Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 51164 |
| ensemblid | ENSG00000132912.13 |
| hgncid | 15518 |
| symbol | DCTN4 |
| name | dynactin subunit 4 |
| refseq_nuc | NM_016221.4 |
| refseq_prot | NP_057305.1 |
| ensembl_nuc | ENST00000447998.7 |
| ensembl_prot | ENSP00000416968.2 |
| mane_status | MANE Select |
| chr | chr5 |
| start | 150708440 |
| end | 150759017 |
| strand | - |
| ver | v1.2 |
| region | chr5:150708440-150759017 |
| region5000 | chr5:150703440-150764017 |
| regionname0 | DCTN4_chr5_150708440_150759017 |
| regionname5000 | DCTN4_chr5_150703440_150764017 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 460 | 155 | 35 | 31 | 61 | 0 | 26 | 49 | DCTN4_chr5_150703440_150764017 | DCTN4 | MASLL others(455): Show |
chr5 | 150703440 | 150764017 |
| a0002 | 0/0 | 460 | 112 | 61 | 13 | 32 | 0 | 6 | 26 | DCTN4_chr5_150703440_150764017 | DCTN4 | MASLL others(455): Show |
chr5 | 150703440 | 150764017 |
| a0003 | 0/0 | 460 | 14 | 0 | 0 | 14 | 0 | 0 | 10 | DCTN4_chr5_150703440_150764017 | DCTN4 | MASLL others(455): Show |
chr5 | 150703440 | 150764017 |
| a0004 | 0/0 | 460 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | DCTN4_chr5_150703440_150764017 | DCTN4 | MASLL others(455): Show |
chr5 | 150703440 | 150764017 |
| a0005 | 0/0 | 460 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | MASLL others(455): Show |
chr5 | 150703440 | 150764017 |
| a0006 | 0/0 | 460 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | MASLL others(455): Show |
chr5 | 150703440 | 150764017 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1380 | 147 | 28 | 31 | 60 | 0 | 26 | DCTN4_chr5_150703440_150764017 | DCTN4 | ATGGC others(1375): Show |
chr5 | 150703440 | 150764017 | ||
| a0001c0005 | 0/0 | 1380 | 7 | 7 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | ATGGC others(1375): Show |
chr5 | 150703440 | 150764017 | ||
| a0001c0010 | 0/0 | 1380 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | ATGGC others(1375): Show |
chr5 | 150703440 | 150764017 | ||
| a0002c0002 | 0/0 | 1380 | 104 | 55 | 11 | 32 | 0 | 6 | DCTN4_chr5_150703440_150764017 | DCTN4 | ATGGC others(1375): Show |
chr5 | 150703440 | 150764017 | ||
| a0002c0004 | 0/0 | 1380 | 7 | 5 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | ATGGC others(1375): Show |
chr5 | 150703440 | 150764017 | ||
| a0002c0007 | 0/0 | 1380 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | ATGGC others(1375): Show |
chr5 | 150703440 | 150764017 | ||
| a0003c0003 | 0/0 | 1380 | 14 | 0 | 0 | 14 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | ATGGC others(1375): Show |
chr5 | 150703440 | 150764017 | ||
| a0004c0006 | 0/0 | 1380 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | ATGGC others(1375): Show |
chr5 | 150703440 | 150764017 | ||
| a0005c0009 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | ATGGC others(1375): Show |
chr5 | 150703440 | 150764017 | ||
| a0006c0008 | 0/0 | 1380 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | ATGGC others(1375): Show |
chr5 | 150703440 | 150764017 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 4116 | 123 | 22 | 26 | 55 | 0 | 19 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0002 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0003 | 0/0 | 4115 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4110): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0007 | 0/0 | 4116 | 6 | 0 | 1 | 0 | 0 | 5 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0010 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0013 | 0/0 | 4116 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0015 | 0/1 | 4116 | 2 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0019 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0020 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0021 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0022 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0023 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0024 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0025 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0026 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0001t0027 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0005t0006 | 0/0 | 4116 | 7 | 7 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0001c0010t0001 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0002t0001 | 0/0 | 4116 | 24 | 12 | 2 | 6 | 0 | 4 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0002t0002 | 0/0 | 4116 | 30 | 1 | 6 | 21 | 0 | 2 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0002t0003 | 0/0 | 4115 | 18 | 16 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4110): Show |
chr5 | 150703440 | 150764017 |
| a0002c0002t0005 | 0/0 | 4116 | 17 | 16 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0002t0009 | 0/0 | 4114 | 4 | 4 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4109): Show |
chr5 | 150703440 | 150764017 |
| a0002c0002t0011 | 0/0 | 4116 | 3 | 3 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0002t0012 | 0/0 | 4116 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0002t0014 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0002t0016 | 0/0 | 4116 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0002t0017 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0004t0001 | 0/0 | 4116 | 3 | 1 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0004t0008 | 0/0 | 4116 | 4 | 4 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0002c0007t0018 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0003c0003t0004 | 0/0 | 4115 | 14 | 0 | 0 | 14 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4110): Show |
chr5 | 150703440 | 150764017 |
| a0004c0006t0004 | 0/0 | 4115 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4110): Show |
chr5 | 150703440 | 150764017 |
| a0005c0009t0001 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| a0006c0008t0010 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | GTCAT others(4111): Show |
chr5 | 150703440 | 150764017 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0002 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0012 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0018 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0003g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0007g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0007g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0007g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0007g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0007g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0007g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0010g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0013g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0013g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0015g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0015g0162 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0019g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0020g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0021g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0022g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0023g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0024g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0025g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0026g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0001t0027g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0005t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0005t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0005t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0005t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0005t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0005t0006g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0005t0006g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0001c0010t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0021 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0009g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0009g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0009g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0009g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0011g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0011g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0011g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0012g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0012g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0014g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0014g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0016g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0016g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0002t0017g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0004t0001g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0004t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0004t0008g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0004t0008g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0004t0008g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0004t0008g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0002c0007t0018g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0003c0003t0004g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0004c0006t0004g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0005c0009t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| a0006c0008t0010g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00408 | hp1 | a0003 | c0003 | t0004 | g0025 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00408 | hp2 | a0002 | c0002 | t0001 | g0204 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00558 | hp2 | a0002 | c0002 | t0001 | g0200 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00597 | hp2 | a0002 | c0002 | t0002 | g0226 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00639 | hp1 | a0002 | c0002 | t0002 | g0021 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00639 | hp2 | a0001 | c0001 | t0023 | g0078 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00642 | hp2 | a0005 | c0009 | t0001 | g0094 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00735 | hp2 | a0002 | c0002 | t0003 | g0007 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG00738 | hp2 | a0002 | c0002 | t0002 | g0230 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01069 | hp1 | a0002 | c0004 | t0001 | g0026 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01071 | hp1 | a0002 | c0004 | t0001 | g0026 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01081 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01167 | hp1 | a0002 | c0002 | t0002 | g0020 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01167 | hp2 | a0001 | c0001 | t0015 | g0161 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01243 | hp1 | a0002 | c0002 | t0001 | g0037 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01243 | hp2 | a0002 | c0002 | t0001 | g0189 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01433 | hp2 | a0006 | c0008 | t0010 | g0103 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01496 | hp1 | a0002 | c0002 | t0003 | g0007 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01496 | hp2 | a0002 | c0002 | t0002 | g0229 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01884 | hp1 | a0002 | c0002 | t0003 | g0040 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01891 | hp1 | a0002 | c0002 | t0005 | g0053 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01891 | hp2 | a0001 | c0001 | t0010 | g0113 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01943 | hp1 | a0002 | c0002 | t0002 | g0218 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01943 | hp2 | a0001 | c0001 | t0027 | g0111 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01978 | hp1 | a0001 | c0001 | t0007 | g0073 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01981 | hp1 | a0002 | c0002 | t0005 | g0062 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02015 | hp2 | a0003 | c0003 | t0004 | g0025 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02040 | hp2 | a0001 | c0001 | t0020 | g0110 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02055 | hp1 | a0002 | c0002 | t0005 | g0050 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02071 | hp2 | a0003 | c0003 | t0004 | g0231 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02080 | hp1 | a0002 | c0002 | t0001 | g0223 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02080 | hp2 | a0003 | c0003 | t0004 | g0205 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02129 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02135 | hp1 | a0001 | c0001 | t0025 | g0083 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02145 | hp1 | a0002 | c0002 | t0005 | g0059 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02145 | hp2 | a0002 | c0002 | t0001 | g0035 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02257 | hp1 | a0002 | c0004 | t0001 | g0244 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02257 | hp2 | a0001 | c0001 | t0010 | g0104 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02258 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02258 | hp2 | a0002 | c0002 | t0003 | g0038 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02280 | hp1 | a0002 | c0002 | t0011 | g0198 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02280 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02300 | hp1 | a0001 | c0001 | t0021 | g0166 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02451 | hp1 | a0002 | c0002 | t0005 | g0052 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02451 | hp2 | a0002 | c0002 | t0005 | g0180 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02523 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02572 | hp2 | a0002 | c0002 | t0003 | g0034 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02602 | hp1 | a0001 | c0001 | t0007 | g0135 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0061 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02615 | hp2 | a0002 | c0002 | t0005 | g0054 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02622 | hp1 | a0002 | c0002 | t0005 | g0057 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02622 | hp2 | a0002 | c0002 | t0014 | g0181 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02630 | hp1 | a0002 | c0002 | t0001 | g0214 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02630 | hp2 | a0002 | c0002 | t0005 | g0056 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02647 | hp1 | a0002 | c0002 | t0003 | g0009 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0196 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02717 | hp1 | a0002 | c0002 | t0003 | g0041 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02717 | hp2 | a0002 | c0002 | t0005 | g0190 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02723 | hp1 | a0002 | c0002 | t0003 | g0030 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02735 | hp1 | a0001 | c0001 | t0007 | g0082 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02738 | hp1 | a0001 | c0001 | t0019 | g0048 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02738 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02809 | hp1 | a0002 | c0002 | t0009 | g0194 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02809 | hp2 | a0002 | c0002 | t0003 | g0039 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02886 | hp1 | a0002 | c0002 | t0003 | g0046 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02886 | hp2 | a0002 | c0002 | t0003 | g0027 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02895 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02896 | hp1 | a0002 | c0004 | t0008 | g0243 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02896 | hp2 | a0001 | c0005 | t0006 | g0207 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02897 | hp1 | a0001 | c0005 | t0006 | g0208 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02922 | hp1 | a0002 | c0002 | t0001 | g0188 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02965 | hp1 | a0002 | c0002 | t0005 | g0064 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02970 | hp1 | a0001 | c0001 | t0003 | g0242 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02970 | hp2 | a0002 | c0002 | t0001 | g0213 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03017 | hp1 | a0002 | c0002 | t0001 | g0206 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03041 | hp1 | a0002 | c0004 | t0008 | g0246 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03098 | hp1 | a0002 | c0002 | t0001 | g0212 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03098 | hp2 | a0002 | c0002 | t0002 | g0232 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03130 | hp1 | a0002 | c0002 | t0017 | g0047 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0036 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03139 | hp1 | a0001 | c0005 | t0006 | g0186 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03139 | hp2 | a0002 | c0002 | t0005 | g0049 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03195 | hp1 | a0002 | c0004 | t0008 | g0247 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03209 | hp1 | a0002 | c0002 | t0011 | g0211 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03209 | hp2 | a0002 | c0002 | t0009 | g0195 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03225 | hp1 | a0001 | c0005 | t0006 | g0187 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03453 | hp1 | a0002 | c0002 | t0001 | g0044 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03453 | hp2 | a0001 | c0005 | t0006 | g0184 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03486 | hp1 | a0001 | c0005 | t0006 | g0185 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03486 | hp2 | a0002 | c0007 | t0018 | g0029 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03492 | hp1 | a0001 | c0001 | t0007 | g0176 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03516 | hp1 | a0002 | c0002 | t0009 | g0193 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03540 | hp1 | a0002 | c0002 | t0005 | g0182 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03540 | hp2 | a0002 | c0002 | t0003 | g0042 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03579 | hp1 | a0001 | c0005 | t0006 | g0183 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03579 | hp2 | a0002 | c0002 | t0005 | g0058 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03654 | hp2 | a0002 | c0002 | t0001 | g0203 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03688 | hp2 | a0002 | c0002 | t0001 | g0202 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | BEB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03831 | hp2 | a0001 | c0001 | t0007 | g0081 | SAS | BEB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03834 | hp1 | a0002 | c0002 | t0002 | g0021 | SAS | BEB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0136 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG04204 | hp2 | a0001 | c0001 | t0007 | g0072 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG04228 | hp1 | a0002 | c0002 | t0002 | g0217 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0013 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18522 | hp1 | a0002 | c0002 | t0003 | g0032 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18906 | hp1 | a0002 | c0002 | t0003 | g0043 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18906 | hp2 | a0001 | c0001 | t0024 | g0087 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18939 | hp1 | a0003 | c0003 | t0004 | g0023 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18944 | hp2 | a0002 | c0002 | t0016 | g0241 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18945 | hp1 | a0002 | c0002 | t0012 | g0019 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18946 | hp1 | a0002 | c0002 | t0002 | g0228 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18947 | hp2 | a0002 | c0002 | t0012 | g0019 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0238 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18951 | hp1 | a0003 | c0003 | t0004 | g0224 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18959 | hp2 | a0002 | c0002 | t0002 | g0209 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18960 | hp1 | a0001 | c0001 | t0013 | g0154 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18960 | hp2 | a0002 | c0002 | t0002 | g0227 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18965 | hp2 | a0003 | c0003 | t0004 | g0220 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18966 | hp1 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18969 | hp2 | a0002 | c0002 | t0002 | g0215 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18974 | hp2 | a0003 | c0003 | t0004 | g0234 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18975 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18977 | hp1 | a0001 | c0001 | t0022 | g0146 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18977 | hp2 | a0001 | c0010 | t0001 | g0125 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18979 | hp2 | a0003 | c0003 | t0004 | g0233 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18982 | hp1 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18983 | hp1 | a0002 | c0002 | t0002 | g0237 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18983 | hp2 | a0004 | c0006 | t0004 | g0006 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18989 | hp2 | a0004 | c0006 | t0004 | g0006 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18990 | hp1 | a0002 | c0002 | t0012 | g0201 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0024 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19003 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19004 | hp2 | a0002 | c0002 | t0002 | g0022 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19009 | hp2 | a0002 | c0002 | t0002 | g0225 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19012 | hp2 | a0002 | c0002 | t0001 | g0199 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19030 | hp2 | a0002 | c0002 | t0005 | g0063 | AFR | LWK | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19043 | hp1 | a0001 | c0001 | t0026 | g0175 | AFR | LWK | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19043 | hp2 | a0002 | c0002 | t0005 | g0051 | AFR | LWK | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19062 | hp1 | a0003 | c0003 | t0004 | g0023 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19067 | hp1 | a0003 | c0003 | t0004 | g0219 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19070 | hp1 | a0003 | c0003 | t0004 | g0222 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19075 | hp2 | a0002 | c0002 | t0002 | g0191 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19080 | hp1 | a0002 | c0002 | t0002 | g0210 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19083 | hp2 | a0003 | c0003 | t0004 | g0236 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19086 | hp1 | a0001 | c0001 | t0013 | g0145 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19086 | hp2 | a0003 | c0003 | t0004 | g0221 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19087 | hp1 | a0002 | c0002 | t0002 | g0004 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19088 | hp2 | a0002 | c0002 | t0002 | g0005 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19089 | hp1 | a0002 | c0002 | t0001 | g0235 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19091 | hp1 | a0004 | c0006 | t0004 | g0006 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19240 | hp1 | a0002 | c0002 | t0003 | g0045 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA20129 | hp1 | a0002 | c0002 | t0005 | g0055 | AFR | ASW | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA20129 | hp2 | a0002 | c0002 | t0014 | g0179 | AFR | ASW | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | GIH | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA20905 | hp2 | a0002 | c0002 | t0001 | g0239 | SAS | GIH | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02109 | hp1 | a0002 | c0002 | t0003 | g0009 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02486 | hp2 | a0002 | c0004 | t0008 | g0245 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG02559 | hp2 | a0002 | c0002 | t0003 | g0028 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03471 | hp1 | a0002 | c0002 | t0001 | g0060 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG06807 | hp1 | a0002 | c0002 | t0011 | g0031 | AFR | USA | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | USA | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18955 | hp1 | a0002 | c0002 | t0016 | g0240 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | USA | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| NA20300 | hp2 | a0002 | c0002 | t0009 | g0192 | AFR | USA | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0015 | g0162 | REF | REF | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0177 | REF | REF | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:150711219 | C | T | 2 | a0003 a0004 |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
missense_variant | MODERATE | c.1313G>A | p.Ser438Asn | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1337/4116 | 1313/1383 | 438/460 | chr5 | 150711219 | |||
| chr5:150718321 | G | C | 3 | a0002 a0003 a0004 |
129 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(126): Show |
missense_variant | MODERATE | c.1026C>G | p.Phe342Leu | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/13 | 1050/4116 | 1026/1383 | 342/460 | chr5 | 150718321 | |||
| chr5:150719768 | T | C | 1 | a0006 | 1 | HG01433.hp2 | missense_variant&splice_region_variant | MODERATE | c.911A>G | p.Asn304Ser | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/13 | 935/4116 | 911/1383 | 304/460 | chr5 | 150719768 | |||
| chr5:150722908 | C | T | 1 | a0004 | 3 | NA18983.hp2 NA18989.hp2 NA19091.hp1 |
missense_variant&splice_region_variant | MODERATE | c.907G>A | p.Val303Ile | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/13 | 931/4116 | 907/1383 | 303/460 | chr5 | 150722908 | |||
| chr5:150730677 | T | C | 1 | a0005 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.788A>G | p.Tyr263Cys | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/13 | 812/4116 | 788/1383 | 263/460 | chr5 | 150730677 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:150711239 | G | T | 1 | a0002c0007 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1293C>A | p.Pro431Pro | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1317/4116 | 1293/1383 | 431/460 | chr5 | 150711239 | |||
| chr5:150715603 | A | G | 1 | a0001c0005 | 7 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
synonymous_variant | LOW | c.1131T>C | p.Asp377Asp | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/13 | 1155/4116 | 1131/1383 | 377/460 | chr5 | 150715603 | |||
| chr5:150719764 | A | G | 1 | a0002c0004 | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
synonymous_variant | LOW | c.915T>C | p.Tyr305Tyr | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/13 | 939/4116 | 915/1383 | 305/460 | chr5 | 150719764 | |||
| chr5:150731436 | G | A | 1 | a0001c0010 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.591C>T | p.Ile197Ile | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 6/13 | 615/4116 | 591/1383 | 197/460 | chr5 | 150731436 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:150708519 | A | G | 8 | a0001c0005t0006 a0002c0002t0005 a0002c0002t0014 others(5): Show |
49 | HG00408.hp1 HG01891.hp1 HG01981.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2630T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2630 | chr5 | 150708519 | ||||||
| chr5:150708557 | A | C | 2 | a0001c0001t0010 a0006c0008t0010 |
3 | HG01433.hp2 HG01891.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2592T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2592 | chr5 | 150708557 | ||||||
| chr5:150708578 | A | G | 1 | a0002c0002t0017 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2571T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2571 | chr5 | 150708578 | ||||||
| chr5:150708647 | C | T | 2 | a0003c0003t0004 a0004c0006t0004 |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2502G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2502 | chr5 | 150708647 | ||||||
| chr5:150708983 | G | A | 3 | a0002c0004t0008 a0003c0003t0004 a0004c0006t0004 |
21 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2166C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2166 | chr5 | 150708983 | ||||||
| chr5:150709012 | A | T | 1 | a0001c0001t0021 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2137T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2137 | chr5 | 150709012 | ||||||
| chr5:150709052 | T | C | 1 | a0001c0005t0006 | 7 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2097A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2097 | chr5 | 150709052 | ||||||
| chr5:150709065 | A | G | 2 | a0003c0003t0004 a0004c0006t0004 |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2084T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2084 | chr5 | 150709065 | ||||||
| chr5:150709208 | G | A | 7 | a0001c0005t0006 a0002c0002t0005 a0002c0002t0014 others(4): Show |
48 | HG00408.hp1 HG01891.hp1 HG01981.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1941C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1941 | chr5 | 150709208 | ||||||
| chr5:150709234 | T | C | 3 | a0002c0004t0008 a0003c0003t0004 a0004c0006t0004 |
21 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1915A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1915 | chr5 | 150709234 | ||||||
| chr5:150709259 | G | A | 2 | a0003c0003t0004 a0004c0006t0004 |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1890C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1890 | chr5 | 150709259 | ||||||
| chr5:150709271 | T | A | 1 | a0002c0002t0011 | 3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1878A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1878 | chr5 | 150709271 | ||||||
| chr5:150709437 | G | A | 1 | a0002c0004t0008 | 4 | HG02486.hp2 HG02896.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1712C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1712 | chr5 | 150709437 | ||||||
| chr5:150709463 | T | C | 1 | a0001c0001t0025 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1686 | chr5 | 150709463 | ||||||
| chr5:150709522 | T | C | 1 | a0001c0001t0013 | 2 | NA18960.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1627A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1627 | chr5 | 150709522 | ||||||
| chr5:150709560 | G | A | 2 | a0003c0003t0004 a0004c0006t0004 |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1589C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1589 | chr5 | 150709560 | ||||||
| chr5:150709581 | AT | A | 2 | a0001c0001t0003 a0002c0002t0003 |
20 | HG00735.hp2 HG01496.hp1 HG01884.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1567delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1567 | chr5 | 150709581 | ||||||
| chr5:150709583 | G | A | 3 | a0001c0001t0022 a0003c0003t0004 a0004c0006t0004 |
18 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1566C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1566 | chr5 | 150709583 | ||||||
| chr5:150709743 | G | A | 2 | a0003c0003t0004 a0004c0006t0004 |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1406C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1406 | chr5 | 150709743 | ||||||
| chr5:150709890 | C | T | 2 | a0001c0001t0015 a0001c0001t0020 |
2 | HG01167.hp2 HG02040.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1259G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1259 | chr5 | 150709890 | ||||||
| chr5:150710204 | G | A | 2 | a0003c0003t0004 a0004c0006t0004 |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*945C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 945 | chr5 | 150710204 | ||||||
| chr5:150710265 | C | A | 1 | a0002c0002t0012 | 3 | NA18945.hp1 NA18947.hp2 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*884G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 884 | chr5 | 150710265 | ||||||
| chr5:150710265 | C | T | 1 | a0001c0001t0019 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*884G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 884 | chr5 | 150710265 | ||||||
| chr5:150710318 | G | A | 1 | a0001c0001t0023 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*831C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 831 | chr5 | 150710318 | ||||||
| chr5:150710327 | G | A | 1 | a0002c0002t0014 | 2 | HG02622.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*822C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 822 | chr5 | 150710327 | ||||||
| chr5:150710398 | C | T | 1 | a0002c0007t0018 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*751G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 751 | chr5 | 150710398 | ||||||
| chr5:150710464 | A | T | 3 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0025 |
8 | HG01167.hp2 HG01978.hp1 HG02135.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*685T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 685 | chr5 | 150710464 | ||||||
| chr5:150710545 | G | A | 1 | a0001c0001t0024 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*604C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 604 | chr5 | 150710545 | ||||||
| chr5:150710580 | G | A | 3 | a0002c0004t0008 a0003c0003t0004 a0004c0006t0004 |
21 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*569C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 569 | chr5 | 150710580 | ||||||
| chr5:150710602 | T | G | 4 | a0001c0001t0007 a0001c0001t0015 a0001c0001t0025 others(1): Show |
9 | HG01167.hp2 HG01978.hp1 HG02135.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*547A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 547 | chr5 | 150710602 | ||||||
| chr5:150710606 | G | A | 2 | a0003c0003t0004 a0004c0006t0004 |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*543C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 543 | chr5 | 150710606 | ||||||
| chr5:150710669 | T | G | 1 | a0001c0001t0027 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*480A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 480 | chr5 | 150710669 | ||||||
| chr5:150710683 | TG | T | 2 | a0003c0003t0004 a0004c0006t0004 |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*465delC | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 465 | chr5 | 150710683 | ||||||
| chr5:150710726 | A | G | 1 | a0002c0002t0016 | 2 | NA18944.hp2 NA18955.hp1 |
3_prime_UTR_variant | MODIFIER | c.*423T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 423 | chr5 | 150710726 | ||||||
| chr5:150710782 | T | C | 3 | a0001c0001t0002 a0002c0002t0002 a0002c0002t0016 |
33 | HG00597.hp2 HG00639.hp1 HG00738.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*367A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 367 | chr5 | 150710782 | ||||||
| chr5:150710786 | A | G | 1 | a0002c0002t0017 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*363T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 363 | chr5 | 150710786 | ||||||
| chr5:150710818 | C | T | 2 | a0003c0003t0004 a0004c0006t0004 |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*331G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 331 | chr5 | 150710818 | ||||||
| chr5:150710914 | AG | A | 1 | a0002c0002t0009 | 4 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*234delC | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 234 | chr5 | 150710914 | ||||||
| chr5:150710922 | GT | G | 1 | a0002c0002t0009 | 4 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*226delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 226 | chr5 | 150710922 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr5:150711395 | G | T | 2 | a0002c0002t0001g0037 a0002c0002t0001g0044 |
2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1170-33C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150711395 | |||||||
| chr5:150711599 | G | A | 13 | a0003c0003t0004g0023 a0003c0003t0004g0025 a0003c0003t0004g0205 others(10): Show |
17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1170-237C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150711599 | |||||||
| chr5:150711673 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1170-311G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150711673 | |||||||
| chr5:150711688 | C | T | 2 | a0002c0002t0009g0194 a0002c0002t0009g0195 |
2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1170-326G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150711688 | |||||||
| chr5:150711917 | A | C | 11 | a0002c0002t0005g0049 a0002c0002t0005g0050 a0002c0002t0005g0051 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1170-555T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150711917 | |||||||
| chr5:150712341 | A | G | 17 | a0002c0004t0008g0243 a0002c0004t0008g0245 a0002c0004t0008g0246 others(14): Show |
21 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1170-979T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150712341 | |||||||
| chr5:150712446 | G | A | 1 | a0002c0002t0003g0039 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1170-1084C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150712446 | |||||||
| chr5:150712490 | C | T | 1 | a0002c0002t0003g0041 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1170-1128G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150712490 | |||||||
| chr5:150712530 | T | C | 17 | a0002c0004t0008g0243 a0002c0004t0008g0245 a0002c0004t0008g0246 others(14): Show |
21 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1170-1168A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150712530 | |||||||
| chr5:150712970 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1170-1608A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150712970 | |||||||
| chr5:150713120 | A | T | 19 | a0001c0001t0001g0010 a0001c0001t0001g0090 a0001c0001t0001g0091 others(16): Show |
20 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1170-1758T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713120 | |||||||
| chr5:150713235 | C | A | 1 | a0001c0001t0001g0124 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1170-1873G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713235 | |||||||
| chr5:150713313 | G | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0002c0002t0001g0060 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1170-1951C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713313 | |||||||
| chr5:150713339 | C | A | 2 | a0002c0002t0011g0198 a0002c0002t0011g0211 |
2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1170-1977G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713339 | |||||||
| chr5:150713394 | T | TA | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1170-2033dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713394 | |||||||
| chr5:150713416 | T | A | 1 | a0001c0001t0003g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1170-2054A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713416 | |||||||
| chr5:150713445 | C | CT | 6 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0064 others(3): Show |
6 | HG02615.hp1 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170-2084dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713445 | |||||||
| chr5:150713445 | CTT | C | 7 | a0002c0002t0001g0008 a0002c0004t0001g0026 a0002c0004t0001g0244 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170-2085_1170-208 others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713445 | |||||||
| chr5:150713450 | T | C | 7 | a0002c0002t0001g0008 a0002c0004t0001g0026 a0002c0004t0001g0244 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170-2088A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713450 | |||||||
| chr5:150713462 | G | GA | 9 | a0001c0005t0006g0183 a0001c0005t0006g0184 a0001c0005t0006g0185 others(6): Show |
9 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170-2101dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713462 | |||||||
| chr5:150713529 | C | G | 1 | a0001c0001t0001g0163 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1169+2036G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713529 | |||||||
| chr5:150713627 | A | G | 1 | a0002c0002t0002g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1169+1938T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713627 | |||||||
| chr5:150713628 | G | C | 15 | a0001c0001t0003g0242 a0001c0005t0006g0183 a0001c0005t0006g0184 others(12): Show |
15 | HG02717.hp1 HG02723.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.1169+1937C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713628 | |||||||
| chr5:150713726 | C | G | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1169+1839G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713726 | |||||||
| chr5:150713732 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1169+1833G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713732 | |||||||
| chr5:150713830 | A | C | 7 | a0002c0002t0001g0008 a0002c0004t0001g0026 a0002c0004t0001g0244 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1169+1735T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713830 | |||||||
| chr5:150714224 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1169+1341A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714224 | |||||||
| chr5:150714225 | G | A | 1 | a0002c0002t0002g0218 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1169+1340C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714225 | |||||||
| chr5:150714271 | C | T | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1169+1294G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714271 | |||||||
| chr5:150714425 | C | A | 1 | a0001c0001t0026g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1169+1140G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714425 | |||||||
| chr5:150714431 | TAC | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1169+1132_1169+113 others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714431 | |||||||
| chr5:150714467 | A | G | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1169+1098T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714467 | |||||||
| chr5:150714470 | G | A | 1 | a0001c0001t0010g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1169+1095C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714470 | |||||||
| chr5:150714574 | TA | T | 120 | a0001c0001t0003g0242 a0001c0005t0006g0183 a0001c0005t0006g0184 others(117): Show |
137 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1169+990delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714574 | |||||||
| chr5:150714640 | G | A | 1 | a0002c0002t0002g0218 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1169+925C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714640 | |||||||
| chr5:150714716 | T | C | 4 | a0001c0001t0001g0147 a0002c0002t0003g0007 a0002c0002t0003g0027 others(1): Show |
5 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169+849A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714716 | |||||||
| chr5:150714757 | T | C | 1 | a0002c0002t0002g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1169+808A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714757 | |||||||
| chr5:150714809 | T | A | 7 | a0002c0002t0001g0008 a0002c0004t0001g0026 a0002c0004t0001g0244 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1169+756A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714809 | |||||||
| chr5:150714829 | A | G | 5 | a0001c0005t0006g0183 a0001c0005t0006g0184 a0001c0005t0006g0185 others(2): Show |
5 | HG03139.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169+736T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714829 | |||||||
| chr5:150714923 | A | G | 7 | a0002c0002t0001g0008 a0002c0004t0001g0026 a0002c0004t0001g0244 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1169+642T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714923 | |||||||
| chr5:150715048 | A | T | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1169+517T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715048 | |||||||
| chr5:150715094 | T | G | 3 | a0002c0002t0005g0056 a0002c0002t0005g0058 a0002c0002t0005g0059 |
3 | HG02145.hp1 HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1169+471A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715094 | |||||||
| chr5:150715117 | A | T | 1 | a0002c0002t0002g0226 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1169+448T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715117 | |||||||
| chr5:150715188 | A | G | 7 | a0002c0002t0001g0008 a0002c0004t0001g0026 a0002c0004t0001g0244 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1169+377T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715188 | |||||||
| chr5:150715270 | A | G | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1169+295T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715270 | |||||||
| chr5:150715472 | T | A | 8 | a0001c0001t0003g0242 a0001c0005t0006g0183 a0001c0005t0006g0184 others(5): Show |
8 | HG02896.hp2 HG02897.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1169+93A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715472 | |||||||
| chr5:150715488 | A | G | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1169+77T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715488 | |||||||
| chr5:150715489 | G | T | 4 | a0002c0002t0005g0180 a0002c0002t0005g0182 a0002c0002t0014g0179 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1169+76C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715489 | |||||||
| chr5:150715524 | T | A | 2 | a0002c0002t0014g0179 a0002c0002t0014g0181 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1169+41A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715524 | |||||||
| chr5:150715540 | T | C | 3 | a0002c0002t0003g0007 a0002c0002t0003g0027 a0002c0002t0003g0028 |
4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+25A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715540 | |||||||
| chr5:150715726 | C | T | 2 | a0001c0001t0001g0010 a0001c0001t0001g0065 |
3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1072-64G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150715726 | |||||||
| chr5:150715896 | T | TAA | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1072-235_1072-234i others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150715896 | |||||||
| chr5:150715916 | T | G | 17 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(14): Show |
18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1072-254A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150715916 | |||||||
| chr5:150715999 | G | T | 2 | a0001c0005t0006g0207 a0001c0005t0006g0208 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1072-337C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150715999 | |||||||
| chr5:150716196 | G | A | 1 | a0001c0001t0001g0152 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1072-534C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716196 | |||||||
| chr5:150716207 | A | T | 1 | a0001c0001t0023g0078 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1072-545T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716207 | |||||||
| chr5:150716218 | C | G | 3 | a0002c0002t0003g0007 a0002c0002t0003g0027 a0002c0002t0003g0028 |
4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1072-556G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716218 | |||||||
| chr5:150716245 | T | C | 1 | a0001c0001t0023g0078 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1072-583A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716245 | |||||||
| chr5:150716259 | C | T | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072-597G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716259 | |||||||
| chr5:150716272 | G | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02135.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1072-610C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716272 | |||||||
| chr5:150716337 | T | C | 1 | a0001c0001t0003g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1072-675A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716337 | |||||||
| chr5:150716415 | A | G | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072-753T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716415 | |||||||
| chr5:150716683 | C | G | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072-1021G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716683 | |||||||
| chr5:150716746 | C | T | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1072-1084G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716746 | |||||||
| chr5:150716747 | G | A | 13 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(10): Show |
17 | HG01255.hp1 HG01433.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1072-1085C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716747 | |||||||
| chr5:150716750 | T | G | 1 | a0001c0001t0001g0155 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1072-1088A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716750 | |||||||
| chr5:150716782 | G | A | 2 | a0001c0001t0001g0100 a0001c0001t0001g0117 |
2 | HG01071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1072-1120C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716782 | |||||||
| chr5:150716833 | C | T | 1 | a0002c0002t0005g0062 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1072-1171G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716833 | |||||||
| chr5:150716850 | C | T | 3 | a0002c0002t0001g0212 a0002c0002t0001g0213 a0002c0002t0001g0239 |
3 | HG02970.hp2 HG03098.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1072-1188G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716850 | |||||||
| chr5:150716881 | T | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0065 |
3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1072-1219A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716881 | |||||||
| chr5:150716917 | C | CA | 81 | a0001c0001t0001g0129 a0001c0001t0001g0156 a0001c0001t0002g0139 others(78): Show |
95 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1072-1256dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716917 | |||||||
| chr5:150716917 | CA | C | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072-1256delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716917 | |||||||
| chr5:150716929 | A | G | 1 | a0001c0005t0006g0184 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1072-1267T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716929 | |||||||
| chr5:150717240 | CTTTAACA others(6): Show |
C | 1 | a0002c0002t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1071+1023_1071+103 others(17): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717240 | |||||||
| chr5:150717431 | T | G | 4 | a0002c0002t0005g0062 a0002c0002t0005g0063 a0002c0002t0005g0064 others(1): Show |
4 | HG01981.hp1 HG02965.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+845A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717431 | |||||||
| chr5:150717499 | T | C | 122 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0003g0242 others(119): Show |
140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.1071+777A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717499 | |||||||
| chr5:150717566 | G | A | 2 | a0002c0002t0002g0237 a0002c0002t0002g0238 |
2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1071+710C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717566 | |||||||
| chr5:150717583 | T | C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1071+693A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717583 | |||||||
| chr5:150717644 | G | C | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1071+632C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717644 | |||||||
| chr5:150717911 | T | G | 1 | a0001c0001t0001g0148 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1071+365A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717911 | |||||||
| chr5:150717985 | T | C | 1 | a0002c0002t0002g0230 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1071+291A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717985 | |||||||
| chr5:150717995 | A | G | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1071+281T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717995 | |||||||
| chr5:150718005 | C | T | 18 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(15): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1071+271G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150718005 | |||||||
| chr5:150718466 | G | A | 4 | a0001c0001t0001g0014 a0001c0001t0001g0112 a0001c0001t0001g0115 others(1): Show |
5 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-83C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718466 | |||||||
| chr5:150718477 | T | G | 1 | a0001c0001t0001g0089 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.964-94A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718477 | |||||||
| chr5:150718544 | T | C | 1 | a0002c0002t0002g0232 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.964-161A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718544 | |||||||
| chr5:150718555 | T | C | 1 | a0002c0002t0003g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.964-172A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718555 | |||||||
| chr5:150718651 | A | G | 1 | a0001c0001t0001g0153 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.964-268T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718651 | |||||||
| chr5:150718711 | G | A | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.964-328C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718711 | |||||||
| chr5:150718816 | ATTAT | A | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.964-437_964-434del others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718816 | |||||||
| chr5:150718994 | A | AT | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.964-612dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718994 | |||||||
| chr5:150719005 | A | C | 63 | a0001c0001t0001g0003 a0001c0001t0001g0018 a0001c0001t0001g0067 others(60): Show |
79 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.964-622T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719005 | |||||||
| chr5:150719008 | T | C | 4 | a0002c0002t0005g0180 a0002c0002t0005g0182 a0002c0002t0014g0179 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-625A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719008 | |||||||
| chr5:150719182 | A | G | 1 | a0001c0001t0001g0160 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.963+534T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719182 | |||||||
| chr5:150719222 | T | C | 1 | a0001c0001t0010g0104 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.963+494A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719222 | |||||||
| chr5:150719294 | CTGGGTGT others(1): Show |
C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.963+414_963+421del others(8): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719294 | |||||||
| chr5:150719406 | C | G | 2 | a0002c0002t0001g0188 a0002c0002t0001g0189 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.963+310G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719406 | |||||||
| chr5:150719782 | TAAA | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.909-15_909-13delTT others(1): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150719782 | |||||||
| chr5:150719804 | T | C | 2 | a0001c0001t0001g0085 a0001c0001t0003g0080 |
2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.909-34A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150719804 | |||||||
| chr5:150719937 | CAT | C | 3 | a0001c0001t0010g0104 a0001c0001t0010g0113 a0006c0008t0010g0103 |
3 | HG01433.hp2 HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.909-169_909-168del others(2): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150719937 | |||||||
| chr5:150719938 | A | G | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.909-168T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150719938 | |||||||
| chr5:150720006 | CCA | C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.909-238_909-237del others(2): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720006 | |||||||
| chr5:150720228 | A | G | 7 | a0002c0002t0001g0008 a0002c0004t0001g0026 a0002c0004t0001g0244 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.909-458T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720228 | |||||||
| chr5:150720481 | AT | A | 15 | a0001c0001t0001g0069 a0001c0001t0001g0092 a0001c0005t0006g0208 others(12): Show |
17 | HG00558.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.909-712delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720481 | |||||||
| chr5:150720754 | C | T | 2 | a0002c0002t0002g0225 a0002c0002t0002g0227 |
2 | NA18960.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.909-984G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720754 | |||||||
| chr5:150720764 | C | A | 1 | a0002c0002t0001g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.909-994G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720764 | |||||||
| chr5:150720962 | T | C | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.909-1192A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720962 | |||||||
| chr5:150721049 | T | C | 1 | a0002c0002t0002g0021 | 2 | HG00639.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.909-1279A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721049 | |||||||
| chr5:150721077 | T | G | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.909-1307A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721077 | |||||||
| chr5:150721099 | C | T | 1 | a0002c0004t0008g0246 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.909-1329G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721099 | |||||||
| chr5:150721124 | T | C | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.909-1354A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721124 | |||||||
| chr5:150721405 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.908+1502T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721405 | |||||||
| chr5:150721406 | T | C | 2 | a0002c0002t0016g0240 a0002c0002t0016g0241 |
2 | NA18944.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.908+1501A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721406 | |||||||
| chr5:150721429 | G | A | 1 | a0001c0001t0001g0156 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.908+1478C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721429 | |||||||
| chr5:150721840 | T | G | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.908+1067A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721840 | |||||||
| chr5:150721893 | T | C | 5 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0062 others(2): Show |
5 | HG01981.hp1 HG02615.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.908+1014A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721893 | |||||||
| chr5:150722085 | C | T | 18 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(15): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.908+822G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722085 | |||||||
| chr5:150722152 | T | A | 1 | a0002c0002t0005g0057 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.908+755A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722152 | |||||||
| chr5:150722275 | T | G | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+632A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722275 | |||||||
| chr5:150722500 | G | A | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.908+407C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722500 | |||||||
| chr5:150722601 | C | A | 1 | a0001c0001t0010g0113 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.908+306G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722601 | |||||||
| chr5:150722682 | T | C | 79 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(76): Show |
93 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.908+225A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722682 | |||||||
| chr5:150723116 | T | C | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.835-136A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723116 | |||||||
| chr5:150723122 | A | G | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-142T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723122 | |||||||
| chr5:150723167 | A | G | 1 | a0003c0003t0004g0233 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.835-187T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723167 | |||||||
| chr5:150723243 | A | G | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.835-263T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723243 | |||||||
| chr5:150723314 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.835-334C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723314 | |||||||
| chr5:150723336 | T | A | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.835-356A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723336 | |||||||
| chr5:150723465 | T | A | 3 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 |
3 | HG02109.hp2 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.835-485A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723465 | |||||||
| chr5:150723556 | A | G | 7 | a0002c0002t0001g0008 a0002c0004t0001g0026 a0002c0004t0001g0244 others(4): Show |
9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.835-576T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723556 | |||||||
| chr5:150723578 | C | T | 1 | a0001c0001t0019g0048 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.835-598G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723578 | |||||||
| chr5:150723830 | C | T | 4 | a0001c0001t0001g0079 a0001c0001t0001g0085 a0001c0001t0001g0086 others(1): Show |
4 | HG02572.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-850G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723830 | |||||||
| chr5:150723895 | A | G | 3 | a0002c0002t0005g0062 a0002c0002t0005g0063 a0002c0002t0005g0064 |
3 | HG01981.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.835-915T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723895 | |||||||
| chr5:150724136 | C | T | 125 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0001g0074 others(122): Show |
143 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.835-1156G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724136 | |||||||
| chr5:150724238 | A | G | 1 | a0001c0001t0001g0109 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.835-1258T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724238 | |||||||
| chr5:150724320 | C | T | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-1340G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724320 | |||||||
| chr5:150724475 | T | C | 1 | a0001c0001t0001g0011 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.835-1495A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724475 | |||||||
| chr5:150724615 | G | A | 2 | a0002c0002t0001g0188 a0002c0002t0001g0189 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.835-1635C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724615 | |||||||
| chr5:150724641 | T | C | 1 | a0002c0002t0014g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.835-1661A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724641 | |||||||
| chr5:150724674 | A | C | 2 | a0001c0001t0001g0089 a0001c0001t0001g0174 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835-1694T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724674 | |||||||
| chr5:150724928 | C | T | 4 | a0001c0001t0003g0242 a0002c0002t0001g0188 a0002c0002t0001g0189 others(1): Show |
4 | HG01243.hp2 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-1948G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724928 | |||||||
| chr5:150724973 | C | T | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.835-1993G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724973 | |||||||
| chr5:150725048 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
5 | HG02129.hp1 NA18988.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.835-2068G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725048 | |||||||
| chr5:150725071 | T | C | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-2091A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725071 | |||||||
| chr5:150725076 | T | C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.835-2096A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725076 | |||||||
| chr5:150725157 | C | CA | 34 | a0001c0001t0001g0065 a0001c0001t0001g0090 a0001c0001t0001g0105 others(31): Show |
34 | HG00738.hp2 HG01071.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.835-2178dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725157 | |||||||
| chr5:150725157 | CA | C | 26 | a0001c0001t0001g0108 a0001c0001t0001g0144 a0001c0001t0001g0151 others(23): Show |
27 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.835-2178delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725157 | |||||||
| chr5:150725181 | G | T | 5 | a0003c0003t0004g0023 a0003c0003t0004g0220 a0003c0003t0004g0221 others(2): Show |
6 | HG02071.hp2 NA18939.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.835-2201C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725181 | |||||||
| chr5:150725230 | G | A | 59 | a0002c0002t0001g0196 a0002c0002t0001g0197 a0002c0002t0001g0199 others(56): Show |
72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.835-2250C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725230 | |||||||
| chr5:150725304 | A | T | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-2324T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725304 | |||||||
| chr5:150725365 | C | A | 77 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(74): Show |
91 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.835-2385G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725365 | |||||||
| chr5:150725569 | T | C | 1 | a0001c0001t0001g0115 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.835-2589A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725569 | |||||||
| chr5:150725784 | C | T | 7 | a0001c0005t0006g0183 a0001c0005t0006g0184 a0001c0005t0006g0185 others(4): Show |
7 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-2804G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725784 | |||||||
| chr5:150725794 | A | T | 1 | a0001c0001t0001g0107 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.835-2814T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725794 | |||||||
| chr5:150725796 | C | G | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.835-2816G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725796 | |||||||
| chr5:150725944 | C | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.835-2964G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725944 | |||||||
| chr5:150725950 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.835-2970G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725950 | |||||||
| chr5:150725964 | G | A | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.835-2984C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725964 | |||||||
| chr5:150726054 | A | T | 4 | a0001c0001t0003g0242 a0002c0002t0003g0007 a0002c0002t0003g0027 others(1): Show |
5 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.835-3074T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726054 | |||||||
| chr5:150726307 | C | T | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.835-3327G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726307 | |||||||
| chr5:150726365 | C | CT | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-3386dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726365 | |||||||
| chr5:150726401 | A | G | 1 | a0001c0001t0001g0075 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.835-3421T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726401 | |||||||
| chr5:150726421 | T | C | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-3441A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726421 | |||||||
| chr5:150726527 | T | C | 10 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(7): Show |
12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-3547A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726527 | |||||||
| chr5:150726562 | T | C | 1 | a0001c0001t0002g0139 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.835-3582A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726562 | |||||||
| chr5:150726657 | G | C | 1 | a0002c0002t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.835-3677C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726657 | |||||||
| chr5:150726774 | A | C | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.835-3794T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726774 | |||||||
| chr5:150726815 | A | G | 1 | a0003c0003t0004g0025 | 2 | HG00408.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.834+3816T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726815 | |||||||
| chr5:150726846 | G | A | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.834+3785C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726846 | |||||||
| chr5:150727011 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0065 |
3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+3620C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727011 | |||||||
| chr5:150727098 | T | A | 2 | a0002c0002t0014g0179 a0002c0002t0014g0181 |
2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.834+3533A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727098 | |||||||
| chr5:150727134 | T | C | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.834+3497A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727134 | |||||||
| chr5:150727162 | T | G | 18 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(15): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.834+3469A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727162 | |||||||
| chr5:150727198 | G | A | 2 | a0001c0005t0006g0207 a0001c0005t0006g0208 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.834+3433C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727198 | |||||||
| chr5:150727293 | G | T | 1 | a0003c0003t0004g0221 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.834+3338C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727293 | |||||||
| chr5:150727339 | T | C | 1 | a0001c0001t0001g0095 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.834+3292A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727339 | |||||||
| chr5:150727422 | A | T | 8 | a0001c0001t0003g0242 a0001c0005t0006g0183 a0001c0005t0006g0184 others(5): Show |
8 | HG02896.hp2 HG02897.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+3209T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727422 | |||||||
| chr5:150727447 | T | G | 54 | a0002c0002t0001g0197 a0002c0002t0001g0199 a0002c0002t0001g0200 others(51): Show |
67 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.834+3184A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727447 | |||||||
| chr5:150727499 | G | A | 1 | a0001c0005t0006g0186 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.834+3132C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727499 | |||||||
| chr5:150727503 | G | A | 2 | a0001c0001t0001g0095 a0001c0001t0001g0116 |
2 | NA18945.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.834+3128C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727503 | |||||||
| chr5:150727531 | T | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.834+3100A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727531 | |||||||
| chr5:150727590 | A | C | 3 | a0002c0002t0001g0212 a0002c0002t0001g0213 a0002c0002t0001g0239 |
3 | HG02970.hp2 HG03098.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.834+3041T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727590 | |||||||
| chr5:150727636 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.834+2995G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727636 | |||||||
| chr5:150727644 | C | T | 1 | a0002c0002t0001g0044 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.834+2987G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727644 | |||||||
| chr5:150727645 | G | A | 1 | a0001c0001t0003g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.834+2986C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727645 | |||||||
| chr5:150727648 | C | T | 1 | a0001c0001t0003g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.834+2983G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727648 | |||||||
| chr5:150727652 | T | C | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.834+2979A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727652 | |||||||
| chr5:150727669 | G | A | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+2962C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727669 | |||||||
| chr5:150727692 | C | T | 1 | a0001c0001t0023g0078 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.834+2939G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727692 | |||||||
| chr5:150727701 | G | A | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.834+2930C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727701 | |||||||
| chr5:150727712 | C | G | 18 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(15): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.834+2919G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727712 | |||||||
| chr5:150727762 | C | T | 3 | a0002c0002t0003g0007 a0002c0002t0003g0027 a0002c0002t0003g0028 |
4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+2869G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727762 | |||||||
| chr5:150727771 | G | A | 85 | a0001c0005t0006g0186 a0002c0002t0001g0033 a0002c0002t0001g0035 others(82): Show |
100 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.834+2860C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727771 | |||||||
| chr5:150727775 | CA | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(116): Show |
140 | HG00558.hp1 HG00597.hp1 HG00639.hp2 others(137): Show |
intron_variant | MODIFIER | c.834+2855delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727775 | |||||||
| chr5:150727792 | AAAAAAC | A | 8 | a0002c0002t0003g0030 a0002c0002t0003g0032 a0002c0002t0003g0041 others(5): Show |
8 | HG02280.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+2833_834+2838d others(8): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727792 | |||||||
| chr5:150727793 | AAAAAC | A | 26 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0044 others(23): Show |
28 | HG00408.hp2 HG00558.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.834+2833_834+2837d others(7): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727793 | |||||||
| chr5:150727794 | AAAAC | A | 40 | a0002c0002t0001g0037 a0002c0002t0001g0188 a0002c0002t0001g0189 others(37): Show |
47 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.834+2833_834+2836d others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727794 | |||||||
| chr5:150727795 | AAAC | A | 18 | a0002c0002t0001g0214 a0002c0002t0001g0235 a0002c0002t0002g0004 others(15): Show |
19 | HG00738.hp2 HG01496.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.834+2833_834+2835d others(5): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727795 | |||||||
| chr5:150728053 | C | A | 120 | a0001c0001t0003g0242 a0001c0005t0006g0183 a0001c0005t0006g0184 others(117): Show |
137 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.834+2578G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728053 | |||||||
| chr5:150728073 | T | C | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.834+2558A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728073 | |||||||
| chr5:150728314 | T | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.834+2317A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728314 | |||||||
| chr5:150728393 | T | C | 7 | a0001c0005t0006g0183 a0001c0005t0006g0184 a0001c0005t0006g0185 others(4): Show |
7 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+2238A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728393 | |||||||
| chr5:150728491 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0065 |
3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+2140C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728491 | |||||||
| chr5:150728534 | T | C | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834+2097A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728534 | |||||||
| chr5:150728651 | T | A | 1 | a0002c0002t0002g0217 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.834+1980A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728651 | |||||||
| chr5:150728789 | T | C | 18 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(15): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.834+1842A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728789 | |||||||
| chr5:150728817 | T | C | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.834+1814A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728817 | |||||||
| chr5:150728847 | G | C | 1 | a0001c0001t0001g0158 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.834+1784C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728847 | |||||||
| chr5:150728873 | C | T | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.834+1758G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728873 | |||||||
| chr5:150728874 | A | G | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.834+1757T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728874 | |||||||
| chr5:150728879 | C | CT | 22 | a0001c0001t0001g0069 a0001c0001t0001g0088 a0001c0001t0001g0089 others(19): Show |
24 | HG00558.hp1 HG00597.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.834+1751dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728879 | |||||||
| chr5:150728956 | C | T | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.834+1675G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728956 | |||||||
| chr5:150729025 | G | A | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.834+1606C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729025 | |||||||
| chr5:150729042 | C | CCTT | 4 | a0002c0002t0001g0197 a0002c0002t0001g0203 a0002c0002t0011g0198 others(1): Show |
4 | HG02129.hp2 HG02280.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(5): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CCTTT | 5 | a0002c0002t0001g0199 a0002c0002t0001g0200 a0002c0002t0001g0204 others(2): Show |
7 | HG00408.hp2 HG00558.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CCTTTT | 16 | a0002c0002t0001g0202 a0002c0002t0001g0223 a0002c0002t0001g0235 others(13): Show |
21 | HG00408.hp1 HG00639.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(7): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CCTTTTT | 16 | a0002c0002t0001g0214 a0002c0002t0002g0005 a0002c0002t0002g0022 others(13): Show |
19 | HG02071.hp2 HG02630.hp1 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(8): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CCTTTTTT | 10 | a0002c0002t0001g0196 a0002c0002t0001g0206 a0002c0002t0002g0004 others(7): Show |
13 | HG00597.hp2 HG00738.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(9): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CCTTTTTT others(1): Show |
4 | a0002c0002t0001g0008 a0002c0002t0002g0217 a0002c0002t0002g0229 others(1): Show |
5 | HG01496.hp2 HG02258.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(10): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CCTTTTTT others(2): Show |
3 | a0002c0002t0001g0212 a0002c0002t0001g0213 a0002c0002t0002g0232 |
3 | HG02970.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.834+1588_834+1589i others(11): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CCTTTTTT others(3): Show |
1 | a0002c0002t0009g0193 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.834+1588_834+1589i others(12): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CT | 43 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(40): Show |
52 | HG00597.hp1 HG00642.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.834+1588dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CTT | 12 | a0001c0001t0001g0018 a0001c0001t0001g0068 a0001c0001t0001g0093 others(9): Show |
13 | HG01433.hp1 HG02300.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+1587_834+1588d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CTTTTTTT others(7): Show |
1 | a0002c0002t0005g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.834+1575_834+1588d others(16): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CTTTTTTT others(10): Show |
1 | a0002c0002t0005g0052 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.834+1572_834+1588d others(19): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CTTTTTTT others(12): Show |
1 | a0002c0002t0005g0051 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.834+1570_834+1588d others(21): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CTTTTTTT others(13): Show |
2 | a0002c0002t0005g0053 a0002c0002t0005g0055 |
2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.834+1569_834+1588d others(22): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CTTTTTTT others(14): Show |
2 | a0002c0002t0005g0050 a0002c0002t0005g0059 |
2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.834+1568_834+1588d others(23): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CTTTTTTT others(16): Show |
1 | a0002c0002t0005g0058 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.834+1566_834+1588d others(25): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CTTTTTTT others(18): Show |
1 | a0002c0002t0005g0049 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.834+1564_834+1588d others(27): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | C | CTTTTTTT others(21): Show |
2 | a0002c0002t0005g0056 a0002c0002t0005g0057 |
2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.834+1561_834+1588d others(30): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | CT | C | 23 | a0001c0001t0001g0086 a0001c0001t0001g0121 a0001c0001t0001g0157 others(20): Show |
24 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.834+1588delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | CTT | C | 6 | a0002c0002t0001g0188 a0002c0002t0005g0190 a0002c0004t0001g0026 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+1587_834+1588d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0005g0062 a0002c0002t0005g0064 |
2 | HG01981.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.834+1578_834+1588d others(13): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0076 a0002c0007t0018g0029 |
2 | HG03486.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.834+1577_834+1588d others(14): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | CTTTTTTT others(7): Show |
C | 1 | a0002c0002t0002g0209 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.834+1575_834+1588d others(16): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0065 |
3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+1574_834+1588d others(17): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729042 | CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0095 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.834+1571_834+1588d others(20): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | |||||||
| chr5:150729043 | T | C | 4 | a0002c0002t0001g0035 a0002c0002t0003g0009 a0002c0002t0003g0036 others(1): Show |
5 | HG02109.hp1 HG02145.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+1588A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729043 | |||||||
| chr5:150729044 | T | C | 16 | a0002c0002t0001g0033 a0002c0002t0001g0037 a0002c0002t0001g0044 others(13): Show |
16 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.834+1587A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729044 | |||||||
| chr5:150729045 | T | C | 6 | a0002c0002t0001g0188 a0002c0002t0005g0190 a0002c0004t0001g0026 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+1586A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729045 | |||||||
| chr5:150729046 | T | C | 1 | a0002c0002t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.834+1585A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729046 | |||||||
| chr5:150729047 | T | C | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.834+1584A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729047 | |||||||
| chr5:150729057 | T | C | 1 | a0002c0002t0002g0209 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.834+1574A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729057 | |||||||
| chr5:150729210 | A | G | 1 | a0002c0002t0016g0240 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.834+1421T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729210 | |||||||
| chr5:150729249 | GT | G | 20 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0021 others(17): Show |
27 | HG00597.hp2 HG00639.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.834+1381delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729249 | |||||||
| chr5:150729292 | A | G | 1 | a0001c0001t0007g0081 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.834+1339T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729292 | |||||||
| chr5:150729333 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.834+1298G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729333 | |||||||
| chr5:150729374 | T | C | 11 | a0002c0002t0005g0049 a0002c0002t0005g0050 a0002c0002t0005g0051 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.834+1257A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729374 | |||||||
| chr5:150729610 | C | CT | 35 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0003g0242 others(32): Show |
38 | HG00735.hp2 HG01496.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.834+1020dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729610 | |||||||
| chr5:150729610 | C | CTT | 82 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(79): Show |
97 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.834+1019_834+1020d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729610 | |||||||
| chr5:150729632 | C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0076 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.834+998_834+999ins others(10): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729632 | |||||||
| chr5:150729652 | T | C | 3 | a0002c0002t0001g0212 a0002c0002t0001g0213 a0002c0002t0001g0239 |
3 | HG02970.hp2 HG03098.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.834+979A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729652 | |||||||
| chr5:150729664 | C | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.834+967G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729664 | |||||||
| chr5:150729695 | A | G | 1 | a0002c0002t0003g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.834+936T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729695 | |||||||
| chr5:150729940 | C | G | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.834+691G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729940 | |||||||
| chr5:150730078 | T | C | 1 | a0001c0001t0001g0132 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.834+553A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730078 | |||||||
| chr5:150730084 | C | A | 1 | a0002c0002t0005g0055 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+547G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730084 | |||||||
| chr5:150730115 | C | T | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.834+516G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730115 | |||||||
| chr5:150730334 | C | G | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+297G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730334 | |||||||
| chr5:150730342 | T | C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.834+289A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730342 | |||||||
| chr5:150730370 | G | GT | 2 | a0001c0001t0001g0010 a0001c0001t0001g0065 |
3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+260dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730370 | |||||||
| chr5:150730376 | C | T | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834+255G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730376 | |||||||
| chr5:150730514 | A | G | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.834+117T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730514 | |||||||
| chr5:150730542 | C | T | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.834+89G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730542 | |||||||
| chr5:150730853 | A | C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.725-113T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 7/12 | chr5 | 150730853 | |||||||
| chr5:150731325 | C | CTG | 38 | a0002c0002t0001g0223 a0002c0002t0001g0235 a0002c0002t0002g0004 others(35): Show |
50 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.611+89_611+90dupCA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 6/12 | chr5 | 150731325 | |||||||
| chr5:150731770 | G | A | 1 | a0001c0001t0007g0072 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.538-281C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150731770 | |||||||
| chr5:150731776 | G | C | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG01884.hp2 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.538-287C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150731776 | |||||||
| chr5:150731974 | C | T | 1 | a0002c0002t0014g0179 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.538-485G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150731974 | |||||||
| chr5:150731982 | G | A | 1 | a0001c0001t0001g0097 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.538-493C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150731982 | |||||||
| chr5:150732051 | C | T | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.538-562G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732051 | |||||||
| chr5:150732235 | C | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.538-746G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732235 | |||||||
| chr5:150732269 | C | A | 1 | a0001c0001t0001g0118 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.538-780G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732269 | |||||||
| chr5:150732282 | T | C | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.538-793A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732282 | |||||||
| chr5:150732308 | C | T | 1 | a0001c0001t0003g0080 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.538-819G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732308 | |||||||
| chr5:150732335 | G | C | 1 | a0002c0002t0002g0230 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.538-846C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732335 | |||||||
| chr5:150732551 | C | T | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.537+817G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732551 | |||||||
| chr5:150732571 | T | C | 1 | a0001c0001t0001g0016 | 2 | NA18950.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.537+797A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732571 | |||||||
| chr5:150732691 | T | C | 4 | a0002c0002t0005g0180 a0002c0002t0005g0182 a0002c0002t0014g0179 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+677A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732691 | |||||||
| chr5:150732810 | C | T | 3 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG01884.hp2 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.537+558G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732810 | |||||||
| chr5:150732847 | T | C | 1 | a0001c0001t0003g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.537+521A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732847 | |||||||
| chr5:150733000 | C | T | 1 | a0001c0005t0006g0183 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.537+368G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150733000 | |||||||
| chr5:150733082 | G | A | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.537+286C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150733082 | |||||||
| chr5:150733523 | A | G | 7 | a0002c0002t0005g0049 a0002c0002t0005g0050 a0002c0002t0005g0051 others(4): Show |
7 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-48T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733523 | |||||||
| chr5:150733556 | A | G | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0174 others(1): Show |
4 | HG03195.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-81T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733556 | |||||||
| chr5:150733568 | G | A | 83 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(80): Show |
98 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.430-93C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733568 | |||||||
| chr5:150733646 | G | A | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.430-171C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733646 | |||||||
| chr5:150733802 | A | G | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.430-327T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733802 | |||||||
| chr5:150733912 | T | C | 120 | a0001c0001t0003g0242 a0001c0005t0006g0183 a0001c0005t0006g0184 others(117): Show |
137 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.430-437A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733912 | |||||||
| chr5:150734024 | C | G | 4 | a0002c0002t0005g0056 a0002c0002t0005g0057 a0002c0002t0005g0058 others(1): Show |
4 | HG02145.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-549G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734024 | |||||||
| chr5:150734181 | C | T | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.430-706G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734181 | |||||||
| chr5:150734418 | T | G | 2 | a0001c0001t0001g0010 a0001c0001t0001g0065 |
3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.430-943A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734418 | |||||||
| chr5:150734483 | G | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0132 |
2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.430-1008C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734483 | |||||||
| chr5:150734536 | C | T | 3 | a0002c0002t0003g0007 a0002c0002t0003g0027 a0002c0002t0003g0028 |
4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-1061G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734536 | |||||||
| chr5:150734617 | G | A | 1 | a0001c0001t0001g0158 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.430-1142C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734617 | |||||||
| chr5:150734930 | A | G | 2 | a0002c0002t0001g0037 a0002c0002t0001g0044 |
2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.430-1455T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734930 | |||||||
| chr5:150734943 | C | T | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430-1468G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734943 | |||||||
| chr5:150735038 | C | A | 5 | a0002c0002t0001g0196 a0002c0002t0009g0192 a0002c0002t0009g0193 others(2): Show |
5 | HG02647.hp2 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-1563G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735038 | |||||||
| chr5:150735219 | C | CTCAAG | 122 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0003g0242 others(119): Show |
140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.430-1745_430-1744i others(7): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735219 | |||||||
| chr5:150735226 | T | C | 2 | a0002c0002t0002g0229 a0002c0002t0002g0230 |
2 | HG00738.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.430-1751A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735226 | |||||||
| chr5:150735247 | C | A | 1 | a0001c0001t0003g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.430-1772G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735247 | |||||||
| chr5:150735328 | C | T | 83 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(80): Show |
98 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.430-1853G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735328 | |||||||
| chr5:150735329 | G | A | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.430-1854C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735329 | |||||||
| chr5:150735377 | G | A | 1 | a0001c0001t0026g0175 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430-1902C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735377 | |||||||
| chr5:150735559 | G | A | 3 | a0002c0002t0005g0062 a0002c0002t0005g0063 a0002c0002t0005g0064 |
3 | HG01981.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.430-2084C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735559 | |||||||
| chr5:150735605 | G | C | 2 | a0001c0001t0001g0119 a0001c0001t0001g0127 |
2 | HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.430-2130C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735605 | |||||||
| chr5:150735749 | T | C | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-2274A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735749 | |||||||
| chr5:150735914 | TA | T | 24 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0001g0075 others(21): Show |
25 | HG00408.hp2 HG01175.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.430-2440delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735914 | |||||||
| chr5:150735914 | TAA | T | 73 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(70): Show |
88 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.430-2441_430-2440d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735914 | |||||||
| chr5:150735914 | TAAA | T | 7 | a0002c0002t0002g0191 a0002c0004t0001g0026 a0002c0004t0001g0244 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-2442_430-2440d others(5): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735914 | |||||||
| chr5:150735965 | A | G | 1 | a0002c0002t0002g0237 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.430-2490T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735965 | |||||||
| chr5:150736084 | A | T | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.430-2609T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736084 | |||||||
| chr5:150736302 | C | CAG | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.430-2829_430-2828d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736302 | |||||||
| chr5:150736373 | A | C | 1 | a0002c0004t0008g0243 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.430-2898T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736373 | |||||||
| chr5:150736416 | C | T | 7 | a0001c0001t0002g0139 a0002c0004t0001g0026 a0002c0004t0001g0244 others(4): Show |
8 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-2941G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736416 | |||||||
| chr5:150736417 | G | A | 1 | a0001c0001t0001g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.430-2942C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736417 | |||||||
| chr5:150736421 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.430-2946G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736421 | |||||||
| chr5:150736609 | G | A | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | HG02135.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.430-3134C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736609 | |||||||
| chr5:150736711 | A | C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.430-3236T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736711 | |||||||
| chr5:150736858 | G | A | 2 | a0001c0001t0001g0089 a0001c0001t0001g0174 |
2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430-3383C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736858 | |||||||
| chr5:150736949 | G | A | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-3474C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736949 | |||||||
| chr5:150736972 | T | C | 1 | a0002c0002t0009g0192 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430-3497A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736972 | |||||||
| chr5:150736975 | C | G | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.430-3500G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736975 | |||||||
| chr5:150737160 | A | T | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.430-3685T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737160 | |||||||
| chr5:150737359 | G | A | 2 | a0002c0002t0009g0194 a0002c0002t0009g0195 |
2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.430-3884C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737359 | |||||||
| chr5:150737418 | G | T | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.430-3943C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737418 | |||||||
| chr5:150737529 | A | C | 3 | a0002c0002t0003g0007 a0002c0002t0003g0027 a0002c0002t0003g0028 |
4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-4054T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737529 | |||||||
| chr5:150737532 | G | GAAATCAG others(12): Show |
3 | a0002c0002t0003g0007 a0002c0002t0003g0027 a0002c0002t0003g0028 |
4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-4076_430-4058d others(21): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737532 | |||||||
| chr5:150737738 | A | C | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.430-4263T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737738 | |||||||
| chr5:150737825 | C | T | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.429+4289G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737825 | |||||||
| chr5:150737848 | A | T | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.429+4266T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737848 | |||||||
| chr5:150738392 | C | T | 4 | a0002c0002t0005g0049 a0002c0002t0005g0050 a0002c0002t0005g0051 others(1): Show |
4 | HG02055.hp1 HG02451.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+3722G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738392 | |||||||
| chr5:150738441 | G | C | 59 | a0002c0002t0001g0196 a0002c0002t0001g0197 a0002c0002t0001g0199 others(56): Show |
72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.429+3673C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738441 | |||||||
| chr5:150738458 | G | A | 120 | a0001c0001t0003g0242 a0001c0005t0006g0183 a0001c0005t0006g0184 others(117): Show |
137 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.429+3656C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738458 | |||||||
| chr5:150738554 | A | G | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429+3560T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738554 | |||||||
| chr5:150738662 | C | T | 59 | a0002c0002t0001g0196 a0002c0002t0001g0197 a0002c0002t0001g0199 others(56): Show |
72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.429+3452G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738662 | |||||||
| chr5:150738672 | T | C | 1 | a0002c0002t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.429+3442A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738672 | |||||||
| chr5:150738783 | T | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG02683.hp1 HG03239.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.429+3331A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738783 | |||||||
| chr5:150738853 | A | G | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+3261T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738853 | |||||||
| chr5:150738866 | G | T | 1 | a0001c0001t0001g0138 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.429+3248C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738866 | |||||||
| chr5:150738959 | C | T | 1 | a0002c0002t0003g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+3155G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738959 | |||||||
| chr5:150738986 | G | A | 4 | a0002c0002t0005g0180 a0002c0002t0005g0182 a0002c0002t0014g0179 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+3128C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738986 | |||||||
| chr5:150739023 | A | G | 133 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(130): Show |
154 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.429+3091T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739023 | |||||||
| chr5:150739100 | G | C | 1 | a0001c0001t0001g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.429+3014C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739100 | |||||||
| chr5:150739162 | CAG | C | 4 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0174 others(1): Show |
4 | HG03195.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+2950_429+2951d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739162 | |||||||
| chr5:150739180 | CA | C | 9 | a0001c0001t0023g0078 a0002c0002t0001g0188 a0002c0002t0001g0189 others(6): Show |
9 | HG00639.hp2 HG01243.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+2933delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739180 | |||||||
| chr5:150739222 | A | G | 1 | a0001c0001t0001g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.429+2892T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739222 | |||||||
| chr5:150739237 | A | C | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.429+2877T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739237 | |||||||
| chr5:150739365 | C | T | 1 | a0002c0002t0005g0190 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.429+2749G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739365 | |||||||
| chr5:150739376 | A | C | 1 | a0001c0001t0001g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.429+2738T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739376 | |||||||
| chr5:150739459 | T | C | 1 | a0002c0002t0011g0211 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.429+2655A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739459 | |||||||
| chr5:150739709 | T | C | 1 | a0002c0002t0001g0197 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.429+2405A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739709 | |||||||
| chr5:150739710 | A | G | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+2404T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739710 | |||||||
| chr5:150739754 | G | A | 1 | a0003c0003t0004g0205 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.429+2360C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739754 | |||||||
| chr5:150739830 | G | A | 1 | a0002c0002t0003g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.429+2284C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739830 | |||||||
| chr5:150740194 | A | G | 4 | a0002c0002t0005g0180 a0002c0002t0005g0182 a0002c0002t0014g0179 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+1920T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740194 | |||||||
| chr5:150740246 | T | C | 122 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0003g0242 others(119): Show |
140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.429+1868A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740246 | |||||||
| chr5:150740266 | T | G | 1 | a0002c0002t0001g0196 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.429+1848A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740266 | |||||||
| chr5:150740287 | T | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+1827A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740287 | |||||||
| chr5:150740600 | G | A | 1 | a0001c0001t0007g0073 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.429+1514C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740600 | |||||||
| chr5:150740626 | G | A | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+1488C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740626 | |||||||
| chr5:150740628 | C | T | 18 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(15): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+1486G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740628 | |||||||
| chr5:150740719 | A | AT | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429+1394dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740719 | |||||||
| chr5:150740811 | A | T | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+1303T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740811 | |||||||
| chr5:150740888 | C | A | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+1226G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740888 | |||||||
| chr5:150741031 | C | G | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.429+1083G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741031 | |||||||
| chr5:150741164 | C | CAAAAA | 58 | a0002c0002t0001g0037 a0002c0002t0001g0197 a0002c0002t0001g0199 others(55): Show |
71 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.429+945_429+949dup others(5): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | |||||||
| chr5:150741164 | C | CAAAAAA | 23 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0044 others(20): Show |
24 | HG01884.hp1 HG02071.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.429+944_429+949dup others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | |||||||
| chr5:150741164 | C | CAAAAAAA others(3): Show |
1 | a0002c0002t0001g0188 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.429+940_429+949dup others(10): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | |||||||
| chr5:150741164 | C | CAAAAAAA others(4): Show |
1 | a0002c0002t0001g0189 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.429+939_429+949dup others(11): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | |||||||
| chr5:150741164 | C | CAAAAAAA others(5): Show |
1 | a0002c0002t0005g0190 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.429+938_429+949dup others(12): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | |||||||
| chr5:150741164 | CA | C | 12 | a0001c0001t0001g0069 a0001c0001t0001g0079 a0001c0001t0001g0124 others(9): Show |
12 | HG00558.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+949delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | |||||||
| chr5:150741193 | C | A | 2 | a0002c0002t0001g0188 a0002c0002t0001g0189 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429+921G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741193 | |||||||
| chr5:150741221 | A | C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429+893T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741221 | |||||||
| chr5:150741352 | T | C | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.429+762A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741352 | |||||||
| chr5:150741518 | T | C | 1 | a0001c0001t0003g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.429+596A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741518 | |||||||
| chr5:150741530 | G | A | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.429+584C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741530 | |||||||
| chr5:150741533 | C | T | 1 | a0002c0002t0003g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+581G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741533 | |||||||
| chr5:150741621 | T | C | 4 | a0002c0002t0005g0056 a0002c0002t0005g0057 a0002c0002t0005g0058 others(1): Show |
4 | HG02145.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+493A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741621 | |||||||
| chr5:150741660 | T | C | 1 | a0001c0001t0001g0159 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.429+454A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741660 | |||||||
| chr5:150741896 | G | C | 1 | a0005c0009t0001g0094 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.429+218C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741896 | |||||||
| chr5:150742007 | A | T | 1 | a0002c0002t0003g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+107T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150742007 | |||||||
| chr5:150742161 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0007g0135 |
2 | HG02602.hp1 HG04115.hp1 |
splice_region_variant&intron_variant | LOW | c.386-4G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742161 | |||||||
| chr5:150742502 | C | T | 3 | a0001c0001t0001g0092 a0001c0001t0001g0129 a0001c0001t0001g0134 |
3 | HG01884.hp2 NA18965.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.386-345G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742502 | |||||||
| chr5:150742513 | T | C | 1 | a0001c0001t0001g0092 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.386-356A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742513 | |||||||
| chr5:150742717 | G | C | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.386-560C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742717 | |||||||
| chr5:150742829 | C | A | 4 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(1): Show |
4 | HG01175.hp1 HG01884.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-672G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742829 | |||||||
| chr5:150742919 | C | T | 7 | a0001c0005t0006g0183 a0001c0005t0006g0184 a0001c0005t0006g0185 others(4): Show |
7 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-762G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742919 | |||||||
| chr5:150742960 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.386-803G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742960 | |||||||
| chr5:150742965 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.386-808G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742965 | |||||||
| chr5:150742965 | C | G | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-808G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742965 | |||||||
| chr5:150742997 | G | A | 1 | a0002c0002t0001g0044 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.386-840C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742997 | |||||||
| chr5:150743000 | C | T | 1 | a0001c0001t0001g0133 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.386-843G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743000 | |||||||
| chr5:150743002 | C | T | 1 | a0002c0002t0009g0194 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.386-845G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743002 | |||||||
| chr5:150743042 | G | A | 54 | a0002c0002t0001g0197 a0002c0002t0001g0199 a0002c0002t0001g0200 others(51): Show |
67 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.386-885C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743042 | |||||||
| chr5:150743082 | G | A | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-925C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743082 | |||||||
| chr5:150743120 | C | T | 1 | a0002c0002t0001g0199 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.386-963G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743120 | |||||||
| chr5:150743122 | G | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-965C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743122 | |||||||
| chr5:150743189 | G | A | 1 | a0002c0002t0003g0045 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.386-1032C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743189 | |||||||
| chr5:150743279 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.386-1122C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743279 | |||||||
| chr5:150743306 | T | TA | 16 | a0002c0002t0001g0197 a0002c0002t0001g0199 a0002c0002t0001g0200 others(13): Show |
17 | HG00408.hp2 HG00558.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.386-1150dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743306 | |||||||
| chr5:150743400 | C | A | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-1243G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743400 | |||||||
| chr5:150743445 | A | G | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-1288T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743445 | |||||||
| chr5:150743481 | C | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-1324G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743481 | |||||||
| chr5:150743587 | C | T | 1 | a0001c0001t0001g0098 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.386-1430G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743587 | |||||||
| chr5:150743689 | G | A | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-1532C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743689 | |||||||
| chr5:150743693 | A | T | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-1536T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743693 | |||||||
| chr5:150743797 | C | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-1640G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743797 | |||||||
| chr5:150743902 | A | C | 4 | a0002c0002t0001g0008 a0002c0002t0001g0188 a0002c0002t0001g0189 others(1): Show |
5 | HG01243.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-1745T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743902 | |||||||
| chr5:150743902 | A | T | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.386-1745T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743902 | |||||||
| chr5:150743948 | T | C | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.386-1791A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743948 | |||||||
| chr5:150743992 | G | A | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-1835C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743992 | |||||||
| chr5:150744044 | A | C | 1 | a0002c0002t0016g0240 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.386-1887T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744044 | |||||||
| chr5:150744099 | G | C | 2 | a0001c0001t0001g0068 a0001c0001t0001g0173 |
2 | NA18992.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.386-1942C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744099 | |||||||
| chr5:150744191 | T | C | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.386-2034A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744191 | |||||||
| chr5:150744192 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.386-2035C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744192 | |||||||
| chr5:150744194 | C | T | 3 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0001g0071 |
4 | HG01975.hp2 HG02723.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-2037G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744194 | |||||||
| chr5:150744195 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.386-2038C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744195 | |||||||
| chr5:150744202 | G | C | 2 | a0001c0001t0001g0010 a0001c0001t0001g0065 |
3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.386-2045C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744202 | |||||||
| chr5:150744220 | C | T | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-2063G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744220 | |||||||
| chr5:150744238 | G | GA | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2082dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744238 | |||||||
| chr5:150744258 | C | T | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.386-2101G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744258 | |||||||
| chr5:150744308 | G | A | 2 | a0002c0002t0009g0194 a0002c0002t0009g0195 |
2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.386-2151C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744308 | |||||||
| chr5:150744315 | T | C | 1 | a0002c0002t0005g0190 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.386-2158A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744315 | |||||||
| chr5:150744440 | T | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2283A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744440 | |||||||
| chr5:150744457 | T | A | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-2300A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744457 | |||||||
| chr5:150744534 | C | T | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.386-2377G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744534 | |||||||
| chr5:150744603 | T | C | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.386-2446A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744603 | |||||||
| chr5:150744651 | C | A | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2494G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744651 | |||||||
| chr5:150744754 | G | A | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-2597C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744754 | |||||||
| chr5:150744763 | C | T | 1 | a0001c0001t0001g0065 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.386-2606G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744763 | |||||||
| chr5:150744887 | G | A | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-2730C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744887 | |||||||
| chr5:150744912 | C | A | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2755G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744912 | |||||||
| chr5:150744935 | C | T | 1 | a0001c0001t0001g0074 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.386-2778G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744935 | |||||||
| chr5:150744998 | A | G | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2841T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744998 | |||||||
| chr5:150745053 | A | G | 59 | a0002c0002t0001g0196 a0002c0002t0001g0197 a0002c0002t0001g0199 others(56): Show |
72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.386-2896T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745053 | |||||||
| chr5:150745107 | A | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2950T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745107 | |||||||
| chr5:150745169 | C | G | 1 | a0001c0001t0023g0078 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.386-3012G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745169 | |||||||
| chr5:150745220 | C | A | 8 | a0001c0001t0003g0242 a0001c0005t0006g0183 a0001c0005t0006g0184 others(5): Show |
8 | HG02896.hp2 HG02897.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.386-3063G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745220 | |||||||
| chr5:150745235 | C | A | 86 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(83): Show |
101 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.386-3078G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745235 | |||||||
| chr5:150745305 | C | T | 1 | a0002c0002t0001g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.386-3148G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745305 | |||||||
| chr5:150745435 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.386-3278G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745435 | |||||||
| chr5:150745436 | C | T | 1 | a0001c0001t0001g0160 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.386-3279G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745436 | |||||||
| chr5:150745437 | A | G | 89 | a0001c0001t0001g0160 a0002c0002t0001g0008 a0002c0002t0001g0033 others(86): Show |
105 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.386-3280T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745437 | |||||||
| chr5:150745443 | T | A | 1 | a0001c0001t0001g0160 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.386-3286A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745443 | |||||||
| chr5:150745514 | A | G | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-3357T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745514 | |||||||
| chr5:150745607 | C | A | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-3450G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745607 | |||||||
| chr5:150745746 | G | C | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-3589C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745746 | |||||||
| chr5:150745788 | A | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-3631T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745788 | |||||||
| chr5:150745824 | C | A | 3 | a0002c0002t0003g0007 a0002c0002t0003g0027 a0002c0002t0003g0028 |
4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-3667G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745824 | |||||||
| chr5:150745825 | C | T | 3 | a0002c0002t0003g0007 a0002c0002t0003g0027 a0002c0002t0003g0028 |
4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-3668G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745825 | |||||||
| chr5:150745826 | A | C | 5 | a0002c0002t0002g0004 a0002c0002t0002g0005 a0002c0002t0002g0022 others(2): Show |
10 | NA18966.hp1 NA18968.hp1 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.386-3669T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745826 | |||||||
| chr5:150745961 | T | C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-3804A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745961 | |||||||
| chr5:150745995 | A | G | 1 | a0002c0002t0002g0237 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.386-3838T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745995 | |||||||
| chr5:150746000 | G | T | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-3843C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746000 | |||||||
| chr5:150746147 | G | C | 2 | a0002c0002t0001g0204 a0003c0003t0004g0205 |
2 | HG00408.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.386-3990C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746147 | |||||||
| chr5:150746169 | T | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-4012A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746169 | |||||||
| chr5:150746179 | C | G | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-4022G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746179 | |||||||
| chr5:150746211 | C | T | 1 | a0001c0001t0001g0097 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.386-4054G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746211 | |||||||
| chr5:150746242 | C | G | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.386-4085G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746242 | |||||||
| chr5:150746266 | C | T | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-4109G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746266 | |||||||
| chr5:150746293 | A | ATAAT | 122 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0003g0242 others(119): Show |
140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.386-4140_386-4137d others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746293 | |||||||
| chr5:150746359 | A | G | 1 | a0001c0001t0001g0096 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.386-4202T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746359 | |||||||
| chr5:150746443 | C | T | 18 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(15): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.386-4286G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746443 | |||||||
| chr5:150746467 | T | C | 112 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(109): Show |
129 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.386-4310A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746467 | |||||||
| chr5:150746481 | A | G | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-4324T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746481 | |||||||
| chr5:150746525 | T | G | 1 | a0002c0002t0005g0190 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.386-4368A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746525 | |||||||
| chr5:150746549 | G | A | 1 | a0002c0002t0001g0206 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.386-4392C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746549 | |||||||
| chr5:150746555 | C | A | 1 | a0001c0001t0001g0123 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.386-4398G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746555 | |||||||
| chr5:150746557 | G | A | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-4400C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746557 | |||||||
| chr5:150746561 | G | C | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-4404C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746561 | |||||||
| chr5:150746588 | A | C | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-4431T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746588 | |||||||
| chr5:150746638 | G | A | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.386-4481C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746638 | |||||||
| chr5:150746704 | T | C | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-4547A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746704 | |||||||
| chr5:150746710 | C | A | 2 | a0001c0001t0001g0124 a0001c0010t0001g0125 |
2 | NA18977.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.386-4553G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746710 | |||||||
| chr5:150746768 | C | A | 11 | a0002c0002t0005g0049 a0002c0002t0005g0050 a0002c0002t0005g0051 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.386-4611G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746768 | |||||||
| chr5:150746769 | G | A | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-4612C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746769 | |||||||
| chr5:150746903 | A | G | 1 | a0001c0001t0001g0095 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.386-4746T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746903 | |||||||
| chr5:150746917 | T | C | 2 | a0002c0002t0002g0237 a0002c0002t0002g0238 |
2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.386-4760A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746917 | |||||||
| chr5:150746926 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.386-4769C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746926 | |||||||
| chr5:150747014 | T | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-4857A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747014 | |||||||
| chr5:150747083 | C | T | 59 | a0002c0002t0001g0196 a0002c0002t0001g0197 a0002c0002t0001g0199 others(56): Show |
72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.386-4926G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747083 | |||||||
| chr5:150747095 | G | A | 1 | a0001c0001t0007g0176 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.386-4938C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747095 | |||||||
| chr5:150747112 | T | G | 59 | a0002c0002t0001g0196 a0002c0002t0001g0197 a0002c0002t0001g0199 others(56): Show |
72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.386-4955A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747112 | |||||||
| chr5:150747146 | C | T | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-4989G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747146 | |||||||
| chr5:150747236 | C | T | 4 | a0001c0001t0001g0130 a0001c0001t0001g0131 a0001c0001t0001g0132 others(1): Show |
4 | HG02109.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-5079G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747236 | |||||||
| chr5:150747471 | C | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-5314G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747471 | |||||||
| chr5:150747635 | G | A | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.386-5478C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747635 | |||||||
| chr5:150747640 | T | C | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.386-5483A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747640 | |||||||
| chr5:150747660 | G | A | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-5503C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747660 | |||||||
| chr5:150747661 | A | G | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-5504T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747661 | |||||||
| chr5:150747925 | C | A | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.385+5554G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747925 | |||||||
| chr5:150747975 | A | G | 1 | a0001c0001t0001g0077 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.385+5504T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747975 | |||||||
| chr5:150747988 | T | A | 4 | a0002c0002t0009g0192 a0002c0002t0009g0193 a0002c0002t0009g0194 others(1): Show |
4 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+5491A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747988 | |||||||
| chr5:150748024 | T | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.385+5455A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748024 | |||||||
| chr5:150748057 | G | T | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.385+5422C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748057 | |||||||
| chr5:150748299 | G | A | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.385+5180C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748299 | |||||||
| chr5:150748359 | C | T | 1 | a0002c0002t0001g0035 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.385+5120G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748359 | |||||||
| chr5:150748385 | C | T | 2 | a0002c0002t0001g0060 a0002c0002t0001g0061 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+5094G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748385 | |||||||
| chr5:150748443 | A | G | 2 | a0002c0002t0001g0060 a0002c0002t0001g0061 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+5036T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748443 | |||||||
| chr5:150748488 | A | G | 3 | a0002c0002t0003g0007 a0002c0002t0003g0027 a0002c0002t0003g0028 |
4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+4991T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748488 | |||||||
| chr5:150748600 | T | C | 5 | a0002c0002t0001g0235 a0003c0003t0004g0025 a0003c0003t0004g0233 others(2): Show |
6 | HG00408.hp1 HG02015.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+4879A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748600 | |||||||
| chr5:150748608 | C | T | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.385+4871G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748608 | |||||||
| chr5:150748639 | G | A | 2 | a0002c0002t0009g0194 a0002c0002t0009g0195 |
2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.385+4840C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748639 | |||||||
| chr5:150748704 | G | A | 1 | a0001c0001t0001g0093 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.385+4775C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748704 | |||||||
| chr5:150748800 | G | T | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+4679C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748800 | |||||||
| chr5:150748843 | C | T | 1 | a0002c0002t0003g0034 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.385+4636G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748843 | |||||||
| chr5:150748953 | G | A | 1 | a0001c0001t0001g0129 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.385+4526C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748953 | |||||||
| chr5:150748954 | A | G | 1 | a0001c0001t0001g0129 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.385+4525T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748954 | |||||||
| chr5:150749162 | G | A | 1 | a0002c0002t0016g0241 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.385+4317C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749162 | |||||||
| chr5:150749245 | A | G | 65 | a0002c0002t0001g0196 a0002c0002t0001g0197 a0002c0002t0001g0199 others(62): Show |
79 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.385+4234T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749245 | |||||||
| chr5:150749332 | C | T | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+4147G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749332 | |||||||
| chr5:150749390 | G | C | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.385+4089C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749390 | |||||||
| chr5:150749392 | G | T | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.385+4087C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749392 | |||||||
| chr5:150749475 | C | T | 1 | a0001c0001t0001g0011 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.385+4004G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749475 | |||||||
| chr5:150749586 | C | T | 1 | a0005c0009t0001g0094 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.385+3893G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749586 | |||||||
| chr5:150749602 | G | T | 4 | a0002c0002t0005g0180 a0002c0002t0005g0182 a0002c0002t0014g0179 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+3877C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749602 | |||||||
| chr5:150749658 | AAAAT | A | 18 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(15): Show |
19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.385+3817_385+3820d others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749658 | |||||||
| chr5:150749659 | AAAT | A | 22 | a0002c0002t0001g0200 a0002c0002t0001g0214 a0002c0002t0001g0235 others(19): Show |
23 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.385+3817_385+3819d others(5): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749659 | |||||||
| chr5:150749660 | AAT | A | 46 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0196 others(43): Show |
57 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.385+3817_385+3818d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749660 | |||||||
| chr5:150749662 | T | A | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.385+3817A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749662 | |||||||
| chr5:150749672 | T | A | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+3807A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749672 | |||||||
| chr5:150749965 | AAGAC | A | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.385+3510_385+3513d others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749965 | |||||||
| chr5:150749989 | G | A | 1 | a0001c0001t0001g0171 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.385+3490C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749989 | |||||||
| chr5:150750045 | A | C | 1 | a0002c0002t0002g0021 | 2 | HG00639.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.385+3434T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750045 | |||||||
| chr5:150750232 | A | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.385+3247T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750232 | |||||||
| chr5:150750246 | C | T | 1 | a0002c0002t0001g0212 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.385+3233G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750246 | |||||||
| chr5:150750324 | G | A | 4 | a0002c0002t0009g0192 a0002c0002t0009g0193 a0002c0002t0009g0194 others(1): Show |
4 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+3155C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750324 | |||||||
| chr5:150750344 | A | T | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+3135T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750344 | |||||||
| chr5:150750414 | G | A | 54 | a0002c0002t0001g0197 a0002c0002t0001g0199 a0002c0002t0001g0200 others(51): Show |
67 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.385+3065C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750414 | |||||||
| chr5:150750479 | T | G | 1 | a0001c0001t0001g0127 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.385+3000A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750479 | |||||||
| chr5:150750522 | A | G | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+2957T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750522 | |||||||
| chr5:150750594 | G | T | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.385+2885C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750594 | |||||||
| chr5:150750721 | C | T | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0076 |
3 | HG02683.hp1 HG03239.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.385+2758G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750721 | |||||||
| chr5:150750867 | A | G | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.385+2612T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750867 | |||||||
| chr5:150751064 | T | C | 1 | a0002c0002t0002g0210 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.385+2415A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751064 | |||||||
| chr5:150751146 | T | C | 88 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(85): Show |
104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.385+2333A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751146 | |||||||
| chr5:150751172 | C | T | 4 | a0001c0001t0001g0017 a0001c0001t0001g0163 a0001c0001t0001g0164 others(1): Show |
5 | HG02129.hp1 NA18988.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+2307G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751172 | |||||||
| chr5:150751280 | G | T | 122 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0003g0242 others(119): Show |
140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.385+2199C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751280 | |||||||
| chr5:150751322 | CCTAGAGG others(10): Show |
C | 1 | a0002c0002t0017g0047 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.385+2140_385+2156d others(19): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751322 | |||||||
| chr5:150751509 | A | G | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.385+1970T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751509 | |||||||
| chr5:150751531 | G | A | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.385+1948C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751531 | |||||||
| chr5:150751754 | G | GA | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.385+1724dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751754 | |||||||
| chr5:150751834 | C | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.385+1645G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751834 | |||||||
| chr5:150752076 | G | A | 1 | a0002c0002t0005g0190 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.385+1403C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752076 | |||||||
| chr5:150752100 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.385+1379T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752100 | |||||||
| chr5:150752106 | A | G | 2 | a0002c0002t0001g0060 a0002c0002t0001g0061 |
2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+1373T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752106 | |||||||
| chr5:150752112 | G | A | 39 | a0001c0001t0001g0012 a0001c0001t0001g0013 a0001c0001t0001g0069 others(36): Show |
41 | HG00558.hp1 HG00597.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.385+1367C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752112 | |||||||
| chr5:150752247 | C | T | 1 | a0002c0002t0001g0214 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.385+1232G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752247 | |||||||
| chr5:150752263 | G | T | 2 | a0001c0001t0007g0072 a0001c0001t0007g0073 |
2 | HG01978.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.385+1216C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752263 | |||||||
| chr5:150752425 | C | T | 187 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(184): Show |
208 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(205): Show |
intron_variant | MODIFIER | c.385+1054G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752425 | |||||||
| chr5:150752445 | T | C | 1 | a0002c0002t0003g0028 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.385+1034A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752445 | |||||||
| chr5:150752495 | G | A | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+984C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752495 | |||||||
| chr5:150752584 | G | A | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+895C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752584 | |||||||
| chr5:150752598 | T | C | 1 | a0001c0001t0015g0161 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.385+881A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752598 | |||||||
| chr5:150752662 | C | T | 87 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(84): Show |
102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+817G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752662 | |||||||
| chr5:150752727 | T | C | 16 | a0001c0001t0001g0003 a0001c0001t0001g0017 a0001c0001t0001g0018 others(13): Show |
20 | HG01255.hp1 HG01433.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.385+752A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752727 | |||||||
| chr5:150752734 | T | G | 2 | a0002c0002t0001g0212 a0002c0002t0001g0213 |
2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.385+745A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752734 | |||||||
| chr5:150752786 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.385+693G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752786 | |||||||
| chr5:150752919 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385+560A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752919 | |||||||
| chr5:150752944 | G | A | 1 | a0002c0002t0003g0046 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.385+535C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752944 | |||||||
| chr5:150753092 | C | A | 2 | a0002c0002t0002g0237 a0002c0002t0002g0238 |
2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.385+387G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150753092 | |||||||
| chr5:150753161 | G | A | 2 | a0001c0001t0001g0068 a0001c0001t0001g0173 |
2 | NA18992.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.385+318C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150753161 | |||||||
| chr5:150753772 | T | A | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.207-115A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150753772 | |||||||
| chr5:150753905 | G | A | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.207-248C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150753905 | |||||||
| chr5:150754159 | C | T | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.207-502G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754159 | |||||||
| chr5:150754422 | A | G | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.207-765T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754422 | |||||||
| chr5:150754435 | C | T | 3 | a0002c0002t0001g0212 a0002c0002t0001g0213 a0002c0002t0001g0239 |
3 | HG02970.hp2 HG03098.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.207-778G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754435 | |||||||
| chr5:150754839 | C | T | 2 | a0002c0002t0009g0192 a0002c0002t0009g0193 |
2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.207-1182G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754839 | |||||||
| chr5:150754856 | A | T | 11 | a0002c0002t0005g0049 a0002c0002t0005g0050 a0002c0002t0005g0051 others(8): Show |
11 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.207-1199T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754856 | |||||||
| chr5:150754877 | T | C | 1 | a0001c0001t0001g0174 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.207-1220A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754877 | |||||||
| chr5:150754879 | C | CT | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.207-1223dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754879 | |||||||
| chr5:150754962 | CA | C | 89 | a0001c0001t0001g0070 a0002c0002t0001g0008 a0002c0002t0001g0033 others(86): Show |
105 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.207-1306delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754962 | |||||||
| chr5:150755128 | C | T | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.206+1289G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755128 | |||||||
| chr5:150755345 | T | C | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.206+1072A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755345 | |||||||
| chr5:150755406 | C | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.206+1011G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755406 | |||||||
| chr5:150755614 | A | G | 1 | a0001c0001t0001g0069 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.206+803T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755614 | |||||||
| chr5:150755622 | C | T | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.206+795G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755622 | |||||||
| chr5:150755655 | T | C | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.206+762A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755655 | |||||||
| chr5:150755665 | G | A | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.206+752C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755665 | |||||||
| chr5:150755862 | G | A | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.206+555C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755862 | |||||||
| chr5:150755935 | C | T | 16 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(13): Show |
16 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.206+482G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755935 | |||||||
| chr5:150756039 | C | CT | 7 | a0001c0001t0001g0066 a0001c0001t0001g0067 a0001c0001t0001g0068 others(4): Show |
8 | HG01081.hp1 HG01167.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.206+377dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756039 | |||||||
| chr5:150756039 | CT | C | 34 | a0001c0001t0003g0242 a0001c0005t0006g0183 a0001c0005t0006g0184 others(31): Show |
35 | HG01243.hp2 HG01891.hp1 HG01981.hp1 others(32): Show |
intron_variant | MODIFIER | c.206+377delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756039 | |||||||
| chr5:150756071 | T | C | 2 | a0002c0002t0001g0188 a0002c0002t0001g0189 |
2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.206+346A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756071 | |||||||
| chr5:150756291 | C | T | 2 | a0002c0002t0002g0209 a0002c0002t0002g0210 |
2 | NA18959.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.206+126G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756291 | |||||||
| chr5:150756338 | C | T | 83 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(80): Show |
98 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.206+79G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756338 | |||||||
| chr5:150756366 | GAGAACAG others(3): Show |
G | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.206+41_206+50delTG others(8): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756366 | |||||||
| chr5:150756368 | G | GAAC | 17 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(14): Show |
18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.206+46_206+48dupGT others(1): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756368 | |||||||
| chr5:150756616 | G | C | 1 | a0004c0006t0004g0006 | 3 | NA18983.hp2 NA18989.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.136-129C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756616 | |||||||
| chr5:150756617 | G | T | 4 | a0002c0002t0009g0192 a0002c0002t0009g0193 a0002c0002t0009g0194 others(1): Show |
4 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-130C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756617 | |||||||
| chr5:150756639 | G | GT | 217 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(214): Show |
254 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(251): Show |
intron_variant | MODIFIER | c.136-153dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756639 | |||||||
| chr5:150756639 | G | GTT | 22 | a0001c0001t0001g0066 a0002c0002t0001g0008 a0002c0002t0001g0060 others(19): Show |
24 | HG00735.hp2 HG01496.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.136-154_136-153dup others(2): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756639 | |||||||
| chr5:150756760 | T | G | 84 | a0002c0002t0001g0033 a0002c0002t0001g0035 a0002c0002t0001g0037 others(81): Show |
99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-273A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756760 | |||||||
| chr5:150756762 | G | C | 2 | a0002c0002t0016g0240 a0002c0002t0016g0241 |
2 | NA18944.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.136-275C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756762 | |||||||
| chr5:150756886 | G | A | 89 | a0002c0002t0001g0008 a0002c0002t0001g0033 a0002c0002t0001g0035 others(86): Show |
105 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.136-399C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756886 | |||||||
| chr5:150757107 | G | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.136-620C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757107 | |||||||
| chr5:150757290 | C | G | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136-803G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757290 | |||||||
| chr5:150757298 | C | T | 1 | a0001c0001t0001g0178 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.136-811G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757298 | |||||||
| chr5:150757498 | C | T | 20 | a0002c0002t0001g0060 a0002c0002t0001g0061 a0002c0002t0005g0049 others(17): Show |
20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.136-1011G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757498 | |||||||
| chr5:150757534 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.136-1047C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757534 | |||||||
| chr5:150757633 | C | T | 1 | a0002c0002t0001g0008 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.136-1146G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757633 | |||||||
| chr5:150757774 | C | T | 1 | a0002c0002t0003g0027 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.135+1085G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757774 | |||||||
| chr5:150757776 | C | T | 10 | a0002c0002t0001g0197 a0002c0002t0001g0199 a0002c0002t0001g0200 others(7): Show |
11 | HG00408.hp2 HG00558.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+1083G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757776 | |||||||
| chr5:150757810 | A | G | 3 | a0002c0002t0003g0030 a0002c0002t0003g0032 a0002c0002t0011g0031 |
3 | HG02723.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.135+1049T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757810 | |||||||
| chr5:150757887 | T | C | 122 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0003g0242 others(119): Show |
140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.135+972A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757887 | |||||||
| chr5:150757937 | C | T | 1 | a0002c0002t0011g0198 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.135+922G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757937 | |||||||
| chr5:150757967 | A | T | 122 | a0001c0001t0001g0010 a0001c0001t0001g0065 a0001c0001t0003g0242 others(119): Show |
140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.135+892T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757967 | |||||||
| chr5:150757968 | A | T | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0001g0197 |
3 | HG01243.hp2 HG02129.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.135+891T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757968 | |||||||
| chr5:150758152 | T | C | 5 | a0001c0005t0006g0183 a0001c0005t0006g0184 a0001c0005t0006g0185 others(2): Show |
5 | HG03139.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+707A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758152 | |||||||
| chr5:150758159 | C | G | 1 | a0001c0001t0019g0048 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.135+700G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758159 | |||||||
| chr5:150758267 | T | C | 4 | a0002c0002t0005g0180 a0002c0002t0005g0182 a0002c0002t0014g0179 others(1): Show |
4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+592A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758267 | |||||||
| chr5:150758278 | C | T | 5 | a0002c0002t0001g0196 a0002c0002t0009g0192 a0002c0002t0009g0193 others(2): Show |
5 | HG02647.hp2 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+581G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758278 | |||||||
| chr5:150758355 | C | T | 1 | a0001c0001t0003g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+504G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758355 | |||||||
| chr5:150758371 | G | A | 5 | a0001c0005t0006g0183 a0001c0005t0006g0184 a0001c0005t0006g0185 others(2): Show |
5 | HG03139.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+488C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758371 | |||||||
| chr5:150758475 | C | T | 91 | a0001c0005t0006g0207 a0001c0005t0006g0208 a0002c0002t0001g0008 others(88): Show |
107 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.135+384G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758475 | |||||||
| chr5:150758481 | C | T | 1 | a0002c0002t0002g0191 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.135+378G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758481 | |||||||
| chr5:150758506 | T | A | 3 | a0002c0002t0001g0188 a0002c0002t0001g0189 a0002c0002t0005g0190 |
3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.135+353A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758506 | |||||||
| chr5:150758528 | C | T | 1 | a0002c0007t0018g0029 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.135+331G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758528 | |||||||
| chr5:150758634 | C | A | 61 | a0001c0005t0006g0207 a0001c0005t0006g0208 a0002c0002t0001g0196 others(58): Show |
74 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.135+225G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758634 | |||||||
| chr5:150758685 | C | G | 3 | a0002c0002t0003g0007 a0002c0002t0003g0027 a0002c0002t0003g0028 |
4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+174G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758685 | |||||||
| chr5:150758746 | G | A | 1 | a0001c0001t0003g0242 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+113C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758746 | |||||||
| chr5:150758768 | G | A | 6 | a0002c0004t0001g0026 a0002c0004t0001g0244 a0002c0004t0008g0243 others(3): Show |
7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+91C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758768 |