_880-1344d others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883209 | ||||||
chr7:158883218 | CT | C | 43 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(40): Show |
43 | HG00140.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.880-1329delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883218 | ||||||
chr7:158883221 | T | C | 1 | a0001c0001t0002g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.880-1343T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883221 | |||||||
chr7:158883257 | G | A | 2 | a0001c0001t0005g0190 a0001c0001t0005g0192 |
2 | HG00544.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.880-1307G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883257 | |||||||
chr7:158883382 | A | AT | 30 | a0001c0001t0002g0125 a0001c0001t0002g0191 a0001c0001t0003g0215 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00544.hp2 others(27): Show |
intron_variant | MODIFIER | c.880-1168dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883382 | ||||||
chr7:158883384 | T | TA | 5 | a0003c0003t0004g0256 a0003c0003t0004g0264 a0003c0003t0004g0265 others(2): Show |
5 | HG02015.hp1 HG02155.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.880-1180_880-1179i others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883384 | |||||||
chr7:158883385 | T | A | 8 | a0001c0001t0001g0006 a0001c0001t0002g0145 a0001c0001t0002g0146 others(5): Show |
8 | HG01167.hp2 HG01169.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.880-1179T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883385 | |||||||
chr7:158883415 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.880-1149C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883415 | |||||||
chr7:158883484 | C | T | 4 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0008c0007t0008g0113 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.880-1080C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883484 | |||||||
chr7:158883513 | T | C | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.880-1051T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883513 | |||||||
chr7:158883586 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.880-978A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883586 | |||||||
chr7:158883598 | T | TAGAA | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.880-963_880-962ins others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883598 | ||||||
chr7:158883631 | T | C | 1 | a0001c0001t0002g0123 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.880-933T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883631 | |||||||
chr7:158883658 | C | CT | 14 | a0001c0001t0001g0271 a0002c0002t0001g0016 a0002c0002t0001g0021 others(11): Show |
14 | HG01175.hp1 HG02080.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.880-883dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883658 | ||||||
chr7:158883658 | CT | C | 146 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(143): Show |
146 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.880-883delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883658 | ||||||
chr7:158883658 | CTT | C | 5 | a0001c0001t0002g0162 a0001c0001t0009g0115 a0001c0001t0009g0227 others(2): Show |
5 | HG01169.hp1 HG01496.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-884_880-883del others(2): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158883658 | ||||||
chr7:158883686 | C | T | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.880-878C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883686 | |||||||
chr7:158883818 | C | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.880-746C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883818 | |||||||
chr7:158883821 | A | G | 159 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(156): Show |
159 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.880-743A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883821 | |||||||
chr7:158883857 | A | G | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.880-707A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883857 | |||||||
chr7:158883944 | G | A | 1 | a0003c0010t0011g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.880-620G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158883944 | |||||||
chr7:158884004 | G | A | 1 | a0001c0001t0002g0125 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.880-560G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884004 | |||||||
chr7:158884046 | A | AT | 27 | a0001c0001t0001g0006 a0001c0001t0013g0116 a0003c0003t0004g0237 others(24): Show |
27 | HG00408.hp1 HG01071.hp2 HG01175.hp2 others(24): Show |
intron_variant | MODIFIER | c.880-502dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158884046 | ||||||
chr7:158884046 | AT | A | 10 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(7): Show |
10 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(7): Show |
intron_variant | MODIFIER | c.880-502delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158884046 | ||||||
chr7:158884075 | C | T | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.880-489C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884075 | |||||||
chr7:158884083 | C | T | 2 | a0002c0002t0001g0109 a0002c0002t0001g0111 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.880-481C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884083 | |||||||
chr7:158884205 | C | T | 3 | a0001c0021t0008g0112 a0008c0007t0008g0113 a0008c0007t0008g0114 |
3 | HG02717.hp1 HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.880-359C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884205 | |||||||
chr7:158884256 | G | T | 1 | a0001c0001t0002g0163 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.880-308G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884256 | |||||||
chr7:158884410 | TAACTGGT others(3): Show |
T | 3 | a0002c0002t0001g0058 a0002c0002t0001g0101 a0002c0005t0010g0100 |
3 | HG02451.hp2 HG02486.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.880-151_880-142del others(10): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | INFO_REALIGN_3_PRIME | chr7 | 158884410 | ||||||
chr7:158884453 | A | G | 1 | a0001c0001t0002g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.880-111A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884453 | |||||||
chr7:158884510 | A | G | 1 | a0001c0001t0002g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.880-54A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 5/24 | chr7 | 158884510 | |||||||
chr7:158884799 | C | T | 1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.935+180C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158884799 | |||||||
chr7:158885112 | C | T | 8 | a0004c0004t0001g0180 a0004c0004t0002g0137 a0004c0004t0002g0138 others(5): Show |
8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.935+493C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885112 | |||||||
chr7:158885137 | A | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.935+518A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885137 | |||||||
chr7:158885303 | G | A | 7 | a0003c0003t0004g0256 a0003c0003t0004g0262 a0003c0003t0004g0264 others(4): Show |
7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.935+684G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885303 | |||||||
chr7:158885345 | C | CT | 16 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(13): Show |
16 | HG00099.hp1 HG00140.hp1 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.935+740dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr7 | 158885345 | ||||||
chr7:158885430 | C | G | 1 | a0001c0001t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.935+811C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885430 | |||||||
chr7:158885494 | A | G | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.935+875A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885494 | |||||||
chr7:158885613 | A | AT | 75 | a0001c0001t0002g0117 a0001c0001t0002g0119 a0001c0001t0002g0120 others(72): Show |
75 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.935+996dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | INFO_REALIGN_3_PRIME | chr7 | 158885613 | ||||||
chr7:158885794 | A | G | 5 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(2): Show |
5 | HG02055.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.935+1175A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885794 | |||||||
chr7:158885915 | C | G | 4 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0008c0007t0008g0113 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.936-1106C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158885915 | |||||||
chr7:158886048 | T | C | 2 | a0003c0003t0004g0243 a0003c0003t0004g0246 |
2 | HG01255.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.936-973T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886048 | |||||||
chr7:158886398 | T | C | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.936-623T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886398 | |||||||
chr7:158886430 | G | A | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.936-591G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886430 | |||||||
chr7:158886434 | G | A | 1 | a0003c0010t0011g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.936-587G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886434 | |||||||
chr7:158886505 | T | C | 1 | a0002c0002t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.936-516T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886505 | |||||||
chr7:158886639 | T | A | 1 | a0002c0002t0001g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.936-382T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886639 | |||||||
chr7:158886862 | A | G | 4 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0008c0007t0008g0113 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.936-159A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886862 | |||||||
chr7:158886928 | T | C | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.936-93T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886928 | |||||||
chr7:158886949 | AT | A | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.936-71delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 6/24 | chr7 | 158886949 | |||||||
chr7:158887130 | A | G | 2 | a0001c0001t0002g0157 a0001c0001t0002g0167 |
2 | NA18969.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.990+55A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887130 | |||||||
chr7:158887167 | C | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.990+92C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887167 | |||||||
chr7:158887224 | G | A | 1 | a0002c0002t0001g0010 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.990+149G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887224 | |||||||
chr7:158887252 | AATTG | A | 96 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(93): Show |
96 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(93): Show |
intron_variant | MODIFIER | c.990+183_990+186del others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158887252 | ||||||
chr7:158887487 | T | C | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.990+412T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887487 | |||||||
chr7:158887506 | A | G | 7 | a0003c0003t0004g0256 a0003c0003t0004g0262 a0003c0003t0004g0264 others(4): Show |
7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.990+431A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887506 | |||||||
chr7:158887958 | G | C | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.990+883G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887958 | |||||||
chr7:158887987 | T | C | 1 | a0002c0002t0001g0009 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.990+912T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158887987 | |||||||
chr7:158888019 | C | CT | 42 | a0001c0001t0001g0006 a0001c0001t0001g0271 a0001c0001t0002g0003 others(39): Show |
42 | HG00423.hp1 HG00621.hp1 HG01175.hp1 others(39): Show |
intron_variant | MODIFIER | c.990+968dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888019 | ||||||
chr7:158888019 | C | CTTTT | 19 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(16): Show |
19 | HG00140.hp2 HG00733.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.990+965_990+968dup others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888019 | ||||||
chr7:158888019 | C | CTTTTT | 11 | a0003c0003t0004g0244 a0003c0003t0004g0251 a0003c0003t0004g0258 others(8): Show |
11 | HG00408.hp1 HG01175.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.990+964_990+968dup others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888019 | ||||||
chr7:158888019 | CT | C | 7 | a0001c0001t0002g0176 a0001c0001t0002g0186 a0001c0001t0003g0206 others(4): Show |
7 | HG01255.hp2 HG02683.hp2 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.990+968delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888019 | ||||||
chr7:158888114 | T | C | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+1039T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888114 | |||||||
chr7:158888185 | C | T | 4 | a0004c0004t0001g0180 a0004c0004t0006g0178 a0004c0004t0006g0179 others(1): Show |
4 | HG02818.hp1 HG03486.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+1110C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888185 | |||||||
chr7:158888297 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.990+1222A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888297 | |||||||
chr7:158888410 | G | A | 1 | a0001c0001t0002g0198 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.990+1335G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888410 | |||||||
chr7:158888468 | C | CAT | 11 | a0001c0001t0002g0233 a0001c0001t0005g0142 a0001c0001t0009g0115 others(8): Show |
11 | HG01175.hp2 HG01255.hp1 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.990+1409_990+1410d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888468 | ||||||
chr7:158888618 | C | T | 6 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0021t0008g0112 others(3): Show |
6 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.990+1543C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888618 | |||||||
chr7:158888630 | C | G | 1 | a0001c0001t0001g0269 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.990+1555C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888630 | |||||||
chr7:158888808 | C | T | 6 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0021t0008g0112 others(3): Show |
6 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.990+1733C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888808 | |||||||
chr7:158888850 | CTGT | C | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+1780_990+1782d others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158888850 | ||||||
chr7:158888918 | G | A | 4 | a0001c0001t0002g0122 a0001c0001t0002g0163 a0001c0001t0002g0171 others(1): Show |
4 | NA18939.hp2 NA18954.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+1843G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888918 | |||||||
chr7:158888966 | T | C | 2 | a0002c0002t0001g0109 a0002c0002t0001g0111 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.990+1891T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158888966 | |||||||
chr7:158889036 | T | TAC | 5 | a0002c0002t0001g0009 a0002c0002t0001g0071 a0002c0002t0001g0082 others(2): Show |
5 | HG01123.hp2 HG01891.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.990+1990_990+1991d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | ||||||
chr7:158889036 | T | TACAC | 3 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0002c0002t0001g0072 |
3 | HG02451.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.990+1988_990+1991d others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | ||||||
chr7:158889036 | T | TACACACA others(3): Show |
4 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0271 others(1): Show |
4 | HG00140.hp1 HG01934.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.990+1982_990+1991d others(12): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | ||||||
chr7:158889036 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.990+1980_990+1991d others(14): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | ||||||
chr7:158889036 | TAC | T | 13 | a0001c0001t0002g0133 a0001c0001t0003g0214 a0001c0021t0008g0112 others(10): Show |
13 | HG01255.hp2 HG01257.hp2 HG02004.hp2 others(10): Show |
intron_variant | MODIFIER | c.990+1990_990+1991d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | ||||||
chr7:158889036 | TACAC | T | 115 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(112): Show |
115 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(112): Show |
intron_variant | MODIFIER | c.990+1988_990+1991d others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | ||||||
chr7:158889036 | TACACAC | T | 3 | a0003c0003t0004g0264 a0003c0003t0004g0266 a0003c0003t0004g0267 |
3 | HG02015.hp1 HG02155.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.990+1986_990+1991d others(8): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | ||||||
chr7:158889036 | TACACACA others(1): Show |
T | 28 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(25): Show |
28 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.990+1984_990+1991d others(10): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889036 | ||||||
chr7:158889065 | A | C | 2 | a0002c0002t0001g0014 a0002c0002t0001g0027 |
2 | HG01255.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.990+1990A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889065 | |||||||
chr7:158889080 | C | CT | 11 | a0001c0001t0002g0166 a0001c0001t0002g0168 a0001c0001t0002g0184 others(8): Show |
11 | HG00408.hp2 HG00741.hp2 HG01099.hp2 others(8): Show |
intron_variant | MODIFIER | c.990+2023dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889080 | ||||||
chr7:158889080 | CT | C | 34 | a0001c0001t0005g0139 a0001c0001t0009g0115 a0001c0001t0009g0227 others(31): Show |
34 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.990+2023delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889080 | ||||||
chr7:158889083 | T | C | 6 | a0001c0001t0002g0124 a0001c0001t0002g0134 a0001c0001t0002g0147 others(3): Show |
6 | HG02165.hp2 NA18942.hp1 NA18982.hp2 others(3): Show |
intron_variant | MODIFIER | c.990+2008T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889083 | |||||||
chr7:158889085 | T | C | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.990+2010T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889085 | |||||||
chr7:158889086 | T | C | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.990+2011T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889086 | |||||||
chr7:158889151 | G | T | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.990+2076G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889151 | |||||||
chr7:158889157 | TGCAAGCT others(5): Show |
T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.990+2083_990+2094d others(14): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889157 | |||||||
chr7:158889174 | G | A | 2 | a0003c0003t0004g0243 a0003c0003t0004g0246 |
2 | HG01255.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.991-2091G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889174 | |||||||
chr7:158889421 | G | A | 1 | a0003c0003t0007g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.991-1844G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889421 | |||||||
chr7:158889428 | C | T | 1 | a0002c0002t0001g0093 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.991-1837C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889428 | |||||||
chr7:158889436 | A | T | 31 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.991-1829A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889436 | |||||||
chr7:158889442 | C | T | 1 | a0001c0001t0019g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.991-1823C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889442 | |||||||
chr7:158889692 | AAAC | A | 4 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0008c0007t0008g0113 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-1558_991-1556d others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889692 | ||||||
chr7:158889794 | A | G | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.991-1471A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158889794 | |||||||
chr7:158889835 | TCTCTA | T | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-1426_991-1422d others(7): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158889835 | ||||||
chr7:158890005 | C | CA | 112 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(109): Show |
112 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.991-1236dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158890005 | ||||||
chr7:158890005 | C | CAA | 7 | a0001c0001t0002g0122 a0001c0001t0002g0136 a0003c0003t0004g0262 others(4): Show |
7 | HG00733.hp1 HG02055.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.991-1237_991-1236d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158890005 | ||||||
chr7:158890005 | CA | C | 23 | a0001c0001t0003g0224 a0001c0022t0018g0229 a0002c0002t0001g0013 others(20): Show |
23 | HG00438.hp1 HG01257.hp1 HG01257.hp2 others(20): Show |
intron_variant | MODIFIER | c.991-1236delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | INFO_REALIGN_3_PRIME | chr7 | 158890005 | ||||||
chr7:158890111 | G | C | 7 | a0003c0003t0004g0256 a0003c0003t0004g0262 a0003c0003t0004g0264 others(4): Show |
7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.991-1154G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890111 | |||||||
chr7:158890226 | A | C | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.991-1039A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890226 | |||||||
chr7:158890331 | G | A | 7 | a0003c0003t0004g0256 a0003c0003t0004g0262 a0003c0003t0004g0264 others(4): Show |
7 | HG02015.hp1 HG02055.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.991-934G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890331 | |||||||
chr7:158890488 | G | T | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.991-777G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890488 | |||||||
chr7:158890628 | G | A | 1 | a0002c0002t0001g0105 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.991-637G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890628 | |||||||
chr7:158890717 | G | A | 1 | a0004c0004t0002g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.991-548G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890717 | |||||||
chr7:158890893 | G | A | 57 | a0002c0002t0001g0002 a0002c0002t0001g0011 a0002c0002t0001g0012 others(54): Show |
57 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(54): Show |
intron_variant | MODIFIER | c.991-372G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890893 | |||||||
chr7:158890991 | C | T | 1 | a0001c0001t0002g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.991-274C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158890991 | |||||||
chr7:158891000 | C | G | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.991-265C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158891000 | |||||||
chr7:158891112 | G | T | 4 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0008c0007t0008g0113 others(1): Show |
4 | HG02717.hp1 HG02809.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.991-153G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158891112 | |||||||
chr7:158891134 | T | C | 169 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(166): Show |
169 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(166): Show |
intron_variant | MODIFIER | c.991-131T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158891134 | |||||||
chr7:158891190 | G | C | 2 | a0001c0001t0002g0154 a0001c0001t0013g0116 |
2 | HG02080.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.991-75G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 7/24 | chr7 | 158891190 | |||||||
chr7:158891392 | A | T | 1 | a0002c0002t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1059+59A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891392 | |||||||
chr7:158891461 | A | G | 98 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(95): Show |
98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1059+128A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891461 | |||||||
chr7:158891494 | C | T | 3 | a0002c0002t0001g0010 a0002c0002t0001g0057 a0012c0015t0001g0056 |
3 | HG02615.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1059+161C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891494 | |||||||
chr7:158891582 | C | T | 15 | a0003c0003t0004g0241 a0003c0003t0004g0243 a0003c0003t0004g0244 others(12): Show |
15 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1059+249C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891582 | |||||||
chr7:158891583 | G | A | 1 | a0003c0003t0004g0237 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1059+250G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891583 | |||||||
chr7:158891613 | A | G | 6 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0021t0008g0112 others(3): Show |
6 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1059+280A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891613 | |||||||
chr7:158891678 | C | A | 1 | a0001c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1059+345C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891678 | |||||||
chr7:158891855 | AAGGGAAG others(63): Show |
A | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+556_1059+625d others(72): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158891855 | ||||||
chr7:158891920 | C | T | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1059+587C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891920 | |||||||
chr7:158891998 | C | T | 1 | a0001c0001t0002g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1059+665C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158891998 | |||||||
chr7:158892025 | G | C | 1 | a0002c0002t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1059+692G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892025 | |||||||
chr7:158892302 | G | T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1059+969G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892302 | |||||||
chr7:158892321 | A | G | 1 | a0007c0009t0020g0222 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1059+988A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892321 | |||||||
chr7:158892404 | A | G | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+1071A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892404 | |||||||
chr7:158892485 | A | T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1059+1152A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892485 | |||||||
chr7:158892509 | A | G | 1 | a0002c0002t0001g0049 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1059+1176A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892509 | |||||||
chr7:158892566 | T | C | 157 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(154): Show |
157 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1059+1233T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892566 | |||||||
chr7:158892615 | A | AT | 97 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(94): Show |
97 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.1059+1292dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158892615 | ||||||
chr7:158892717 | G | T | 1 | a0001c0001t0005g0142 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1059+1384G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892717 | |||||||
chr7:158892805 | G | A | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+1472G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892805 | |||||||
chr7:158892812 | G | A | 1 | a0001c0001t0006g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1059+1479G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892812 | |||||||
chr7:158892907 | T | C | 157 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(154): Show |
157 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1059+1574T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892907 | |||||||
chr7:158892938 | C | CA | 15 | a0002c0002t0001g0027 a0002c0002t0001g0028 a0003c0003t0004g0241 others(12): Show |
15 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.1059+1623dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158892938 | ||||||
chr7:158892938 | CA | C | 120 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(117): Show |
120 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(117): Show |
intron_variant | MODIFIER | c.1059+1623delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158892938 | ||||||
chr7:158892962 | A | G | 2 | a0008c0007t0008g0113 a0008c0007t0008g0114 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1059+1629A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158892962 | |||||||
chr7:158893167 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1059+1834C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893167 | |||||||
chr7:158893215 | A | G | 1 | a0002c0002t0001g0013 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1059+1882A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893215 | |||||||
chr7:158893291 | G | T | 1 | a0001c0001t0002g0186 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1059+1958G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893291 | |||||||
chr7:158893379 | T | A | 1 | a0003c0003t0004g0256 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1059+2046T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893379 | |||||||
chr7:158893646 | C | T | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+2313C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893646 | |||||||
chr7:158893663 | C | T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1059+2330C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893663 | |||||||
chr7:158893699 | T | TGCATATC others(5): Show |
4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1059+2367_1059+237 others(16): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158893699 | ||||||
chr7:158893718 | C | T | 1 | a0001c0001t0006g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1059+2385C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893718 | |||||||
chr7:158893863 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1059+2530G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893863 | |||||||
chr7:158893928 | A | G | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+2595A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893928 | |||||||
chr7:158893935 | T | A | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+2602T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158893935 | |||||||
chr7:158894004 | C | T | 85 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(82): Show |
85 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1059+2671C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894004 | |||||||
chr7:158894089 | G | A | 1 | a0001c0001t0003g0199 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1059+2756G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894089 | |||||||
chr7:158894112 | T | C | 1 | a0002c0002t0001g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1059+2779T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894112 | |||||||
chr7:158894112 | T | TGCATATC others(5): Show |
1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1059+2787_1059+279 others(16): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894112 | ||||||
chr7:158894112 | T | TGCATATC others(17): Show |
4 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0002c0002t0001g0046 others(1): Show |
4 | HG00642.hp2 HG01496.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1059+2798_1059+279 others(28): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894112 | ||||||
chr7:158894120 | C | CTACCGCA others(17): Show |
125 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(122): Show |
125 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(122): Show |
intron_variant | MODIFIER | c.1059+2798_1059+279 others(28): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894120 | ||||||
chr7:158894120 | C | CTACTGCA others(17): Show |
2 | a0002c0002t0001g0095 a0002c0002t0001g0096 |
2 | NA18943.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1059+2790_1059+279 others(28): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894120 | ||||||
chr7:158894120 | C | CTACTGCA others(17): Show |
3 | a0003c0003t0004g0264 a0003c0003t0004g0266 a0003c0003t0004g0267 |
3 | HG02015.hp1 HG02155.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.1059+2790_1059+279 others(28): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894120 | ||||||
chr7:158894132 | A | ATACCGCA others(5): Show |
12 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(9): Show |
12 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.1059+2804_1059+281 others(16): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894132 | ||||||
chr7:158894132 | A | ATACCGCA others(17): Show |
102 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(99): Show |
102 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.1059+2815_1059+281 others(28): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894132 | ||||||
chr7:158894172 | G | C | 3 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0014g0087 |
3 | HG03017.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.1059+2839G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894172 | |||||||
chr7:158894182 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1059+2849G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894182 | |||||||
chr7:158894216 | GCATATCC others(53): Show |
G | 1 | a0003c0029t0004g0249 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1059+2887_1059+294 others(64): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894216 | ||||||
chr7:158894463 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1059+3130T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894463 | |||||||
chr7:158894824 | C | T | 2 | a0002c0002t0001g0109 a0002c0002t0001g0111 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1059+3491C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158894824 | |||||||
chr7:158894865 | GT | G | 121 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(118): Show |
121 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1059+3534delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158894865 | ||||||
chr7:158895102 | T | G | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1059+3769T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895102 | |||||||
chr7:158895118 | T | C | 1 | a0001c0001t0012g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1059+3785T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895118 | |||||||
chr7:158895136 | A | G | 1 | a0002c0002t0001g0011 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1059+3803A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895136 | |||||||
chr7:158895184 | G | T | 1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1059+3851G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895184 | |||||||
chr7:158895236 | C | G | 1 | a0001c0001t0002g0194 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1059+3903C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895236 | |||||||
chr7:158895307 | C | T | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+3974C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895307 | |||||||
chr7:158895712 | C | T | 2 | a0007c0009t0003g0220 a0007c0009t0020g0222 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1059+4379C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895712 | |||||||
chr7:158895809 | G | A | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+4476G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895809 | |||||||
chr7:158895934 | G | A | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1059+4601G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158895934 | |||||||
chr7:158896134 | T | A | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1059+4801T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896134 | |||||||
chr7:158896575 | A | G | 1 | a0001c0021t0008g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1060-5164A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896575 | |||||||
chr7:158896654 | G | A | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1060-5085G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896654 | |||||||
chr7:158896738 | G | T | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1060-5001G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896738 | |||||||
chr7:158896776 | T | G | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1060-4963T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896776 | |||||||
chr7:158896856 | T | C | 1 | a0001c0001t0002g0164 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.1060-4883T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896856 | |||||||
chr7:158896866 | GT | G | 161 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(158): Show |
161 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.1060-4859delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158896866 | ||||||
chr7:158896884 | G | A | 1 | a0003c0029t0004g0249 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1060-4855G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896884 | |||||||
chr7:158896985 | C | CT | 28 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(25): Show |
28 | HG00140.hp1 HG00642.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.1060-4738dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158896985 | ||||||
chr7:158896985 | CT | C | 24 | a0001c0001t0002g0151 a0001c0001t0002g0182 a0001c0001t0003g0199 others(21): Show |
24 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1060-4738delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158896985 | ||||||
chr7:158896994 | T | A | 1 | a0001c0001t0002g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1060-4745T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158896994 | |||||||
chr7:158897058 | G | A | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1060-4681G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897058 | |||||||
chr7:158897288 | C | T | 4 | a0004c0004t0001g0180 a0004c0004t0006g0178 a0004c0004t0006g0179 others(1): Show |
4 | HG02818.hp1 HG03486.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-4451C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897288 | |||||||
chr7:158897433 | C | T | 2 | a0001c0001t0006g0007 a0001c0001t0006g0008 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1060-4306C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897433 | |||||||
chr7:158897511 | T | C | 1 | a0004c0004t0002g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1060-4228T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897511 | |||||||
chr7:158897596 | A | G | 3 | a0001c0001t0002g0005 a0006c0006t0002g0118 a0006c0006t0002g0219 |
3 | HG01891.hp2 HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1060-4143A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897596 | |||||||
chr7:158897624 | A | G | 106 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(103): Show |
106 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1060-4115A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897624 | |||||||
chr7:158897659 | A | G | 1 | a0004c0004t0002g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1060-4080A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897659 | |||||||
chr7:158897768 | T | G | 1 | a0001c0001t0002g0186 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1060-3971T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897768 | |||||||
chr7:158897776 | C | T | 35 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(32): Show |
35 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(32): Show |
intron_variant | MODIFIER | c.1060-3963C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897776 | |||||||
chr7:158897885 | G | A | 176 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(173): Show |
176 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.1060-3854G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158897885 | |||||||
chr7:158898087 | A | C | 6 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0021t0008g0112 others(3): Show |
6 | HG02055.hp1 HG02717.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.1060-3652A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158898087 | |||||||
chr7:158898175 | A | G | 115 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(112): Show |
115 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(112): Show |
intron_variant | MODIFIER | c.1060-3564A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158898175 | |||||||
chr7:158898530 | G | A | 12 | a0002c0002t0001g0016 a0002c0002t0001g0019 a0002c0002t0001g0024 others(9): Show |
12 | HG00438.hp1 HG02027.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.1060-3209G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158898530 | |||||||
chr7:158898726 | G | A | 164 | a0001c0001t0001g0006 a0001c0001t0002g0003 a0001c0001t0002g0004 others(161): Show |
164 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.1060-3013G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158898726 | |||||||
chr7:158898936 | A | G | 1 | a0002c0002t0001g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1060-2803A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158898936 | |||||||
chr7:158899312 | A | G | 2 | a0003c0003t0004g0255 a0003c0003t0004g0258 |
2 | HG01358.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1060-2427A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899312 | |||||||
chr7:158899351 | C | T | 1 | a0002c0002t0001g0022 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1060-2388C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899351 | |||||||
chr7:158899359 | T | C | 121 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(118): Show |
121 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.1060-2380T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899359 | |||||||
chr7:158899455 | T | C | 3 | a0004c0004t0006g0178 a0004c0004t0006g0179 a0004c0004t0006g0181 |
3 | HG02818.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1060-2284T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899455 | |||||||
chr7:158899777 | T | G | 1 | a0002c0002t0001g0098 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1060-1962T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899777 | |||||||
chr7:158899807 | T | C | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1060-1932T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899807 | |||||||
chr7:158899823 | A | G | 1 | a0006c0006t0002g0118 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.1060-1916A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899823 | |||||||
chr7:158899952 | C | T | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1060-1787C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158899952 | |||||||
chr7:158900068 | C | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(90): Show |
93 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1060-1671C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158900068 | |||||||
chr7:158900116 | C | CT | 5 | a0001c0001t0002g0003 a0001c0001t0002g0173 a0002c0002t0001g0044 others(2): Show |
5 | HG01175.hp1 HG02109.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1060-1607dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900116 | ||||||
chr7:158900116 | CT | C | 22 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(19): Show |
22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1060-1607delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900116 | ||||||
chr7:158900433 | T | A | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1060-1306T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158900433 | |||||||
chr7:158900731 | G | GT | 67 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(64): Show |
67 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.1060-990dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900731 | ||||||
chr7:158900731 | G | GTT | 85 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(82): Show |
85 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1060-991_1060-990d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900731 | ||||||
chr7:158900731 | G | GTTT | 11 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0123 others(8): Show |
11 | HG01243.hp2 HG02071.hp1 HG03654.hp2 others(8): Show |
intron_variant | MODIFIER | c.1060-992_1060-990d others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900731 | ||||||
chr7:158900731 | GT | G | 10 | a0001c0001t0006g0008 a0002c0002t0001g0021 a0002c0002t0001g0039 others(7): Show |
10 | HG01943.hp2 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.1060-990delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | INFO_REALIGN_3_PRIME | chr7 | 158900731 | ||||||
chr7:158900788 | G | A | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1060-951G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158900788 | |||||||
chr7:158900974 | A | G | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1060-765A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158900974 | |||||||
chr7:158901073 | C | A | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1060-666C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158901073 | |||||||
chr7:158901282 | C | T | 5 | a0002c0002t0001g0010 a0002c0002t0001g0057 a0002c0002t0001g0109 others(2): Show |
5 | HG02280.hp2 HG02615.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.1060-457C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 8/24 | chr7 | 158901282 | |||||||
chr7:158901839 | T | C | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1137+23T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 9/24 | chr7 | 158901839 | |||||||
chr7:158902050 | A | G | 1 | a0002c0002t0001g0103 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1137+234A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 9/24 | chr7 | 158902050 | |||||||
chr7:158902110 | G | A | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1138-266G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 9/24 | chr7 | 158902110 | |||||||
chr7:158902216 | C | T | 1 | a0001c0001t0002g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1138-160C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 9/24 | chr7 | 158902216 | |||||||
chr7:158902873 | C | G | 1 | a0001c0001t0002g0120 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1357+278C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158902873 | |||||||
chr7:158902893 | G | C | 2 | a0002c0002t0001g0036 a0002c0002t0001g0037 |
2 | NA18994.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.1357+298G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158902893 | |||||||
chr7:158903341 | C | CTG | 171 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(168): Show |
171 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(168): Show |
intron_variant | MODIFIER | c.1357+747_1357+748d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158903341 | ||||||
chr7:158903728 | C | T | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1357+1133C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158903728 | |||||||
chr7:158904123 | C | T | 31 | a0001c0001t0002g0197 a0003c0003t0004g0237 a0003c0003t0004g0238 others(28): Show |
31 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(28): Show |
intron_variant | MODIFIER | c.1357+1528C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904123 | |||||||
chr7:158904364 | C | T | 1 | a0001c0001t0002g0130 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1358-1625C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904364 | |||||||
chr7:158904412 | A | C | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1358-1577A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904412 | |||||||
chr7:158904526 | T | A | 1 | a0001c0001t0002g0129 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1358-1463T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904526 | |||||||
chr7:158904874 | G | A | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1358-1115G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158904874 | |||||||
chr7:158905140 | C | CT | 16 | a0001c0001t0002g0123 a0001c0001t0012g0217 a0001c0001t0012g0218 others(13): Show |
16 | HG01257.hp2 HG02055.hp1 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.1358-831dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158905140 | ||||||
chr7:158905140 | C | CTTTTTTT others(3): Show |
3 | a0003c0003t0004g0254 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG02976.hp2 HG03491.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1358-840_1358-831d others(12): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158905140 | ||||||
chr7:158905140 | C | CTTTTTTT others(4): Show |
26 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(23): Show |
26 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(23): Show |
intron_variant | MODIFIER | c.1358-841_1358-831d others(13): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158905140 | ||||||
chr7:158905140 | C | CTTTTTTT others(5): Show |
1 | a0003c0003t0004g0251 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1358-842_1358-831d others(14): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158905140 | ||||||
chr7:158905140 | CT | C | 10 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0162 others(7): Show |
10 | HG01070.hp2 HG01081.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1358-831delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | INFO_REALIGN_3_PRIME | chr7 | 158905140 | ||||||
chr7:158905184 | G | A | 1 | a0001c0001t0006g0008 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1358-805G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905184 | |||||||
chr7:158905200 | G | A | 1 | a0002c0002t0001g0097 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1358-789G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905200 | |||||||
chr7:158905372 | C | T | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1358-617C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905372 | |||||||
chr7:158905431 | G | A | 2 | a0001c0001t0006g0007 a0001c0001t0006g0008 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1358-558G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905431 | |||||||
chr7:158905618 | T | G | 1 | a0001c0001t0001g0269 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1358-371T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905618 | |||||||
chr7:158905784 | G | T | 4 | a0001c0021t0008g0112 a0002c0005t0010g0100 a0008c0007t0008g0113 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1358-205G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 10/24 | chr7 | 158905784 | |||||||
chr7:158906121 | G | A | 4 | a0004c0004t0001g0180 a0004c0004t0006g0178 a0004c0004t0006g0179 others(1): Show |
4 | HG02818.hp1 HG03486.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.1460+30G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906121 | |||||||
chr7:158906271 | C | T | 1 | a0002c0002t0001g0037 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1460+180C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906271 | |||||||
chr7:158906276 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1460+185C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906276 | |||||||
chr7:158906410 | T | C | 1 | a0002c0002t0001g0016 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1460+319T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906410 | |||||||
chr7:158906521 | C | T | 1 | a0001c0001t0002g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1460+430C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906521 | |||||||
chr7:158906686 | G | A | 1 | a0002c0002t0001g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1460+595G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906686 | |||||||
chr7:158906865 | A | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+774A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158906865 | |||||||
chr7:158907106 | T | C | 158 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(155): Show |
158 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.1460+1015T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907106 | |||||||
chr7:158907164 | GA | G | 132 | a0001c0001t0001g0006 a0001c0001t0002g0003 a0001c0001t0002g0004 others(129): Show |
132 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.1460+1086delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158907164 | ||||||
chr7:158907273 | C | CT | 106 | a0001c0001t0001g0268 a0001c0001t0002g0003 a0001c0001t0002g0004 others(103): Show |
106 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.1460+1207dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158907273 | ||||||
chr7:158907273 | C | CTT | 7 | a0001c0001t0002g0173 a0001c0001t0002g0188 a0001c0001t0002g0194 others(4): Show |
7 | HG02080.hp1 HG02683.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1460+1206_1460+120 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158907273 | ||||||
chr7:158907273 | CT | C | 6 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(3): Show |
6 | HG01169.hp2 HG01255.hp2 HG01433.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+1207delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158907273 | ||||||
chr7:158907273 | CTT | C | 29 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(26): Show |
29 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.1460+1206_1460+120 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158907273 | ||||||
chr7:158907418 | T | C | 8 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0245 others(5): Show |
8 | HG00140.hp2 HG01071.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1460+1327T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907418 | |||||||
chr7:158907586 | C | T | 6 | a0002c0002t0001g0026 a0002c0002t0001g0054 a0002c0002t0001g0055 others(3): Show |
6 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.1460+1495C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907586 | |||||||
chr7:158907648 | C | T | 1 | a0002c0002t0001g0047 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1460+1557C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907648 | |||||||
chr7:158907669 | G | A | 1 | a0001c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1460+1578G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907669 | |||||||
chr7:158907852 | A | G | 98 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(95): Show |
98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1460+1761A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907852 | |||||||
chr7:158907891 | G | A | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1460+1800G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907891 | |||||||
chr7:158907908 | C | T | 98 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(95): Show |
98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1460+1817C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158907908 | |||||||
chr7:158908398 | G | A | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1460+2307G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158908398 | |||||||
chr7:158908490 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1460+2399G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158908490 | |||||||
chr7:158908691 | G | A | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1460+2600G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158908691 | |||||||
chr7:158908733 | C | G | 98 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(95): Show |
98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1460+2642C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158908733 | |||||||
chr7:158908860 | C | T | 1 | a0001c0001t0002g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1461-2690C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158908860 | |||||||
chr7:158909017 | A | T | 30 | a0003c0003t0004g0237 a0003c0003t0004g0238 a0003c0003t0004g0241 others(27): Show |
30 | HG00140.hp2 HG00408.hp1 HG00733.hp1 others(27): Show |
intron_variant | MODIFIER | c.1461-2533A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909017 | |||||||
chr7:158909277 | G | A | 1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1461-2273G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909277 | |||||||
chr7:158909305 | T | C | 1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1461-2245T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909305 | |||||||
chr7:158909330 | C | CA | 33 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0202 others(30): Show |
33 | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(30): Show |
intron_variant | MODIFIER | c.1461-2195dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158909330 | ||||||
chr7:158909330 | C | CAA | 6 | a0001c0001t0001g0006 a0001c0001t0003g0201 a0001c0001t0003g0226 others(3): Show |
6 | HG00423.hp2 HG00544.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461-2196_1461-219 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158909330 | ||||||
chr7:158909330 | CA | C | 94 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0271 others(91): Show |
94 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1461-2195delA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158909330 | ||||||
chr7:158909330 | CAA | C | 9 | a0001c0001t0002g0145 a0001c0001t0002g0197 a0001c0001t0005g0161 others(6): Show |
9 | HG01167.hp2 HG02015.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.1461-2196_1461-219 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158909330 | ||||||
chr7:158909416 | A | G | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1461-2134A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909416 | |||||||
chr7:158909588 | C | T | 5 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0002c0005t0010g0100 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1461-1962C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909588 | |||||||
chr7:158909653 | A | G | 1 | a0012c0015t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1461-1897A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909653 | |||||||
chr7:158909891 | G | C | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1461-1659G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909891 | |||||||
chr7:158909931 | C | G | 1 | a0003c0003t0004g0238 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1461-1619C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909931 | |||||||
chr7:158909955 | C | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1461-1595C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909955 | |||||||
chr7:158909985 | C | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1461-1565C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158909985 | |||||||
chr7:158910250 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1461-1300G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910250 | |||||||
chr7:158910328 | T | C | 242 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1461-1222T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910328 | |||||||
chr7:158910402 | ACCTGTGG others(22): Show |
A | 98 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(95): Show |
98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1461-1139_1461-111 others(33): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158910402 | ||||||
chr7:158910413 | C | G | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1461-1137C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910413 | |||||||
chr7:158910435 | G | T | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1461-1115G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910435 | |||||||
chr7:158910437 | G | T | 4 | a0001c0021t0008g0112 a0002c0005t0010g0100 a0008c0007t0008g0113 others(1): Show |
4 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.1461-1113G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910437 | |||||||
chr7:158910574 | G | T | 1 | a0001c0001t0002g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1461-976G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910574 | |||||||
chr7:158910613 | G | C | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1461-937G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910613 | |||||||
chr7:158910644 | C | CGAGGGCA others(4): Show |
1 | a0002c0002t0016g0034 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1461-893_1461-883d others(13): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | INFO_REALIGN_3_PRIME | chr7 | 158910644 | ||||||
chr7:158910757 | T | C | 242 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1461-793T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910757 | |||||||
chr7:158910863 | C | A | 10 | a0002c0002t0001g0016 a0002c0002t0001g0019 a0002c0002t0001g0024 others(7): Show |
10 | HG00438.hp1 HG02027.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.1461-687C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910863 | |||||||
chr7:158910983 | A | G | 1 | a0013c0014t0001g0106 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1461-567A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910983 | |||||||
chr7:158910984 | G | A | 1 | a0013c0014t0001g0106 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1461-566G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158910984 | |||||||
chr7:158911023 | G | T | 8 | a0004c0004t0001g0180 a0004c0004t0002g0137 a0004c0004t0002g0138 others(5): Show |
8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1461-527G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158911023 | |||||||
chr7:158911127 | G | A | 1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1461-423G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158911127 | |||||||
chr7:158911363 | G | A | 98 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(95): Show |
98 | HG00099.hp1 HG00438.hp2 HG00544.hp2 others(95): Show |
intron_variant | MODIFIER | c.1461-187G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 11/24 | chr7 | 158911363 | |||||||
chr7:158911914 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1590+235C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158911914 | |||||||
chr7:158911984 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1590+305T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158911984 | |||||||
chr7:158912308 | C | T | 2 | a0001c0001t0001g0269 a0001c0001t0001g0271 |
2 | HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1590+629C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158912308 | |||||||
chr7:158912424 | G | C | 2 | a0002c0002t0001g0109 a0002c0002t0001g0111 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1591-561G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158912424 | |||||||
chr7:158912576 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1591-409G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158912576 | |||||||
chr7:158912720 | C | CCTAAGAA others(31): Show |
1 | a0003c0003t0007g0242 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1591-264_1591-227d others(40): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | INFO_REALIGN_3_PRIME | chr7 | 158912720 | ||||||
chr7:158912752 | G | A | 1 | a0002c0005t0010g0100 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1591-233G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 12/24 | chr7 | 158912752 | |||||||
chr7:158913353 | A | T | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1702+257A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913353 | |||||||
chr7:158913475 | C | T | 242 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1702+379C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913475 | |||||||
chr7:158913556 | G | A | 1 | a0001c0001t0002g0234 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1702+460G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913556 | |||||||
chr7:158913559 | T | G | 8 | a0004c0004t0001g0180 a0004c0004t0002g0137 a0004c0004t0002g0138 others(5): Show |
8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1702+463T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913559 | |||||||
chr7:158913563 | A | G | 1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1702+467A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913563 | |||||||
chr7:158913702 | G | T | 242 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1703-531G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913702 | |||||||
chr7:158913715 | A | AT | 5 | a0001c0021t0008g0112 a0001c0022t0018g0229 a0002c0005t0010g0100 others(2): Show |
5 | HG02451.hp2 HG02717.hp1 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1703-518_1703-517i others(3): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913715 | |||||||
chr7:158913716 | A | T | 136 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(133): Show |
136 | HG00099.hp1 HG00140.hp1 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.1703-517A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913716 | |||||||
chr7:158913794 | C | T | 1 | a0005c0008t0003g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1703-439C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913794 | |||||||
chr7:158913801 | T | C | 242 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(239): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.1703-432T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913801 | |||||||
chr7:158913959 | C | T | 108 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(105): Show |
108 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1703-274C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913959 | |||||||
chr7:158913989 | C | T | 7 | a0001c0001t0005g0161 a0002c0002t0001g0002 a0002c0002t0001g0022 others(4): Show |
7 | HG01358.hp2 HG02015.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.1703-244C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 13/24 | chr7 | 158913989 | |||||||
chr7:158914340 | T | C | 2 | a0002c0002t0001g0109 a0002c0002t0001g0111 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1791+19T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914340 | |||||||
chr7:158914380 | A | G | 11 | a0001c0001t0002g0123 a0001c0001t0005g0161 a0001c0001t0012g0217 others(8): Show |
11 | HG01358.hp2 HG02015.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1791+59A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914380 | |||||||
chr7:158914381 | T | C | 1 | a0001c0001t0002g0230 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1791+60T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914381 | |||||||
chr7:158914546 | G | A | 11 | a0004c0004t0001g0180 a0004c0004t0002g0137 a0004c0004t0006g0178 others(8): Show |
11 | HG01257.hp2 HG01934.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1791+225G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914546 | |||||||
chr7:158914608 | G | GC | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1791+288dupC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158914608 | ||||||
chr7:158914616 | G | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(6): Show |
9 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.1791+295G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914616 | |||||||
chr7:158914703 | A | T | 4 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0162 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG01257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+382A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914703 | |||||||
chr7:158914734 | C | T | 1 | a0001c0001t0006g0007 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1791+413C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914734 | |||||||
chr7:158914784 | C | G | 1 | a0001c0001t0003g0205 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1791+463C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914784 | |||||||
chr7:158914798 | G | A | 1 | a0001c0001t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1791+477G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914798 | |||||||
chr7:158914874 | A | G | 1 | a0003c0003t0007g0242 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1791+553A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914874 | |||||||
chr7:158914968 | G | C | 1 | a0001c0001t0002g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1791+647G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158914968 | |||||||
chr7:158915048 | A | G | 33 | a0002c0002t0001g0001 a0002c0002t0001g0009 a0002c0002t0001g0020 others(30): Show |
33 | HG00408.hp2 HG00597.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.1791+727A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915048 | |||||||
chr7:158915052 | CGCTAGTT others(31): Show |
C | 17 | a0003c0003t0004g0241 a0003c0003t0004g0243 a0003c0003t0004g0244 others(14): Show |
17 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(14): Show |
intron_variant | MODIFIER | c.1791+735_1791+772d others(40): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915052 | ||||||
chr7:158915090 | T | TGCTGGTT others(69): Show |
2 | a0002c0002t0001g0009 a0002c0002t0001g0066 |
2 | HG01943.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.1791+810_1791+811i others(78): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915090 | ||||||
chr7:158915128 | C | T | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+807C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915128 | |||||||
chr7:158915196 | G | A | 2 | a0002c0002t0001g0014 a0002c0002t0001g0027 |
2 | HG01255.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1791+875G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915196 | |||||||
chr7:158915216 | G | A | 1 | a0001c0001t0012g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1791+895G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915216 | |||||||
chr7:158915222 | C | T | 3 | a0001c0022t0018g0229 a0002c0002t0001g0069 a0002c0002t0001g0073 |
3 | NA18945.hp1 NA19002.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1791+901C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915222 | |||||||
chr7:158915231 | A | C | 2 | a0002c0002t0001g0069 a0002c0002t0001g0073 |
2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+910A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915231 | |||||||
chr7:158915234 | G | A | 1 | a0002c0002t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1791+913G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915234 | |||||||
chr7:158915238 | T | C | 2 | a0002c0002t0001g0069 a0002c0002t0001g0073 |
2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+917T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915238 | |||||||
chr7:158915240 | C | G | 2 | a0002c0002t0001g0069 a0002c0002t0001g0073 |
2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+919C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915240 | |||||||
chr7:158915248 | C | G | 2 | a0002c0002t0001g0069 a0002c0002t0001g0073 |
2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+927C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915248 | |||||||
chr7:158915251 | T | A | 2 | a0002c0002t0001g0069 a0002c0002t0001g0073 |
2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+930T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915251 | |||||||
chr7:158915255 | A | G | 2 | a0002c0002t0001g0069 a0002c0002t0001g0073 |
2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+934A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915255 | |||||||
chr7:158915261 | T | G | 2 | a0002c0002t0001g0069 a0002c0002t0001g0073 |
2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+940T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915261 | |||||||
chr7:158915278 | G | C | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1791+957G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915278 | |||||||
chr7:158915278 | G | GTGGTTGA others(943): Show |
1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+964_1791+965i others(952): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915278 | ||||||
chr7:158915286 | G | C | 4 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 others(1): Show |
4 | HG00140.hp1 HG02257.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+965G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915286 | |||||||
chr7:158915307 | C | G | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+986C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915307 | |||||||
chr7:158915309 | G | C | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+988G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915309 | |||||||
chr7:158915309 | G | GGACACGC others(31): Show |
8 | a0004c0004t0001g0180 a0004c0004t0002g0137 a0004c0004t0002g0138 others(5): Show |
8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1791+1031_1791+106 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915309 | ||||||
chr7:158915347 | C | CGACACGC others(183): Show |
95 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(92): Show |
95 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1791+1064_1791+106 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915347 | ||||||
chr7:158915347 | C | CGACACGC others(183): Show |
2 | a0002c0002t0001g0010 a0002c0002t0001g0057 |
2 | HG02615.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1791+1064_1791+106 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915347 | ||||||
chr7:158915347 | C | CGACACGC others(183): Show |
2 | a0002c0002t0001g0075 a0002c0002t0001g0077 |
2 | HG01516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1791+1068_1791+106 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915347 | ||||||
chr7:158915348 | G | GACACGCT others(449): Show |
2 | a0001c0001t0005g0161 a0002c0018t0015g0048 |
2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1061_1791+106 others(460): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915348 | ||||||
chr7:158915352 | CGCTGGTT others(31): Show |
C | 2 | a0002c0002t0001g0069 a0002c0002t0001g0073 |
2 | NA18945.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.1791+1069_1791+110 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915352 | ||||||
chr7:158915362 | C | G | 1 | a0001c0001t0002g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1041C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915362 | |||||||
chr7:158915383 | G | C | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1062G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915383 | |||||||
chr7:158915386 | G | A | 1 | a0002c0002t0001g0030 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1791+1065G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915386 | |||||||
chr7:158915390 | T | C | 239 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(236): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.1791+1069T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915390 | |||||||
chr7:158915392 | C | CTGGTTGA others(369): Show |
1 | a0002c0002t0001g0088 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1791+1098_1791+109 others(380): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915392 | ||||||
chr7:158915400 | C | CATTAAGG others(863): Show |
1 | a0001c0001t0002g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1099_1791+110 others(874): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915400 | ||||||
chr7:158915400 | C | CATTAAGG others(4799): Show |
1 | a0001c0001t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1791+1251_1791+125 others(4810): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915400 | ||||||
chr7:158915400 | C | G | 4 | a0001c0001t0005g0161 a0002c0002t0001g0030 a0002c0018t0015g0048 others(1): Show |
4 | HG00140.hp1 HG01081.hp2 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1079C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915400 | |||||||
chr7:158915421 | G | C | 2 | a0001c0001t0003g0199 a0001c0001t0003g0225 |
2 | HG00597.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.1791+1100G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915421 | |||||||
chr7:158915423 | C | T | 1 | a0002c0002t0001g0088 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1791+1102C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915423 | |||||||
chr7:158915424 | G | GACACGCT others(297): Show |
1 | a0002c0002t0001g0030 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1791+1116_1791+111 others(308): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915424 | ||||||
chr7:158915424 | G | T | 1 | a0002c0002t0001g0088 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1791+1103G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915424 | |||||||
chr7:158915428 | C | T | 1 | a0002c0002t0001g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1791+1107C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915428 | |||||||
chr7:158915429 | G | A | 1 | a0001c0001t0002g0147 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1791+1108G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915429 | |||||||
chr7:158915438 | G | C | 11 | a0001c0001t0002g0185 a0001c0001t0005g0161 a0002c0002t0001g0030 others(8): Show |
11 | HG00140.hp1 HG01081.hp2 HG02015.hp2 others(8): Show |
intron_variant | MODIFIER | c.1791+1117G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915438 | |||||||
chr7:158915458 | C | T | 3 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 |
3 | HG01891.hp2 HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1791+1137C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915458 | |||||||
chr7:158915459 | G | A | 2 | a0001c0001t0005g0161 a0002c0018t0015g0048 |
2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1138G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915459 | |||||||
chr7:158915459 | G | C | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1138G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915459 | |||||||
chr7:158915466 | C | T | 4 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0003c0010t0011g0252 others(1): Show |
4 | HG02976.hp2 HG03654.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1145C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915466 | |||||||
chr7:158915467 | G | A | 2 | a0001c0001t0005g0161 a0002c0018t0015g0048 |
2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1146G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915467 | |||||||
chr7:158915483 | G | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1162G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915483 | |||||||
chr7:158915499 | C | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1178C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915499 | |||||||
chr7:158915500 | G | A | 22 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(19): Show |
22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1791+1179G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915500 | |||||||
chr7:158915506 | G | C | 3 | a0003c0003t0004g0255 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG01358.hp1 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1185G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915506 | |||||||
chr7:158915514 | G | C | 4 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0003c0010t0011g0252 others(1): Show |
4 | HG02976.hp2 HG03654.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1193G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915514 | |||||||
chr7:158915517 | A | T | 10 | a0001c0001t0002g0185 a0001c0001t0003g0216 a0001c0001t0005g0161 others(7): Show |
10 | HG00140.hp1 HG01081.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+1196A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915517 | |||||||
chr7:158915527 | G | T | 8 | a0001c0001t0002g0185 a0001c0001t0003g0216 a0002c0002t0001g0030 others(5): Show |
8 | HG00140.hp1 HG01358.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.1791+1206G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915527 | |||||||
chr7:158915534 | C | T | 1 | a0003c0003t0004g0255 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1791+1213C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915534 | |||||||
chr7:158915535 | C | A | 1 | a0001c0001t0003g0216 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1791+1214C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915535 | |||||||
chr7:158915535 | C | G | 1 | a0003c0003t0004g0255 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1791+1214C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915535 | |||||||
chr7:158915537 | C | T | 1 | a0003c0003t0004g0255 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1791+1216C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915537 | |||||||
chr7:158915538 | G | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1217G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915538 | |||||||
chr7:158915543 | G | A | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1222G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915543 | |||||||
chr7:158915544 | G | C | 5 | a0001c0001t0003g0216 a0002c0002t0001g0030 a0002c0002t0001g0088 others(2): Show |
5 | HG02976.hp2 HG03654.hp1 NA18957.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+1223G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915544 | |||||||
chr7:158915552 | G | C | 4 | a0001c0001t0003g0216 a0003c0003t0004g0255 a0003c0010t0011g0252 others(1): Show |
4 | HG01358.hp1 HG02976.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1231G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915552 | |||||||
chr7:158915573 | C | A | 1 | a0001c0001t0002g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1252C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915573 | |||||||
chr7:158915573 | C | G | 6 | a0001c0001t0003g0216 a0002c0002t0001g0030 a0002c0002t0001g0088 others(3): Show |
6 | HG01358.hp1 HG02976.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1791+1252C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915573 | |||||||
chr7:158915582 | C | G | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1261C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915582 | |||||||
chr7:158915590 | G | C | 4 | a0001c0001t0002g0185 a0001c0001t0003g0216 a0003c0010t0011g0252 others(1): Show |
4 | HG02976.hp2 HG04204.hp2 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1269G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915590 | |||||||
chr7:158915611 | A | C | 3 | a0003c0003t0004g0238 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG01071.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1290A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915611 | |||||||
chr7:158915611 | A | G | 4 | a0001c0001t0002g0185 a0001c0001t0003g0216 a0001c0001t0005g0161 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1290A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915611 | |||||||
chr7:158915613 | C | T | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1292C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915613 | |||||||
chr7:158915619 | G | A | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1298G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915619 | |||||||
chr7:158915620 | C | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1299C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915620 | |||||||
chr7:158915628 | C | A | 2 | a0001c0001t0005g0161 a0002c0018t0015g0048 |
2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1307C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915628 | |||||||
chr7:158915628 | C | CATTA | 5 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0003c0010t0011g0252 others(2): Show |
5 | HG00140.hp1 HG02976.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+1308_1791+130 others(8): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915628 | ||||||
chr7:158915628 | C | CATTAAGG others(1619): Show |
1 | a0001c0001t0002g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1308_1791+130 others(1630): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915628 | ||||||
chr7:158915628 | C | CATTAAGG others(2033): Show |
1 | a0001c0001t0003g0216 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1791+1308_1791+130 others(2044): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915628 | ||||||
chr7:158915645 | C | G | 3 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0010c0023t0001g0272 |
3 | HG00140.hp1 HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1324C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915645 | |||||||
chr7:158915647 | C | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1326C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915647 | |||||||
chr7:158915647 | C | T | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1326C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915647 | |||||||
chr7:158915648 | G | T | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1327G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915648 | |||||||
chr7:158915654 | G | C | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1333G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915654 | |||||||
chr7:158915655 | T | TGGTTGAC others(210): Show |
1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1362_1791+136 others(221): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915655 | ||||||
chr7:158915662 | C | G | 4 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0003c0010t0011g0252 others(1): Show |
4 | HG02976.hp2 HG03654.hp1 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1341C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915662 | |||||||
chr7:158915683 | G | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1362G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915683 | |||||||
chr7:158915685 | C | T | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1364C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915685 | |||||||
chr7:158915686 | G | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1365G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915686 | |||||||
chr7:158915690 | C | T | 185 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(182): Show |
185 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.1791+1369C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915690 | |||||||
chr7:158915691 | G | A | 3 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0022t0018g0229 |
3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1791+1370G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915691 | |||||||
chr7:158915699 | A | G | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1378A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915699 | |||||||
chr7:158915721 | G | A | 3 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0022t0018g0229 |
3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1791+1400G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915721 | |||||||
chr7:158915723 | C | T | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1402C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915723 | |||||||
chr7:158915724 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1403G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915724 | |||||||
chr7:158915724 | G | T | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1403G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915724 | |||||||
chr7:158915728 | C | T | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1407C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915728 | |||||||
chr7:158915730 | C | G | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1409C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915730 | |||||||
chr7:158915732 | G | C | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1411G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915732 | |||||||
chr7:158915738 | C | G | 1 | a0002c0002t0001g0088 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1791+1417C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915738 | |||||||
chr7:158915759 | G | C | 3 | a0001c0001t0003g0206 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG02976.hp2 NA18990.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1438G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915759 | |||||||
chr7:158915761 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1440C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915761 | |||||||
chr7:158915762 | T | A | 1 | a0001c0001t0003g0206 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1791+1441T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915762 | |||||||
chr7:158915762 | T | G | 7 | a0001c0001t0005g0161 a0002c0002t0001g0030 a0002c0002t0001g0088 others(4): Show |
7 | HG00140.hp1 HG02015.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.1791+1441T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915762 | |||||||
chr7:158915766 | C | CGCTGGCT others(145): Show |
1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1450_1791+145 others(156): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915766 | ||||||
chr7:158915768 | C | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1447C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915768 | |||||||
chr7:158915776 | G | C | 3 | a0001c0001t0003g0206 a0002c0018t0015g0048 a0010c0023t0001g0272 |
3 | HG00140.hp1 HG01081.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.1791+1455G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915776 | |||||||
chr7:158915797 | G | A | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1476G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915797 | |||||||
chr7:158915797 | G | C | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1476G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915797 | |||||||
chr7:158915799 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1478C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915799 | |||||||
chr7:158915800 | G | A | 3 | a0002c0018t0015g0048 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG01081.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1479G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915800 | |||||||
chr7:158915814 | C | G | 2 | a0001c0001t0002g0185 a0001c0001t0003g0216 |
2 | HG04204.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1791+1493C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915814 | |||||||
chr7:158915835 | G | C | 2 | a0001c0001t0002g0185 a0001c0001t0003g0216 |
2 | HG04204.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.1791+1514G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915835 | |||||||
chr7:158915836 | T | TCGACACG others(104): Show |
1 | a0001c0001t0003g0216 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1791+1516_1791+151 others(115): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915836 | ||||||
chr7:158915838 | A | ACGGTGGT others(1339): Show |
1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1517_1791+151 others(1350): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915838 | |||||||
chr7:158915838 | A | G | 13 | a0001c0001t0002g0185 a0001c0001t0002g0197 a0001c0001t0005g0161 others(10): Show |
13 | HG01081.hp1 HG02015.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1791+1517A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915838 | |||||||
chr7:158915842 | C | CGGTGGTT others(26): Show |
1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1522_1791+152 others(37): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915842 | ||||||
chr7:158915845 | T | C | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1524T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915845 | |||||||
chr7:158915851 | A | G | 91 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
91 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1791+1530A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915851 | |||||||
chr7:158915852 | C | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1531C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915852 | |||||||
chr7:158915873 | G | C | 4 | a0001c0001t0002g0185 a0001c0001t0005g0161 a0002c0002t0001g0030 others(1): Show |
4 | HG02015.hp2 HG03654.hp1 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1552G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915873 | |||||||
chr7:158915875 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1554C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915875 | |||||||
chr7:158915880 | C | T | 2 | a0002c0002t0001g0020 a0002c0002t0001g0051 |
2 | HG04184.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1791+1559C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915880 | |||||||
chr7:158915881 | G | A | 1 | a0001c0001t0003g0216 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1791+1560G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915881 | |||||||
chr7:158915882 | C | G | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1561C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915882 | |||||||
chr7:158915886 | T | C | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1791+1565T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915886 | |||||||
chr7:158915890 | G | C | 6 | a0001c0001t0002g0185 a0001c0001t0005g0161 a0002c0018t0015g0048 others(3): Show |
6 | HG00140.hp1 HG01081.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1791+1569G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915890 | |||||||
chr7:158915890 | G | GATTAAGG others(366): Show |
1 | a0002c0002t0001g0093 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1791+1588_1791+158 others(377): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915890 | ||||||
chr7:158915911 | G | C | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1590G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915911 | |||||||
chr7:158915914 | G | A | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1593G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915914 | |||||||
chr7:158915914 | G | T | 1 | a0001c0001t0002g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1593G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915914 | |||||||
chr7:158915918 | C | T | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1597C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915918 | |||||||
chr7:158915919 | G | A | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1598G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915919 | |||||||
chr7:158915920 | C | G | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1599C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915920 | |||||||
chr7:158915928 | C | G | 4 | a0001c0001t0003g0216 a0002c0002t0001g0030 a0002c0002t0001g0088 others(1): Show |
4 | HG03654.hp1 HG03688.hp1 NA18957.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1607C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915928 | |||||||
chr7:158915949 | G | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1628G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915949 | |||||||
chr7:158915949 | G | C | 5 | a0001c0001t0003g0216 a0001c0001t0005g0161 a0003c0010t0011g0252 others(2): Show |
5 | HG00140.hp1 HG02015.hp2 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1791+1628G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915949 | |||||||
chr7:158915949 | G | GTCAACAC others(107): Show |
1 | a0001c0001t0002g0185 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1791+1629_1791+163 others(118): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915949 | ||||||
chr7:158915951 | T | C | 9 | a0001c0001t0002g0185 a0001c0001t0003g0216 a0001c0001t0005g0161 others(6): Show |
9 | HG00140.hp1 HG02015.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1791+1630T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915951 | |||||||
chr7:158915957 | A | AGTGGTTG others(3282): Show |
1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3293): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915957 | ||||||
chr7:158915957 | A | G | 9 | a0001c0001t0002g0185 a0001c0001t0003g0216 a0001c0001t0005g0161 others(6): Show |
9 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(6): Show |
intron_variant | MODIFIER | c.1791+1636A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915957 | |||||||
chr7:158915958 | G | C | 4 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0002c0002t0001g0093 others(1): Show |
4 | HG01081.hp2 HG03654.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1637G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915958 | |||||||
chr7:158915958 | G | GTGGTTGA others(598): Show |
1 | a0002c0002t0001g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(609): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | ||||||
chr7:158915958 | G | GTGGTTGA others(2634): Show |
2 | a0001c0001t0001g0268 a0001c0001t0001g0273 |
2 | HG01934.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2645): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | ||||||
chr7:158915958 | G | GTGGTTGA others(2634): Show |
2 | a0001c0001t0001g0269 a0001c0001t0001g0270 |
2 | HG01433.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2645): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | ||||||
chr7:158915958 | G | GTGGTTGA others(2634): Show |
1 | a0001c0001t0001g0271 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2645): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | ||||||
chr7:158915958 | G | GTGGTTGA others(2748): Show |
2 | a0001c0001t0003g0208 a0001c0001t0003g0211 |
2 | HG02129.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2759): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | ||||||
chr7:158915958 | G | GTGGTTGA others(3200): Show |
1 | a0001c0001t0003g0214 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3211): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915958 | ||||||
chr7:158915962 | T | C | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1641T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915962 | |||||||
chr7:158915965 | A | ACATGAAG others(294): Show |
1 | a0002c0002t0001g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1791+1647_1791+164 others(305): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915965 | ||||||
chr7:158915966 | C | CATTAAGG others(3125): Show |
1 | a0001c0001t0003g0207 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3348): Show |
1 | a0001c0001t0003g0215 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3359): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3125): Show |
3 | a0001c0001t0003g0202 a0001c0001t0003g0204 a0001c0001t0003g0226 |
3 | NA18944.hp2 NA19079.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3125): Show |
1 | a0001c0001t0003g0206 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7257): Show |
1 | a0001c0001t0002g0188 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7268): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2641): Show |
5 | a0004c0004t0002g0137 a0004c0004t0006g0178 a0004c0004t0006g0181 others(2): Show |
5 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2641): Show |
1 | a0004c0004t0001g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2641): Show |
1 | a0004c0004t0002g0138 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2641): Show |
1 | a0004c0004t0006g0179 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7523): Show |
1 | a0001c0001t0005g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2682): Show |
1 | a0001c0001t0002g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2693): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(6394): Show |
1 | a0001c0001t0002g0173 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(6405): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0171 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2641): Show |
1 | a0001c0001t0002g0150 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2641): Show |
1 | a0001c0001t0002g0177 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2679): Show |
23 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0124 others(20): Show |
23 | HG00741.hp2 HG01192.hp1 HG01517.hp1 others(20): Show |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(6766): Show |
1 | a0001c0001t0002g0187 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(6777): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7596): Show |
2 | a0001c0001t0002g0182 a0001c0001t0002g0183 |
2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(7607): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2679): Show |
9 | a0001c0001t0002g0117 a0001c0001t0002g0132 a0001c0001t0002g0158 others(6): Show |
9 | HG01243.hp2 HG02486.hp2 HG02523.hp2 others(6): Show |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0143 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7520): Show |
1 | a0009c0024t0002g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7531): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7520): Show |
1 | a0001c0001t0002g0163 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7531): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7520): Show |
1 | a0001c0001t0002g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7531): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0121 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0135 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7523): Show |
3 | a0001c0001t0002g0126 a0001c0001t0002g0195 a0001c0001t0002g0198 |
3 | HG02273.hp2 HG03654.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7520): Show |
1 | a0001c0001t0002g0130 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7531): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7485): Show |
1 | a0001c0001t0002g0157 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7496): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7941): Show |
2 | a0001c0001t0002g0153 a0001c0001t0002g0191 |
2 | HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(7952): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7941): Show |
1 | a0001c0001t0002g0168 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7952): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7941): Show |
1 | a0001c0001t0002g0160 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7952): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2641): Show |
1 | a0001c0001t0002g0141 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2652): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2680): Show |
1 | a0001c0001t0002g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2691): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2983): Show |
1 | a0001c0001t0002g0233 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2994): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2679): Show |
1 | a0001c0001t0002g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7941): Show |
1 | a0001c0001t0002g0125 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7952): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7748): Show |
1 | a0001c0001t0002g0196 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7759): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(1999): Show |
1 | a0001c0001t0002g0166 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2010): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7523): Show |
1 | a0001c0013t0002g0175 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2679): Show |
1 | a0001c0001t0002g0127 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2679): Show |
2 | a0001c0001t0002g0003 a0001c0001t0002g0004 |
2 | HG02109.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(8242): Show |
2 | a0001c0001t0002g0123 a0002c0002t0001g0108 |
2 | NA18992.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(8253): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7523): Show |
1 | a0001c0001t0002g0197 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7534): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(4612): Show |
1 | a0001c0001t0002g0133 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(4623): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2676): Show |
3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0162 |
3 | HG01167.hp2 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(2687): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2679): Show |
1 | a0001c0001t0002g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2690): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2718): Show |
1 | a0001c0001t0012g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2729): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(2718): Show |
1 | a0001c0001t0012g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(2729): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3166): Show |
2 | a0001c0001t0006g0007 a0001c0001t0006g0008 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(3177): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3166): Show |
1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3177): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3125): Show |
10 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0203 others(7): Show |
10 | HG00423.hp1 HG00597.hp2 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3125): Show |
1 | a0001c0001t0003g0224 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3125): Show |
1 | a0001c0001t0003g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3505): Show |
1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3516): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7979): Show |
1 | a0001c0001t0002g0172 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(7990): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3432): Show |
1 | a0001c0001t0009g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3443): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3356): Show |
1 | a0001c0001t0009g0115 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3367): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(3356): Show |
1 | a0001c0001t0009g0228 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(3367): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | CATTAAGG others(7561): Show |
1 | a0001c0001t0002g0194 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.1791+1663_1791+166 others(7572): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915966 | ||||||
chr7:158915966 | C | G | 5 | a0001c0001t0002g0185 a0001c0001t0003g0216 a0002c0002t0001g0093 others(2): Show |
5 | HG02976.hp2 HG03688.hp1 HG04204.hp2 others(2): Show |
intron_variant | MODIFIER | c.1791+1645C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915966 | |||||||
chr7:158915979 | T | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1658T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915979 | |||||||
chr7:158915987 | G | A | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1666G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915987 | |||||||
chr7:158915987 | G | C | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1666G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915987 | |||||||
chr7:158915987 | G | GTTTACAC others(69): Show |
9 | a0001c0001t0002g0193 a0002c0002t0001g0044 a0002c0002t0001g0045 others(6): Show |
9 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1791+1667_1791+166 others(80): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915987 | ||||||
chr7:158915987 | G | GTTTACAC others(4000): Show |
1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1791+1667_1791+166 others(4011): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158915987 | ||||||
chr7:158915989 | C | A | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1791+1668C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915989 | |||||||
chr7:158915989 | C | T | 92 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(89): Show |
92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1791+1668C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915989 | |||||||
chr7:158915990 | G | A | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1669G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915990 | |||||||
chr7:158915990 | G | T | 92 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(89): Show |
92 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1791+1669G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915990 | |||||||
chr7:158915996 | C | G | 12 | a0001c0001t0002g0193 a0001c0022t0018g0229 a0002c0002t0001g0044 others(9): Show |
12 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1791+1675C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158915996 | |||||||
chr7:158916004 | C | G | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(90): Show |
93 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.1791+1683C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916004 | |||||||
chr7:158916021 | A | C | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1700A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916021 | |||||||
chr7:158916025 | G | C | 12 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0002c0002t0001g0044 others(9): Show |
12 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(9): Show |
intron_variant | MODIFIER | c.1791+1704G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916025 | |||||||
chr7:158916025 | G | GTCGACAT others(446): Show |
4 | a0002c0002t0001g0074 a0002c0002t0001g0076 a0002c0002t0001g0082 others(1): Show |
4 | HG01123.hp2 HG01346.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1706_1791+170 others(457): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916025 | ||||||
chr7:158916025 | G | GTCGACAT others(484): Show |
1 | a0002c0002t0001g0038 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1791+1706_1791+170 others(495): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916025 | ||||||
chr7:158916026 | T | TCGACATG others(142): Show |
1 | a0002c0002t0001g0097 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1791+1706_1791+170 others(153): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916026 | ||||||
chr7:158916026 | T | TCGACATG others(142): Show |
1 | a0002c0002t0017g0029 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1791+1706_1791+170 others(153): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916026 | ||||||
chr7:158916026 | T | TCGACATG others(142): Show |
82 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(79): Show |
82 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1791+1706_1791+170 others(153): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916026 | ||||||
chr7:158916026 | T | TCGACATG others(329): Show |
1 | a0002c0002t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1791+1706_1791+170 others(340): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916026 | ||||||
chr7:158916027 | C | CGACATGC others(3087): Show |
1 | a0005c0008t0003g0223 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1791+1706_1791+170 others(3098): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916027 | |||||||
chr7:158916027 | C | CGACATGC others(3090): Show |
3 | a0005c0008t0003g0221 a0007c0009t0003g0220 a0007c0009t0020g0222 |
3 | HG02258.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1791+1706_1791+170 others(3101): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916027 | |||||||
chr7:158916027 | C | T | 118 | a0001c0001t0001g0006 a0001c0001t0002g0003 a0001c0001t0002g0004 others(115): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1791+1706C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916027 | |||||||
chr7:158916028 | T | A | 9 | a0001c0001t0002g0193 a0002c0002t0001g0044 a0002c0002t0001g0045 others(6): Show |
9 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.1791+1707T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916028 | |||||||
chr7:158916028 | T | G | 228 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(225): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.1791+1707T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916028 | |||||||
chr7:158916028 | T | TACACGCT others(4238): Show |
1 | a0003c0027t0022g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4238): Show |
1 | a0003c0003t0004g0241 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4577): Show |
1 | a0003c0003t0004g0266 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4588): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4574): Show |
1 | a0003c0003t0004g0267 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4585): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4238): Show |
1 | a0003c0003t0004g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4613): Show |
2 | a0003c0003t0004g0256 a0003c0003t0004g0265 |
2 | HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1791+1743_1791+174 others(4624): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4276): Show |
1 | a0003c0003t0007g0242 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4287): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4238): Show |
8 | a0003c0003t0004g0243 a0003c0003t0004g0244 a0003c0003t0004g0251 others(5): Show |
8 | HG00408.hp1 HG00733.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(3747): Show |
1 | a0003c0003t0007g0248 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(3758): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4537): Show |
2 | a0008c0007t0008g0113 a0008c0007t0008g0114 |
2 | HG02809.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1791+1743_1791+174 others(4548): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4233): Show |
1 | a0003c0003t0004g0255 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4244): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(5176): Show |
1 | a0003c0003t0004g0237 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(5187): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(5100): Show |
1 | a0003c0003t0004g0245 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(5111): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(5214): Show |
2 | a0003c0003t0004g0253 a0003c0003t0004g0257 |
2 | HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1791+1743_1791+174 others(5225): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(5176): Show |
1 | a0003c0003t0004g0254 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(5187): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4577): Show |
1 | a0003c0003t0004g0264 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4588): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4238): Show |
1 | a0003c0003t0007g0239 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(4238): Show |
1 | a0003c0003t0004g0246 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(4249): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(5176): Show |
1 | a0003c0003t0004g0238 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(5187): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916028 | T | TACACGCT others(5179): Show |
1 | a0003c0003t0004g0258 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1791+1743_1791+174 others(5190): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916028 | ||||||
chr7:158916034 | C | G | 5 | a0001c0001t0005g0161 a0002c0002t0001g0074 a0002c0002t0001g0076 others(2): Show |
5 | HG01123.hp2 HG01346.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1791+1713C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916034 | |||||||
chr7:158916042 | G | C | 96 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(93): Show |
96 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(93): Show |
intron_variant | MODIFIER | c.1791+1721G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916042 | |||||||
chr7:158916062 | C | T | 3 | a0001c0001t0002g0126 a0001c0001t0002g0133 a0002c0018t0015g0048 |
3 | HG01081.hp2 NA19065.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.1791+1741C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916062 | |||||||
chr7:158916063 | G | A | 4 | a0002c0002t0001g0074 a0002c0002t0001g0076 a0002c0002t0001g0082 others(1): Show |
4 | HG01123.hp2 HG01346.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1742G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916063 | |||||||
chr7:158916063 | G | C | 87 | a0001c0001t0005g0161 a0001c0001t0005g0190 a0001c0001t0005g0192 others(84): Show |
87 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1791+1742G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916063 | |||||||
chr7:158916063 | G | GTCGACAC others(6316): Show |
2 | a0001c0021t0008g0112 a0002c0005t0010g0100 |
2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1791+1743_1791+174 others(6327): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916063 | ||||||
chr7:158916064 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1791+1743T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916064 | |||||||
chr7:158916065 | T | C | 118 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.1791+1744T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916065 | |||||||
chr7:158916066 | G | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1791+1745G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916066 | |||||||
chr7:158916070 | C | T | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1749C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916070 | |||||||
chr7:158916071 | G | A | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1750G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916071 | |||||||
chr7:158916072 | C | G | 87 | a0001c0001t0005g0161 a0001c0001t0005g0190 a0001c0001t0005g0192 others(84): Show |
87 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1791+1751C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916072 | |||||||
chr7:158916080 | G | C | 7 | a0002c0002t0001g0038 a0002c0002t0001g0062 a0002c0002t0001g0074 others(4): Show |
7 | HG01081.hp2 HG01123.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1791+1759G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916080 | |||||||
chr7:158916086 | G | GGAT | 107 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(104): Show |
107 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1791+1766_1791+176 others(7): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916086 | ||||||
chr7:158916086 | G | GGATGATT others(34): Show |
1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1768_1791+176 others(45): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916086 | ||||||
chr7:158916086 | G | GGATGATT others(107): Show |
8 | a0002c0002t0001g0044 a0002c0002t0001g0045 a0002c0002t0001g0046 others(5): Show |
8 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.1791+1768_1791+176 others(118): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916086 | ||||||
chr7:158916086 | G | GGATGATT others(110): Show |
1 | a0001c0001t0002g0193 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1791+1768_1791+176 others(121): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916086 | ||||||
chr7:158916086 | G | GGATGATT others(148): Show |
1 | a0002c0002t0001g0062 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1791+1768_1791+176 others(159): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916086 | ||||||
chr7:158916097 | C | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1791+1776C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916097 | |||||||
chr7:158916098 | G | A | 178 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(175): Show |
178 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(175): Show |
intron_variant | MODIFIER | c.1791+1777G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916098 | |||||||
chr7:158916098 | G | C | 11 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(8): Show |
11 | HG01081.hp2 HG01433.hp1 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.1791+1777G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916098 | |||||||
chr7:158916100 | C | G | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1779C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916100 | |||||||
chr7:158916100 | C | T | 3 | a0001c0001t0005g0161 a0003c0003t0004g0255 a0003c0003t0004g0258 |
3 | HG01358.hp1 HG02015.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.1791+1779C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916100 | |||||||
chr7:158916101 | G | A | 85 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(82): Show |
85 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1791+1780G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916101 | |||||||
chr7:158916107 | C | CTGGTTGA others(145): Show |
1 | a0002c0002t0001g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1791+1814_1791+181 others(156): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916107 | ||||||
chr7:158916107 | C | G | 1 | a0002c0002t0001g0093 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1791+1786C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916107 | |||||||
chr7:158916114 | A | G | 85 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(82): Show |
85 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1791+1793A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916114 | |||||||
chr7:158916115 | C | G | 15 | a0001c0001t0002g0193 a0002c0002t0001g0030 a0002c0002t0001g0044 others(12): Show |
15 | HG00140.hp1 HG00733.hp2 HG01175.hp1 others(12): Show |
intron_variant | MODIFIER | c.1791+1794C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916115 | |||||||
chr7:158916124 | T | TGATTGTG others(329): Show |
3 | a0001c0001t0003g0208 a0001c0001t0003g0211 a0001c0001t0003g0214 |
3 | HG02083.hp1 HG02129.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.1791+1814_1791+181 others(340): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916124 | ||||||
chr7:158916136 | G | A | 1 | a0002c0002t0001g0093 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1791+1815G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916136 | |||||||
chr7:158916136 | G | C | 4 | a0003c0010t0011g0252 a0003c0010t0011g0261 a0003c0028t0023g0260 others(1): Show |
4 | HG00140.hp1 HG02922.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+1815G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916136 | |||||||
chr7:158916143 | T | C | 129 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(126): Show |
129 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(126): Show |
intron_variant | MODIFIER | c.1791+1822T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916143 | |||||||
chr7:158916144 | G | T | 1 | a0001c0001t0002g0193 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1791+1823G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916144 | |||||||
chr7:158916145 | G | C | 116 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(113): Show |
116 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.1791+1824G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916145 | |||||||
chr7:158916145 | G | GTGGTTGA others(31): Show |
1 | a0003c0029t0004g0249 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1791+1856_1791+189 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916145 | ||||||
chr7:158916146 | T | TCGTTGAC others(590): Show |
1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1825_1791+182 others(601): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916146 | |||||||
chr7:158916153 | C | G | 84 | a0001c0001t0002g0193 a0001c0001t0005g0190 a0001c0001t0005g0192 others(81): Show |
84 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1791+1832C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916153 | |||||||
chr7:158916157 | A | T | 2 | a0003c0003t0004g0262 a0003c0027t0022g0263 |
2 | HG02055.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1791+1836A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916157 | |||||||
chr7:158916174 | G | A | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1853G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916174 | |||||||
chr7:158916174 | G | C | 4 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0002c0018t0015g0048 others(1): Show |
4 | HG01081.hp2 HG02922.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+1853G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916174 | |||||||
chr7:158916176 | C | G | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1855C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916176 | |||||||
chr7:158916177 | G | A | 5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG01433.hp1 HG01934.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+1856G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916177 | |||||||
chr7:158916183 | C | G | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1862C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916183 | |||||||
chr7:158916191 | C | G | 88 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(85): Show |
88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1791+1870C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916191 | |||||||
chr7:158916212 | G | C | 7 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(4): Show |
7 | HG01433.hp1 HG01934.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1791+1891G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916212 | |||||||
chr7:158916214 | C | CGACACGC others(780): Show |
1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+1893_1791+189 others(791): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916214 | |||||||
chr7:158916215 | T | A | 3 | a0001c0001t0005g0161 a0002c0002t0001g0067 a0010c0023t0001g0272 |
3 | HG00140.hp1 HG01975.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.1791+1894T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916215 | |||||||
chr7:158916215 | T | G | 112 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(109): Show |
112 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1791+1894T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916215 | |||||||
chr7:158916221 | C | G | 7 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(4): Show |
7 | HG01433.hp1 HG01934.hp1 HG01981.hp1 others(4): Show |
intron_variant | MODIFIER | c.1791+1900C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916221 | |||||||
chr7:158916229 | C | G | 14 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(11): Show |
14 | HG01123.hp2 HG01243.hp1 HG01346.hp2 others(11): Show |
intron_variant | MODIFIER | c.1791+1908C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916229 | |||||||
chr7:158916242 | T | G | 5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG01433.hp1 HG01934.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+1921T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916242 | |||||||
chr7:158916242 | T | TGTGAAAC others(31): Show |
1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1791+1928_1791+192 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916242 | ||||||
chr7:158916250 | G | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1929G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916250 | |||||||
chr7:158916250 | G | C | 10 | a0001c0001t0002g0193 a0002c0002t0001g0038 a0002c0002t0001g0044 others(7): Show |
10 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+1929G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916250 | |||||||
chr7:158916252 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1931C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916252 | |||||||
chr7:158916253 | T | G | 131 | a0001c0001t0002g0193 a0001c0001t0003g0199 a0001c0001t0003g0200 others(128): Show |
131 | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1791+1932T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916253 | |||||||
chr7:158916257 | C | T | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+1936C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916257 | |||||||
chr7:158916259 | C | G | 10 | a0001c0001t0002g0193 a0002c0002t0001g0038 a0002c0002t0001g0044 others(7): Show |
10 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+1938C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916259 | |||||||
chr7:158916263 | T | C | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1942T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916263 | |||||||
chr7:158916267 | C | G | 11 | a0001c0001t0002g0193 a0002c0002t0001g0038 a0002c0002t0001g0044 others(8): Show |
11 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(8): Show |
intron_variant | MODIFIER | c.1791+1946C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916267 | |||||||
chr7:158916271 | T | A | 108 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(105): Show |
108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1791+1950T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916271 | |||||||
chr7:158916288 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1967C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916288 | |||||||
chr7:158916288 | C | G | 6 | a0002c0002t0001g0030 a0002c0002t0001g0081 a0002c0002t0001g0088 others(3): Show |
6 | HG01257.hp1 HG02976.hp2 HG03654.hp1 others(3): Show |
intron_variant | MODIFIER | c.1791+1967C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916288 | |||||||
chr7:158916290 | C | T | 3 | a0002c0002t0001g0030 a0002c0002t0001g0081 a0002c0002t0001g0088 |
3 | HG01257.hp1 HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1969C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916290 | |||||||
chr7:158916291 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+1970G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916291 | |||||||
chr7:158916291 | G | T | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+1970G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916291 | |||||||
chr7:158916297 | G | C | 27 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(24): Show |
27 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.1791+1976G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916297 | |||||||
chr7:158916305 | G | C | 6 | a0002c0002t0001g0030 a0002c0002t0001g0081 a0002c0002t0001g0088 others(3): Show |
6 | HG01081.hp2 HG01257.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1791+1984G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916305 | |||||||
chr7:158916305 | G | GATTAAGG others(107): Show |
1 | a0002c0002t0001g0082 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1791+2004_1791+200 others(118): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916305 | ||||||
chr7:158916326 | G | A | 10 | a0001c0001t0002g0193 a0002c0002t0001g0038 a0002c0002t0001g0044 others(7): Show |
10 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.1791+2005G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916326 | |||||||
chr7:158916326 | G | C | 91 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(88): Show |
91 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1791+2005G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916326 | |||||||
chr7:158916328 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1791+2007C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916328 | |||||||
chr7:158916329 | T | G | 107 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(104): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1791+2008T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916329 | |||||||
chr7:158916333 | C | T | 3 | a0002c0002t0001g0030 a0002c0002t0001g0082 a0002c0002t0001g0088 |
3 | HG01123.hp2 HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1791+2012C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916333 | |||||||
chr7:158916335 | C | G | 91 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(88): Show |
91 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1791+2014C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916335 | |||||||
chr7:158916343 | C | G | 91 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(88): Show |
91 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1791+2022C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916343 | |||||||
chr7:158916363 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+2042C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916363 | |||||||
chr7:158916364 | G | A | 89 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(86): Show |
89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1791+2043G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916364 | |||||||
chr7:158916364 | G | C | 3 | a0002c0002t0001g0093 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG02976.hp2 HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+2043G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916364 | |||||||
chr7:158916366 | C | T | 1 | a0002c0002t0001g0038 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1791+2045C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916366 | |||||||
chr7:158916367 | G | A | 2 | a0002c0002t0001g0049 a0002c0002t0001g0064 |
2 | NA19070.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1791+2046G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916367 | |||||||
chr7:158916367 | G | T | 47 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(44): Show |
47 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.1791+2046G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916367 | |||||||
chr7:158916371 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+2050C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916371 | |||||||
chr7:158916373 | C | G | 4 | a0002c0002t0001g0038 a0002c0002t0001g0093 a0003c0010t0011g0252 others(1): Show |
4 | HG02976.hp2 HG03017.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+2052C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916373 | |||||||
chr7:158916381 | C | G | 4 | a0001c0001t0005g0142 a0002c0002t0001g0093 a0003c0010t0011g0252 others(1): Show |
4 | HG01517.hp1 HG02976.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+2060C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916381 | |||||||
chr7:158916402 | G | A | 1 | a0002c0002t0001g0027 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1791+2081G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916402 | |||||||
chr7:158916402 | G | C | 4 | a0001c0001t0005g0161 a0002c0002t0001g0093 a0003c0010t0011g0252 others(1): Show |
4 | HG02015.hp2 HG02976.hp2 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1791+2081G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916402 | |||||||
chr7:158916402 | G | GTCGCTGG others(1125): Show |
1 | a0002c0002t0001g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1791+2084_1791+208 others(1136): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916402 | ||||||
chr7:158916404 | C | CGGCATGC others(31): Show |
1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+2084_1791+208 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916404 | ||||||
chr7:158916404 | C | T | 6 | a0002c0002t0001g0062 a0002c0002t0001g0074 a0002c0002t0001g0076 others(3): Show |
6 | HG01243.hp1 HG01346.hp2 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1791+2083C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916404 | |||||||
chr7:158916405 | G | T | 4 | a0002c0002t0001g0062 a0002c0002t0001g0074 a0002c0002t0001g0076 others(1): Show |
4 | HG01243.hp1 HG01346.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+2084G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916405 | |||||||
chr7:158916409 | C | T | 1 | a0002c0002t0001g0038 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1791+2088C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916409 | |||||||
chr7:158916411 | C | G | 5 | a0002c0002t0001g0062 a0002c0002t0001g0074 a0002c0002t0001g0076 others(2): Show |
5 | HG01243.hp1 HG01346.hp2 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1791+2090C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916411 | |||||||
chr7:158916419 | C | G | 3 | a0002c0002t0001g0093 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG02976.hp2 HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+2098C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916419 | |||||||
chr7:158916440 | G | A | 1 | a0002c0002t0001g0093 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1791+2119G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916440 | |||||||
chr7:158916440 | G | GTCGACAC others(183): Show |
1 | a0002c0002t0001g0101 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1791+2135_1791+213 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916440 | ||||||
chr7:158916443 | G | T | 25 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(22): Show |
25 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1791+2122G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916443 | |||||||
chr7:158916447 | C | T | 4 | a0002c0002t0001g0062 a0002c0002t0001g0074 a0002c0002t0001g0076 others(1): Show |
4 | HG01243.hp1 HG01346.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.1791+2126C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916447 | |||||||
chr7:158916449 | C | CTGGTTGA others(221): Show |
3 | a0002c0002t0001g0045 a0002c0002t0001g0053 a0002c0002t0001g0075 |
3 | HG00733.hp2 HG01516.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1791+2135_1791+213 others(232): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916449 | ||||||
chr7:158916457 | C | G | 8 | a0001c0001t0002g0193 a0002c0002t0001g0010 a0002c0002t0001g0044 others(5): Show |
8 | HG01175.hp1 HG01496.hp1 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.1791+2136C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916457 | |||||||
chr7:158916459 | T | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+2138T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916459 | |||||||
chr7:158916461 | T | A | 108 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(105): Show |
108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1791+2140T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916461 | |||||||
chr7:158916469 | T | C | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+2148T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916469 | |||||||
chr7:158916478 | G | A | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+2157G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916478 | |||||||
chr7:158916478 | G | C | 3 | a0001c0001t0005g0161 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG02015.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+2157G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916478 | |||||||
chr7:158916480 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1791+2159C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916480 | |||||||
chr7:158916480 | C | T | 5 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0002c0002t0001g0093 others(2): Show |
5 | HG02976.hp2 HG03654.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+2159C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916480 | |||||||
chr7:158916481 | T | G | 107 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(104): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1791+2160T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916481 | |||||||
chr7:158916485 | T | C | 198 | a0001c0001t0001g0006 a0001c0001t0002g0003 a0001c0001t0002g0004 others(195): Show |
198 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.1791+2164T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916485 | |||||||
chr7:158916485 | T | G | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+2164T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916485 | |||||||
chr7:158916487 | C | G | 5 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0002c0002t0001g0093 others(2): Show |
5 | HG02976.hp2 HG03654.hp1 HG03688.hp1 others(2): Show |
intron_variant | MODIFIER | c.1791+2166C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916487 | |||||||
chr7:158916490 | G | A | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1791+2169G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916490 | |||||||
chr7:158916495 | C | G | 89 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(86): Show |
89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1791+2174C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916495 | |||||||
chr7:158916499 | A | T | 1 | a0001c0001t0002g0177 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.1791+2178A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916499 | |||||||
chr7:158916516 | G | C | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1791+2195G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916516 | |||||||
chr7:158916518 | C | T | 6 | a0002c0002t0001g0025 a0002c0002t0001g0030 a0002c0002t0001g0050 others(3): Show |
6 | HG02486.hp1 HG03654.hp1 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.1791+2197C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916518 | |||||||
chr7:158916519 | T | G | 107 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(104): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1791+2198T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916519 | |||||||
chr7:158916523 | C | T | 6 | a0002c0002t0001g0093 a0003c0003t0004g0256 a0003c0003t0004g0264 others(3): Show |
6 | HG02015.hp1 HG02155.hp1 HG03491.hp2 others(3): Show |
intron_variant | MODIFIER | c.1791+2202C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916523 | |||||||
chr7:158916525 | C | G | 1 | a0002c0002t0001g0101 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1791+2204C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916525 | |||||||
chr7:158916533 | C | CATTAAGG others(183): Show |
1 | a0001c0001t0002g0193 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1792-2185_1792-218 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916533 | ||||||
chr7:158916533 | C | G | 87 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(84): Show |
87 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1792-2207C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916533 | |||||||
chr7:158916540 | G | A | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1792-2200G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916540 | |||||||
chr7:158916554 | G | C | 6 | a0001c0001t0005g0161 a0002c0002t0001g0044 a0002c0002t0001g0046 others(3): Show |
6 | HG01081.hp2 HG01175.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-2186G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916554 | |||||||
chr7:158916561 | C | T | 1 | a0002c0002t0001g0101 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1792-2179C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916561 | |||||||
chr7:158916562 | G | A | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-2178G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916562 | |||||||
chr7:158916563 | C | G | 6 | a0001c0001t0005g0161 a0002c0002t0001g0044 a0002c0002t0001g0046 others(3): Show |
6 | HG01081.hp2 HG01175.hp1 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-2177C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916563 | |||||||
chr7:158916571 | C | CATTAAGG others(69): Show |
1 | a0002c0002t0001g0066 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-2149_1792-214 others(80): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916571 | ||||||
chr7:158916571 | C | G | 5 | a0002c0002t0001g0044 a0002c0002t0001g0046 a0002c0002t0001g0077 others(2): Show |
5 | HG01175.hp1 HG01257.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792-2169C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916571 | |||||||
chr7:158916571 | C | T | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-2169C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916571 | |||||||
chr7:158916592 | G | A | 1 | a0002c0002t0001g0066 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-2148G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916592 | |||||||
chr7:158916592 | G | C | 218 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(215): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.1792-2148G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916592 | |||||||
chr7:158916592 | G | GTCGCTGG others(26): Show |
2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2145_1792-214 others(37): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916592 | ||||||
chr7:158916595 | G | A | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1792-2145G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916595 | |||||||
chr7:158916599 | C | G | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2141C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916599 | |||||||
chr7:158916601 | C | G | 88 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(85): Show |
88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1792-2139C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916601 | |||||||
chr7:158916609 | C | G | 88 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(85): Show |
88 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.1792-2131C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916609 | |||||||
chr7:158916630 | G | A | 4 | a0002c0002t0001g0044 a0002c0002t0001g0046 a0002c0002t0001g0077 others(1): Show |
4 | HG01175.hp1 HG01496.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-2110G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916630 | |||||||
chr7:158916630 | G | C | 89 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(86): Show |
89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1792-2110G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916630 | |||||||
chr7:158916632 | C | G | 1 | a0001c0001t0005g0142 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1792-2108C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916632 | |||||||
chr7:158916632 | C | T | 2 | a0002c0002t0001g0053 a0002c0002t0001g0066 |
2 | HG01943.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.1792-2108C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916632 | |||||||
chr7:158916633 | T | A | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-2107T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916633 | |||||||
chr7:158916633 | T | G | 106 | a0001c0001t0001g0270 a0001c0001t0002g0193 a0001c0001t0005g0161 others(103): Show |
106 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1792-2107T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916633 | |||||||
chr7:158916637 | C | T | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2103C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916637 | |||||||
chr7:158916639 | C | G | 89 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(86): Show |
89 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1792-2101C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916639 | |||||||
chr7:158916647 | C | G | 90 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(87): Show |
90 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1792-2093C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916647 | |||||||
chr7:158916651 | T | A | 108 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(105): Show |
108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1792-2089T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916651 | |||||||
chr7:158916655 | G | A | 108 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(105): Show |
108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.1792-2085G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916655 | |||||||
chr7:158916668 | C | A | 84 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(81): Show |
84 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(81): Show |
intron_variant | MODIFIER | c.1792-2072C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916668 | |||||||
chr7:158916668 | C | G | 16 | a0002c0002t0001g0038 a0002c0002t0001g0044 a0002c0002t0001g0045 others(13): Show |
16 | HG00733.hp2 HG01123.hp2 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1792-2072C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916668 | |||||||
chr7:158916670 | C | T | 7 | a0002c0002t0001g0044 a0002c0002t0001g0045 a0002c0002t0001g0046 others(4): Show |
7 | HG00733.hp2 HG01175.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-2070C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916670 | |||||||
chr7:158916671 | G | A | 4 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0003c0010t0011g0252 others(1): Show |
4 | HG02055.hp1 HG02723.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-2069G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916671 | |||||||
chr7:158916671 | G | T | 4 | a0002c0002t0001g0044 a0002c0002t0001g0046 a0002c0002t0001g0077 others(1): Show |
4 | HG01175.hp1 HG01496.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-2069G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916671 | |||||||
chr7:158916676 | G | A | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2064G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916676 | |||||||
chr7:158916677 | G | C | 86 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(83): Show |
86 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1792-2063G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916677 | |||||||
chr7:158916685 | G | C | 101 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(98): Show |
101 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(98): Show |
intron_variant | MODIFIER | c.1792-2055G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916685 | |||||||
chr7:158916685 | G | T | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2055G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916685 | |||||||
chr7:158916693 | A | G | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1792-2047A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916693 | |||||||
chr7:158916706 | G | A | 2 | a0001c0001t0002g0193 a0002c0002t0001g0081 |
2 | HG01257.hp1 HG02071.hp1 |
intron_variant | MODIFIER | c.1792-2034G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916706 | |||||||
chr7:158916706 | G | C | 4 | a0001c0001t0005g0161 a0002c0002t0001g0030 a0002c0002t0001g0088 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.1792-2034G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916706 | |||||||
chr7:158916708 | C | T | 87 | a0001c0001t0005g0161 a0001c0001t0005g0190 a0001c0001t0005g0192 others(84): Show |
87 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1792-2032C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916708 | |||||||
chr7:158916709 | T | G | 11 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0002c0002t0001g0044 others(8): Show |
11 | HG01081.hp2 HG01175.hp1 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1792-2031T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916709 | |||||||
chr7:158916710 | G | A | 106 | a0001c0001t0002g0193 a0001c0001t0005g0161 a0001c0001t0005g0190 others(103): Show |
106 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1792-2030G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916710 | |||||||
chr7:158916713 | C | T | 6 | a0002c0002t0001g0044 a0002c0002t0001g0046 a0002c0002t0001g0077 others(3): Show |
6 | HG01175.hp1 HG01496.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792-2027C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916713 | |||||||
chr7:158916715 | C | G | 86 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(83): Show |
86 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(83): Show |
intron_variant | MODIFIER | c.1792-2025C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916715 | |||||||
chr7:158916723 | C | G | 3 | a0001c0001t0005g0161 a0002c0002t0001g0030 a0002c0002t0001g0088 |
3 | HG02015.hp2 HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-2017C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916723 | |||||||
chr7:158916744 | G | GTCGCTGG others(140): Show |
1 | a0002c0002t0001g0053 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1792-1994_1792-199 others(151): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916744 | ||||||
chr7:158916746 | C | T | 3 | a0002c0002t0001g0081 a0002c0002t0001g0101 a0002c0018t0015g0048 |
3 | HG01081.hp2 HG01257.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.1792-1994C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916746 | |||||||
chr7:158916747 | T | G | 199 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(196): Show |
199 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(196): Show |
intron_variant | MODIFIER | c.1792-1993T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916747 | |||||||
chr7:158916747 | T | TACACGCT others(31): Show |
1 | a0001c0001t0019g0235 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1792-1917_1792-188 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916747 | ||||||
chr7:158916748 | A | G | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1792-1992A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916748 | |||||||
chr7:158916751 | C | T | 82 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(79): Show |
82 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1792-1989C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916751 | |||||||
chr7:158916753 | C | G | 1 | a0002c0002t0001g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1792-1987C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916753 | |||||||
chr7:158916761 | C | CAGTAAGG others(400): Show |
1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1978_1792-197 others(411): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916761 | ||||||
chr7:158916761 | C | G | 3 | a0002c0002t0001g0030 a0002c0002t0001g0053 a0002c0002t0001g0088 |
3 | HG03654.hp1 HG03942.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-1979C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916761 | |||||||
chr7:158916764 | T | C | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-1976T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916764 | |||||||
chr7:158916764 | T | TAAGGATG others(178): Show |
7 | a0002c0002t0001g0045 a0002c0002t0001g0062 a0002c0002t0001g0074 others(4): Show |
7 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-1955_1792-195 others(189): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916764 | ||||||
chr7:158916764 | T | TAAGGATG others(178): Show |
1 | a0002c0002t0001g0038 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1792-1955_1792-195 others(189): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916764 | ||||||
chr7:158916782 | G | C | 2 | a0002c0002t0001g0030 a0002c0002t0001g0088 |
2 | HG03654.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-1958G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916782 | |||||||
chr7:158916782 | G | GTCGCTGG others(216): Show |
1 | a0002c0002t0001g0093 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1792-1955_1792-195 others(227): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916782 | ||||||
chr7:158916785 | G | A | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1955G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916785 | |||||||
chr7:158916789 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1792-1951C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916789 | |||||||
chr7:158916799 | C | G | 12 | a0002c0002t0001g0038 a0002c0002t0001g0045 a0002c0002t0001g0053 others(9): Show |
12 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.1792-1941C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916799 | |||||||
chr7:158916800 | A | G | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1792-1940A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916800 | |||||||
chr7:158916802 | T | C | 9 | a0002c0002t0001g0038 a0002c0002t0001g0045 a0002c0002t0001g0053 others(6): Show |
9 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(6): Show |
intron_variant | MODIFIER | c.1792-1938T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916802 | |||||||
chr7:158916819 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1921C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916819 | |||||||
chr7:158916820 | G | C | 10 | a0002c0002t0001g0038 a0002c0002t0001g0045 a0002c0002t0001g0053 others(7): Show |
10 | HG00733.hp2 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1792-1920G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916820 | |||||||
chr7:158916820 | G | GTCGCTGG others(216): Show |
1 | a0002c0002t0001g0101 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1792-1917_1792-191 others(227): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916820 | ||||||
chr7:158916820 | G | T | 1 | a0001c0001t0002g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1792-1920G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916820 | |||||||
chr7:158916822 | C | T | 1 | a0002c0002t0001g0066 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-1918C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916822 | |||||||
chr7:158916823 | G | GACACGCT others(3472): Show |
1 | a0001c0001t0002g0193 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1792-1904_1792-190 others(3483): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916823 | ||||||
chr7:158916827 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1913C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916827 | |||||||
chr7:158916829 | C | G | 1 | a0002c0002t0001g0066 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-1911C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916829 | |||||||
chr7:158916837 | C | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1903C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916837 | |||||||
chr7:158916858 | G | C | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1882G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916858 | |||||||
chr7:158916858 | G | GTCGCTGG others(216): Show |
1 | a0012c0015t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1792-1880_1792-187 others(227): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916858 | ||||||
chr7:158916860 | C | T | 1 | a0002c0002t0001g0066 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-1880C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916860 | |||||||
chr7:158916861 | T | G | 106 | a0001c0001t0005g0161 a0001c0001t0005g0190 a0001c0001t0005g0192 others(103): Show |
106 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.1792-1879T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916861 | |||||||
chr7:158916862 | A | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1878A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916862 | |||||||
chr7:158916865 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1875C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916865 | |||||||
chr7:158916867 | C | G | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1873C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916867 | |||||||
chr7:158916875 | C | G | 9 | a0001c0001t0005g0161 a0002c0002t0001g0021 a0002c0002t0001g0030 others(6): Show |
9 | HG02015.hp2 HG02109.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1792-1865C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916875 | |||||||
chr7:158916879 | T | A | 107 | a0001c0001t0005g0161 a0001c0001t0005g0190 a0001c0001t0005g0192 others(104): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.1792-1861T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916879 | |||||||
chr7:158916896 | C | G | 103 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(100): Show |
103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.1792-1844C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916896 | |||||||
chr7:158916898 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1842C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916898 | |||||||
chr7:158916898 | C | T | 87 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(84): Show |
87 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1792-1842C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916898 | |||||||
chr7:158916899 | G | T | 3 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0002c0002t0001g0093 |
3 | HG03654.hp1 HG03688.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-1841G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916899 | |||||||
chr7:158916905 | G | C | 17 | a0001c0001t0005g0161 a0002c0002t0001g0030 a0002c0002t0001g0038 others(14): Show |
17 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.1792-1835G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916905 | |||||||
chr7:158916913 | G | C | 96 | a0001c0001t0005g0161 a0001c0001t0005g0190 a0001c0001t0005g0192 others(93): Show |
96 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.1792-1827G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916913 | |||||||
chr7:158916914 | A | G | 3 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0002c0002t0001g0093 |
3 | HG03654.hp1 HG03688.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.1792-1826A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916914 | |||||||
chr7:158916926 | T | G | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1814T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916926 | |||||||
chr7:158916934 | G | C | 4 | a0002c0002t0001g0030 a0002c0002t0001g0088 a0002c0002t0001g0093 others(1): Show |
4 | HG01081.hp2 HG03654.hp1 HG03688.hp1 others(1): Show |
intron_variant | MODIFIER | c.1792-1806G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916934 | |||||||
chr7:158916934 | G | GTCGCTGG others(368): Show |
1 | a0002c0002t0001g0066 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1792-1804_1792-180 others(379): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916934 | ||||||
chr7:158916936 | C | T | 87 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(84): Show |
87 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(84): Show |
intron_variant | MODIFIER | c.1792-1804C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916936 | |||||||
chr7:158916937 | T | G | 10 | a0001c0001t0005g0161 a0002c0002t0001g0030 a0002c0002t0001g0066 others(7): Show |
10 | HG01081.hp2 HG01257.hp1 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.1792-1803T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916937 | |||||||
chr7:158916941 | C | T | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1799C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916941 | |||||||
chr7:158916943 | C | CTGGTTGA others(442): Show |
1 | a0002c0002t0001g0022 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1792-1775_1792-177 others(453): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916943 | ||||||
chr7:158916943 | C | CTGGTTGA others(31): Show |
2 | a0002c0002t0001g0053 a0002c0002t0001g0101 |
2 | HG02486.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1792-1789_1792-178 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916943 | ||||||
chr7:158916943 | C | G | 5 | a0002c0002t0001g0030 a0002c0002t0001g0066 a0002c0002t0001g0081 others(2): Show |
5 | HG01257.hp1 HG01943.hp2 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792-1797C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916943 | |||||||
chr7:158916951 | C | G | 1 | a0012c0015t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1792-1789C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916951 | |||||||
chr7:158916952 | A | G | 8 | a0002c0002t0001g0038 a0002c0002t0001g0045 a0002c0002t0001g0062 others(5): Show |
8 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1788A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916952 | |||||||
chr7:158916963 | T | G | 1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1792-1777T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916963 | |||||||
chr7:158916963 | TTG | T | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1774_1792-177 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158916963 | ||||||
chr7:158916971 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1792-1769C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916971 | |||||||
chr7:158916972 | G | C | 10 | a0001c0001t0005g0161 a0002c0002t0001g0038 a0002c0002t0001g0045 others(7): Show |
10 | HG00733.hp2 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1792-1768G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916972 | |||||||
chr7:158916974 | C | A | 88 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(85): Show |
88 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(85): Show |
intron_variant | MODIFIER | c.1792-1766C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916974 | |||||||
chr7:158916974 | C | T | 1 | a0002c0002t0001g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1792-1766C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916974 | |||||||
chr7:158916975 | T | G | 203 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(200): Show |
203 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(200): Show |
intron_variant | MODIFIER | c.1792-1765T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916975 | |||||||
chr7:158916981 | C | G | 10 | a0001c0001t0005g0161 a0002c0002t0001g0038 a0002c0002t0001g0045 others(7): Show |
10 | HG00733.hp2 HG01081.hp2 HG01123.hp2 others(7): Show |
intron_variant | MODIFIER | c.1792-1759C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916981 | |||||||
chr7:158916989 | C | G | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1751C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916989 | |||||||
chr7:158916990 | A | G | 1 | a0012c0015t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1792-1750A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158916990 | |||||||
chr7:158917001 | TTG | T | 7 | a0002c0002t0001g0022 a0002c0002t0001g0030 a0002c0002t0001g0053 others(4): Show |
7 | HG01943.hp2 HG02486.hp1 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1792-1736_1792-173 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917001 | ||||||
chr7:158917002 | T | G | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1738T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917002 | |||||||
chr7:158917003 | G | GTGAAACG others(442): Show |
3 | a0002c0002t0001g0044 a0002c0002t0001g0046 a0002c0002t0001g0077 |
3 | HG01175.hp1 HG01496.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1792-1727_1792-172 others(453): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917003 | ||||||
chr7:158917003 | G | GTGAAACG others(442): Show |
82 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(79): Show |
82 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.1792-1727_1792-172 others(453): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917003 | ||||||
chr7:158917010 | G | C | 4 | a0002c0018t0015g0048 a0003c0010t0011g0252 a0003c0010t0011g0261 others(1): Show |
4 | HG01081.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1730G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917010 | |||||||
chr7:158917017 | C | T | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1723C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917017 | |||||||
chr7:158917019 | C | G | 1 | a0012c0015t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1792-1721C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917019 | |||||||
chr7:158917039 | TTG | T | 8 | a0002c0002t0001g0038 a0002c0002t0001g0045 a0002c0002t0001g0062 others(5): Show |
8 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1698_1792-169 others(6): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917039 | ||||||
chr7:158917048 | G | A | 1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1792-1692G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917048 | |||||||
chr7:158917048 | G | C | 95 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(92): Show |
95 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1792-1692G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917048 | |||||||
chr7:158917048 | G | GTCGCTGG others(480): Show |
1 | a0002c0002t0001g0081 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1792-1689_1792-168 others(491): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917048 | ||||||
chr7:158917048 | G | GTCTACAC others(221): Show |
1 | a0001c0001t0002g0171 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1792-1690_1792-168 others(232): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917048 | ||||||
chr7:158917050 | C | T | 5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792-1690C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917050 | |||||||
chr7:158917051 | G | GACACGCT others(31): Show |
2 | a0001c0001t0009g0115 a0001c0001t0009g0227 |
2 | HG02280.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1792-1654_1792-161 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917051 | ||||||
chr7:158917055 | C | G | 1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1792-1685C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917055 | |||||||
chr7:158917055 | C | T | 1 | a0001c0001t0002g0186 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1792-1685C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917055 | |||||||
chr7:158917057 | C | G | 97 | a0001c0001t0002g0171 a0001c0001t0005g0190 a0001c0001t0005g0192 others(94): Show |
97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.1792-1683C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917057 | |||||||
chr7:158917065 | C | CATTAAGG others(485): Show |
1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.1792-1664_1792-166 others(496): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917065 | ||||||
chr7:158917065 | C | CATTAAGG others(67): Show |
1 | a0012c0015t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1792-1661_1792-166 others(78): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917065 | ||||||
chr7:158917065 | C | CATTAAGG others(31): Show |
8 | a0002c0002t0001g0038 a0002c0002t0001g0045 a0002c0002t0001g0062 others(5): Show |
8 | HG00733.hp2 HG01123.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1655_1792-165 others(42): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917065 | ||||||
chr7:158917065 | C | CATTTAGG others(449): Show |
1 | a0001c0001t0002g0193 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1792-1672_1792-167 others(460): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917065 | ||||||
chr7:158917065 | C | G | 95 | a0001c0001t0002g0171 a0001c0001t0005g0190 a0001c0001t0005g0192 others(92): Show |
95 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1792-1675C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917065 | |||||||
chr7:158917086 | G | C | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1654G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917086 | |||||||
chr7:158917088 | C | T | 2 | a0002c0002t0001g0075 a0002c0002t0001g0077 |
2 | HG01516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1792-1652C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917088 | |||||||
chr7:158917089 | T | G | 110 | a0001c0001t0002g0171 a0001c0001t0002g0193 a0001c0001t0005g0161 others(107): Show |
110 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(107): Show |
intron_variant | MODIFIER | c.1792-1651T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917089 | |||||||
chr7:158917089 | T | TACACGCT others(259): Show |
2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(270): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(943): Show |
2 | a0001c0001t0006g0007 a0001c0001t0006g0008 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(954): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(943): Show |
1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(954): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(942): Show |
1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(953): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(942): Show |
5 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(2): Show |
5 | HG01433.hp1 HG01934.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(953): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(259): Show |
66 | a0001c0001t0002g0119 a0001c0001t0002g0120 a0001c0001t0002g0121 others(63): Show |
66 | HG00099.hp1 HG00438.hp2 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(270): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0232 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(3890): Show |
1 | a0001c0001t0002g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(3901): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(3890): Show |
1 | a0001c0001t0002g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(3901): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5027): Show |
1 | a0001c0001t0002g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5038): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0162 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0131 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0132 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0136 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5065): Show |
1 | a0001c0001t0002g0141 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5076): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(4002): Show |
1 | a0001c0001t0002g0003 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(4013): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0128 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
2 | a0001c0001t0002g0150 a0001c0001t0002g0189 |
2 | HG00741.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0186 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(6467): Show |
1 | a0001c0001t0002g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(6478): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(676): Show |
1 | a0004c0004t0001g0180 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(687): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
1 | a0001c0001t0002g0233 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917089 | T | TACACGCT others(5103): Show |
3 | a0001c0001t0002g0230 a0001c0001t0002g0231 a0001c0001t0002g0234 |
3 | HG01243.hp2 HG02486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(5114): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917089 | ||||||
chr7:158917093 | C | T | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1647C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917093 | |||||||
chr7:158917094 | G | GCTGGTTG others(183): Show |
3 | a0005c0008t0003g0221 a0007c0009t0003g0220 a0007c0009t0020g0222 |
3 | HG02258.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1792-1638_1792-163 others(194): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917094 | ||||||
chr7:158917094 | G | GCTGGTTG others(259): Show |
1 | a0005c0008t0003g0223 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(270): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917094 | ||||||
chr7:158917095 | C | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1645C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917095 | |||||||
chr7:158917096 | T | TGGTTGAG others(256): Show |
1 | a0001c0001t0002g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1792-1638_1792-163 others(267): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917096 | ||||||
chr7:158917103 | C | CATTAAGG others(102): Show |
1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1617_1792-161 others(113): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917103 | ||||||
chr7:158917103 | C | G | 26 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(23): Show |
26 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1792-1637C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917103 | |||||||
chr7:158917107 | A | T | 3 | a0005c0008t0003g0221 a0007c0009t0003g0220 a0007c0009t0020g0222 |
3 | HG02258.hp1 HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1792-1633A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917107 | |||||||
chr7:158917116 | T | G | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1624T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917116 | |||||||
chr7:158917124 | C | G | 26 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(23): Show |
26 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1792-1616C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917124 | |||||||
chr7:158917127 | G | T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1792-1613G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917127 | |||||||
chr7:158917131 | C | T | 3 | a0002c0018t0015g0048 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG01081.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1609C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917131 | |||||||
chr7:158917132 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1608G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917132 | |||||||
chr7:158917133 | C | G | 4 | a0001c0001t0005g0161 a0005c0008t0003g0221 a0007c0009t0003g0220 others(1): Show |
4 | HG02015.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1607C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917133 | |||||||
chr7:158917141 | G | C | 26 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(23): Show |
26 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(23): Show |
intron_variant | MODIFIER | c.1792-1599G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917141 | |||||||
chr7:158917141 | G | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1599G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917141 | |||||||
chr7:158917154 | T | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1586T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917154 | |||||||
chr7:158917161 | T | C | 31 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(28): Show |
31 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1792-1579T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917161 | |||||||
chr7:158917162 | G | C | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1578G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917162 | |||||||
chr7:158917164 | T | C | 31 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(28): Show |
31 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.1792-1576T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917164 | |||||||
chr7:158917169 | C | CGCTGGTT others(143): Show |
1 | a0001c0001t0003g0203 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1792-1570_1792-156 others(154): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917169 | ||||||
chr7:158917169 | C | CGCTGGTT others(146): Show |
22 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(19): Show |
22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1792-1570_1792-156 others(157): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917169 | ||||||
chr7:158917169 | C | T | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1571C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917169 | |||||||
chr7:158917170 | G | GC | 7 | a0001c0001t0005g0161 a0001c0022t0018g0229 a0003c0010t0011g0252 others(4): Show |
7 | HG02015.hp2 HG02258.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1792-1570_1792-156 others(5): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917170 | |||||||
chr7:158917178 | C | G | 25 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(22): Show |
25 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(22): Show |
intron_variant | MODIFIER | c.1792-1562C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917178 | |||||||
chr7:158917182 | A | G | 8 | a0004c0004t0001g0180 a0004c0004t0002g0137 a0004c0004t0002g0138 others(5): Show |
8 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.1792-1558A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917182 | |||||||
chr7:158917199 | G | C | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1541G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917199 | |||||||
chr7:158917202 | G | T | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1792-1538G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917202 | |||||||
chr7:158917208 | C | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1532C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917208 | |||||||
chr7:158917215 | A | G | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1792-1525A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917215 | |||||||
chr7:158917216 | G | C | 24 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
24 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.1792-1524G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917216 | |||||||
chr7:158917216 | G | GATTAAGG others(220): Show |
1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1792-1505_1792-150 others(231): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917216 | ||||||
chr7:158917229 | T | C | 95 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(92): Show |
95 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1792-1511T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917229 | |||||||
chr7:158917236 | T | C | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1504T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917236 | |||||||
chr7:158917237 | G | C | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1503G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917237 | |||||||
chr7:158917239 | T | C | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1501T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917239 | |||||||
chr7:158917244 | C | T | 2 | a0001c0001t0001g0006 a0002c0002t0001g0053 |
2 | HG02257.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1792-1496C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917244 | |||||||
chr7:158917248 | C | G | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1492C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917248 | |||||||
chr7:158917249 | G | A | 2 | a0001c0001t0002g0146 a0001c0001t0002g0162 |
2 | HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1792-1491G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917249 | |||||||
chr7:158917249 | G | GTTGACAT others(4837): Show |
1 | a0001c0001t0002g0145 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1792-1431_1792-143 others(4848): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917249 | ||||||
chr7:158917253 | A | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1487A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917253 | |||||||
chr7:158917275 | G | C | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1465G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917275 | |||||||
chr7:158917282 | T | C | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1458T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917282 | |||||||
chr7:158917284 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1456C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917284 | |||||||
chr7:158917292 | A | C | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1448A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917292 | |||||||
chr7:158917292 | A | G | 3 | a0002c0018t0015g0048 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG01081.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1448A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917292 | |||||||
chr7:158917307 | T | G | 3 | a0002c0002t0001g0010 a0002c0002t0001g0057 a0012c0015t0001g0056 |
3 | HG02615.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1792-1433T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917307 | |||||||
chr7:158917310 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1430G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917310 | |||||||
chr7:158917316 | A | ACTAAACA others(161): Show |
5 | a0002c0002t0001g0021 a0002c0002t0001g0058 a0002c0002t0001g0059 others(2): Show |
5 | HG02486.hp1 HG02976.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.1792-1370_1792-136 others(172): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917316 | ||||||
chr7:158917316 | ACTAAACA others(245): Show |
A | 3 | a0002c0018t0015g0048 a0003c0010t0011g0252 a0003c0010t0011g0261 |
3 | HG01081.hp2 HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1792-1348_1792-109 others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917316 | ||||||
chr7:158917317 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1423C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917317 | |||||||
chr7:158917318 | T | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1422T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917318 | |||||||
chr7:158917320 | A | C | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1420A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917320 | |||||||
chr7:158917323 | A | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1417A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917323 | |||||||
chr7:158917325 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1415C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917325 | |||||||
chr7:158917326 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1414C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917326 | |||||||
chr7:158917327 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1413C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917327 | |||||||
chr7:158917328 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1412C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917328 | |||||||
chr7:158917331 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1409C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917331 | |||||||
chr7:158917331 | CCCTCCAC others(119): Show |
C | 8 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(5): Show |
8 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1288_1792-116 others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917331 | ||||||
chr7:158917333 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1407C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917333 | |||||||
chr7:158917335 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1405C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917335 | |||||||
chr7:158917336 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1404C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917336 | |||||||
chr7:158917338 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1402C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917338 | |||||||
chr7:158917340 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1400C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917340 | |||||||
chr7:158917342 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1398C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917342 | |||||||
chr7:158917343 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1397C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917343 | |||||||
chr7:158917345 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1395C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917345 | |||||||
chr7:158917347 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1393C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917347 | |||||||
chr7:158917350 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1390C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917350 | |||||||
chr7:158917354 | T | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1386T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917354 | |||||||
chr7:158917359 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1381C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917359 | |||||||
chr7:158917363 | A | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1377A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917363 | |||||||
chr7:158917364 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1376C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917364 | |||||||
chr7:158917374 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1366C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917374 | |||||||
chr7:158917375 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1365C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917375 | |||||||
chr7:158917377 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1363C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917377 | |||||||
chr7:158917378 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1362C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917378 | |||||||
chr7:158917380 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1360C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917380 | |||||||
chr7:158917381 | A | C | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1359A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917381 | |||||||
chr7:158917385 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1355C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917385 | |||||||
chr7:158917388 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1352C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917388 | |||||||
chr7:158917390 | T | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1350T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917390 | |||||||
chr7:158917392 | T | C | 6 | a0002c0002t0001g0021 a0002c0002t0001g0032 a0002c0002t0001g0058 others(3): Show |
6 | HG02486.hp1 HG02976.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1348T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917392 | |||||||
chr7:158917392 | T | TGCCTCTC others(119): Show |
85 | a0001c0001t0005g0190 a0001c0001t0005g0192 a0002c0002t0001g0001 others(82): Show |
85 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(82): Show |
intron_variant | MODIFIER | c.1792-1289_1792-128 others(130): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917392 | ||||||
chr7:158917392 | T | TGCCTCTC others(161): Show |
1 | a0002c0002t0001g0068 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1792-1307_1792-130 others(172): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917392 | ||||||
chr7:158917393 | G | GCCTCTCA others(77): Show |
2 | a0002c0002t0001g0095 a0002c0002t0001g0096 |
2 | NA18943.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.1792-1289_1792-128 others(88): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917393 | ||||||
chr7:158917394 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1346C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917394 | |||||||
chr7:158917395 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1345C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917395 | |||||||
chr7:158917397 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1343C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917397 | |||||||
chr7:158917398 | T | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1342T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917398 | |||||||
chr7:158917401 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1339C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917401 | |||||||
chr7:158917404 | A | AACACCTC others(287): Show |
22 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(19): Show |
22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.1792-1289_1792-128 others(298): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917404 | ||||||
chr7:158917405 | A | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1335A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917405 | |||||||
chr7:158917406 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1334C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917406 | |||||||
chr7:158917416 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1324C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917416 | |||||||
chr7:158917417 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1323C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917417 | |||||||
chr7:158917419 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1321C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917419 | |||||||
chr7:158917420 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1320C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917420 | |||||||
chr7:158917422 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1318C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917422 | |||||||
chr7:158917423 | A | C | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1317A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917423 | |||||||
chr7:158917427 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1313C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917427 | |||||||
chr7:158917430 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1310C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917430 | |||||||
chr7:158917432 | T | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1308T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917432 | |||||||
chr7:158917433 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1307C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917433 | |||||||
chr7:158917434 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1306C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917434 | |||||||
chr7:158917435 | G | A | 2 | a0002c0002t0001g0067 a0002c0002t0001g0097 |
2 | HG00741.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1792-1305G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917435 | |||||||
chr7:158917436 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1304C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917436 | |||||||
chr7:158917437 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1303C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917437 | |||||||
chr7:158917439 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1301C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917439 | |||||||
chr7:158917440 | T | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1300T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917440 | |||||||
chr7:158917442 | G | A | 4 | a0001c0001t0005g0161 a0002c0002t0001g0067 a0002c0002t0001g0097 others(1): Show |
4 | HG00741.hp1 HG01975.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1298G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917442 | |||||||
chr7:158917442 | G | GCTAAACA others(161): Show |
1 | a0002c0002t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1792-1289_1792-128 others(172): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917442 | ||||||
chr7:158917442 | GCTAAACA others(77): Show |
G | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1792-1263_1792-118 others(88): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917442 | ||||||
chr7:158917443 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1297C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917443 | |||||||
chr7:158917447 | A | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1293A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917447 | |||||||
chr7:158917448 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1292C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917448 | |||||||
chr7:158917450 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1290C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917450 | |||||||
chr7:158917451 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1289C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917451 | |||||||
chr7:158917452 | T | C | 220 | a0001c0001t0001g0006 a0001c0001t0002g0003 a0001c0001t0002g0004 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1792-1288T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917452 | |||||||
chr7:158917453 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1287C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917453 | |||||||
chr7:158917454 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1286C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917454 | |||||||
chr7:158917457 | T | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1283T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917457 | |||||||
chr7:158917457 | T | C | 220 | a0001c0001t0001g0006 a0001c0001t0002g0003 a0001c0001t0002g0004 others(217): Show |
220 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.1792-1283T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917457 | |||||||
chr7:158917457 | T | TCCTCCAC others(35): Show |
1 | a0011c0012t0001g0043 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1792-1264_1792-126 others(46): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917457 | ||||||
chr7:158917462 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1278C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917462 | |||||||
chr7:158917466 | C | CGGTGGTT others(93): Show |
1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1274_1792-127 others(104): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917466 | |||||||
chr7:158917468 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1272C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917468 | |||||||
chr7:158917469 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1271C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917469 | |||||||
chr7:158917471 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1269C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917471 | |||||||
chr7:158917476 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1264C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917476 | |||||||
chr7:158917476 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1792-1264C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917476 | |||||||
chr7:158917477 | A | G | 4 | a0002c0002t0001g0015 a0002c0002t0001g0067 a0002c0002t0001g0085 others(1): Show |
4 | HG00741.hp1 HG01099.hp1 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1792-1263A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917477 | |||||||
chr7:158917477 | ACCTCTCA others(35): Show |
A | 2 | a0003c0003t0007g0248 a0003c0003t0007g0259 |
2 | NA18964.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1792-1222_1792-118 others(46): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917477 | ||||||
chr7:158917479 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1261C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917479 | |||||||
chr7:158917485 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1255C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917485 | |||||||
chr7:158917489 | A | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1251A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917489 | |||||||
chr7:158917490 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1250C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917490 | |||||||
chr7:158917492 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1248C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917492 | |||||||
chr7:158917493 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1247C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917493 | |||||||
chr7:158917495 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1245C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917495 | |||||||
chr7:158917496 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1244C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917496 | |||||||
chr7:158917499 | T | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1241T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917499 | |||||||
chr7:158917499 | T | TCCTCCAC others(119): Show |
1 | a0002c0002t0001g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1792-1223_1792-122 others(130): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917499 | ||||||
chr7:158917504 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1236C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917504 | |||||||
chr7:158917508 | C | CGGTGGTT others(138): Show |
1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1232_1792-123 others(149): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917508 | |||||||
chr7:158917511 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1229C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917511 | |||||||
chr7:158917514 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1226C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917514 | |||||||
chr7:158917516 | T | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1224T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917516 | |||||||
chr7:158917518 | T | C | 8 | a0001c0001t0003g0215 a0002c0002t0001g0009 a0002c0002t0001g0010 others(5): Show |
8 | HG01943.hp2 HG02074.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1792-1222T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917518 | |||||||
chr7:158917519 | G | A | 1 | a0002c0002t0001g0015 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1792-1221G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917519 | |||||||
chr7:158917519 | G | GCCTCTCA others(749): Show |
1 | a0001c0001t0003g0215 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1792-1089_1792-108 others(760): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917519 | ||||||
chr7:158917519 | GCCTCTCA others(77): Show |
G | 1 | a0002c0002t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1792-1120_1792-103 others(88): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917519 | ||||||
chr7:158917520 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1220C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917520 | |||||||
chr7:158917521 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1219C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917521 | |||||||
chr7:158917523 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1217C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917523 | |||||||
chr7:158917524 | T | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1216T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917524 | |||||||
chr7:158917526 | A | G | 1 | a0004c0004t0006g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1792-1214A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917526 | |||||||
chr7:158917527 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1213C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917527 | |||||||
chr7:158917531 | A | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1209A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917531 | |||||||
chr7:158917532 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1208C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917532 | |||||||
chr7:158917534 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1206C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917534 | |||||||
chr7:158917535 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1205C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917535 | |||||||
chr7:158917536 | T | C | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1792-1204T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917536 | |||||||
chr7:158917537 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1203C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917537 | |||||||
chr7:158917538 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1202C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917538 | |||||||
chr7:158917541 | T | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1199T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917541 | |||||||
chr7:158917541 | T | C | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1792-1199T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917541 | |||||||
chr7:158917541 | T | TCCTCCAC others(35): Show |
91 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
91 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1792-1179_1792-113 others(46): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917541 | ||||||
chr7:158917541 | T | TCCTCCAC others(455): Show |
1 | a0004c0004t0006g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1792-1181_1792-118 others(466): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917541 | ||||||
chr7:158917543 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1197C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917543 | |||||||
chr7:158917546 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1194C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917546 | |||||||
chr7:158917551 | T | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1189T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917551 | |||||||
chr7:158917552 | C | CTGGTTGA others(10): Show |
1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1188_1792-118 others(21): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917552 | |||||||
chr7:158917553 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1187C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917553 | |||||||
chr7:158917555 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1185C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917555 | |||||||
chr7:158917556 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1184C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917556 | |||||||
chr7:158917557 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1183C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917557 | |||||||
chr7:158917559 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1181C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917559 | |||||||
chr7:158917560 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1180C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917560 | |||||||
chr7:158917562 | C | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1178C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917562 | |||||||
chr7:158917565 | C | G | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1175C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917565 | |||||||
chr7:158917568 | G | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1792-1172G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917568 | |||||||
chr7:158917568 | G | GCTAAACA others(119): Show |
1 | a0002c0002t0014g0087 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1792-1138_1792-101 others(130): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917568 | ||||||
chr7:158917603 | A | G | 2 | a0006c0006t0002g0118 a0006c0006t0002g0219 |
2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1792-1137A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917603 | |||||||
chr7:158917610 | A | G | 2 | a0006c0006t0002g0118 a0006c0006t0002g0219 |
2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1792-1130A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917610 | |||||||
chr7:158917620 | T | C | 2 | a0006c0006t0002g0118 a0006c0006t0002g0219 |
2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1792-1120T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917620 | |||||||
chr7:158917625 | T | C | 2 | a0006c0006t0002g0118 a0006c0006t0002g0219 |
2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1792-1115T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917625 | |||||||
chr7:158917625 | TCCTCCAC others(35): Show |
T | 3 | a0002c0002t0001g0010 a0002c0002t0001g0057 a0012c0015t0001g0056 |
3 | HG02615.hp1 HG02922.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1792-1095_1792-105 others(46): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | INFO_REALIGN_3_PRIME | chr7 | 158917625 | ||||||
chr7:158917644 | C | T | 6 | a0004c0004t0001g0180 a0004c0004t0002g0137 a0004c0004t0002g0138 others(3): Show |
6 | HG02258.hp2 HG02818.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792-1096C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917644 | |||||||
chr7:158917645 | G | A | 2 | a0006c0006t0002g0118 a0006c0006t0002g0219 |
2 | HG01934.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.1792-1095G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917645 | |||||||
chr7:158917652 | G | A | 6 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(3): Show |
6 | HG01081.hp2 HG01934.hp2 HG02015.hp2 others(3): Show |
intron_variant | MODIFIER | c.1792-1088G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917652 | |||||||
chr7:158917686 | C | T | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-1054C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917686 | |||||||
chr7:158917687 | A | G | 8 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(5): Show |
8 | HG01081.hp2 HG01257.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1792-1053A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917687 | |||||||
chr7:158917698 | A | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1042A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917698 | |||||||
chr7:158917704 | C | T | 6 | a0002c0002t0001g0021 a0002c0002t0001g0058 a0002c0002t0001g0059 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1792-1036C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917704 | |||||||
chr7:158917732 | T | C | 118 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(115): Show |
118 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(115): Show |
intron_variant | MODIFIER | c.1792-1008T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917732 | |||||||
chr7:158917744 | C | T | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-996C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917744 | |||||||
chr7:158917783 | T | G | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-957T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917783 | |||||||
chr7:158917805 | T | A | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1792-935T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917805 | |||||||
chr7:158917951 | A | G | 8 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(5): Show |
8 | HG01081.hp2 HG01257.hp2 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.1792-789A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158917951 | |||||||
chr7:158918075 | T | C | 2 | a0002c0002t0001g0075 a0002c0002t0001g0077 |
2 | HG01516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1792-665T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918075 | |||||||
chr7:158918121 | C | T | 23 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(20): Show |
23 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(20): Show |
intron_variant | MODIFIER | c.1792-619C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918121 | |||||||
chr7:158918188 | G | A | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1792-552G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918188 | |||||||
chr7:158918250 | C | T | 2 | a0001c0001t0005g0161 a0002c0018t0015g0048 |
2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1792-490C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918250 | |||||||
chr7:158918363 | C | T | 1 | a0002c0002t0001g0032 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1792-377C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918363 | |||||||
chr7:158918604 | T | C | 95 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(92): Show |
95 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1792-136T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918604 | |||||||
chr7:158918735 | G | C | 1 | a0001c0001t0001g0270 | 1 | HG01433.hp1 | splice_region_variant&intron_variant | LOW | c.1792-5G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 14/24 | chr7 | 158918735 | |||||||
chr7:158918893 | A | G | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1921+24A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158918893 | |||||||
chr7:158918952 | AT | A | 91 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(88): Show |
91 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(88): Show |
intron_variant | MODIFIER | c.1921+87delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr7 | 158918952 | ||||||
chr7:158918963 | A | G | 1 | a0001c0001t0002g0188 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1921+94A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158918963 | |||||||
chr7:158919112 | T | A | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1921+243T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919112 | |||||||
chr7:158919251 | A | T | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1921+382A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919251 | |||||||
chr7:158919259 | T | G | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1921+390T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919259 | |||||||
chr7:158919379 | C | CAA | 3 | a0002c0002t0001g0002 a0002c0002t0001g0047 a0002c0002t0001g0105 |
3 | HG01358.hp2 NA18939.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.1921+512_1921+513d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr7 | 158919379 | ||||||
chr7:158919496 | G | A | 1 | a0001c0001t0002g0231 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1921+627G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919496 | |||||||
chr7:158919548 | G | C | 3 | a0002c0002t0001g0074 a0002c0002t0001g0076 a0002c0002t0001g0089 |
3 | HG01346.hp2 HG01975.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1921+679G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919548 | |||||||
chr7:158919561 | G | A | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1921+692G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919561 | |||||||
chr7:158919881 | GC | G | 95 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(92): Show |
95 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.1921+1017delC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr7 | 158919881 | ||||||
chr7:158919895 | G | A | 3 | a0001c0001t0002g0164 a0001c0001t0012g0217 a0001c0001t0012g0218 |
3 | HG02055.hp1 HG02723.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.1921+1026G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919895 | |||||||
chr7:158919945 | C | T | 1 | a0001c0001t0005g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1921+1076C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919945 | |||||||
chr7:158919952 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1921+1083G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158919952 | |||||||
chr7:158919954 | AGAACACG others(90): Show |
A | 1 | a0003c0003t0007g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1921+1110_1921+120 others(101): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr7 | 158919954 | ||||||
chr7:158920047 | A | G | 2 | a0001c0001t0005g0161 a0002c0018t0015g0048 |
2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1921+1178A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920047 | |||||||
chr7:158920073 | G | T | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1921+1204G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920073 | |||||||
chr7:158920076 | T | C | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1921+1207T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920076 | |||||||
chr7:158920083 | G | A | 1 | a0001c0001t0002g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1921+1214G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920083 | |||||||
chr7:158920141 | C | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1921+1272C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920141 | |||||||
chr7:158920160 | T | A | 2 | a0001c0001t0006g0007 a0001c0001t0006g0008 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1921+1291T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920160 | |||||||
chr7:158920190 | G | A | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1921+1321G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920190 | |||||||
chr7:158920227 | G | A | 1 | a0002c0002t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1921+1358G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920227 | |||||||
chr7:158920229 | C | T | 1 | a0001c0001t0002g0165 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1921+1360C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920229 | |||||||
chr7:158920385 | G | A | 1 | a0001c0001t0002g0197 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.1921+1516G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920385 | |||||||
chr7:158920439 | C | T | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.1921+1570C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920439 | |||||||
chr7:158920574 | G | A | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1921+1705G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920574 | |||||||
chr7:158920621 | C | T | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1921+1752C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920621 | |||||||
chr7:158920633 | CGTG | C | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-1743_1922-174 others(7): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920633 | |||||||
chr7:158920901 | A | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1922-1476A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920901 | |||||||
chr7:158920967 | G | A | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1922-1410G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920967 | |||||||
chr7:158920995 | C | T | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-1382C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158920995 | |||||||
chr7:158921082 | C | T | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-1295C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921082 | |||||||
chr7:158921123 | AC | A | 4 | a0004c0004t0002g0137 a0004c0004t0002g0138 a0006c0006t0002g0118 others(1): Show |
4 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-1253delC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921123 | |||||||
chr7:158921238 | T | C | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-1139T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921238 | |||||||
chr7:158921311 | G | A | 2 | a0001c0001t0005g0161 a0002c0018t0015g0048 |
2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.1922-1066G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921311 | |||||||
chr7:158921321 | C | T | 1 | a0001c0001t0002g0168 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1922-1056C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921321 | |||||||
chr7:158921407 | G | A | 4 | a0005c0008t0003g0221 a0005c0008t0003g0223 a0007c0009t0003g0220 others(1): Show |
4 | HG01257.hp2 HG02258.hp1 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-970G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921407 | |||||||
chr7:158921428 | G | A | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-949G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921428 | |||||||
chr7:158921467 | A | G | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1922-910A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921467 | |||||||
chr7:158921525 | C | T | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-852C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921525 | |||||||
chr7:158921547 | C | T | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1922-830C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921547 | |||||||
chr7:158921552 | G | T | 3 | a0001c0001t0002g0145 a0001c0001t0002g0146 a0001c0001t0002g0162 |
3 | HG01167.hp2 HG01169.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1922-825G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921552 | |||||||
chr7:158921635 | G | A | 2 | a0003c0003t0004g0253 a0003c0003t0004g0257 |
2 | HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.1922-742G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921635 | |||||||
chr7:158921751 | C | T | 3 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0022t0018g0229 |
3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1922-626C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921751 | |||||||
chr7:158921800 | A | G | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1922-577A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158921800 | |||||||
chr7:158922051 | G | A | 1 | a0001c0001t0002g0004 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1922-326G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158922051 | |||||||
chr7:158922174 | A | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1922-203A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158922174 | |||||||
chr7:158922187 | C | T | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1922-190C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158922187 | |||||||
chr7:158922230 | A | C | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.1922-147A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158922230 | |||||||
chr7:158922361 | T | C | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1922-16T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | chr7 | 158922361 | |||||||
chr7:158922370 | TC | T | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
splice_region_variant&intron_variant | LOW | c.1922-4delC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 15/24 | INFO_REALIGN_3_PRIME | chr7 | 158922370 | ||||||
chr7:158922571 | G | C | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+22G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922571 | |||||||
chr7:158922573 | A | G | 125 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(122): Show |
125 | HG00099.hp1 HG00423.hp1 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.2094+24A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922573 | |||||||
chr7:158922575 | G | A | 2 | a0003c0003t0004g0253 a0003c0003t0004g0257 |
2 | HG01346.hp1 HG01496.hp2 |
intron_variant | MODIFIER | c.2094+26G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922575 | |||||||
chr7:158922655 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2094+106G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922655 | |||||||
chr7:158922878 | G | T | 264 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(261): Show |
264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.2094+329G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922878 | |||||||
chr7:158922896 | T | G | 1 | a0004c0004t0006g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2094+347T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922896 | |||||||
chr7:158922931 | C | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2094+382C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922931 | |||||||
chr7:158922952 | A | C | 3 | a0004c0004t0006g0178 a0004c0004t0006g0179 a0004c0004t0006g0181 |
3 | HG02818.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2094+403A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158922952 | |||||||
chr7:158923028 | C | A | 4 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0010t0011g0252 others(1): Show |
4 | HG01081.hp2 HG02015.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2094+479C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158923028 | |||||||
chr7:158923073 | G | C | 1 | a0003c0010t0011g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2095-498G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158923073 | |||||||
chr7:158923294 | C | T | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2095-277C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158923294 | |||||||
chr7:158923336 | G | A | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2095-235G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 16/24 | chr7 | 158923336 | |||||||
chr7:158923943 | C | T | 1 | a0002c0002t0001g0070 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.2257+210C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158923943 | |||||||
chr7:158924059 | C | T | 1 | a0002c0002t0001g0011 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.2257+326C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924059 | |||||||
chr7:158924221 | T | C | 237 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(234): Show |
237 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(234): Show |
intron_variant | MODIFIER | c.2257+488T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924221 | |||||||
chr7:158924452 | C | T | 1 | a0002c0002t0001g0066 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.2257+719C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924452 | |||||||
chr7:158924493 | A | G | 2 | a0001c0001t0005g0161 a0002c0018t0015g0048 |
2 | HG01081.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.2257+760A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924493 | |||||||
chr7:158924587 | C | T | 2 | a0002c0002t0001g0014 a0002c0002t0001g0027 |
2 | HG01255.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.2257+854C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924587 | |||||||
chr7:158924603 | C | T | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2257+870C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924603 | |||||||
chr7:158924614 | T | TAAAAGAT others(316): Show |
1 | a0001c0001t0012g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2257+895_2257+896i others(325): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr7 | 158924614 | ||||||
chr7:158924614 | T | TAAAAGAT others(326): Show |
1 | a0001c0001t0012g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2257+895_2257+896i others(335): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr7 | 158924614 | ||||||
chr7:158924623 | T | C | 3 | a0001c0001t0001g0006 a0001c0001t0006g0007 a0001c0001t0006g0008 |
3 | HG02257.hp1 HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2257+890T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924623 | |||||||
chr7:158924798 | A | G | 1 | a0001c0001t0002g0005 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2257+1065A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158924798 | |||||||
chr7:158925170 | G | A | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2258-1017G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158925170 | |||||||
chr7:158925223 | C | G | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2258-964C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158925223 | |||||||
chr7:158925531 | A | T | 1 | a0004c0004t0002g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2258-656A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158925531 | |||||||
chr7:158925564 | A | G | 3 | a0002c0002t0001g0044 a0002c0002t0001g0045 a0002c0002t0001g0046 |
3 | HG00733.hp2 HG01175.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.2258-623A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158925564 | |||||||
chr7:158925707 | G | C | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2258-480G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158925707 | |||||||
chr7:158926102 | A | G | 103 | a0001c0001t0001g0268 a0001c0001t0005g0139 a0001c0001t0005g0142 others(100): Show |
103 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(100): Show |
intron_variant | MODIFIER | c.2258-85A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158926102 | |||||||
chr7:158926114 | T | C | 32 | a0001c0001t0005g0139 a0001c0001t0005g0190 a0001c0001t0005g0192 others(29): Show |
32 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(29): Show |
intron_variant | MODIFIER | c.2258-73T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 17/24 | chr7 | 158926114 | |||||||
chr7:158926304 | C | T | 30 | a0001c0001t0002g0176 a0001c0001t0003g0199 a0001c0001t0003g0200 others(27): Show |
30 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(27): Show |
splice_region_variant&intron_variant | LOW | c.2371+4C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 18/24 | chr7 | 158926304 | |||||||
chr7:158926358 | C | G | 1 | a0001c0001t0002g0187 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2372-44C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 18/24 | chr7 | 158926358 | |||||||
chr7:158926370 | C | T | 1 | a0001c0001t0002g0117 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2372-32C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 18/24 | chr7 | 158926370 | |||||||
chr7:158926393 | C | T | 219 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(216): Show |
219 | HG00099.hp1 HG00099.hp2 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.2372-9C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 18/24 | chr7 | 158926393 | |||||||
chr7:158926562 | G | A | 124 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(121): Show |
124 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(121): Show |
intron_variant | MODIFIER | c.2433+99G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 19/24 | chr7 | 158926562 | |||||||
chr7:158926734 | T | A | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2434-258T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 19/24 | chr7 | 158926734 | |||||||
chr7:158926765 | G | A | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2434-227G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 19/24 | chr7 | 158926765 | |||||||
chr7:158927100 | A | C | 1 | a0001c0001t0002g0196 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.2485+57A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927100 | |||||||
chr7:158927231 | G | A | 1 | a0001c0001t0003g0213 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.2485+188G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927231 | |||||||
chr7:158927306 | G | A | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(90): Show |
93 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.2485+263G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927306 | |||||||
chr7:158927310 | G | A | 21 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(18): Show |
21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2485+267G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927310 | |||||||
chr7:158927396 | TTG | T | 2 | a0002c0018t0015g0048 a0003c0027t0022g0263 |
2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2485+355_2485+356d others(4): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158927396 | ||||||
chr7:158927408 | T | TA | 121 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(118): Show |
121 | HG00099.hp1 HG00408.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.2485+379dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158927408 | ||||||
chr7:158927446 | A | C | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2485+403A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927446 | |||||||
chr7:158927557 | AT | A | 94 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(91): Show |
94 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(91): Show |
intron_variant | MODIFIER | c.2485+528delT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158927557 | ||||||
chr7:158927712 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2485+669C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927712 | |||||||
chr7:158927827 | C | T | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2485+784C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927827 | |||||||
chr7:158927834 | GAGCCACC others(4): Show |
G | 2 | a0002c0002t0001g0109 a0002c0002t0001g0111 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.2485+796_2485+806d others(13): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158927834 | ||||||
chr7:158927875 | G | A | 2 | a0001c0001t0006g0007 a0001c0001t0006g0008 |
2 | HG03486.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2485+832G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158927875 | |||||||
chr7:158928037 | A | C | 2 | a0001c0001t0005g0161 a0001c0001t0006g0008 |
2 | HG02015.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.2485+994A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928037 | |||||||
chr7:158928108 | G | A | 92 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(89): Show |
92 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(89): Show |
intron_variant | MODIFIER | c.2485+1065G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928108 | |||||||
chr7:158928110 | G | T | 1 | a0001c0001t0002g0135 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2485+1067G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928110 | |||||||
chr7:158928271 | T | TGATCTCA others(311): Show |
1 | a0001c0001t0003g0216 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2485+1243_2485+124 others(322): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158928271 | ||||||
chr7:158928271 | T | TGATCTCA others(312): Show |
14 | a0001c0001t0003g0200 a0001c0001t0003g0203 a0001c0001t0003g0204 others(11): Show |
14 | HG00423.hp1 HG00597.hp2 HG02056.hp2 others(11): Show |
intron_variant | MODIFIER | c.2485+1243_2485+124 others(323): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158928271 | ||||||
chr7:158928271 | T | TGATCTCA others(313): Show |
6 | a0001c0001t0003g0199 a0001c0001t0003g0201 a0001c0001t0003g0202 others(3): Show |
6 | HG00544.hp1 HG03688.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.2485+1243_2485+124 others(324): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158928271 | ||||||
chr7:158928296 | T | A | 1 | a0001c0001t0003g0204 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.2485+1253T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928296 | |||||||
chr7:158928310 | C | T | 1 | a0001c0001t0002g0122 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2485+1267C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928310 | |||||||
chr7:158928333 | C | A | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2485+1290C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928333 | |||||||
chr7:158928401 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2485+1358C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928401 | |||||||
chr7:158928589 | G | C | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2485+1546G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928589 | |||||||
chr7:158928682 | G | A | 1 | a0001c0013t0002g0175 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2485+1639G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928682 | |||||||
chr7:158928748 | A | G | 143 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(140): Show |
143 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2485+1705A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928748 | |||||||
chr7:158928776 | TAGTC | T | 135 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(132): Show |
135 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.2486-1674_2486-167 others(8): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158928776 | ||||||
chr7:158928808 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2486-1647C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928808 | |||||||
chr7:158928813 | A | G | 238 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2486-1642A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928813 | |||||||
chr7:158928835 | C | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2486-1620C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928835 | |||||||
chr7:158928856 | G | A | 95 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(92): Show |
95 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(92): Show |
intron_variant | MODIFIER | c.2486-1599G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158928856 | |||||||
chr7:158929030 | A | G | 21 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(18): Show |
21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2486-1425A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929030 | |||||||
chr7:158929255 | C | A | 2 | a0002c0018t0015g0048 a0003c0027t0022g0263 |
2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2486-1200C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929255 | |||||||
chr7:158929288 | C | T | 1 | a0002c0002t0001g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2486-1167C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929288 | |||||||
chr7:158929385 | A | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2486-1070A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929385 | |||||||
chr7:158929385 | AGGCCTGG others(49): Show |
A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.2486-1048_2486-993 others(59): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr7 | 158929385 | ||||||
chr7:158929391 | G | A | 7 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(4): Show |
7 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(4): Show |
intron_variant | MODIFIER | c.2486-1064G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929391 | |||||||
chr7:158929408 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2486-1047G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929408 | |||||||
chr7:158929441 | G | A | 3 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 |
3 | HG01433.hp1 HG01981.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.2486-1014G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929441 | |||||||
chr7:158929459 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2486-996T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929459 | |||||||
chr7:158929487 | A | G | 10 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0022t0018g0229 others(7): Show |
10 | HG01255.hp2 HG01257.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.2486-968A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929487 | |||||||
chr7:158929499 | C | G | 2 | a0007c0009t0003g0220 a0007c0009t0020g0222 |
2 | HG02615.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2486-956C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929499 | |||||||
chr7:158929501 | G | C | 113 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(110): Show |
113 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.2486-954G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929501 | |||||||
chr7:158929555 | G | A | 1 | a0001c0001t0002g0232 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2486-900G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929555 | |||||||
chr7:158929624 | G | A | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2486-831G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929624 | |||||||
chr7:158929630 | C | T | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2486-825C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929630 | |||||||
chr7:158929837 | G | A | 2 | a0001c0001t0002g0145 a0001c0001t0002g0162 |
2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2486-618G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158929837 | |||||||
chr7:158930062 | T | A | 141 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(138): Show |
141 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.2486-393T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158930062 | |||||||
chr7:158930132 | T | G | 2 | a0003c0010t0011g0252 a0003c0010t0011g0261 |
2 | HG02976.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2486-323T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158930132 | |||||||
chr7:158930322 | G | A | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2486-133G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158930322 | |||||||
chr7:158930323 | T | C | 142 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(139): Show |
142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.2486-132T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 20/24 | chr7 | 158930323 | |||||||
chr7:158930624 | A | G | 1 | a0002c0002t0001g0013 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2546+109A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930624 | |||||||
chr7:158930643 | T | C | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2546+128T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930643 | |||||||
chr7:158930648 | G | A | 4 | a0004c0004t0001g0180 a0004c0004t0006g0178 a0004c0004t0006g0179 others(1): Show |
4 | HG02818.hp1 HG03486.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.2546+133G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930648 | |||||||
chr7:158930661 | A | G | 1 | a0004c0004t0006g0178 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2546+146A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930661 | |||||||
chr7:158930713 | G | A | 2 | a0002c0018t0015g0048 a0003c0027t0022g0263 |
2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2546+198G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930713 | |||||||
chr7:158930763 | G | A | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2546+248G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930763 | |||||||
chr7:158930767 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2546+252C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930767 | |||||||
chr7:158930772 | G | A | 6 | a0002c0002t0001g0021 a0002c0002t0001g0058 a0002c0002t0001g0059 others(3): Show |
6 | HG02109.hp1 HG02486.hp1 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.2546+257G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158930772 | |||||||
chr7:158931015 | G | A | 1 | a0005c0008t0003g0223 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2546+500G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931015 | |||||||
chr7:158931093 | A | C | 3 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0027t0022g0263 |
3 | HG01081.hp2 HG02015.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2546+578A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931093 | |||||||
chr7:158931228 | T | C | 1 | a0003c0010t0011g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2546+713T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931228 | |||||||
chr7:158931244 | A | G | 22 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(19): Show |
22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.2546+729A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931244 | |||||||
chr7:158931305 | C | G | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2546+790C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931305 | |||||||
chr7:158931318 | T | C | 24 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
24 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.2546+803T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931318 | |||||||
chr7:158931472 | C | T | 117 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.2546+957C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931472 | |||||||
chr7:158931544 | C | T | 1 | a0004c0004t0002g0137 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.2546+1029C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931544 | |||||||
chr7:158931636 | A | G | 22 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(19): Show |
22 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(19): Show |
intron_variant | MODIFIER | c.2546+1121A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931636 | |||||||
chr7:158931910 | G | T | 1 | a0012c0015t0001g0056 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2546+1395G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931910 | |||||||
chr7:158931914 | A | T | 1 | a0003c0003t0007g0240 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.2546+1399A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158931914 | |||||||
chr7:158932027 | A | G | 145 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(142): Show |
145 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.2546+1512A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932027 | |||||||
chr7:158932098 | G | C | 144 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(141): Show |
144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2546+1583G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932098 | |||||||
chr7:158932123 | G | A | 1 | a0001c0001t0005g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2546+1608G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932123 | |||||||
chr7:158932198 | C | T | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
82 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.2546+1683C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932198 | |||||||
chr7:158932214 | C | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2546+1699C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932214 | |||||||
chr7:158932448 | A | G | 1 | a0003c0003t0007g0259 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2547-1681A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932448 | |||||||
chr7:158932449 | C | T | 1 | a0001c0001t0002g0171 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.2547-1680C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932449 | |||||||
chr7:158932563 | C | CCGA | 24 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
24 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.2547-1564_2547-156 others(7): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | INFO_REALIGN_3_PRIME | chr7 | 158932563 | ||||||
chr7:158932898 | T | A | 3 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0022t0018g0229 |
3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2547-1231T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932898 | |||||||
chr7:158932932 | G | A | 3 | a0003c0010t0011g0252 a0003c0010t0011g0261 a0004c0004t0001g0180 |
3 | HG02976.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2547-1197G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158932932 | |||||||
chr7:158933043 | C | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.2547-1086C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933043 | |||||||
chr7:158933073 | TC | T | 4 | a0002c0002t0001g0012 a0002c0002t0001g0068 a0002c0002t0001g0081 others(1): Show |
4 | HG01167.hp1 HG01169.hp2 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2547-1055delC | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933073 | |||||||
chr7:158933177 | G | A | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2547-952G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933177 | |||||||
chr7:158933216 | C | G | 117 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(114): Show |
117 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.2547-913C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933216 | |||||||
chr7:158933498 | G | A | 1 | a0003c0003t0007g0242 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.2547-631G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933498 | |||||||
chr7:158933523 | C | T | 3 | a0004c0004t0006g0178 a0004c0004t0006g0179 a0004c0004t0006g0181 |
3 | HG02818.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2547-606C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933523 | |||||||
chr7:158933601 | A | G | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2547-528A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933601 | |||||||
chr7:158933763 | T | C | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2547-366T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933763 | |||||||
chr7:158933771 | T | C | 145 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(142): Show |
145 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.2547-358T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933771 | |||||||
chr7:158933785 | G | A | 21 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(18): Show |
21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2547-344G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933785 | |||||||
chr7:158933964 | G | A | 108 | a0001c0001t0005g0139 a0001c0001t0005g0142 a0001c0001t0005g0161 others(105): Show |
108 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(105): Show |
intron_variant | MODIFIER | c.2547-165G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933964 | |||||||
chr7:158933993 | G | A | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2547-136G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158933993 | |||||||
chr7:158934107 | T | TC | 241 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2547-22_2547-21ins others(1): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 21/24 | chr7 | 158934107 | |||||||
chr7:158934323 | T | C | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2646+95T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 22/24 | chr7 | 158934323 | |||||||
chr7:158934324 | C | CT | 238 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.2647-91dupT | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr7 | 158934324 | ||||||
chr7:158934332 | A | C | 3 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0022t0018g0229 |
3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2647-86A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 22/24 | chr7 | 158934332 | |||||||
chr7:158934387 | G | A | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2647-31G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 22/24 | chr7 | 158934387 | |||||||
chr7:158934578 | A | G | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2778+29A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934578 | |||||||
chr7:158934585 | T | A | 119 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2778+36T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934585 | |||||||
chr7:158934612 | G | T | 107 | a0001c0001t0005g0139 a0001c0001t0005g0142 a0001c0001t0005g0190 others(104): Show |
107 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.2778+63G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934612 | |||||||
chr7:158934781 | G | A | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2778+232G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934781 | |||||||
chr7:158934813 | T | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2778+264T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934813 | |||||||
chr7:158934900 | C | G | 119 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2778+351C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934900 | |||||||
chr7:158934922 | C | T | 94 | a0001c0001t0005g0139 a0001c0001t0005g0190 a0001c0001t0005g0192 others(91): Show |
94 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.2778+373C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934922 | |||||||
chr7:158934981 | A | G | 1 | a0001c0013t0002g0175 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2778+432A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158934981 | |||||||
chr7:158935209 | C | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2778+660C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158935209 | |||||||
chr7:158935219 | A | G | 2 | a0002c0018t0015g0048 a0003c0027t0022g0263 |
2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2778+670A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158935219 | |||||||
chr7:158935246 | C | T | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2778+697C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158935246 | |||||||
chr7:158935460 | T | C | 1 | a0001c0001t0002g0195 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.2778+911T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158935460 | |||||||
chr7:158935485 | C | T | 1 | a0001c0001t0003g0201 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2778+936C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158935485 | |||||||
chr7:158935926 | ACGGTGGC others(16): Show |
A | 1 | a0002c0002t0001g0069 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.2778+1381_2778+140 others(27): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158935926 | ||||||
chr7:158936052 | G | A | 144 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(141): Show |
144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2778+1503G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936052 | |||||||
chr7:158936185 | C | T | 1 | a0001c0001t0009g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2778+1636C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936185 | |||||||
chr7:158936283 | A | G | 72 | a0001c0001t0002g0117 a0001c0001t0002g0119 a0001c0001t0002g0120 others(69): Show |
72 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(69): Show |
intron_variant | MODIFIER | c.2778+1734A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936283 | |||||||
chr7:158936417 | C | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2778+1868C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936417 | |||||||
chr7:158936447 | G | A | 1 | a0001c0001t0001g0273 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.2778+1898G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936447 | |||||||
chr7:158936550 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2778+2001C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936550 | |||||||
chr7:158936645 | C | T | 3 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0001c0022t0018g0229 |
3 | HG02055.hp1 HG02723.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2778+2096C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936645 | |||||||
chr7:158936831 | A | G | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2778+2282A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936831 | |||||||
chr7:158936840 | C | T | 1 | a0001c0001t0005g0139 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2778+2291C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158936840 | |||||||
chr7:158937237 | T | C | 143 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(140): Show |
143 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2778+2688T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937237 | |||||||
chr7:158937242 | G | T | 1 | a0005c0008t0003g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2778+2693G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937242 | |||||||
chr7:158937352 | C | T | 3 | a0003c0010t0011g0252 a0003c0010t0011g0261 a0004c0004t0001g0180 |
3 | HG02976.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2778+2803C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937352 | |||||||
chr7:158937423 | G | A | 1 | a0001c0001t0002g0159 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2778+2874G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937423 | |||||||
chr7:158937499 | G | A | 3 | a0003c0010t0011g0252 a0003c0010t0011g0261 a0004c0004t0001g0180 |
3 | HG02976.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2778+2950G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937499 | |||||||
chr7:158937622 | G | GA | 7 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 others(4): Show |
7 | HG01257.hp2 HG02258.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.2778+3086dupA | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAA | 20 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(17): Show |
20 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.2778+3083_2778+308 others(8): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA | 97 | a0001c0001t0005g0139 a0001c0001t0005g0142 a0001c0001t0005g0161 others(94): Show |
97 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(94): Show |
intron_variant | MODIFIER | c.2778+3080_2778+308 others(11): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA others(6): Show |
1 | a0002c0002t0001g0058 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2778+3074_2778+308 others(17): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA others(7): Show |
5 | a0002c0002t0001g0021 a0002c0002t0001g0059 a0002c0002t0001g0078 others(2): Show |
5 | HG02109.hp1 HG02486.hp1 NA18906.hp2 others(2): Show |
intron_variant | MODIFIER | c.2778+3086_2778+308 others(18): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA others(8): Show |
3 | a0003c0010t0011g0252 a0003c0010t0011g0261 a0004c0004t0001g0180 |
3 | HG02976.hp2 NA19030.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2778+3086_2778+308 others(19): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA others(9): Show |
1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2778+3086_2778+308 others(20): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA others(10): Show |
1 | a0003c0027t0022g0263 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.2778+3086_2778+308 others(21): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA others(11): Show |
1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2778+3086_2778+308 others(22): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA others(19): Show |
1 | a0001c0001t0012g0217 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2778+3086_2778+308 others(30): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA others(20): Show |
2 | a0001c0001t0001g0268 a0001c0001t0012g0218 |
2 | HG01934.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.2778+3086_2778+308 others(31): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA others(21): Show |
4 | a0001c0001t0001g0269 a0001c0001t0001g0271 a0001c0001t0001g0273 others(1): Show |
4 | HG01981.hp1 HG02148.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.2778+3086_2778+308 others(32): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937622 | G | GAAAAAAA others(22): Show |
1 | a0001c0001t0001g0270 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2778+3086_2778+308 others(33): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158937622 | ||||||
chr7:158937756 | A | T | 93 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(90): Show |
93 | HG00099.hp1 HG00438.hp2 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.2778+3207A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937756 | |||||||
chr7:158937888 | A | C | 143 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(140): Show |
143 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2778+3339A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158937888 | |||||||
chr7:158938101 | A | G | 21 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(18): Show |
21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2778+3552A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938101 | |||||||
chr7:158938115 | A | T | 1 | a0001c0001t0002g0194 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2778+3566A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938115 | |||||||
chr7:158938157 | C | T | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2778+3608C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938157 | |||||||
chr7:158938263 | C | G | 1 | a0005c0008t0003g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2779-3662C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938263 | |||||||
chr7:158938476 | G | A | 3 | a0001c0001t0005g0161 a0002c0018t0015g0048 a0003c0027t0022g0263 |
3 | HG01081.hp2 HG02015.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2779-3449G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938476 | |||||||
chr7:158938506 | G | T | 118 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.2779-3419G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938506 | |||||||
chr7:158938605 | A | C | 21 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(18): Show |
21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2779-3320A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938605 | |||||||
chr7:158938625 | G | A | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.2779-3300G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938625 | |||||||
chr7:158938695 | G | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2779-3230G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938695 | |||||||
chr7:158938741 | G | T | 1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.2779-3184G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938741 | |||||||
chr7:158938842 | T | C | 1 | a0002c0002t0001g0057 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2779-3083T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158938842 | |||||||
chr7:158939233 | C | A | 21 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(18): Show |
21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.2779-2692C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939233 | |||||||
chr7:158939239 | G | C | 1 | a0002c0002t0001g0080 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2779-2686G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939239 | |||||||
chr7:158939272 | C | A | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0002c0002t0021g0092 others(1): Show |
4 | HG01433.hp1 HG01981.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2779-2653C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939272 | |||||||
chr7:158939273 | C | CCAAA | 138 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0271 others(135): Show |
138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.2779-2647_2779-264 others(8): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158939273 | ||||||
chr7:158939273 | C | CCCAAA | 4 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0002c0002t0021g0092 others(1): Show |
4 | HG01433.hp1 HG01981.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.2779-2651_2779-265 others(9): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr7 | 158939273 | ||||||
chr7:158939422 | G | T | 1 | a0002c0002t0001g0088 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2779-2503G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939422 | |||||||
chr7:158939514 | T | C | 1 | a0005c0008t0003g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2779-2411T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939514 | |||||||
chr7:158939756 | C | T | 119 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2779-2169C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939756 | |||||||
chr7:158939867 | A | G | 119 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.2779-2058A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939867 | |||||||
chr7:158939991 | G | A | 1 | a0003c0010t0011g0252 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2779-1934G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158939991 | |||||||
chr7:158940063 | A | T | 1 | a0001c0001t0002g0141 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2779-1862A>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940063 | |||||||
chr7:158940158 | C | T | 6 | a0001c0001t0001g0268 a0001c0001t0001g0269 a0001c0001t0001g0270 others(3): Show |
6 | HG00140.hp1 HG01433.hp1 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.2779-1767C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940158 | |||||||
chr7:158940180 | A | C | 1 | a0010c0023t0001g0272 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2779-1745A>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940180 | |||||||
chr7:158940216 | A | G | 2 | a0002c0018t0015g0048 a0003c0027t0022g0263 |
2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.2779-1709A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940216 | |||||||
chr7:158940268 | G | A | 241 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(238): Show |
241 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(238): Show |
intron_variant | MODIFIER | c.2779-1657G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940268 | |||||||
chr7:158940344 | C | T | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.2779-1581C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940344 | |||||||
chr7:158940387 | C | T | 1 | a0003c0003t0007g0248 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.2779-1538C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940387 | |||||||
chr7:158940492 | C | T | 1 | a0003c0003t0004g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2779-1433C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940492 | |||||||
chr7:158940599 | C | T | 3 | a0001c0001t0002g0124 a0001c0001t0002g0134 a0001c0001t0002g0149 |
3 | NA18942.hp1 NA19060.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.2779-1326C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940599 | |||||||
chr7:158940836 | C | T | 1 | a0002c0018t0015g0048 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2779-1089C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158940836 | |||||||
chr7:158941363 | G | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.2779-562G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941363 | |||||||
chr7:158941386 | G | A | 118 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(115): Show |
118 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(115): Show |
intron_variant | MODIFIER | c.2779-539G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941386 | |||||||
chr7:158941582 | C | T | 24 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
24 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(21): Show |
intron_variant | MODIFIER | c.2779-343C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941582 | |||||||
chr7:158941591 | C | A | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2779-334C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941591 | |||||||
chr7:158941722 | C | T | 1 | a0001c0001t0002g0144 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2779-203C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941722 | |||||||
chr7:158941778 | C | T | 1 | a0001c0013t0002g0175 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2779-147C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 23/24 | chr7 | 158941778 | |||||||
chr7:158942432 | C | G | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3002+284C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158942432 | |||||||
chr7:158942448 | G | A | 1 | a0001c0001t0002g0146 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.3002+300G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158942448 | |||||||
chr7:158942569 | G | A | 238 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(235): Show |
238 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(235): Show |
intron_variant | MODIFIER | c.3002+421G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158942569 | |||||||
chr7:158942670 | T | C | 1 | a0003c0028t0023g0260 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3002+522T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158942670 | |||||||
chr7:158942898 | A | G | 1 | a0001c0001t0009g0227 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3002+750A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158942898 | |||||||
chr7:158943037 | C | T | 1 | a0001c0001t0002g0141 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.3002+889C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943037 | |||||||
chr7:158943060 | C | T | 1 | a0001c0022t0018g0229 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3002+912C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943060 | |||||||
chr7:158943106 | G | A | 1 | a0003c0003t0004g0262 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3002+958G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943106 | |||||||
chr7:158943342 | C | A | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3002+1194C>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943342 | |||||||
chr7:158943346 | C | T | 1 | a0001c0001t0002g0173 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3002+1198C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943346 | |||||||
chr7:158943421 | C | G | 2 | a0002c0018t0015g0048 a0003c0027t0022g0263 |
2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3002+1273C>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943421 | |||||||
chr7:158943576 | G | T | 1 | a0001c0001t0001g0006 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3002+1428G>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943576 | |||||||
chr7:158943633 | G | C | 21 | a0001c0001t0003g0199 a0001c0001t0003g0200 a0001c0001t0003g0201 others(18): Show |
21 | HG00423.hp1 HG00544.hp1 HG00597.hp2 others(18): Show |
intron_variant | MODIFIER | c.3002+1485G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943633 | |||||||
chr7:158943684 | C | T | 1 | a0005c0008t0003g0221 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3002+1536C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943684 | |||||||
chr7:158943694 | AGCATGTT others(4): Show |
A | 4 | a0001c0001t0012g0217 a0001c0001t0012g0218 a0002c0018t0015g0048 others(1): Show |
4 | HG01081.hp2 HG02055.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.3002+1548_3002+155 others(15): Show |
DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr7 | 158943694 | ||||||
chr7:158943757 | T | C | 3 | a0003c0003t0004g0243 a0003c0003t0004g0246 a0003c0029t0004g0249 |
3 | HG00733.hp1 HG01255.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3002+1609T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943757 | |||||||
chr7:158943819 | C | T | 1 | a0001c0001t0003g0205 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3002+1671C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943819 | |||||||
chr7:158943870 | C | T | 2 | a0003c0003t0004g0256 a0003c0003t0004g0265 |
2 | HG03491.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.3003-1711C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943870 | |||||||
chr7:158943871 | G | A | 9 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0004c0004t0002g0137 others(6): Show |
9 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.3003-1710G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943871 | |||||||
chr7:158943901 | G | C | 4 | a0001c0001t0002g0130 a0001c0001t0002g0182 a0001c0001t0002g0183 others(1): Show |
4 | HG00642.hp1 HG01070.hp2 HG01071.hp1 others(1): Show |
intron_variant | MODIFIER | c.3003-1680G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158943901 | |||||||
chr7:158944004 | G | C | 1 | a0001c0001t0002g0158 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.3003-1577G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944004 | |||||||
chr7:158944065 | G | A | 1 | a0001c0001t0002g0121 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.3003-1516G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944065 | |||||||
chr7:158944123 | G | A | 3 | a0002c0002t0001g0052 a0002c0002t0001g0053 a0002c0002t0014g0087 |
3 | HG03017.hp2 HG03942.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.3003-1458G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944123 | |||||||
chr7:158944150 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3003-1431G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944150 | |||||||
chr7:158944172 | G | A | 102 | a0001c0001t0005g0139 a0001c0001t0005g0142 a0001c0001t0005g0190 others(99): Show |
102 | HG00099.hp2 HG00408.hp2 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.3003-1409G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944172 | |||||||
chr7:158944187 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.3003-1394C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944187 | |||||||
chr7:158944212 | G | A | 1 | a0001c0001t0003g0212 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3003-1369G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944212 | |||||||
chr7:158944422 | G | A | 144 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(141): Show |
144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.3003-1159G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944422 | |||||||
chr7:158944505 | G | C | 2 | a0001c0001t0012g0217 a0001c0001t0012g0218 |
2 | HG02055.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.3003-1076G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944505 | |||||||
chr7:158944628 | G | A | 1 | a0004c0004t0006g0179 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3003-953G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944628 | |||||||
chr7:158944674 | A | G | 9 | a0001c0001t0006g0007 a0001c0001t0006g0008 a0004c0004t0002g0137 others(6): Show |
9 | HG01934.hp2 HG02257.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.3003-907A>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944674 | |||||||
chr7:158944763 | T | C | 119 | a0001c0001t0001g0006 a0001c0001t0001g0268 a0001c0001t0001g0269 others(116): Show |
119 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(116): Show |
intron_variant | MODIFIER | c.3003-818T>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944763 | |||||||
chr7:158944870 | G | A | 2 | a0002c0018t0015g0048 a0003c0027t0022g0263 |
2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3003-711G>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944870 | |||||||
chr7:158944907 | C | T | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3003-674C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158944907 | |||||||
chr7:158945026 | C | T | 2 | a0002c0018t0015g0048 a0003c0027t0022g0263 |
2 | HG01081.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.3003-555C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945026 | |||||||
chr7:158945112 | T | A | 1 | a0001c0001t0005g0161 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.3003-469T>A | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945112 | |||||||
chr7:158945141 | G | C | 1 | a0002c0002t0001g0009 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.3003-440G>C | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945141 | |||||||
chr7:158945178 | C | T | 2 | a0002c0002t0001g0109 a0002c0002t0001g0111 |
2 | HG02280.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.3003-403C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945178 | |||||||
chr7:158945435 | T | G | 1 | a0002c0016t0001g0018 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3003-146T>G | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945435 | |||||||
chr7:158945529 | C | T | 3 | a0001c0001t0009g0115 a0001c0001t0009g0227 a0001c0001t0009g0228 |
3 | HG02280.hp1 HG02647.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.3003-52C>T | DYNC2I1 | ENSG00000126870.16 | transcript | ENST00000407559.8 | protein_coding | 24/24 | chr7 | 158945529 |