Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51626 |
| ensemblid | ENSG00000138036.18 |
| hgncid | 24595 |
| symbol | DYNC2LI1 |
| name | dynein cytoplasmic 2 light intermediate chain 1 |
| refseq_nuc | NM_016008.4 |
| refseq_prot | NP_057092.2 |
| ensembl_nuc | ENST00000260605.12 |
| ensembl_prot | ENSP00000260605.8 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 43774039 |
| end | 43810010 |
| strand | + |
| ver | v1.2 |
| region | chr2:43774039-43810010 |
| region5000 | chr2:43769039-43815010 |
| regionname0 | DYNC2LI1_chr2_43774039_43810010 |
| regionname5000 | DYNC2LI1_chr2_43769039_43815010 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 351 | 104 | 10 | 32 | 37 | 7 | 16 | 27 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0002 | 0/0 | 351 | 101 | 46 | 20 | 27 | 1 | 7 | 22 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0003 | 0/0 | 351 | 72 | 30 | 16 | 6 | 6 | 14 | 2 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0004 | 0/0 | 351 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0005 | 0/0 | 351 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0006 | 0/0 | 351 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0007 | 0/0 | 351 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0008 | 0/0 | 351 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0009 | 0/0 | 351 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0010 | 0/0 | 351 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0011 | 0/0 | 351 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| a0012 | 0/0 | 351 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | MPSET others(346): Show |
chr2 | 43769039 | 43815010 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1053 | 104 | 10 | 32 | 37 | 7 | 16 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0002c0002 | 0/0 | 1053 | 100 | 45 | 20 | 27 | 1 | 7 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0002c0008 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0003c0003 | 0/0 | 1053 | 72 | 30 | 16 | 6 | 6 | 14 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0004c0004 | 0/0 | 1053 | 6 | 6 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0005c0005 | 0/0 | 1053 | 3 | 3 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0006c0006 | 0/0 | 1053 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0007c0013 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0008c0012 | 0/0 | 1053 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0009c0007 | 0/0 | 1053 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0010c0009 | 0/0 | 1053 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0011c0010 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 | ||
| a0012c0011 | 0/0 | 1053 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | ATGCC others(1048): Show |
chr2 | 43769039 | 43815010 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1399 | 103 | 10 | 31 | 37 | 7 | 16 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0001c0001t0002 | 0/0 | 1399 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0002c0002t0001 | 0/0 | 1399 | 15 | 11 | 1 | 1 | 0 | 2 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0002c0002t0002 | 0/0 | 1399 | 61 | 22 | 17 | 19 | 0 | 3 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0002c0002t0003 | 0/0 | 1399 | 7 | 5 | 0 | 0 | 0 | 2 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0002c0002t0004 | 0/0 | 1399 | 16 | 6 | 2 | 7 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0002c0002t0008 | 0/0 | 1399 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0002c0008t0001 | 0/0 | 1399 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0003c0003t0002 | 0/0 | 1399 | 21 | 9 | 3 | 0 | 3 | 6 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0003c0003t0003 | 0/0 | 1399 | 31 | 8 | 7 | 6 | 2 | 8 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0003c0003t0005 | 0/0 | 1399 | 15 | 11 | 4 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0003c0003t0006 | 0/0 | 1399 | 3 | 0 | 2 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0003c0003t0007 | 0/0 | 1399 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0004c0004t0002 | 0/0 | 1399 | 6 | 6 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0005c0005t0001 | 0/0 | 1399 | 3 | 3 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0006c0006t0002 | 0/0 | 1399 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0007c0013t0003 | 0/0 | 1399 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0008c0012t0001 | 0/0 | 1399 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0009c0007t0005 | 0/0 | 1399 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0010c0009t0002 | 0/0 | 1399 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0011c0010t0002 | 0/0 | 1399 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| a0012c0011t0003 | 0/0 | 1399 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | AGAAG others(1394): Show |
chr2 | 43769039 | 43815010 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 13 | 1 | 5 | 3 | 2 | 2 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0005 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0030 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0228 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0015 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0003g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0003g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0003g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0002t0008g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0002c0008t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0012 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0013 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0002 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0005g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0006g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0006g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0007g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0003c0003t0007g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0004c0004t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0004c0004t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0004c0004t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0004c0004t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0004c0004t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0004c0004t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0005c0005t0001g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0005c0005t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0006c0006t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0006c0006t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0007c0013t0003g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0008c0012t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0009c0007t0005g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0010c0009t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0011c0010t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| a0012c0011t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0238 | EUR | GBR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0031 | EUR | FIN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00323 | hp2 | a0003 | c0003 | t0006 | g0072 | EUR | FIN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00438 | hp1 | a0002 | c0002 | t0002 | g0140 | EAS | CHS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00544 | hp1 | a0007 | c0013 | t0003 | g0202 | EAS | CHS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | CHS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00597 | hp1 | a0003 | c0003 | t0003 | g0076 | EAS | CHS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0020 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00639 | hp2 | a0003 | c0003 | t0002 | g0013 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00642 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0199 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00733 | hp1 | a0003 | c0003 | t0003 | g0073 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00733 | hp2 | a0002 | c0002 | t0002 | g0157 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00738 | hp1 | a0002 | c0002 | t0004 | g0110 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00738 | hp2 | a0003 | c0003 | t0005 | g0060 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01074 | hp1 | a0003 | c0003 | t0002 | g0094 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01074 | hp2 | a0003 | c0003 | t0005 | g0053 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01081 | hp2 | a0002 | c0002 | t0002 | g0147 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01099 | hp1 | a0002 | c0002 | t0002 | g0007 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01099 | hp2 | a0003 | c0003 | t0005 | g0054 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01106 | hp2 | a0003 | c0003 | t0005 | g0056 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01109 | hp1 | a0003 | c0003 | t0006 | g0052 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01109 | hp2 | a0006 | c0006 | t0002 | g0242 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01168 | hp1 | a0002 | c0002 | t0002 | g0148 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01175 | hp2 | a0003 | c0003 | t0003 | g0064 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01192 | hp2 | a0003 | c0003 | t0002 | g0012 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01243 | hp1 | a0002 | c0002 | t0002 | g0122 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0030 | AMR | PUR | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01256 | hp2 | a0003 | c0003 | t0003 | g0066 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01257 | hp2 | a0003 | c0003 | t0003 | g0081 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0028 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01258 | hp2 | a0003 | c0003 | t0003 | g0065 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01261 | hp2 | a0002 | c0002 | t0004 | g0117 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01346 | hp1 | a0002 | c0002 | t0001 | g0217 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0138 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01496 | hp1 | a0008 | c0012 | t0001 | g0166 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | CLM | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01515 | hp1 | a0003 | c0003 | t0002 | g0095 | EUR | IBS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0025 | EUR | IBS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01516 | hp2 | a0003 | c0003 | t0003 | g0082 | EUR | IBS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01517 | hp1 | a0003 | c0003 | t0002 | g0097 | EUR | IBS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01884 | hp1 | a0004 | c0004 | t0002 | g0033 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01884 | hp2 | a0002 | c0002 | t0002 | g0126 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01891 | hp1 | a0003 | c0003 | t0005 | g0162 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01928 | hp2 | a0003 | c0003 | t0003 | g0002 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01934 | hp2 | a0002 | c0002 | t0002 | g0137 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01943 | hp2 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01952 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01975 | hp1 | a0002 | c0002 | t0002 | g0130 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01975 | hp2 | a0002 | c0002 | t0002 | g0015 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01978 | hp1 | a0002 | c0002 | t0002 | g0139 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01981 | hp2 | a0003 | c0003 | t0006 | g0058 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01993 | hp1 | a0002 | c0002 | t0002 | g0004 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02004 | hp1 | a0002 | c0002 | t0002 | g0160 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0020 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02027 | hp1 | a0003 | c0003 | t0003 | g0078 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02040 | hp2 | a0003 | c0003 | t0003 | g0069 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02055 | hp2 | a0002 | c0002 | t0003 | g0048 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02071 | hp1 | a0003 | c0003 | t0003 | g0075 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0155 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02132 | hp1 | a0002 | c0002 | t0002 | g0133 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02132 | hp2 | a0002 | c0002 | t0004 | g0109 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02145 | hp1 | a0002 | c0002 | t0001 | g0237 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0207 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CDX | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02155 | hp2 | a0002 | c0002 | t0002 | g0158 | EAS | CDX | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02257 | hp1 | a0002 | c0002 | t0004 | g0115 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02257 | hp2 | a0002 | c0002 | t0001 | g0222 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02258 | hp2 | a0003 | c0003 | t0005 | g0090 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02273 | hp2 | a0002 | c0002 | t0002 | g0131 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02280 | hp1 | a0002 | c0002 | t0001 | g0236 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02300 | hp2 | a0003 | c0003 | t0003 | g0079 | AMR | PEL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02451 | hp1 | a0003 | c0003 | t0007 | g0070 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02451 | hp2 | a0002 | c0002 | t0001 | g0220 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02572 | hp2 | a0002 | c0002 | t0004 | g0003 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02615 | hp1 | a0003 | c0003 | t0003 | g0088 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02615 | hp2 | a0002 | c0002 | t0001 | g0216 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02622 | hp1 | a0002 | c0002 | t0002 | g0145 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02622 | hp2 | a0003 | c0003 | t0005 | g0057 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02630 | hp1 | a0003 | c0003 | t0003 | g0009 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02630 | hp2 | a0002 | c0002 | t0002 | g0124 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02647 | hp1 | a0002 | c0002 | t0002 | g0043 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02647 | hp2 | a0003 | c0003 | t0005 | g0055 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02698 | hp1 | a0003 | c0003 | t0002 | g0099 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02698 | hp2 | a0003 | c0003 | t0003 | g0002 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02717 | hp1 | a0002 | c0002 | t0002 | g0125 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02717 | hp2 | a0002 | c0002 | t0003 | g0040 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02738 | hp1 | a0002 | c0002 | t0002 | g0136 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02809 | hp2 | a0002 | c0002 | t0002 | g0121 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02818 | hp1 | a0002 | c0002 | t0008 | g0061 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02818 | hp2 | a0003 | c0003 | t0003 | g0010 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02886 | hp1 | a0003 | c0003 | t0003 | g0089 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02886 | hp2 | a0002 | c0002 | t0002 | g0152 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02895 | hp2 | a0005 | c0005 | t0001 | g0026 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02896 | hp1 | a0003 | c0003 | t0003 | g0009 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02896 | hp2 | a0002 | c0002 | t0002 | g0041 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02897 | hp1 | a0002 | c0002 | t0002 | g0037 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02897 | hp2 | a0005 | c0005 | t0001 | g0026 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02922 | hp1 | a0003 | c0003 | t0002 | g0107 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02922 | hp2 | a0002 | c0002 | t0004 | g0116 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02965 | hp1 | a0003 | c0003 | t0005 | g0063 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02965 | hp2 | a0003 | c0003 | t0005 | g0068 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02970 | hp1 | a0003 | c0003 | t0003 | g0067 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02970 | hp2 | a0004 | c0004 | t0002 | g0032 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02976 | hp1 | a0004 | c0004 | t0002 | g0035 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02976 | hp2 | a0002 | c0002 | t0002 | g0146 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0015 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03041 | hp1 | a0003 | c0003 | t0005 | g0062 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03041 | hp2 | a0002 | c0002 | t0003 | g0084 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03098 | hp1 | a0003 | c0003 | t0002 | g0105 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03130 | hp1 | a0003 | c0003 | t0002 | g0093 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03130 | hp2 | a0002 | c0002 | t0002 | g0044 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03139 | hp1 | a0003 | c0003 | t0002 | g0098 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03139 | hp2 | a0003 | c0003 | t0007 | g0071 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03195 | hp1 | a0004 | c0004 | t0002 | g0046 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03195 | hp2 | a0003 | c0003 | t0002 | g0102 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03209 | hp1 | a0002 | c0002 | t0002 | g0151 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03225 | hp1 | a0002 | c0002 | t0001 | g0176 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03225 | hp2 | a0002 | c0002 | t0002 | g0153 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03239 | hp1 | a0003 | c0003 | t0002 | g0104 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03453 | hp1 | a0004 | c0004 | t0002 | g0034 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03453 | hp2 | a0003 | c0003 | t0005 | g0091 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03486 | hp1 | a0003 | c0003 | t0002 | g0092 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03486 | hp2 | a0002 | c0002 | t0004 | g0003 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03490 | hp1 | a0002 | c0002 | t0003 | g0011 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03490 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03491 | hp2 | a0003 | c0003 | t0002 | g0240 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0027 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03516 | hp1 | a0002 | c0002 | t0001 | g0177 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03516 | hp2 | a0002 | c0002 | t0002 | g0156 | AFR | ESN | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03540 | hp1 | a0002 | c0002 | t0001 | g0219 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03540 | hp2 | a0002 | c0002 | t0002 | g0039 | AFR | GWD | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03579 | hp1 | a0005 | c0005 | t0001 | g0221 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03579 | hp2 | a0006 | c0006 | t0002 | g0243 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03654 | hp2 | a0002 | c0002 | t0002 | g0241 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03669 | hp1 | a0003 | c0003 | t0003 | g0087 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03688 | hp1 | a0003 | c0003 | t0003 | g0002 | SAS | STU | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03688 | hp2 | a0003 | c0003 | t0002 | g0096 | SAS | STU | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03704 | hp1 | a0002 | c0002 | t0003 | g0011 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03831 | hp1 | a0003 | c0003 | t0003 | g0080 | SAS | BEB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0209 | SAS | BEB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03834 | hp2 | a0003 | c0003 | t0003 | g0002 | SAS | BEB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03942 | hp2 | a0003 | c0003 | t0003 | g0245 | SAS | BEB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG04115 | hp1 | a0003 | c0003 | t0003 | g0074 | SAS | STU | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG04115 | hp2 | a0003 | c0003 | t0002 | g0103 | SAS | STU | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG04184 | hp1 | a0003 | c0003 | t0002 | g0100 | SAS | BEB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | BEB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0168 | SAS | STU | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG04199 | hp2 | a0003 | c0003 | t0003 | g0085 | SAS | STU | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | STU | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG04204 | hp2 | a0009 | c0007 | t0005 | g0051 | SAS | STU | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18522 | hp1 | a0002 | c0002 | t0004 | g0003 | AFR | YRI | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18522 | hp2 | a0002 | c0002 | t0003 | g0049 | AFR | YRI | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18906 | hp1 | a0002 | c0002 | t0004 | g0113 | AFR | YRI | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18906 | hp2 | a0003 | c0003 | t0003 | g0010 | AFR | YRI | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18943 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18952 | hp2 | a0002 | c0002 | t0002 | g0132 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18962 | hp1 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18964 | hp1 | a0002 | c0002 | t0002 | g0135 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18972 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18977 | hp2 | a0002 | c0002 | t0002 | g0142 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18978 | hp1 | a0002 | c0002 | t0002 | g0161 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18978 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18979 | hp2 | a0002 | c0002 | t0002 | g0159 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0128 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18986 | hp2 | a0002 | c0002 | t0002 | g0017 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18994 | hp1 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0143 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19001 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19001 | hp2 | a0002 | c0002 | t0004 | g0111 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19002 | hp2 | a0010 | c0009 | t0002 | g0127 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19009 | hp1 | a0002 | c0002 | t0002 | g0016 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19010 | hp1 | a0002 | c0002 | t0004 | g0114 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19012 | hp1 | a0002 | c0002 | t0004 | g0118 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0144 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19030 | hp1 | a0011 | c0010 | t0002 | g0119 | AFR | LWK | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19030 | hp2 | a0002 | c0002 | t0002 | g0045 | AFR | LWK | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19043 | hp1 | a0002 | c0008 | t0001 | g0244 | AFR | LWK | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19043 | hp2 | a0002 | c0002 | t0002 | g0123 | AFR | LWK | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19054 | hp1 | a0003 | c0003 | t0003 | g0086 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19056 | hp2 | a0002 | c0002 | t0004 | g0014 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19060 | hp2 | a0002 | c0002 | t0004 | g0108 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19067 | hp1 | a0002 | c0002 | t0002 | g0141 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19068 | hp2 | a0002 | c0002 | t0002 | g0134 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19082 | hp1 | a0003 | c0003 | t0003 | g0077 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19085 | hp2 | a0002 | c0002 | t0002 | g0149 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19240 | hp1 | a0002 | c0002 | t0001 | g0174 | AFR | YRI | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA19240 | hp2 | a0003 | c0003 | t0002 | g0012 | AFR | YRI | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA20129 | hp1 | a0002 | c0002 | t0002 | g0150 | AFR | ASW | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA20129 | hp2 | a0003 | c0003 | t0002 | g0101 | AFR | ASW | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA20752 | hp1 | a0003 | c0003 | t0002 | g0013 | EUR | TSI | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA20752 | hp2 | a0003 | c0003 | t0003 | g0002 | EUR | TSI | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | TSI | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA20805 | hp2 | a0002 | c0002 | t0004 | g0112 | EUR | TSI | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02109 | hp1 | a0002 | c0002 | t0002 | g0120 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02109 | hp2 | a0002 | c0002 | t0003 | g0047 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02486 | hp1 | a0003 | c0003 | t0003 | g0083 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0230 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02559 | hp1 | a0002 | c0002 | t0002 | g0038 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG02559 | hp2 | a0003 | c0003 | t0002 | g0106 | AFR | ACB | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG03471 | hp2 | a0002 | c0002 | t0002 | g0154 | AFR | MSL | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG06807 | hp1 | a0002 | c0002 | t0002 | g0042 | AFR | USA | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| HG06807 | hp2 | a0003 | c0003 | t0005 | g0008 | AFR | USA | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA18955 | hp2 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA20300 | hp1 | a0012 | c0011 | t0003 | g0050 | AFR | USA | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA20300 | hp2 | a0003 | c0003 | t0005 | g0008 | AFR | USA | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA21309 | hp1 | a0003 | c0003 | t0005 | g0059 | AFR | LWK | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| NA21309 | hp2 | a0004 | c0004 | t0002 | g0036 | AFR | LWK | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0228 | REF | REF | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0005 | REF | REF | DYNC2LI1_chr2_43769039_43815010 | DYNC2LI1 | chr2 | 43769039 | 43815010 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43776871 | T | C | 9 | a0002 a0003 a0004 others(6): Show |
188 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(185): Show |
missense_variant | MODERATE | c.98T>C | p.Phe33Ser | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/13 | 198/1399 | 98/1056 | 33/351 | chr2 | 43776871 | |||
| chr2:43789685 | A | C | 1 | a0005 | 3 | HG02895.hp2 HG02897.hp2 HG03579.hp1 |
missense_variant | MODERATE | c.284A>C | p.Asp95Ala | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/13 | 384/1399 | 284/1056 | 95/351 | chr2 | 43789685 | |||
| chr2:43794537 | C | T | 2 | a0011 a0012 |
2 | NA19030.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.401C>T | p.Thr134Ile | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/13 | 501/1399 | 401/1056 | 134/351 | chr2 | 43794537 | |||
| chr2:43794627 | T | C | 1 | a0006 | 2 | HG01109.hp2 HG03579.hp2 |
missense_variant | MODERATE | c.491T>C | p.Met164Thr | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/13 | 591/1399 | 491/1056 | 164/351 | chr2 | 43794627 | |||
| chr2:43795896 | G | A | 1 | a0009 | 1 | HG04204.hp2 | missense_variant | MODERATE | c.514G>A | p.Glu172Lys | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/13 | 614/1399 | 514/1056 | 172/351 | chr2 | 43795896 | |||
| chr2:43800874 | A | T | 4 | a0003 a0007 a0009 others(1): Show |
75 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(72): Show |
missense_variant | MODERATE | c.688A>T | p.Ile230Leu | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/13 | 788/1399 | 688/1056 | 230/351 | chr2 | 43800874 | |||
| chr2:43801700 | G | A | 2 | a0004 a0011 |
7 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(4): Show |
missense_variant | MODERATE | c.793G>A | p.Gly265Ser | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/13 | 893/1399 | 793/1056 | 265/351 | chr2 | 43801700 | |||
| chr2:43809725 | A | T | 1 | a0010 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.1014A>T | p.Arg338Ser | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 13/13 | 1114/1399 | 1014/1056 | 338/351 | chr2 | 43809725 | |||
| chr2:43809726 | A | T | 1 | a0010 | 1 | NA19002.hp2 | missense_variant | MODERATE | c.1015A>T | p.Ser339Cys | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 13/13 | 1115/1399 | 1015/1056 | 339/351 | chr2 | 43809726 | |||
| chr2:43809753 | G | C | 1 | a0008 | 1 | HG01496.hp1 | missense_variant | MODERATE | c.1042G>C | p.Glu348Gln | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 13/13 | 1142/1399 | 1042/1056 | 348/351 | chr2 | 43809753 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43801669 | G | A | 1 | a0002c0008 | 1 | NA19043.hp1 | synonymous_variant | LOW | c.762G>A | p.Pro254Pro | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/13 | 862/1399 | 762/1056 | 254/351 | chr2 | 43801669 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43774046 | C | T | 1 | a0003c0003t0006 | 3 | HG00323.hp2 HG01109.hp1 HG01981.hp2 |
5_prime_UTR_variant | MODIFIER | c.-93C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/13 | 93 | chr2 | 43774046 | ||||||
| chr2:43774077 | C | T | 4 | a0002c0002t0008 a0003c0003t0005 a0003c0003t0006 others(1): Show |
20 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(17): Show |
5_prime_UTR_variant | MODIFIER | c.-62C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/13 | 62 | chr2 | 43774077 | ||||||
| chr2:43809774 | T | C | 8 | a0002c0002t0003 a0003c0003t0003 a0003c0003t0005 others(5): Show |
61 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*7T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 13/13 | 7 | chr2 | 43809774 | ||||||
| chr2:43809783 | T | C | 7 | a0001c0001t0002 a0002c0002t0002 a0003c0003t0002 others(4): Show |
93 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(90): Show |
3_prime_UTR_variant | MODIFIER | c.*16T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 13/13 | 16 | chr2 | 43809783 | ||||||
| chr2:43809908 | T | G | 1 | a0002c0002t0004 | 16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*141T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 13/13 | 141 | chr2 | 43809908 | ||||||
| chr2:43809946 | A | G | 1 | a0003c0003t0007 | 2 | HG02451.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*179A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 13/13 | 179 | chr2 | 43809946 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr2:43774161 | C | G | 2 | a0002c0008t0001g0244 a0003c0003t0003g0245 |
2 | HG03942.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8+15C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43774161 | |||||||
| chr2:43774303 | G | C | 5 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(2): Show |
5 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.8+157G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43774303 | |||||||
| chr2:43774352 | G | T | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.8+206G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43774352 | |||||||
| chr2:43774447 | A | G | 2 | a0002c0008t0001g0244 a0003c0003t0003g0245 |
2 | HG03942.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.8+301A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43774447 | |||||||
| chr2:43774596 | A | G | 1 | a0002c0002t0002g0241 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.8+450A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43774596 | |||||||
| chr2:43774658 | C | G | 1 | a0003c0003t0002g0240 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.8+512C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43774658 | |||||||
| chr2:43774790 | T | TAC | 16 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(13): Show |
17 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.8+645_8+646insCA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43774790 | ||||||
| chr2:43775015 | C | G | 2 | a0001c0001t0001g0238 a0001c0001t0001g0239 |
2 | HG00099.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.8+869C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775015 | |||||||
| chr2:43775043 | T | TA | 151 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(148): Show |
170 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(167): Show |
intron_variant | MODIFIER | c.8+898dupA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775043 | ||||||
| chr2:43775099 | A | C | 1 | a0001c0001t0001g0031 | 2 | HG00323.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.8+953A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775099 | |||||||
| chr2:43775388 | A | G | 1 | a0003c0003t0005g0162 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.8+1242A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775388 | |||||||
| chr2:43775484 | C | CT | 46 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(43): Show |
51 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(48): Show |
intron_variant | MODIFIER | c.9-1295dupT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775484 | ||||||
| chr2:43775484 | C | T | 1 | a0002c0002t0002g0161 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.9-1298C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775484 | |||||||
| chr2:43775511 | C | T | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.9-1271C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775511 | |||||||
| chr2:43775539 | C | T | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.9-1243C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775539 | |||||||
| chr2:43775596 | C | T | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.9-1186C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775596 | |||||||
| chr2:43775602 | A | G | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.9-1180A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775602 | |||||||
| chr2:43775604 | C | A | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.9-1178C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775604 | |||||||
| chr2:43775628 | G | A | 3 | a0002c0002t0003g0047 a0002c0002t0003g0048 a0002c0002t0003g0049 |
3 | HG02055.hp2 HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.9-1154G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775628 | |||||||
| chr2:43775668 | CTTTTCT | C | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.9-1103_9-1098delCT others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775668 | ||||||
| chr2:43775687 | A | C | 1 | a0002c0002t0002g0160 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.9-1095A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775687 | |||||||
| chr2:43775692 | C | A | 1 | a0004c0004t0002g0046 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.9-1090C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775692 | |||||||
| chr2:43775692 | C | CT | 30 | a0002c0002t0002g0007 a0002c0002t0002g0038 a0002c0002t0002g0039 others(27): Show |
34 | HG00639.hp2 HG00642.hp1 HG01074.hp1 others(31): Show |
intron_variant | MODIFIER | c.9-1076dupT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775692 | ||||||
| chr2:43775769 | C | T | 1 | a0002c0002t0001g0237 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.9-1013C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775769 | |||||||
| chr2:43775846 | C | T | 2 | a0003c0003t0005g0090 a0003c0003t0005g0091 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.9-936C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775846 | |||||||
| chr2:43775852 | C | T | 16 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(13): Show |
17 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.9-930C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775852 | |||||||
| chr2:43775854 | A | AT | 74 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0019 others(71): Show |
99 | HG00323.hp1 HG00544.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.9-898dupT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATT | 27 | a0001c0001t0001g0028 a0001c0001t0001g0029 a0001c0001t0001g0030 others(24): Show |
32 | HG00438.hp2 HG00741.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.9-899_9-898dupTT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(4): Show |
2 | a0002c0002t0002g0128 a0010c0009t0002g0127 |
2 | NA18982.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.9-908_9-898dupTTTT others(7): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(5): Show |
12 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(9): Show |
17 | HG01943.hp2 HG01952.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.9-909_9-898dupTTTT others(8): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(6): Show |
16 | a0002c0002t0002g0136 a0002c0002t0002g0137 a0002c0002t0002g0138 others(13): Show |
17 | HG00438.hp1 HG00738.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.9-910_9-898dupTTTT others(9): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(7): Show |
4 | a0002c0002t0002g0144 a0002c0002t0004g0003 a0002c0002t0004g0114 others(1): Show |
6 | HG02572.hp2 HG03486.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.9-911_9-898dupTTTT others(10): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(8): Show |
1 | a0002c0002t0004g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.9-912_9-898dupTTTT others(11): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(9): Show |
8 | a0002c0002t0002g0145 a0002c0002t0002g0146 a0002c0002t0002g0147 others(5): Show |
8 | HG01081.hp2 HG01168.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.9-913_9-898dupTTTT others(12): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(10): Show |
5 | a0002c0002t0002g0153 a0002c0002t0002g0154 a0002c0002t0002g0155 others(2): Show |
5 | HG02129.hp2 HG02922.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.9-914_9-898dupTTTT others(13): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(11): Show |
4 | a0002c0002t0002g0156 a0002c0002t0002g0157 a0002c0002t0002g0158 others(1): Show |
4 | HG00733.hp2 HG01261.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.9-915_9-898dupTTTT others(14): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(12): Show |
1 | a0002c0002t0002g0159 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.9-916_9-898dupTTTT others(15): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(13): Show |
1 | a0003c0003t0002g0106 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.9-917_9-898dupTTTT others(16): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | A | ATTTTTTT others(14): Show |
1 | a0003c0003t0002g0107 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.9-918_9-898dupTTTT others(17): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | AT | A | 27 | a0002c0002t0002g0120 a0002c0002t0002g0121 a0002c0002t0002g0122 others(24): Show |
30 | HG00738.hp2 HG01074.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.9-898delT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | ATTTTTTT others(5): Show |
A | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.9-909_9-898delTTTT others(8): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775854 | ATTTTTTT others(8): Show |
A | 6 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(3): Show |
7 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.9-912_9-898delTTTT others(11): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43775854 | ||||||
| chr2:43775909 | T | G | 1 | a0002c0002t0001g0237 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.9-873T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43775909 | |||||||
| chr2:43776032 | TTTC | T | 2 | a0003c0003t0003g0010 a0003c0003t0005g0068 |
3 | HG02818.hp2 HG02965.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.9-738_9-736delCTT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr2 | 43776032 | ||||||
| chr2:43776083 | C | T | 2 | a0003c0003t0003g0009 a0003c0003t0003g0067 |
3 | HG02630.hp1 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.9-699C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43776083 | |||||||
| chr2:43776109 | A | T | 6 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(3): Show |
7 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.9-673A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43776109 | |||||||
| chr2:43776239 | C | T | 1 | a0001c0001t0001g0215 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.9-543C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43776239 | |||||||
| chr2:43776450 | C | G | 1 | a0002c0002t0001g0237 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.9-332C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43776450 | |||||||
| chr2:43776454 | A | T | 17 | a0002c0002t0002g0120 a0002c0002t0002g0121 a0002c0002t0002g0122 others(14): Show |
20 | HG00738.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.9-328A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43776454 | |||||||
| chr2:43776581 | A | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG02523.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.9-201A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43776581 | |||||||
| chr2:43776687 | A | G | 2 | a0003c0003t0003g0088 a0003c0003t0003g0089 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.9-95A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 1/12 | chr2 | 43776687 | |||||||
| chr2:43776958 | G | T | 12 | a0002c0002t0002g0037 a0002c0002t0002g0041 a0002c0002t0002g0042 others(9): Show |
12 | HG01884.hp1 HG02647.hp1 HG02896.hp2 others(9): Show |
intron_variant | MODIFIER | c.126+59G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43776958 | |||||||
| chr2:43776960 | T | G | 50 | a0002c0002t0002g0007 a0002c0002t0002g0038 a0002c0002t0002g0039 others(47): Show |
58 | HG00323.hp2 HG00597.hp1 HG00642.hp1 others(55): Show |
intron_variant | MODIFIER | c.126+61T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43776960 | |||||||
| chr2:43777029 | A | G | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+130A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777029 | |||||||
| chr2:43777115 | A | C | 1 | a0002c0002t0001g0236 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.126+216A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777115 | |||||||
| chr2:43777151 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.126+252G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777151 | |||||||
| chr2:43777262 | G | A | 17 | a0002c0002t0002g0120 a0002c0002t0002g0121 a0002c0002t0002g0122 others(14): Show |
20 | HG00738.hp1 HG01243.hp1 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.126+363G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777262 | |||||||
| chr2:43777359 | T | C | 1 | a0001c0001t0001g0163 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.126+460T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777359 | |||||||
| chr2:43777411 | C | T | 3 | a0002c0002t0003g0047 a0002c0002t0003g0048 a0002c0002t0003g0049 |
3 | HG02055.hp2 HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.126+512C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777411 | |||||||
| chr2:43777506 | G | A | 1 | a0003c0003t0002g0096 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.126+607G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777506 | |||||||
| chr2:43777507 | G | A | 2 | a0002c0008t0001g0244 a0003c0003t0003g0245 |
2 | HG03942.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.126+608G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777507 | |||||||
| chr2:43777721 | G | A | 43 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(40): Show |
48 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.126+822G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777721 | |||||||
| chr2:43777755 | A | G | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.126+856A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777755 | |||||||
| chr2:43777974 | T | A | 1 | a0003c0003t0003g0088 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.126+1075T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43777974 | |||||||
| chr2:43778051 | C | T | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.126+1152C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778051 | |||||||
| chr2:43778077 | A | T | 1 | a0002c0002t0004g0116 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.126+1178A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778077 | |||||||
| chr2:43778175 | T | C | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+1276T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778175 | |||||||
| chr2:43778194 | G | A | 1 | a0006c0006t0002g0242 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.126+1295G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778194 | |||||||
| chr2:43778262 | C | A | 1 | a0003c0003t0003g0069 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.126+1363C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778262 | |||||||
| chr2:43778319 | A | G | 46 | a0002c0002t0008g0061 a0003c0003t0003g0002 a0003c0003t0003g0009 others(43): Show |
53 | HG00323.hp2 HG00597.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.126+1420A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778319 | |||||||
| chr2:43778591 | C | G | 34 | a0002c0002t0003g0011 a0002c0002t0004g0003 a0002c0002t0004g0014 others(31): Show |
40 | HG00639.hp2 HG00738.hp1 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.126+1692C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778591 | |||||||
| chr2:43778807 | T | C | 72 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(69): Show |
80 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.126+1908T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778807 | |||||||
| chr2:43778886 | A | G | 1 | a0003c0003t0003g0083 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.126+1987A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778886 | |||||||
| chr2:43778944 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.126+2045G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778944 | |||||||
| chr2:43778952 | T | G | 1 | a0001c0001t0001g0173 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.126+2053T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43778952 | |||||||
| chr2:43779089 | C | A | 10 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(7): Show |
11 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(8): Show |
intron_variant | MODIFIER | c.126+2190C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779089 | |||||||
| chr2:43779107 | C | T | 4 | a0002c0002t0002g0125 a0002c0002t0002g0150 a0002c0002t0002g0151 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+2208C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779107 | |||||||
| chr2:43779116 | G | A | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.126+2217G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779116 | |||||||
| chr2:43779118 | G | A | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.126+2219G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779118 | |||||||
| chr2:43779120 | G | A | 1 | a0001c0001t0001g0019 | 2 | NA18977.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.126+2221G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779120 | |||||||
| chr2:43779325 | A | C | 79 | a0001c0001t0002g0212 a0002c0002t0001g0129 a0002c0002t0002g0004 others(76): Show |
87 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(84): Show |
intron_variant | MODIFIER | c.126+2426A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779325 | |||||||
| chr2:43779516 | C | T | 19 | a0003c0003t0002g0012 a0003c0003t0002g0013 a0003c0003t0002g0092 others(16): Show |
21 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.126+2617C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779516 | |||||||
| chr2:43779883 | A | G | 1 | a0001c0001t0001g0211 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.126+2984A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779883 | |||||||
| chr2:43779936 | A | G | 150 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(147): Show |
169 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.126+3037A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779936 | |||||||
| chr2:43779957 | G | T | 9 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0110 others(6): Show |
12 | HG00738.hp1 HG01261.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.126+3058G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779957 | |||||||
| chr2:43779988 | G | A | 167 | a0002c0002t0001g0027 a0002c0002t0001g0129 a0002c0002t0001g0164 others(164): Show |
188 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(185): Show |
intron_variant | MODIFIER | c.126+3089G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779988 | |||||||
| chr2:43779989 | T | C | 1 | a0002c0002t0002g0125 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.126+3090T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43779989 | |||||||
| chr2:43780080 | C | T | 5 | a0002c0002t0003g0047 a0002c0002t0003g0048 a0002c0002t0003g0049 others(2): Show |
5 | HG02055.hp2 HG02109.hp2 HG03942.hp2 others(2): Show |
intron_variant | MODIFIER | c.126+3181C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780080 | |||||||
| chr2:43780171 | G | A | 10 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0110 others(7): Show |
13 | HG00738.hp1 HG01261.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.126+3272G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780171 | |||||||
| chr2:43780254 | C | G | 47 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(44): Show |
52 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.127-3266C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780254 | |||||||
| chr2:43780267 | A | G | 150 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(147): Show |
169 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.127-3253A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780267 | |||||||
| chr2:43780501 | G | A | 13 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(10): Show |
14 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.127-3019G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780501 | |||||||
| chr2:43780613 | C | T | 1 | a0003c0003t0002g0107 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.127-2907C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780613 | |||||||
| chr2:43780646 | G | A | 9 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0110 others(6): Show |
12 | HG00738.hp1 HG01261.hp2 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.127-2874G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780646 | |||||||
| chr2:43780715 | A | C | 2 | a0002c0002t0002g0135 a0002c0002t0002g0144 |
2 | NA18964.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.127-2805A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780715 | |||||||
| chr2:43780733 | C | T | 19 | a0003c0003t0003g0002 a0003c0003t0003g0064 a0003c0003t0003g0065 others(16): Show |
23 | HG00597.hp1 HG00733.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.127-2787C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780733 | |||||||
| chr2:43780761 | A | C | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG00741.hp1 HG01175.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.127-2759A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780761 | |||||||
| chr2:43780825 | A | G | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-2695A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780825 | |||||||
| chr2:43780923 | G | T | 150 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(147): Show |
169 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.127-2597G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780923 | |||||||
| chr2:43780952 | T | G | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-2568T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43780952 | |||||||
| chr2:43781089 | A | G | 23 | a0002c0002t0004g0108 a0002c0002t0004g0109 a0002c0002t0004g0118 others(20): Show |
25 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.127-2431A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781089 | |||||||
| chr2:43781106 | A | G | 43 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(40): Show |
48 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.127-2414A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781106 | |||||||
| chr2:43781229 | C | T | 3 | a0003c0003t0007g0070 a0003c0003t0007g0071 a0012c0011t0003g0050 |
3 | HG02451.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.127-2291C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781229 | |||||||
| chr2:43781359 | T | A | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-2161T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781359 | |||||||
| chr2:43781366 | C | CA | 39 | a0001c0001t0001g0028 a0001c0001t0001g0223 a0001c0001t0001g0233 others(36): Show |
43 | HG00639.hp2 HG00642.hp1 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.127-2143dupA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43781366 | ||||||
| chr2:43781366 | CA | C | 49 | a0002c0002t0004g0108 a0002c0002t0004g0109 a0002c0002t0004g0118 others(46): Show |
56 | HG00323.hp2 HG00597.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.127-2143delA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43781366 | ||||||
| chr2:43781411 | G | C | 101 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(98): Show |
113 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(110): Show |
intron_variant | MODIFIER | c.127-2109G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781411 | |||||||
| chr2:43781426 | A | G | 47 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(44): Show |
52 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.127-2094A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781426 | |||||||
| chr2:43781467 | C | T | 1 | a0002c0002t0001g0222 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.127-2053C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781467 | |||||||
| chr2:43781522 | C | T | 6 | a0002c0002t0008g0061 a0003c0003t0005g0008 a0003c0003t0005g0059 others(3): Show |
7 | HG00738.hp2 HG02818.hp1 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-1998C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781522 | |||||||
| chr2:43781546 | A | G | 1 | a0002c0002t0004g0116 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.127-1974A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781546 | |||||||
| chr2:43781601 | C | CT | 7 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(4): Show |
8 | HG01981.hp2 HG02630.hp1 HG02647.hp1 others(5): Show |
intron_variant | MODIFIER | c.127-1914dupT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43781601 | ||||||
| chr2:43781606 | TC | T | 98 | a0002c0002t0002g0004 a0002c0002t0002g0015 a0002c0002t0002g0016 others(95): Show |
113 | HG00438.hp1 HG00597.hp1 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.127-1913delC | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781606 | |||||||
| chr2:43781607 | C | T | 52 | a0002c0002t0001g0129 a0002c0002t0002g0007 a0002c0002t0002g0037 others(49): Show |
56 | HG00323.hp2 HG00642.hp1 HG00738.hp1 others(53): Show |
intron_variant | MODIFIER | c.127-1913C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781607 | |||||||
| chr2:43781625 | CAG | C | 6 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(3): Show |
7 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-1892_127-1891d others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43781625 | ||||||
| chr2:43781769 | T | A | 1 | a0002c0002t0001g0216 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.127-1751T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781769 | |||||||
| chr2:43781837 | C | T | 1 | a0003c0003t0003g0087 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.127-1683C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781837 | |||||||
| chr2:43781847 | C | T | 71 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(68): Show |
78 | HG00438.hp1 HG00639.hp2 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.127-1673C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781847 | |||||||
| chr2:43781848 | C | T | 49 | a0002c0002t0004g0108 a0002c0002t0004g0109 a0002c0002t0004g0118 others(46): Show |
56 | HG00323.hp2 HG00597.hp1 HG00733.hp1 others(53): Show |
intron_variant | MODIFIER | c.127-1672C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781848 | |||||||
| chr2:43781882 | G | A | 1 | a0002c0002t0003g0084 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.127-1638G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781882 | |||||||
| chr2:43781902 | G | A | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1618G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781902 | |||||||
| chr2:43781955 | A | G | 2 | a0003c0003t0003g0009 a0003c0003t0003g0067 |
3 | HG02630.hp1 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.127-1565A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781955 | |||||||
| chr2:43781958 | A | C | 13 | a0002c0002t0001g0027 a0002c0002t0001g0164 a0002c0002t0001g0176 others(10): Show |
15 | HG01981.hp1 HG02257.hp2 HG02280.hp1 others(12): Show |
intron_variant | MODIFIER | c.127-1562A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43781958 | |||||||
| chr2:43782009 | C | CTGTGTGT others(7): Show |
1 | a0006c0006t0002g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-1510_127-1509i others(16): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782009 | ||||||
| chr2:43782011 | A | ATG | 4 | a0001c0001t0001g0232 a0002c0002t0001g0027 a0002c0002t0001g0217 others(1): Show |
5 | HG01346.hp1 HG03490.hp2 HG03492.hp2 others(2): Show |
intron_variant | MODIFIER | c.127-1485_127-1484d others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782011 | ||||||
| chr2:43782011 | A | ATGTGTGT others(5): Show |
12 | a0002c0002t0002g0015 a0002c0002t0002g0136 a0002c0002t0002g0137 others(9): Show |
13 | HG00733.hp2 HG01081.hp2 HG01934.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-1495_127-1484d others(14): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782011 | ||||||
| chr2:43782011 | A | ATGTGTGT others(7): Show |
5 | a0002c0002t0002g0007 a0002c0002t0002g0038 a0002c0002t0002g0039 others(2): Show |
6 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1497_127-1484d others(16): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782011 | ||||||
| chr2:43782011 | A | ATGTGTGT others(9): Show |
39 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0016 others(36): Show |
43 | HG00438.hp1 HG01109.hp2 HG01168.hp1 others(40): Show |
intron_variant | MODIFIER | c.127-1499_127-1484d others(18): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782011 | ||||||
| chr2:43782011 | A | ATGTGTGT others(11): Show |
9 | a0002c0002t0002g0037 a0002c0002t0002g0041 a0002c0002t0002g0125 others(6): Show |
9 | HG02055.hp2 HG02717.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.127-1501_127-1484d others(20): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782011 | ||||||
| chr2:43782011 | A | ATGTGTGT others(13): Show |
5 | a0002c0002t0002g0151 a0002c0002t0003g0011 a0002c0002t0003g0047 others(2): Show |
6 | HG02109.hp2 HG03209.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-1503_127-1484d others(22): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782011 | ||||||
| chr2:43782011 | A | ATGTGTGT others(15): Show |
1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.127-1505_127-1484d others(24): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782011 | ||||||
| chr2:43782011 | A | G | 1 | a0006c0006t0002g0243 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.127-1509A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782011 | |||||||
| chr2:43782011 | ATG | A | 10 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0110 others(7): Show |
13 | HG00738.hp1 HG01261.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-1485_127-1484d others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782011 | ||||||
| chr2:43782026 | T | C | 1 | a0001c0001t0002g0212 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.127-1494T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782026 | |||||||
| chr2:43782244 | C | T | 19 | a0003c0003t0002g0012 a0003c0003t0002g0013 a0003c0003t0002g0092 others(16): Show |
21 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.127-1276C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782244 | |||||||
| chr2:43782260 | A | G | 3 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0001g0217 |
3 | HG01346.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.127-1260A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782260 | |||||||
| chr2:43782277 | A | T | 18 | a0003c0003t0003g0002 a0003c0003t0003g0064 a0003c0003t0003g0065 others(15): Show |
22 | HG00597.hp1 HG00733.hp1 HG01175.hp2 others(19): Show |
intron_variant | MODIFIER | c.127-1243A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782277 | |||||||
| chr2:43782288 | C | A | 12 | a0002c0002t0001g0027 a0002c0002t0001g0164 a0002c0002t0001g0176 others(9): Show |
14 | HG01981.hp1 HG02257.hp2 HG02280.hp1 others(11): Show |
intron_variant | MODIFIER | c.127-1232C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782288 | |||||||
| chr2:43782306 | A | G | 10 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0110 others(7): Show |
13 | HG00738.hp1 HG01261.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.127-1214A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782306 | |||||||
| chr2:43782337 | C | T | 1 | a0001c0001t0001g0028 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.127-1183C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782337 | |||||||
| chr2:43782338 | G | A | 3 | a0001c0001t0001g0020 a0001c0001t0001g0178 a0001c0001t0001g0224 |
4 | HG00639.hp1 HG01993.hp2 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.127-1182G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782338 | |||||||
| chr2:43782547 | TA | T | 23 | a0001c0001t0001g0025 a0001c0001t0001g0173 a0001c0001t0001g0210 others(20): Show |
25 | HG00323.hp2 HG01256.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.127-954delA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782547 | ||||||
| chr2:43782547 | TAA | T | 6 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(3): Show |
7 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.127-955_127-954del others(2): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43782547 | ||||||
| chr2:43782583 | T | A | 1 | a0002c0002t0002g0130 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.127-937T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782583 | |||||||
| chr2:43782696 | T | C | 2 | a0003c0003t0002g0095 a0003c0003t0002g0097 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.127-824T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782696 | |||||||
| chr2:43782713 | G | A | 23 | a0002c0002t0004g0108 a0002c0002t0004g0109 a0002c0002t0004g0118 others(20): Show |
25 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(22): Show |
intron_variant | MODIFIER | c.127-807G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782713 | |||||||
| chr2:43782791 | A | T | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.127-729A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782791 | |||||||
| chr2:43782871 | A | G | 1 | a0001c0001t0001g0209 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.127-649A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782871 | |||||||
| chr2:43782890 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.127-630G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782890 | |||||||
| chr2:43782905 | C | T | 14 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(11): Show |
16 | HG00642.hp1 HG01099.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.127-615C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43782905 | |||||||
| chr2:43783125 | TTTTC | T | 2 | a0003c0003t0003g0009 a0003c0003t0003g0067 |
3 | HG02630.hp1 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.127-391_127-388del others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr2 | 43783125 | ||||||
| chr2:43783202 | C | A | 58 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(55): Show |
63 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(60): Show |
intron_variant | MODIFIER | c.127-318C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43783202 | |||||||
| chr2:43783449 | A | G | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.127-71A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43783449 | |||||||
| chr2:43783481 | G | A | 149 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(146): Show |
168 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(165): Show |
intron_variant | MODIFIER | c.127-39G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 2/12 | chr2 | 43783481 | |||||||
| chr2:43783696 | C | A | 1 | a0003c0003t0002g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161+142C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43783696 | |||||||
| chr2:43783722 | C | G | 12 | a0002c0002t0002g0017 a0002c0002t0002g0128 a0002c0002t0002g0130 others(9): Show |
13 | HG01168.hp1 HG01975.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.161+168C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43783722 | |||||||
| chr2:43783748 | G | T | 63 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(60): Show |
69 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.161+194G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43783748 | |||||||
| chr2:43783808 | T | C | 4 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0001g0217 others(1): Show |
4 | HG01346.hp1 HG02145.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.161+254T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43783808 | |||||||
| chr2:43784129 | T | C | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.161+575T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784129 | |||||||
| chr2:43784181 | C | T | 58 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(55): Show |
64 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.161+627C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784181 | |||||||
| chr2:43784470 | G | A | 1 | a0003c0003t0005g0008 | 2 | HG06807.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.161+916G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784470 | |||||||
| chr2:43784484 | G | A | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.161+930G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784484 | |||||||
| chr2:43784508 | C | T | 1 | a0002c0002t0002g0152 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.161+954C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784508 | |||||||
| chr2:43784526 | G | A | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.161+972G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784526 | |||||||
| chr2:43784591 | C | T | 43 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(40): Show |
48 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.161+1037C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784591 | |||||||
| chr2:43784665 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.161+1111G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784665 | |||||||
| chr2:43784677 | G | A | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.161+1123G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784677 | |||||||
| chr2:43784725 | C | G | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.161+1171C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784725 | |||||||
| chr2:43784893 | C | G | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG02523.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.161+1339C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784893 | |||||||
| chr2:43784925 | G | A | 20 | a0002c0002t0008g0061 a0003c0003t0003g0010 a0003c0003t0005g0008 others(17): Show |
22 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.161+1371G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43784925 | |||||||
| chr2:43785048 | A | T | 1 | a0001c0001t0001g0210 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.161+1494A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785048 | |||||||
| chr2:43785067 | G | A | 45 | a0002c0002t0008g0061 a0003c0003t0003g0002 a0003c0003t0003g0009 others(42): Show |
52 | HG00323.hp2 HG00597.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.161+1513G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785067 | |||||||
| chr2:43785105 | T | C | 77 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(74): Show |
89 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.161+1551T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785105 | |||||||
| chr2:43785105 | T | G | 73 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(70): Show |
80 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.161+1551T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785105 | |||||||
| chr2:43785129 | C | G | 64 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(61): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.161+1575C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785129 | |||||||
| chr2:43785131 | G | C | 1 | a0001c0001t0001g0179 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.161+1577G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785131 | |||||||
| chr2:43785261 | T | C | 47 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(44): Show |
52 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.161+1707T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785261 | |||||||
| chr2:43785449 | T | C | 1 | a0002c0002t0002g0007 | 2 | HG00642.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.162-1732T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785449 | |||||||
| chr2:43785481 | C | A | 58 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(55): Show |
64 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.162-1700C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785481 | |||||||
| chr2:43785531 | C | T | 1 | a0002c0002t0002g0144 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.162-1650C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785531 | |||||||
| chr2:43785548 | A | G | 7 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.162-1633A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785548 | |||||||
| chr2:43785594 | C | T | 1 | a0002c0002t0002g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.162-1587C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785594 | |||||||
| chr2:43785612 | T | C | 47 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(44): Show |
52 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.162-1569T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785612 | |||||||
| chr2:43785646 | A | G | 1 | a0002c0002t0001g0177 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.162-1535A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785646 | |||||||
| chr2:43785690 | T | C | 73 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(70): Show |
80 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.162-1491T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785690 | |||||||
| chr2:43785697 | G | A | 3 | a0003c0003t0002g0099 a0003c0003t0002g0100 a0003c0003t0002g0240 |
3 | HG02698.hp1 HG03491.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.162-1484G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785697 | |||||||
| chr2:43785707 | T | A | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-1474T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785707 | |||||||
| chr2:43785711 | T | TAAATA | 102 | a0001c0001t0002g0212 a0002c0002t0002g0007 a0002c0002t0002g0037 others(99): Show |
116 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(113): Show |
intron_variant | MODIFIER | c.162-1454_162-1450d others(7): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43785711 | ||||||
| chr2:43785744 | T | G | 64 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(61): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.162-1437T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785744 | |||||||
| chr2:43785765 | A | G | 58 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(55): Show |
64 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.162-1416A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785765 | |||||||
| chr2:43785779 | C | G | 1 | a0001c0001t0001g0235 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.162-1402C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785779 | |||||||
| chr2:43785905 | GTGAATAA others(12): Show |
G | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-1270_162-1252d others(21): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr2 | 43785905 | ||||||
| chr2:43785948 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.162-1233T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43785948 | |||||||
| chr2:43786184 | C | T | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.162-997C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786184 | |||||||
| chr2:43786462 | G | A | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.162-719G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786462 | |||||||
| chr2:43786472 | A | G | 6 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(3): Show |
7 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.162-709A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786472 | |||||||
| chr2:43786488 | T | G | 1 | a0008c0012t0001g0166 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.162-693T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786488 | |||||||
| chr2:43786509 | C | G | 1 | a0001c0001t0001g0031 | 2 | HG00323.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.162-672C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786509 | |||||||
| chr2:43786531 | A | G | 1 | a0003c0003t0003g0086 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.162-650A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786531 | |||||||
| chr2:43786570 | G | A | 1 | a0001c0001t0001g0031 | 2 | HG00323.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.162-611G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786570 | |||||||
| chr2:43786572 | C | A | 18 | a0003c0003t0002g0012 a0003c0003t0002g0013 a0003c0003t0002g0092 others(15): Show |
20 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(17): Show |
intron_variant | MODIFIER | c.162-609C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786572 | |||||||
| chr2:43786646 | A | G | 3 | a0002c0002t0004g0003 a0002c0002t0004g0110 a0002c0002t0004g0113 |
5 | HG00738.hp1 HG02572.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.162-535A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786646 | |||||||
| chr2:43786659 | C | T | 7 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(4): Show |
8 | HG02055.hp2 HG02109.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.162-522C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786659 | |||||||
| chr2:43786698 | T | C | 150 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(147): Show |
169 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(166): Show |
intron_variant | MODIFIER | c.162-483T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786698 | |||||||
| chr2:43786699 | G | A | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162-482G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786699 | |||||||
| chr2:43786768 | G | A | 18 | a0002c0002t0008g0061 a0003c0003t0005g0008 a0003c0003t0005g0053 others(15): Show |
19 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(16): Show |
intron_variant | MODIFIER | c.162-413G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786768 | |||||||
| chr2:43786877 | A | G | 5 | a0002c0002t0002g0017 a0002c0002t0002g0128 a0002c0002t0002g0130 others(2): Show |
6 | HG01975.hp1 NA18962.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.162-304A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43786877 | |||||||
| chr2:43787018 | G | A | 1 | a0002c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.162-163G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43787018 | |||||||
| chr2:43787060 | T | C | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.162-121T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43787060 | |||||||
| chr2:43787162 | A | G | 64 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(61): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.162-19A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 3/12 | chr2 | 43787162 | |||||||
| chr2:43787460 | T | G | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.231+210T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787460 | |||||||
| chr2:43787476 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.231+226A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787476 | |||||||
| chr2:43787580 | T | A | 64 | a0002c0002t0008g0061 a0003c0003t0002g0012 a0003c0003t0002g0013 others(61): Show |
73 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.231+330T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787580 | |||||||
| chr2:43787758 | T | C | 1 | a0004c0004t0002g0036 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.231+508T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787758 | |||||||
| chr2:43787798 | T | G | 4 | a0002c0002t0003g0047 a0002c0002t0003g0048 a0002c0002t0003g0049 others(1): Show |
4 | HG02055.hp2 HG02109.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+548T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787798 | |||||||
| chr2:43787857 | A | G | 2 | a0002c0002t0002g0037 a0002c0002t0002g0041 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.231+607A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787857 | |||||||
| chr2:43787907 | C | T | 5 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0205 others(2): Show |
7 | HG01243.hp2 HG02055.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.231+657C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787907 | |||||||
| chr2:43787914 | T | G | 1 | a0002c0002t0001g0174 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.231+664T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787914 | |||||||
| chr2:43787924 | T | G | 2 | a0003c0003t0003g0009 a0003c0003t0003g0067 |
3 | HG02630.hp1 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.231+674T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787924 | |||||||
| chr2:43787981 | T | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0180 a0001c0001t0001g0181 |
4 | HG00735.hp1 HG01081.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+731T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787981 | |||||||
| chr2:43787998 | G | C | 1 | a0003c0003t0007g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.231+748G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43787998 | |||||||
| chr2:43788017 | A | G | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG00741.hp1 HG01175.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.231+767A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788017 | |||||||
| chr2:43788119 | C | T | 2 | a0003c0003t0003g0009 a0003c0003t0003g0067 |
3 | HG02630.hp1 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.231+869C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788119 | |||||||
| chr2:43788121 | T | C | 1 | a0012c0011t0003g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.231+871T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788121 | |||||||
| chr2:43788139 | C | T | 4 | a0003c0003t0005g0055 a0003c0003t0005g0056 a0003c0003t0005g0057 others(1): Show |
4 | HG01106.hp2 HG01891.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.231+889C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788139 | |||||||
| chr2:43788158 | T | G | 9 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(6): Show |
10 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+908T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788158 | |||||||
| chr2:43788189 | A | C | 1 | a0001c0001t0001g0231 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.231+939A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788189 | |||||||
| chr2:43788252 | A | C | 19 | a0003c0003t0002g0104 a0003c0003t0003g0002 a0003c0003t0003g0064 others(16): Show |
23 | HG00597.hp1 HG00733.hp1 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.231+1002A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788252 | |||||||
| chr2:43788256 | T | C | 9 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(6): Show |
10 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+1006T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788256 | |||||||
| chr2:43788270 | A | G | 26 | a0003c0003t0002g0104 a0003c0003t0003g0002 a0003c0003t0003g0009 others(23): Show |
31 | HG00597.hp1 HG00733.hp1 HG01175.hp2 others(28): Show |
intron_variant | MODIFIER | c.231+1020A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788270 | |||||||
| chr2:43788409 | C | T | 9 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(6): Show |
10 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.231+1159C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788409 | |||||||
| chr2:43788411 | G | T | 86 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(83): Show |
96 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.231+1161G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788411 | |||||||
| chr2:43788458 | G | A | 85 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(82): Show |
95 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.232-1175G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788458 | |||||||
| chr2:43788637 | G | A | 64 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(61): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.232-996G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788637 | |||||||
| chr2:43788731 | C | T | 1 | a0001c0001t0001g0181 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.232-902C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788731 | |||||||
| chr2:43788789 | A | T | 64 | a0002c0002t0008g0061 a0003c0003t0002g0012 a0003c0003t0002g0013 others(61): Show |
73 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(70): Show |
intron_variant | MODIFIER | c.232-844A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788789 | |||||||
| chr2:43788844 | G | T | 3 | a0002c0002t0004g0003 a0002c0002t0004g0110 a0002c0002t0004g0113 |
5 | HG00738.hp1 HG02572.hp2 HG03486.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-789G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788844 | |||||||
| chr2:43788915 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.232-718G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788915 | |||||||
| chr2:43788987 | A | G | 2 | a0003c0003t0007g0070 a0003c0003t0007g0071 |
2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.232-646A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43788987 | |||||||
| chr2:43789048 | C | G | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-585C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789048 | |||||||
| chr2:43789049 | G | A | 4 | a0003c0003t0002g0092 a0003c0003t0002g0105 a0003c0003t0002g0106 others(1): Show |
4 | HG02559.hp2 HG02922.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-584G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789049 | |||||||
| chr2:43789099 | C | T | 1 | a0003c0003t0007g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.232-534C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789099 | |||||||
| chr2:43789152 | G | A | 3 | a0002c0002t0002g0150 a0002c0002t0002g0151 a0002c0002t0002g0152 |
3 | HG02886.hp2 HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.232-481G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789152 | |||||||
| chr2:43789292 | C | T | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.232-341C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789292 | |||||||
| chr2:43789293 | G | A | 21 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(18): Show |
25 | HG00738.hp1 HG01109.hp2 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.232-340G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789293 | |||||||
| chr2:43789332 | A | G | 8 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(5): Show |
9 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.232-301A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789332 | |||||||
| chr2:43789369 | G | A | 4 | a0002c0002t0002g0120 a0002c0002t0002g0121 a0002c0002t0002g0122 others(1): Show |
4 | HG01243.hp1 HG01884.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-264G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789369 | |||||||
| chr2:43789408 | G | A | 4 | a0003c0003t0002g0012 a0003c0003t0002g0093 a0003c0003t0002g0101 others(1): Show |
5 | HG01192.hp2 HG03130.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-225G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789408 | |||||||
| chr2:43789412 | A | G | 64 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(61): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.232-221A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789412 | |||||||
| chr2:43789463 | G | A | 85 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(82): Show |
95 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.232-170G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789463 | |||||||
| chr2:43789465 | A | C | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.232-168A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789465 | |||||||
| chr2:43789540 | G | T | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.232-93G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 4/12 | chr2 | 43789540 | |||||||
| chr2:43789746 | C | G | 86 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(83): Show |
96 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.320+25C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43789746 | |||||||
| chr2:43789768 | C | T | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+47C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43789768 | |||||||
| chr2:43789840 | G | T | 1 | a0003c0003t0005g0062 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.320+119G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43789840 | |||||||
| chr2:43789928 | G | C | 20 | a0002c0002t0008g0061 a0003c0003t0003g0010 a0003c0003t0005g0008 others(17): Show |
22 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.320+207G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43789928 | |||||||
| chr2:43789985 | A | G | 64 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(61): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.320+264A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43789985 | |||||||
| chr2:43790001 | G | A | 20 | a0002c0002t0008g0061 a0003c0003t0003g0010 a0003c0003t0005g0008 others(17): Show |
22 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.320+280G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790001 | |||||||
| chr2:43790002 | C | G | 20 | a0002c0002t0008g0061 a0003c0003t0003g0010 a0003c0003t0005g0008 others(17): Show |
22 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.320+281C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790002 | |||||||
| chr2:43790038 | C | T | 77 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(74): Show |
86 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.320+317C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790038 | |||||||
| chr2:43790049 | T | C | 77 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(74): Show |
86 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.320+328T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790049 | |||||||
| chr2:43790088 | T | G | 2 | a0002c0002t0003g0047 a0002c0002t0003g0048 |
2 | HG02055.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.320+367T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790088 | |||||||
| chr2:43790104 | A | G | 5 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(2): Show |
5 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.320+383A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790104 | |||||||
| chr2:43790127 | G | A | 77 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(74): Show |
86 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.320+406G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790127 | |||||||
| chr2:43790197 | G | A | 1 | a0004c0004t0002g0032 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.320+476G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790197 | |||||||
| chr2:43790272 | C | A | 77 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(74): Show |
86 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.320+551C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790272 | |||||||
| chr2:43790470 | G | C | 3 | a0001c0001t0001g0171 a0001c0001t0001g0172 a0001c0001t0001g0183 |
3 | HG03239.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.320+749G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790470 | |||||||
| chr2:43790499 | G | A | 5 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(2): Show |
6 | HG02055.hp2 HG02109.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.320+778G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790499 | |||||||
| chr2:43790541 | G | A | 1 | a0002c0002t0002g0218 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.320+820G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790541 | |||||||
| chr2:43790543 | CT | C | 64 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(61): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.320+833delT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 43790543 | ||||||
| chr2:43790610 | G | T | 77 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(74): Show |
86 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(83): Show |
intron_variant | MODIFIER | c.320+889G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790610 | |||||||
| chr2:43790794 | TTTCTC | T | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.320+1075_320+1079d others(7): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 43790794 | ||||||
| chr2:43790833 | C | T | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+1112C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790833 | |||||||
| chr2:43790866 | T | C | 1 | a0003c0003t0002g0103 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.320+1145T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790866 | |||||||
| chr2:43790982 | G | A | 7 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(4): Show |
8 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.320+1261G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43790982 | |||||||
| chr2:43791156 | G | A | 1 | a0002c0002t0002g0148 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.320+1435G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43791156 | |||||||
| chr2:43791423 | G | T | 3 | a0001c0001t0001g0233 a0001c0001t0001g0234 a0001c0001t0001g0235 |
3 | HG00741.hp1 HG01175.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.320+1702G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43791423 | |||||||
| chr2:43791457 | C | T | 7 | a0002c0002t0001g0129 a0002c0002t0002g0016 a0002c0002t0002g0132 others(4): Show |
8 | HG02155.hp2 NA18943.hp1 NA18952.hp2 others(5): Show |
intron_variant | MODIFIER | c.320+1736C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43791457 | |||||||
| chr2:43791501 | G | A | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.320+1780G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43791501 | |||||||
| chr2:43791517 | G | GGA | 7 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(4): Show |
8 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.320+1802_320+1803d others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 43791517 | ||||||
| chr2:43791666 | G | A | 2 | a0003c0003t0003g0088 a0003c0003t0003g0089 |
2 | HG02615.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.320+1945G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43791666 | |||||||
| chr2:43791698 | G | A | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.320+1977G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43791698 | |||||||
| chr2:43791709 | C | T | 1 | a0001c0001t0001g0204 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.320+1988C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43791709 | |||||||
| chr2:43791878 | T | G | 9 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(6): Show |
10 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.320+2157T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43791878 | |||||||
| chr2:43791879 | T | C | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.320+2158T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43791879 | |||||||
| chr2:43792060 | T | C | 1 | a0001c0001t0001g0225 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.320+2339T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792060 | |||||||
| chr2:43792212 | C | T | 20 | a0002c0002t0008g0061 a0003c0003t0003g0010 a0003c0003t0005g0008 others(17): Show |
22 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(19): Show |
intron_variant | MODIFIER | c.321-2245C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792212 | |||||||
| chr2:43792223 | A | T | 6 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(3): Show |
7 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.321-2234A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792223 | |||||||
| chr2:43792263 | A | T | 1 | a0012c0011t0003g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.321-2194A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792263 | |||||||
| chr2:43792284 | A | T | 6 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(3): Show |
7 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.321-2173A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792284 | |||||||
| chr2:43792354 | T | C | 1 | a0003c0003t0007g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.321-2103T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792354 | |||||||
| chr2:43792413 | T | A | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.321-2044T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792413 | |||||||
| chr2:43792473 | T | A | 64 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(61): Show |
70 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(67): Show |
intron_variant | MODIFIER | c.321-1984T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792473 | |||||||
| chr2:43792487 | C | G | 47 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(44): Show |
52 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.321-1970C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792487 | |||||||
| chr2:43792487 | C | T | 1 | a0001c0001t0001g0203 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.321-1970C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792487 | |||||||
| chr2:43792520 | A | G | 8 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(5): Show |
9 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.321-1937A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792520 | |||||||
| chr2:43792580 | A | G | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.321-1877A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792580 | |||||||
| chr2:43792660 | G | A | 85 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(82): Show |
95 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.321-1797G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792660 | |||||||
| chr2:43792791 | C | T | 85 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(82): Show |
95 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(92): Show |
intron_variant | MODIFIER | c.321-1666C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792791 | |||||||
| chr2:43792797 | C | T | 72 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(69): Show |
79 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(76): Show |
intron_variant | MODIFIER | c.321-1660C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43792797 | |||||||
| chr2:43793018 | G | T | 1 | a0002c0002t0002g0007 | 2 | HG00642.hp1 HG01099.hp1 |
intron_variant | MODIFIER | c.321-1439G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793018 | |||||||
| chr2:43793051 | T | C | 1 | a0002c0002t0001g0176 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.321-1406T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793051 | |||||||
| chr2:43793108 | A | G | 2 | a0011c0010t0002g0119 a0012c0011t0003g0050 |
2 | NA19030.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.321-1349A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793108 | |||||||
| chr2:43793237 | G | T | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.321-1220G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793237 | |||||||
| chr2:43793501 | T | A | 1 | a0001c0001t0001g0184 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.321-956T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793501 | |||||||
| chr2:43793517 | T | C | 1 | a0001c0001t0001g0184 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.321-940T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793517 | |||||||
| chr2:43793553 | ATCTGTAT others(136): Show |
A | 1 | a0001c0001t0001g0184 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.321-901_321-759del | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 43793553 | ||||||
| chr2:43793600 | C | CT | 83 | a0001c0001t0001g0208 a0001c0001t0001g0231 a0001c0001t0002g0212 others(80): Show |
93 | HG00323.hp2 HG00597.hp1 HG00639.hp2 others(90): Show |
intron_variant | MODIFIER | c.321-842dupT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 43793600 | ||||||
| chr2:43793750 | A | G | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.321-707A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793750 | |||||||
| chr2:43793843 | A | G | 20 | a0003c0003t0003g0002 a0003c0003t0003g0064 a0003c0003t0003g0065 others(17): Show |
24 | HG00544.hp1 HG00597.hp1 HG00733.hp1 others(21): Show |
intron_variant | MODIFIER | c.321-614A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793843 | |||||||
| chr2:43793877 | G | C | 1 | a0012c0011t0003g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.321-580G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793877 | |||||||
| chr2:43793984 | C | T | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.321-473C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793984 | |||||||
| chr2:43793985 | A | G | 87 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(84): Show |
97 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.321-472A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43793985 | |||||||
| chr2:43794083 | A | G | 19 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(16): Show |
23 | HG00642.hp1 HG00738.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.321-374A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43794083 | |||||||
| chr2:43794195 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.321-262T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43794195 | |||||||
| chr2:43794268 | A | G | 61 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(58): Show |
67 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.321-189A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43794268 | |||||||
| chr2:43794341 | G | GT | 15 | a0002c0002t0002g0124 a0002c0002t0004g0003 a0002c0002t0004g0014 others(12): Show |
18 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(15): Show |
intron_variant | MODIFIER | c.321-107dupT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr2 | 43794341 | ||||||
| chr2:43794417 | T | C | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.321-40T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43794417 | |||||||
| chr2:43794431 | T | C | 1 | a0003c0003t0002g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.321-26T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 5/12 | chr2 | 43794431 | |||||||
| chr2:43794687 | T | A | 150 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(147): Show |
169 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.507+44T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43794687 | |||||||
| chr2:43794690 | T | C | 7 | a0002c0002t0002g0123 a0002c0002t0002g0124 a0002c0002t0002g0145 others(4): Show |
7 | HG02622.hp1 HG02630.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.507+47T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43794690 | |||||||
| chr2:43794870 | G | T | 1 | a0002c0002t0004g0116 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.507+227G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43794870 | |||||||
| chr2:43794905 | G | C | 1 | a0003c0003t0002g0094 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.507+262G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43794905 | |||||||
| chr2:43794920 | T | C | 1 | a0001c0001t0001g0185 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.507+277T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43794920 | |||||||
| chr2:43794953 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.507+310A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43794953 | |||||||
| chr2:43795039 | T | C | 1 | a0003c0003t0007g0070 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.507+396T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795039 | |||||||
| chr2:43795181 | T | G | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.507+538T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795181 | |||||||
| chr2:43795189 | G | A | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.507+546G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795189 | |||||||
| chr2:43795280 | C | T | 19 | a0003c0003t0002g0012 a0003c0003t0002g0013 a0003c0003t0002g0092 others(16): Show |
21 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.508-610C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795280 | |||||||
| chr2:43795373 | A | G | 87 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(84): Show |
97 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.508-517A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795373 | |||||||
| chr2:43795452 | C | T | 43 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(40): Show |
48 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.508-438C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795452 | |||||||
| chr2:43795522 | G | A | 1 | a0003c0003t0003g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.508-368G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795522 | |||||||
| chr2:43795566 | T | C | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.508-324T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795566 | |||||||
| chr2:43795571 | A | G | 2 | a0003c0003t0005g0053 a0003c0003t0005g0054 |
2 | HG01074.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.508-319A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795571 | |||||||
| chr2:43795605 | A | T | 66 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(63): Show |
73 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(70): Show |
intron_variant | MODIFIER | c.508-285A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795605 | |||||||
| chr2:43795614 | C | A | 6 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(3): Show |
7 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.508-276C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795614 | |||||||
| chr2:43795831 | T | C | 45 | a0003c0003t0003g0002 a0003c0003t0003g0009 a0003c0003t0003g0010 others(42): Show |
52 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.508-59T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795831 | |||||||
| chr2:43795861 | A | G | 2 | a0002c0002t0003g0011 a0003c0003t0003g0245 |
3 | HG03490.hp1 HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.508-29A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 6/12 | chr2 | 43795861 | |||||||
| chr2:43795990 | G | T | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG02523.hp1 NA18972.hp2 |
intron_variant | MODIFIER | c.576+32G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/12 | chr2 | 43795990 | |||||||
| chr2:43796126 | G | A | 2 | a0001c0001t0001g0186 a0001c0001t0001g0187 |
2 | NA18979.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.576+168G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/12 | chr2 | 43796126 | |||||||
| chr2:43796282 | G | A | 1 | a0009c0007t0005g0051 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.576+324G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/12 | chr2 | 43796282 | |||||||
| chr2:43796333 | C | CA | 58 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(55): Show |
64 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(61): Show |
intron_variant | MODIFIER | c.577-369dupA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 43796333 | ||||||
| chr2:43796333 | C | CAA | 16 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(13): Show |
17 | HG00642.hp1 HG01099.hp1 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.577-370_577-369dup others(2): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 43796333 | ||||||
| chr2:43796333 | CA | C | 32 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(29): Show |
37 | HG00323.hp2 HG00738.hp1 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.577-369delA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr2 | 43796333 | ||||||
| chr2:43796397 | A | C | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.577-321A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/12 | chr2 | 43796397 | |||||||
| chr2:43796450 | G | A | 4 | a0002c0002t0002g0125 a0002c0002t0002g0150 a0002c0002t0002g0151 others(1): Show |
4 | HG02717.hp1 HG02886.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.577-268G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/12 | chr2 | 43796450 | |||||||
| chr2:43796624 | A | T | 1 | a0012c0011t0003g0050 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.577-94A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/12 | chr2 | 43796624 | |||||||
| chr2:43796677 | A | G | 9 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(6): Show |
10 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.577-41A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 7/12 | chr2 | 43796677 | |||||||
| chr2:43796873 | C | T | 1 | a0002c0002t0002g0152 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.654+78C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43796873 | |||||||
| chr2:43797029 | A | G | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+234A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797029 | |||||||
| chr2:43797084 | G | A | 2 | a0002c0002t0003g0011 a0003c0003t0003g0245 |
3 | HG03490.hp1 HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.654+289G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797084 | |||||||
| chr2:43797143 | T | A | 152 | a0001c0001t0002g0212 a0002c0002t0001g0129 a0002c0002t0002g0004 others(149): Show |
171 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(168): Show |
intron_variant | MODIFIER | c.654+348T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797143 | |||||||
| chr2:43797145 | A | C | 1 | a0002c0002t0002g0140 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.654+350A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797145 | |||||||
| chr2:43797275 | G | A | 5 | a0002c0002t0002g0017 a0002c0002t0002g0128 a0002c0002t0002g0130 others(2): Show |
6 | HG01975.hp1 NA18962.hp1 NA18977.hp2 others(3): Show |
intron_variant | MODIFIER | c.654+480G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797275 | |||||||
| chr2:43797399 | G | C | 3 | a0002c0002t0004g0014 a0002c0002t0004g0111 a0002c0002t0004g0114 |
4 | NA18994.hp1 NA19001.hp2 NA19010.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+604G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797399 | |||||||
| chr2:43797403 | C | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.654+608C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797403 | |||||||
| chr2:43797409 | C | T | 87 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(84): Show |
97 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.654+614C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797409 | |||||||
| chr2:43797429 | G | T | 47 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(44): Show |
52 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(49): Show |
intron_variant | MODIFIER | c.654+634G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797429 | |||||||
| chr2:43797436 | A | G | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.654+641A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797436 | |||||||
| chr2:43797449 | T | TA | 2 | a0003c0003t0002g0013 a0003c0003t0002g0096 |
3 | HG00639.hp2 HG03688.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.654+655dupA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43797449 | ||||||
| chr2:43797470 | G | A | 19 | a0003c0003t0003g0010 a0003c0003t0005g0008 a0003c0003t0005g0053 others(16): Show |
21 | HG00323.hp2 HG00738.hp2 HG01074.hp2 others(18): Show |
intron_variant | MODIFIER | c.654+675G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797470 | |||||||
| chr2:43797515 | C | CT | 18 | a0001c0001t0001g0023 a0001c0001t0001g0183 a0001c0001t0001g0199 others(15): Show |
20 | HG00544.hp2 HG00642.hp2 HG02155.hp1 others(17): Show |
intron_variant | MODIFIER | c.654+744dupT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43797515 | ||||||
| chr2:43797515 | CT | C | 15 | a0001c0001t0001g0021 a0001c0001t0001g0188 a0001c0001t0001g0189 others(12): Show |
17 | HG00642.hp1 HG01081.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.654+744delT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43797515 | ||||||
| chr2:43797515 | CTT | C | 53 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(50): Show |
59 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(56): Show |
intron_variant | MODIFIER | c.654+743_654+744del others(2): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43797515 | ||||||
| chr2:43797515 | CTTT | C | 11 | a0002c0002t0002g0042 a0002c0002t0002g0123 a0004c0004t0002g0032 others(8): Show |
11 | HG01109.hp2 HG01884.hp1 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.654+742_654+744del others(3): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43797515 | ||||||
| chr2:43797588 | C | T | 2 | a0002c0002t0002g0150 a0002c0002t0002g0151 |
2 | HG03209.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.654+793C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797588 | |||||||
| chr2:43797720 | A | G | 1 | a0002c0002t0002g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.654+925A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797720 | |||||||
| chr2:43797770 | G | A | 1 | a0001c0001t0001g0238 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.654+975G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797770 | |||||||
| chr2:43797788 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.654+993G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797788 | |||||||
| chr2:43797903 | A | G | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.654+1108A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797903 | |||||||
| chr2:43797928 | C | G | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.654+1133C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797928 | |||||||
| chr2:43797959 | C | G | 1 | a0001c0001t0001g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.654+1164C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797959 | |||||||
| chr2:43797965 | A | T | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.654+1170A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43797965 | |||||||
| chr2:43797989 | TG | T | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+1196delG | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43797989 | ||||||
| chr2:43798043 | C | T | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.654+1248C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798043 | |||||||
| chr2:43798044 | A | G | 87 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(84): Show |
97 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.654+1249A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798044 | |||||||
| chr2:43798049 | C | T | 87 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(84): Show |
97 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.654+1254C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798049 | |||||||
| chr2:43798050 | T | G | 87 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(84): Show |
97 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.654+1255T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798050 | |||||||
| chr2:43798057 | G | A | 1 | a0003c0003t0003g0067 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.654+1262G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798057 | |||||||
| chr2:43798093 | C | G | 83 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(80): Show |
93 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.654+1298C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798093 | |||||||
| chr2:43798112 | C | CA | 47 | a0001c0001t0001g0191 a0002c0002t0002g0138 a0003c0003t0003g0002 others(44): Show |
54 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.654+1330dupA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43798112 | ||||||
| chr2:43798128 | T | G | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+1333T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798128 | |||||||
| chr2:43798216 | G | C | 150 | a0001c0001t0002g0212 a0002c0002t0001g0129 a0002c0002t0002g0004 others(147): Show |
169 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(166): Show |
intron_variant | MODIFIER | c.654+1421G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798216 | |||||||
| chr2:43798235 | A | G | 3 | a0002c0002t0003g0011 a0002c0008t0001g0244 a0003c0003t0003g0245 |
4 | HG03490.hp1 HG03704.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.654+1440A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798235 | |||||||
| chr2:43798304 | A | G | 2 | a0003c0003t0003g0009 a0003c0003t0003g0067 |
3 | HG02630.hp1 HG02896.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.654+1509A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798304 | |||||||
| chr2:43798450 | TAC | T | 86 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(83): Show |
96 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(93): Show |
intron_variant | MODIFIER | c.654+1657_654+1658d others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43798450 | ||||||
| chr2:43798489 | T | C | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.654+1694T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798489 | |||||||
| chr2:43798571 | A | G | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.654+1776A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798571 | |||||||
| chr2:43798679 | G | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG03209.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.654+1884G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798679 | |||||||
| chr2:43798753 | T | C | 2 | a0002c0002t0002g0135 a0002c0002t0002g0144 |
2 | NA18964.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.654+1958T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43798753 | |||||||
| chr2:43798917 | GT | G | 65 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(62): Show |
72 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.655-1912delT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr2 | 43798917 | ||||||
| chr2:43799034 | G | C | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.655-1807G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43799034 | |||||||
| chr2:43799091 | G | A | 2 | a0002c0002t0001g0176 a0002c0002t0001g0177 |
2 | HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.655-1750G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43799091 | |||||||
| chr2:43799531 | A | G | 2 | a0001c0001t0001g0171 a0001c0001t0001g0172 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.655-1310A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43799531 | |||||||
| chr2:43799581 | G | A | 73 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(70): Show |
80 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(77): Show |
intron_variant | MODIFIER | c.655-1260G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43799581 | |||||||
| chr2:43799836 | A | G | 6 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(3): Show |
7 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.655-1005A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43799836 | |||||||
| chr2:43800063 | A | G | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.655-778A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800063 | |||||||
| chr2:43800085 | A | G | 8 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(5): Show |
9 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.655-756A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800085 | |||||||
| chr2:43800121 | T | G | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655-720T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800121 | |||||||
| chr2:43800141 | A | G | 2 | a0002c0002t0001g0177 a0002c0002t0002g0123 |
2 | HG03516.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.655-700A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800141 | |||||||
| chr2:43800159 | T | A | 7 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(4): Show |
8 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.655-682T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800159 | |||||||
| chr2:43800163 | G | A | 64 | a0003c0003t0002g0012 a0003c0003t0002g0013 a0003c0003t0002g0092 others(61): Show |
73 | HG00323.hp2 HG00544.hp1 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.655-678G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800163 | |||||||
| chr2:43800252 | C | A | 84 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(81): Show |
94 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(91): Show |
intron_variant | MODIFIER | c.655-589C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800252 | |||||||
| chr2:43800278 | C | T | 1 | a0002c0002t0002g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.655-563C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800278 | |||||||
| chr2:43800356 | A | G | 1 | a0002c0002t0004g0110 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.655-485A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800356 | |||||||
| chr2:43800404 | C | T | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655-437C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800404 | |||||||
| chr2:43800453 | C | G | 7 | a0002c0002t0002g0007 a0002c0002t0002g0037 a0002c0002t0002g0038 others(4): Show |
8 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.655-388C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800453 | |||||||
| chr2:43800539 | A | G | 12 | a0002c0002t0002g0017 a0002c0002t0002g0128 a0002c0002t0002g0130 others(9): Show |
13 | HG01168.hp1 HG01975.hp1 HG02132.hp1 others(10): Show |
intron_variant | MODIFIER | c.655-302A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800539 | |||||||
| chr2:43800545 | A | T | 1 | a0002c0002t0002g0218 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.655-296A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800545 | |||||||
| chr2:43800642 | A | T | 2 | a0003c0003t0002g0095 a0003c0003t0002g0097 |
2 | HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.655-199A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800642 | |||||||
| chr2:43800809 | G | A | 43 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0015 others(40): Show |
48 | HG00438.hp1 HG00733.hp2 HG01081.hp2 others(45): Show |
intron_variant | MODIFIER | c.655-32G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 8/12 | chr2 | 43800809 | |||||||
| chr2:43800970 | G | A | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.731+53G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43800970 | |||||||
| chr2:43801041 | C | T | 71 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(68): Show |
78 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.731+124C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43801041 | |||||||
| chr2:43801349 | T | G | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.732-290T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43801349 | |||||||
| chr2:43801410 | G | T | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.732-229G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43801410 | |||||||
| chr2:43801460 | A | G | 9 | a0002c0002t0001g0164 a0002c0002t0001g0216 a0002c0002t0001g0219 others(6): Show |
10 | HG02257.hp2 HG02280.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.732-179A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43801460 | |||||||
| chr2:43801497 | A | C | 1 | a0003c0003t0002g0102 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.732-142A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43801497 | |||||||
| chr2:43801512 | C | T | 1 | a0001c0001t0001g0197 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.732-127C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43801512 | |||||||
| chr2:43801583 | C | T | 5 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(2): Show |
5 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.732-56C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43801583 | |||||||
| chr2:43801584 | G | A | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.732-55G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43801584 | |||||||
| chr2:43801600 | T | C | 3 | a0003c0003t0007g0070 a0003c0003t0007g0071 a0012c0011t0003g0050 |
3 | HG02451.hp1 HG03139.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.732-39T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43801600 | |||||||
| chr2:43801634 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG02486.hp2 | splice_region_variant&intron_variant | LOW | c.732-5C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 9/12 | chr2 | 43801634 | |||||||
| chr2:43801833 | C | T | 1 | a0002c0002t0002g0131 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.802+124C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43801833 | |||||||
| chr2:43801983 | A | C | 2 | a0003c0003t0007g0070 a0003c0003t0007g0071 |
2 | HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.802+274A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43801983 | |||||||
| chr2:43802314 | G | A | 1 | a0001c0001t0001g0167 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.802+605G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43802314 | |||||||
| chr2:43802374 | G | GT | 26 | a0001c0001t0001g0178 a0001c0001t0001g0187 a0001c0001t0001g0207 others(23): Show |
29 | HG00738.hp1 HG01261.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.802+681dupT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 43802374 | ||||||
| chr2:43802516 | G | A | 70 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(67): Show |
77 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.802+807G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43802516 | |||||||
| chr2:43802633 | T | C | 1 | a0002c0002t0001g0237 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.802+924T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43802633 | |||||||
| chr2:43802661 | T | A | 1 | a0003c0003t0003g0069 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.802+952T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43802661 | |||||||
| chr2:43802682 | C | T | 83 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(80): Show |
93 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(90): Show |
intron_variant | MODIFIER | c.802+973C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43802682 | |||||||
| chr2:43802742 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.802+1033C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43802742 | |||||||
| chr2:43802884 | G | C | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.802+1175G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43802884 | |||||||
| chr2:43802893 | C | A | 147 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(144): Show |
166 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.802+1184C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43802893 | |||||||
| chr2:43802971 | TCACTATA others(36): Show |
T | 1 | a0003c0003t0003g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.802+1264_802+1306d others(45): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr2 | 43802971 | ||||||
| chr2:43802999 | A | T | 6 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(3): Show |
7 | HG01109.hp2 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.802+1290A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43802999 | |||||||
| chr2:43803120 | C | T | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.802+1411C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43803120 | |||||||
| chr2:43803176 | C | T | 3 | a0002c0002t0001g0174 a0002c0002t0001g0175 a0002c0002t0001g0217 |
3 | HG01346.hp1 HG03098.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.803-1466C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43803176 | |||||||
| chr2:43803325 | A | G | 1 | a0002c0002t0002g0122 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.803-1317A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43803325 | |||||||
| chr2:43803443 | T | C | 11 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(8): Show |
14 | HG00738.hp1 HG02132.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.803-1199T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43803443 | |||||||
| chr2:43803510 | C | T | 145 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(142): Show |
164 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(161): Show |
intron_variant | MODIFIER | c.803-1132C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43803510 | |||||||
| chr2:43803565 | A | T | 70 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(67): Show |
77 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(74): Show |
intron_variant | MODIFIER | c.803-1077A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43803565 | |||||||
| chr2:43803905 | A | T | 2 | a0003c0003t0005g0090 a0003c0003t0005g0091 |
2 | HG02258.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.803-737A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43803905 | |||||||
| chr2:43803910 | A | T | 4 | a0002c0002t0002g0042 a0002c0002t0002g0043 a0002c0002t0002g0044 others(1): Show |
4 | HG02647.hp1 HG03130.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.803-732A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43803910 | |||||||
| chr2:43803937 | G | A | 1 | a0003c0003t0003g0073 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.803-705G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43803937 | |||||||
| chr2:43804036 | G | A | 147 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(144): Show |
166 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.803-606G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43804036 | |||||||
| chr2:43804044 | G | A | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.803-598G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43804044 | |||||||
| chr2:43804114 | T | C | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.803-528T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43804114 | |||||||
| chr2:43804148 | T | A | 7 | a0003c0003t0003g0010 a0003c0003t0005g0008 a0003c0003t0005g0059 others(4): Show |
9 | HG00738.hp2 HG02818.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.803-494T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43804148 | |||||||
| chr2:43804158 | G | A | 82 | a0002c0002t0001g0129 a0002c0002t0002g0004 a0002c0002t0002g0007 others(79): Show |
92 | HG00438.hp1 HG00642.hp1 HG00733.hp2 others(89): Show |
intron_variant | MODIFIER | c.803-484G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43804158 | |||||||
| chr2:43804556 | A | G | 1 | a0002c0002t0002g0218 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.803-86A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 10/12 | chr2 | 43804556 | |||||||
| chr2:43804823 | T | C | 4 | a0002c0002t0003g0011 a0002c0002t0003g0047 a0002c0002t0003g0048 others(1): Show |
5 | HG02055.hp2 HG02109.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+84T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 11/12 | chr2 | 43804823 | |||||||
| chr2:43804898 | T | TA | 45 | a0002c0002t0002g0152 a0002c0002t0003g0040 a0003c0003t0003g0002 others(42): Show |
52 | HG00323.hp2 HG00597.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.900+172dupA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 43804898 | ||||||
| chr2:43804898 | TA | T | 6 | a0002c0002t0002g0041 a0002c0002t0003g0011 a0002c0002t0003g0047 others(3): Show |
7 | HG02055.hp2 HG02109.hp2 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.900+172delA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr2 | 43804898 | ||||||
| chr2:43804945 | G | C | 88 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0015 others(85): Show |
97 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(94): Show |
intron_variant | MODIFIER | c.900+206G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 11/12 | chr2 | 43804945 | |||||||
| chr2:43805050 | C | G | 102 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0015 others(99): Show |
114 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(111): Show |
intron_variant | MODIFIER | c.901-104C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 11/12 | chr2 | 43805050 | |||||||
| chr2:43805056 | T | G | 1 | a0004c0004t0002g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.901-98T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 11/12 | chr2 | 43805056 | |||||||
| chr2:43805124 | G | A | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.901-30G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 11/12 | chr2 | 43805124 | |||||||
| chr2:43805345 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.993+99G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43805345 | |||||||
| chr2:43805349 | A | G | 1 | a0003c0003t0003g0077 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.993+103A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43805349 | |||||||
| chr2:43805398 | A | C | 1 | a0003c0003t0003g0077 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.993+152A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43805398 | |||||||
| chr2:43805455 | T | G | 1 | a0003c0003t0005g0059 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.993+209T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43805455 | |||||||
| chr2:43805483 | C | A | 6 | a0002c0002t0002g0016 a0002c0002t0002g0132 a0002c0002t0002g0141 others(3): Show |
7 | HG02155.hp2 NA18943.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.993+237C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43805483 | |||||||
| chr2:43805485 | T | G | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.993+239T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43805485 | |||||||
| chr2:43805884 | C | CT | 17 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(14): Show |
20 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(17): Show |
intron_variant | MODIFIER | c.993+643dupT | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43805884 | ||||||
| chr2:43805889 | TC | T | 4 | a0002c0002t0002g0041 a0003c0003t0002g0240 a0003c0003t0003g0082 others(1): Show |
4 | HG01516.hp2 HG02896.hp2 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.993+644delC | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43805889 | |||||||
| chr2:43805890 | C | T | 142 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0015 others(139): Show |
161 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(158): Show |
intron_variant | MODIFIER | c.993+644C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43805890 | |||||||
| chr2:43805905 | C | A | 75 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0015 others(72): Show |
83 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(80): Show |
intron_variant | MODIFIER | c.993+659C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43805905 | |||||||
| chr2:43805941 | G | T | 19 | a0003c0003t0002g0012 a0003c0003t0002g0013 a0003c0003t0002g0092 others(16): Show |
21 | HG00639.hp2 HG01074.hp1 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.993+695G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43805941 | |||||||
| chr2:43806100 | T | C | 1 | a0003c0003t0005g0063 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.993+854T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806100 | |||||||
| chr2:43806128 | C | T | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.993+882C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806128 | |||||||
| chr2:43806140 | C | T | 12 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(9): Show |
15 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.993+894C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806140 | |||||||
| chr2:43806283 | G | C | 3 | a0002c0002t0003g0040 a0003c0003t0003g0088 a0003c0003t0003g0089 |
3 | HG02615.hp1 HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.993+1037G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806283 | |||||||
| chr2:43806330 | C | T | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.993+1084C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806330 | |||||||
| chr2:43806448 | G | T | 1 | a0004c0004t0002g0033 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.993+1202G>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806448 | |||||||
| chr2:43806569 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.993+1323C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806569 | |||||||
| chr2:43806615 | T | G | 46 | a0002c0002t0003g0040 a0003c0003t0003g0002 a0003c0003t0003g0009 others(43): Show |
53 | HG00323.hp2 HG00597.hp1 HG00733.hp1 others(50): Show |
intron_variant | MODIFIER | c.993+1369T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806615 | |||||||
| chr2:43806636 | T | C | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.993+1390T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806636 | |||||||
| chr2:43806728 | G | C | 3 | a0002c0002t0002g0007 a0002c0002t0002g0038 a0002c0002t0002g0039 |
4 | HG00642.hp1 HG01099.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.993+1482G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806728 | |||||||
| chr2:43806757 | G | A | 147 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0015 others(144): Show |
166 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(163): Show |
intron_variant | MODIFIER | c.993+1511G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806757 | |||||||
| chr2:43806836 | A | C | 1 | a0005c0005t0001g0221 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.993+1590A>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806836 | |||||||
| chr2:43806892 | C | T | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.993+1646C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806892 | |||||||
| chr2:43806897 | T | C | 1 | a0011c0010t0002g0119 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.993+1651T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806897 | |||||||
| chr2:43806974 | G | A | 3 | a0002c0002t0003g0040 a0003c0003t0003g0088 a0003c0003t0003g0089 |
3 | HG02615.hp1 HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.993+1728G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43806974 | |||||||
| chr2:43807009 | A | G | 1 | a0001c0001t0001g0195 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.993+1763A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43807009 | |||||||
| chr2:43807562 | C | G | 82 | a0002c0002t0002g0004 a0002c0002t0002g0007 a0002c0002t0002g0015 others(79): Show |
90 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(87): Show |
intron_variant | MODIFIER | c.994-2143C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43807562 | |||||||
| chr2:43807626 | C | G | 3 | a0002c0002t0003g0040 a0003c0003t0003g0088 a0003c0003t0003g0089 |
3 | HG02615.hp1 HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.994-2079C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43807626 | |||||||
| chr2:43807643 | T | G | 1 | a0001c0001t0001g0192 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.994-2062T>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43807643 | |||||||
| chr2:43807708 | T | C | 1 | a0003c0003t0003g0069 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.994-1997T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43807708 | |||||||
| chr2:43807728 | T | C | 1 | a0001c0001t0001g0226 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.994-1977T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43807728 | |||||||
| chr2:43807743 | C | CA | 27 | a0001c0001t0001g0006 a0001c0001t0001g0168 a0001c0001t0001g0171 others(24): Show |
29 | HG00544.hp2 HG00597.hp2 HG00642.hp2 others(26): Show |
intron_variant | MODIFIER | c.994-1932dupA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43807743 | ||||||
| chr2:43807743 | C | CAA | 4 | a0001c0001t0001g0018 a0001c0001t0001g0223 a0002c0002t0001g0027 others(1): Show |
6 | HG02145.hp1 HG02738.hp2 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.994-1933_994-1932d others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43807743 | ||||||
| chr2:43807743 | CA | C | 61 | a0001c0001t0001g0022 a0001c0001t0001g0208 a0001c0001t0001g0233 others(58): Show |
69 | HG00323.hp2 HG00597.hp1 HG00733.hp1 others(66): Show |
intron_variant | MODIFIER | c.994-1932delA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43807743 | ||||||
| chr2:43807743 | CAA | C | 73 | a0001c0001t0002g0212 a0002c0002t0002g0004 a0002c0002t0002g0007 others(70): Show |
84 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(81): Show |
intron_variant | MODIFIER | c.994-1933_994-1932d others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43807743 | ||||||
| chr2:43807743 | CAAAAAAA others(8): Show |
C | 5 | a0003c0003t0007g0070 a0003c0003t0007g0071 a0006c0006t0002g0242 others(2): Show |
5 | HG01109.hp2 HG02451.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.994-1946_994-1932d others(17): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43807743 | ||||||
| chr2:43807932 | T | TGGGGGGG others(36): Show |
1 | a0003c0003t0003g0080 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.994-1771_994-1770i others(45): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43807932 | ||||||
| chr2:43807984 | C | G | 47 | a0002c0002t0003g0040 a0003c0003t0003g0002 a0003c0003t0003g0009 others(44): Show |
54 | HG00323.hp2 HG00597.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.994-1721C>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43807984 | |||||||
| chr2:43808264 | G | GA | 137 | a0001c0001t0001g0188 a0001c0001t0002g0212 a0002c0002t0002g0004 others(134): Show |
156 | HG00323.hp2 HG00438.hp1 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.994-1430dupA | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43808264 | ||||||
| chr2:43808304 | A | G | 1 | a0003c0003t0002g0092 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.994-1401A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43808304 | |||||||
| chr2:43808364 | G | C | 45 | a0002c0002t0003g0040 a0003c0003t0003g0002 a0003c0003t0003g0009 others(42): Show |
52 | HG00323.hp2 HG00597.hp1 HG00733.hp1 others(49): Show |
intron_variant | MODIFIER | c.994-1341G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43808364 | |||||||
| chr2:43808416 | A | G | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.994-1289A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43808416 | |||||||
| chr2:43808429 | G | A | 103 | a0001c0001t0002g0212 a0002c0002t0002g0004 a0002c0002t0002g0007 others(100): Show |
115 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(112): Show |
intron_variant | MODIFIER | c.994-1276G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43808429 | |||||||
| chr2:43808531 | A | G | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-1174A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43808531 | |||||||
| chr2:43808609 | T | C | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.994-1096T>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43808609 | |||||||
| chr2:43808778 | G | A | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.994-927G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43808778 | |||||||
| chr2:43808887 | C | T | 6 | a0004c0004t0002g0032 a0004c0004t0002g0033 a0004c0004t0002g0034 others(3): Show |
6 | HG01884.hp1 HG02970.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.994-818C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43808887 | |||||||
| chr2:43808900 | C | T | 1 | a0002c0002t0001g0217 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.994-805C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43808900 | |||||||
| chr2:43808911 | C | T | 1 | a0003c0003t0002g0101 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.994-794C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43808911 | |||||||
| chr2:43808964 | T | TAC | 20 | a0001c0001t0001g0024 a0001c0001t0001g0030 a0001c0001t0001g0183 others(17): Show |
22 | HG00642.hp2 HG01243.hp2 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.994-706_994-705dup others(2): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43808964 | ||||||
| chr2:43808964 | T | TACAC | 3 | a0003c0003t0003g0009 a0003c0003t0003g0067 a0004c0004t0002g0032 |
4 | HG02630.hp1 HG02896.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.994-708_994-705dup others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43808964 | ||||||
| chr2:43808964 | T | TACACACA others(5): Show |
2 | a0002c0002t0003g0048 a0002c0002t0003g0049 |
2 | HG02055.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.994-716_994-705dup others(12): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43808964 | ||||||
| chr2:43808964 | TAC | T | 81 | a0001c0001t0001g0023 a0001c0001t0001g0198 a0001c0001t0001g0201 others(78): Show |
91 | HG00438.hp1 HG00597.hp2 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.994-706_994-705del others(2): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43808964 | ||||||
| chr2:43808964 | TACAC | T | 41 | a0002c0002t0001g0177 a0002c0002t0001g0236 a0002c0002t0001g0237 others(38): Show |
44 | HG00597.hp1 HG00738.hp1 HG01175.hp2 others(41): Show |
intron_variant | MODIFIER | c.994-708_994-705del others(4): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43808964 | ||||||
| chr2:43808964 | TACACAC | T | 29 | a0002c0002t0001g0220 a0002c0002t0002g0007 a0002c0002t0002g0037 others(26): Show |
32 | HG00323.hp2 HG00642.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.994-710_994-705del others(6): Show |
DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr2 | 43808964 | ||||||
| chr2:43809066 | G | C | 5 | a0001c0001t0001g0169 a0001c0001t0001g0193 a0001c0001t0001g0194 others(2): Show |
5 | NA18943.hp2 NA18955.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.994-639G>C | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809066 | |||||||
| chr2:43809099 | C | A | 1 | a0002c0002t0004g0118 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.994-606C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809099 | |||||||
| chr2:43809103 | C | T | 1 | a0002c0002t0003g0040 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.994-602C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809103 | |||||||
| chr2:43809108 | A | T | 13 | a0002c0002t0004g0003 a0002c0002t0004g0014 a0002c0002t0004g0108 others(10): Show |
16 | HG00738.hp1 HG01261.hp2 HG02132.hp2 others(13): Show |
intron_variant | MODIFIER | c.994-597A>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809108 | |||||||
| chr2:43809281 | C | T | 2 | a0006c0006t0002g0242 a0006c0006t0002g0243 |
2 | HG01109.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.994-424C>T | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809281 | |||||||
| chr2:43809299 | G | A | 98 | a0001c0001t0002g0212 a0002c0002t0002g0004 a0002c0002t0002g0007 others(95): Show |
109 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.994-406G>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809299 | |||||||
| chr2:43809341 | T | A | 98 | a0001c0001t0002g0212 a0002c0002t0002g0004 a0002c0002t0002g0007 others(95): Show |
109 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.994-364T>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809341 | |||||||
| chr2:43809352 | A | G | 83 | a0001c0001t0002g0212 a0002c0002t0002g0004 a0002c0002t0002g0007 others(80): Show |
91 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(88): Show |
intron_variant | MODIFIER | c.994-353A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809352 | |||||||
| chr2:43809544 | C | A | 3 | a0002c0002t0003g0040 a0003c0003t0003g0088 a0003c0003t0003g0089 |
3 | HG02615.hp1 HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.994-161C>A | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809544 | |||||||
| chr2:43809550 | A | G | 86 | a0001c0001t0002g0212 a0002c0002t0002g0004 a0002c0002t0002g0007 others(83): Show |
94 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(91): Show |
intron_variant | MODIFIER | c.994-155A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809550 | |||||||
| chr2:43809661 | A | G | 98 | a0001c0001t0002g0212 a0002c0002t0002g0004 a0002c0002t0002g0007 others(95): Show |
109 | HG00438.hp1 HG00639.hp2 HG00642.hp1 others(106): Show |
intron_variant | MODIFIER | c.994-44A>G | DYNC2LI1 | ENSG00000138036.18 | transcript | ENST00000260605.12 | protein_coding | 12/12 | chr2 | 43809661 |