Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 4690 |
| ensemblid | ENSG00000158092.7 |
| hgncid | 7664 |
| symbol | NCK1 |
| name | NCK adaptor protein 1 |
| refseq_nuc | NM_001291999.2 |
| refseq_prot | NP_001278928.1 |
| ensembl_nuc | ENST00000481752.6 |
| ensembl_prot | ENSP00000417273.1 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 136862208 |
| end | 136951606 |
| strand | + |
| ver | v1.2 |
| region | chr3:136862208-136951606 |
| region5000 | chr3:136857208-136956606 |
| regionname0 | NCK1_chr3_136862208_136951606 |
| regionname5000 | NCK1_chr3_136857208_136956606 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 377 | 220 | 59 | 41 | 71 | 11 | 36 | 51 | NCK1_chr3_136857208_136956606 | NCK1 | MAEEV others(372): Show |
chr3 | 136857208 | 136956606 |
| a0002 | 0/0 | 377 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | MAEEV others(372): Show |
chr3 | 136857208 | 136956606 |
| a0003 | 0/0 | 377 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | MAEEV others(372): Show |
chr3 | 136857208 | 136956606 |
| a0004 | 0/0 | 377 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | MAEEV others(372): Show |
chr3 | 136857208 | 136956606 |
| a0005 | 0/0 | 377 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | MAEEV others(372): Show |
chr3 | 136857208 | 136956606 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1131 | 219 | 59 | 41 | 70 | 11 | 36 | NCK1_chr3_136857208_136956606 | NCK1 | ATGGC others(1126): Show |
chr3 | 136857208 | 136956606 | ||
| a0001c0004 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ATGGC others(1126): Show |
chr3 | 136857208 | 136956606 | ||
| a0002c0002 | 0/0 | 1131 | 7 | 7 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ATGGC others(1126): Show |
chr3 | 136857208 | 136956606 | ||
| a0003c0003 | 0/0 | 1131 | 3 | 0 | 3 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ATGGC others(1126): Show |
chr3 | 136857208 | 136956606 | ||
| a0004c0006 | 0/0 | 1131 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ATGGC others(1126): Show |
chr3 | 136857208 | 136956606 | ||
| a0005c0005 | 0/0 | 1131 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ATGGC others(1126): Show |
chr3 | 136857208 | 136956606 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 4448 | 125 | 27 | 24 | 42 | 7 | 24 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4443): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0002 | 1/0 | 4451 | 52 | 15 | 11 | 14 | 3 | 8 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4446): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0003 | 0/0 | 4451 | 25 | 5 | 4 | 12 | 1 | 3 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4446): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0004 | 0/0 | 4448 | 4 | 4 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4443): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0005 | 0/0 | 4449 | 4 | 2 | 2 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4444): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0007 | 0/0 | 4451 | 2 | 2 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4446): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0009 | 0/0 | 4451 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4446): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0010 | 0/0 | 4448 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4443): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0011 | 0/0 | 4448 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4443): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0012 | 0/0 | 4448 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4443): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0013 | 0/0 | 4448 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4443): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0014 | 0/0 | 4448 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4443): Show |
chr3 | 136857208 | 136956606 |
| a0001c0001t0015 | 0/0 | 4448 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4443): Show |
chr3 | 136857208 | 136956606 |
| a0001c0004t0001 | 0/0 | 4448 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4443): Show |
chr3 | 136857208 | 136956606 |
| a0002c0002t0002 | 0/0 | 4451 | 4 | 4 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4446): Show |
chr3 | 136857208 | 136956606 |
| a0002c0002t0006 | 0/0 | 4451 | 3 | 3 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4446): Show |
chr3 | 136857208 | 136956606 |
| a0003c0003t0001 | 0/0 | 4448 | 3 | 0 | 3 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4443): Show |
chr3 | 136857208 | 136956606 |
| a0004c0006t0002 | 0/0 | 4451 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4446): Show |
chr3 | 136857208 | 136956606 |
| a0005c0005t0008 | 0/0 | 4451 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | ACCGC others(4446): Show |
chr3 | 136857208 | 136956606 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 0 | 1 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0002 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0048 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0190 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0002g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0004g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0005g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0005g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0005g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0007g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0009g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0010g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0011g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0012g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0013g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0014g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0001t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0001c0004t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0002g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0002g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0002c0002t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0003c0003t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0003c0003t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0003c0003t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0004c0006t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| a0005c0005t0008g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00099 | hp2 | a0004 | c0006 | t0002 | g0148 | EUR | GBR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0168 | EUR | GBR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | GBR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0173 | EUR | FIN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00408 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00423 | hp1 | a0001 | c0001 | t0002 | g0146 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00544 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00639 | hp2 | a0001 | c0001 | t0002 | g0165 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00738 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01070 | hp2 | a0003 | c0003 | t0001 | g0025 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01081 | hp2 | a0001 | c0001 | t0002 | g0155 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01106 | hp1 | a0001 | c0001 | t0003 | g0217 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01167 | hp1 | a0001 | c0001 | t0005 | g0188 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01169 | hp2 | a0001 | c0001 | t0005 | g0189 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0213 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0151 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01257 | hp1 | a0001 | c0001 | t0002 | g0156 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01261 | hp1 | a0003 | c0003 | t0001 | g0026 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0166 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01358 | hp1 | a0003 | c0003 | t0001 | g0024 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01358 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01433 | hp2 | a0001 | c0001 | t0003 | g0205 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01517 | hp1 | a0001 | c0001 | t0003 | g0219 | EUR | IBS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0111 | EUR | IBS | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01891 | hp1 | a0001 | c0001 | t0002 | g0194 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0147 | AMR | PEL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0206 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0185 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02135 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02280 | hp1 | a0002 | c0002 | t0002 | g0196 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0142 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02523 | hp1 | a0001 | c0004 | t0001 | g0110 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0175 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0073 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02615 | hp2 | a0001 | c0001 | t0009 | g0179 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02630 | hp1 | a0001 | c0001 | t0004 | g0018 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0067 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02683 | hp2 | a0001 | c0001 | t0010 | g0093 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0123 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0006 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02818 | hp1 | a0002 | c0002 | t0002 | g0197 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0192 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02896 | hp2 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0028 | AFR | GWD | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0176 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02965 | hp2 | a0002 | c0002 | t0002 | g0195 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02976 | hp1 | a0001 | c0001 | t0014 | g0023 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0005 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03139 | hp2 | a0002 | c0002 | t0006 | g0191 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03195 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03195 | hp2 | a0001 | c0001 | t0007 | g0005 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0224 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03486 | hp1 | a0002 | c0002 | t0006 | g0199 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03486 | hp2 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03491 | hp1 | a0001 | c0001 | t0002 | g0138 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03492 | hp1 | a0001 | c0001 | t0002 | g0140 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03516 | hp1 | a0001 | c0001 | t0004 | g0020 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0007 | AFR | ESN | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0139 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03669 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0162 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03927 | hp2 | a0001 | c0001 | t0003 | g0200 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0172 | SAS | BEB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0207 | SAS | STU | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | CHB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0212 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18954 | hp2 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18959 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18963 | hp1 | a0005 | c0005 | t0008 | g0128 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18963 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18964 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18967 | hp2 | a0001 | c0001 | t0011 | g0109 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18973 | hp1 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0220 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18987 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0153 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0004 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19012 | hp1 | a0001 | c0001 | t0003 | g0221 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0198 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19043 | hp1 | a0001 | c0001 | t0002 | g0183 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19043 | hp2 | a0001 | c0001 | t0002 | g0141 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19060 | hp1 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19065 | hp1 | a0001 | c0001 | t0013 | g0131 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0158 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19079 | hp1 | a0001 | c0001 | t0002 | g0145 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19090 | hp2 | a0001 | c0001 | t0003 | g0222 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19240 | hp1 | a0002 | c0002 | t0006 | g0193 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0059 | AFR | YRI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | ASW | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0150 | AFR | ASW | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | TSI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | TSI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0015 | EUR | TSI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20805 | hp2 | a0001 | c0001 | t0002 | g0149 | EUR | TSI | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | GIH | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20905 | hp2 | a0001 | c0001 | t0003 | g0204 | SAS | GIH | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0182 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02486 | hp1 | a0001 | c0001 | t0005 | g0180 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ACB | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | MSL | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | USA | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | USA | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | USA | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | USA | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| NA21309 | hp2 | a0002 | c0002 | t0002 | g0178 | AFR | LWK | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0048 | REF | REF | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0002 | g0190 | REF | REF | NCK1_chr3_136857208_136956606 | NCK1 | chr3 | 136857208 | 136956606 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136945634 | C | G | 1 | a0004 | 1 | HG00099.hp2 | missense_variant | MODERATE | c.278C>G | p.Ala93Gly | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 442/4451 | 278/1134 | 93/377 | chr3 | 136945634 | |||
| chr3:136945895 | C | T | 1 | a0003 | 3 | HG01070.hp2 HG01261.hp1 HG01358.hp1 |
missense_variant | MODERATE | c.539C>T | p.Ala180Val | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 703/4451 | 539/1134 | 180/377 | chr3 | 136945895 | |||
| chr3:136946128 | G | C | 1 | a0002 | 7 | HG02280.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
missense_variant | MODERATE | c.772G>C | p.Gly258Arg | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 936/4451 | 772/1134 | 258/377 | chr3 | 136946128 | |||
| chr3:136946267 | A | G | 1 | a0005 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.911A>G | p.Asp304Gly | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 1075/4451 | 911/1134 | 304/377 | chr3 | 136946267 | |||
| chr3:136946268 | T | A | 1 | a0005 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.912T>A | p.Asp304Glu | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 1076/4451 | 912/1134 | 304/377 | chr3 | 136946268 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136945611 | T | C | 1 | a0001c0004 | 1 | HG02523.hp1 | synonymous_variant | LOW | c.255T>C | p.Ser85Ser | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 419/4451 | 255/1134 | 85/377 | chr3 | 136945611 | |||
| chr3:136946079 | A | C | 1 | a0005c0005 | 1 | NA18963.hp1 | synonymous_variant | LOW | c.723A>C | p.Leu241Leu | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/4 | 887/4451 | 723/1134 | 241/377 | chr3 | 136946079 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136862230 | C | T | 1 | a0001c0001t0015 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-142C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/4 | 65772 | chr3 | 136862230 | ||||||
| chr3:136948563 | T | C | 1 | a0001c0001t0003 | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*110T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 110 | chr3 | 136948563 | ||||||
| chr3:136948826 | T | C | 1 | a0002c0002t0006 | 3 | HG03139.hp2 HG03486.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*373T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 373 | chr3 | 136948826 | ||||||
| chr3:136948883 | GGA | G | 1 | a0001c0001t0005 | 4 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*434_*435delAG | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 434 | INFO_REALIGN_3_PRIME | chr3 | 136948883 | |||||
| chr3:136949079 | A | G | 1 | a0001c0001t0004 | 4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*626A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 626 | chr3 | 136949079 | ||||||
| chr3:136949227 | A | C | 1 | a0001c0001t0001 | 1 | HG01496.hp1 | 3_prime_UTR_variant | MODIFIER | c.*774A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 774 | chr3 | 136949227 | ||||||
| chr3:136949418 | TAA | T | 10 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(7): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*966_*967delAA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 966 | chr3 | 136949418 | ||||||
| chr3:136949422 | T | G | 1 | a0005c0005t0008 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*969T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 969 | chr3 | 136949422 | ||||||
| chr3:136949570 | T | C | 1 | a0001c0001t0003 | 25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*1117T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1117 | chr3 | 136949570 | ||||||
| chr3:136949783 | T | C | 11 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(8): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*1330T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1330 | chr3 | 136949783 | ||||||
| chr3:136949840 | AT | A | 10 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(7): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
3_prime_UTR_variant | MODIFIER | c.*1395delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1395 | INFO_REALIGN_3_PRIME | chr3 | 136949840 | |||||
| chr3:136950036 | C | A | 1 | a0001c0001t0010 | 1 | HG02683.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1583C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1583 | chr3 | 136950036 | ||||||
| chr3:136950119 | A | T | 1 | a0005c0005t0008 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1666A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1666 | chr3 | 136950119 | ||||||
| chr3:136950180 | T | C | 1 | a0001c0001t0011 | 1 | NA18967.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1727T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1727 | chr3 | 136950180 | ||||||
| chr3:136950237 | C | T | 11 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0010 others(8): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
3_prime_UTR_variant | MODIFIER | c.*1784C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 1784 | chr3 | 136950237 | ||||||
| chr3:136950546 | T | A | 1 | a0005c0005t0008 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2093T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 2093 | chr3 | 136950546 | ||||||
| chr3:136950602 | A | G | 1 | a0001c0001t0014 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2149A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 2149 | chr3 | 136950602 | ||||||
| chr3:136951025 | C | T | 1 | a0001c0001t0013 | 1 | NA19065.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2572C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 2572 | chr3 | 136951025 | ||||||
| chr3:136951069 | T | C | 1 | a0001c0001t0007 | 2 | HG03139.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2616T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 2616 | chr3 | 136951069 | ||||||
| chr3:136951443 | A | T | 2 | a0001c0001t0005 a0001c0001t0009 |
5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2990A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 2990 | chr3 | 136951443 | ||||||
| chr3:136951497 | A | T | 1 | a0001c0001t0012 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3044A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 4/4 | 3044 | chr3 | 136951497 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:136862391 | C | A | 1 | a0001c0001t0001g0006 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-19+38C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862391 | |||||||
| chr3:136862395 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+42C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862395 | |||||||
| chr3:136862451 | C | T | 1 | a0001c0001t0001g0223 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-19+98C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862451 | |||||||
| chr3:136862644 | CCGCCCGT others(15): Show |
C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+294_-19+315del others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136862644 | ||||||
| chr3:136862682 | C | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+329C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862682 | |||||||
| chr3:136862760 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+407G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862760 | |||||||
| chr3:136862769 | G | A | 38 | a0001c0001t0002g0003 a0001c0001t0002g0138 a0001c0001t0002g0139 others(35): Show |
39 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(36): Show |
intron_variant | MODIFIER | c.-19+416G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862769 | |||||||
| chr3:136862780 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+427C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862780 | |||||||
| chr3:136862808 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+455C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862808 | |||||||
| chr3:136862853 | C | G | 2 | a0001c0001t0002g0173 a0001c0001t0002g0174 |
2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-19+500C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862853 | |||||||
| chr3:136862856 | T | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | NA18939.hp2 NA18955.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+503T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862856 | |||||||
| chr3:136862894 | GC | G | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+542delC | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136862894 | |||||||
| chr3:136863001 | C | T | 1 | a0001c0001t0002g0172 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-19+648C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863001 | |||||||
| chr3:136863013 | T | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+660T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863013 | |||||||
| chr3:136863016 | CCTTT | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+667_-19+670del others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136863016 | ||||||
| chr3:136863048 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-19+695C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863048 | |||||||
| chr3:136863073 | G | GTT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+723_-19+724dup others(2): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136863073 | ||||||
| chr3:136863111 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-19+758C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863111 | |||||||
| chr3:136863195 | G | T | 24 | a0001c0001t0003g0004 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-19+842G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863195 | |||||||
| chr3:136863314 | G | A | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | HG03491.hp1 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-19+961G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863314 | |||||||
| chr3:136863917 | C | T | 2 | a0001c0001t0001g0012 a0001c0001t0001g0133 |
2 | HG00099.hp1 NA18939.hp2 |
intron_variant | MODIFIER | c.-19+1564C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136863917 | |||||||
| chr3:136864029 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-19+1676A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864029 | |||||||
| chr3:136864030 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-19+1677G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864030 | |||||||
| chr3:136864080 | G | A | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-19+1727G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864080 | |||||||
| chr3:136864089 | A | G | 1 | a0001c0001t0013g0131 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-19+1736A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864089 | |||||||
| chr3:136864144 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+1791C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864144 | |||||||
| chr3:136864153 | G | C | 1 | a0001c0001t0003g0200 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19+1800G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864153 | |||||||
| chr3:136864240 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19+1887C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864240 | |||||||
| chr3:136864318 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+1965G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864318 | |||||||
| chr3:136864362 | G | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 |
3 | HG01256.hp1 HG02738.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-19+2009G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864362 | |||||||
| chr3:136864423 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+2070G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864423 | |||||||
| chr3:136864484 | T | TCA | 102 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(99): Show |
107 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(104): Show |
intron_variant | MODIFIER | c.-19+2142_-19+2143d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136864484 | ||||||
| chr3:136864496 | A | ACAC | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
4 | HG01243.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+2143_-19+2144i others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864496 | |||||||
| chr3:136864497 | A | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-19+2144A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864497 | |||||||
| chr3:136864499 | A | C | 4 | a0001c0001t0001g0127 a0001c0001t0001g0129 a0001c0001t0001g0130 others(1): Show |
4 | HG00408.hp1 NA18955.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+2146A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864499 | |||||||
| chr3:136864573 | A | T | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+2220A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864573 | |||||||
| chr3:136864625 | A | G | 1 | a0002c0002t0006g0199 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-19+2272A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864625 | |||||||
| chr3:136864668 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-19+2315C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864668 | |||||||
| chr3:136864708 | A | T | 14 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(11): Show |
14 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+2355A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864708 | |||||||
| chr3:136864752 | T | A | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+2399T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864752 | |||||||
| chr3:136864761 | C | CT | 6 | a0001c0001t0002g0170 a0001c0001t0002g0171 a0001c0001t0003g0220 others(3): Show |
6 | NA18963.hp2 NA18964.hp2 NA18984.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+2426dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136864761 | ||||||
| chr3:136864761 | CT | C | 6 | a0001c0001t0001g0027 a0001c0001t0001g0045 a0001c0001t0002g0141 others(3): Show |
7 | HG01243.hp2 HG02280.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+2426delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136864761 | ||||||
| chr3:136864761 | CTT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-19+2425_-19+2426d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136864761 | ||||||
| chr3:136864768 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+2415T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864768 | |||||||
| chr3:136864845 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+2492C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864845 | |||||||
| chr3:136864903 | G | A | 1 | a0001c0001t0002g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-19+2550G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864903 | |||||||
| chr3:136864942 | A | G | 1 | a0001c0001t0003g0219 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-19+2589A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864942 | |||||||
| chr3:136864944 | A | T | 3 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 |
3 | HG01070.hp2 HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-19+2591A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864944 | |||||||
| chr3:136864981 | C | T | 1 | a0001c0001t0001g0125 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-19+2628C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136864981 | |||||||
| chr3:136865039 | A | G | 3 | a0002c0002t0002g0195 a0002c0002t0002g0196 a0002c0002t0002g0197 |
3 | HG02280.hp1 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19+2686A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865039 | |||||||
| chr3:136865114 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-19+2761C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865114 | |||||||
| chr3:136865192 | G | A | 1 | a0001c0001t0001g0134 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-19+2839G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865192 | |||||||
| chr3:136865319 | A | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+2966A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865319 | |||||||
| chr3:136865368 | C | T | 1 | a0001c0001t0002g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+3015C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865368 | |||||||
| chr3:136865374 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+3021C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865374 | |||||||
| chr3:136865378 | G | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-19+3025G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865378 | |||||||
| chr3:136865391 | C | A | 2 | a0001c0001t0001g0029 a0001c0001t0001g0030 |
2 | HG02523.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.-19+3038C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865391 | |||||||
| chr3:136865482 | G | T | 1 | a0001c0001t0001g0124 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-19+3129G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865482 | |||||||
| chr3:136865619 | A | G | 1 | a0001c0001t0014g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-19+3266A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865619 | |||||||
| chr3:136865725 | T | C | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+3372T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865725 | |||||||
| chr3:136865778 | A | G | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0132 |
3 | HG01433.hp1 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-19+3425A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865778 | |||||||
| chr3:136865930 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-19+3577T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865930 | |||||||
| chr3:136865975 | C | A | 2 | a0001c0001t0001g0046 a0001c0001t0001g0047 |
2 | NA18939.hp1 NA18969.hp1 |
intron_variant | MODIFIER | c.-19+3622C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136865975 | |||||||
| chr3:136866097 | C | G | 1 | a0002c0002t0006g0193 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-19+3744C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136866097 | |||||||
| chr3:136866287 | A | G | 1 | a0001c0001t0002g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+3934A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136866287 | |||||||
| chr3:136866312 | C | CT | 26 | a0001c0001t0001g0041 a0001c0001t0003g0004 a0001c0001t0003g0200 others(23): Show |
28 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(25): Show |
intron_variant | MODIFIER | c.-19+3972dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136866312 | ||||||
| chr3:136866736 | TC | T | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | NA18952.hp1 NA18967.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-19+4385delC | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136866736 | ||||||
| chr3:136866861 | C | T | 3 | a0001c0001t0001g0011 a0001c0001t0001g0120 a0001c0001t0001g0121 |
3 | NA18955.hp1 NA18994.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-19+4508C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136866861 | |||||||
| chr3:136866932 | AT | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+4589delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136866932 | ||||||
| chr3:136866989 | C | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+4636C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136866989 | |||||||
| chr3:136867046 | GCTTTTCT others(14): Show |
G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0049 a0001c0001t0001g0127 |
3 | HG03195.hp1 HG03491.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-19+4698_-19+4718d others(23): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | ||||||
| chr3:136867046 | GCTTTTCT others(18): Show |
G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0029 others(10): Show |
13 | HG00609.hp1 HG01891.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+4698_-19+4722d others(27): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | ||||||
| chr3:136867046 | GCTTTTCT others(22): Show |
G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0056 others(5): Show |
8 | HG00140.hp2 HG01070.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+4698_-19+4726d others(31): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | ||||||
| chr3:136867046 | GCTTTTCT others(26): Show |
G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG01361.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-19+4698_-19+4730d others(35): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | ||||||
| chr3:136867046 | GCTTTTCT others(30): Show |
G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0034 others(1): Show |
4 | HG00544.hp1 HG01256.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+4698_-19+4734d others(39): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | ||||||
| chr3:136867046 | GCTTTTCT others(34): Show |
G | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-19+4698_-19+4738d others(43): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867046 | ||||||
| chr3:136867049 | T | TG | 16 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0047 others(13): Show |
16 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+4696_-19+4697i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867049 | |||||||
| chr3:136867050 | T | C | 16 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0047 others(13): Show |
16 | HG00621.hp1 HG01106.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+4697T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867050 | |||||||
| chr3:136867050 | T | G | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(83): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-19+4697T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867050 | |||||||
| chr3:136867051 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(83): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-19+4698T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867051 | |||||||
| chr3:136867052 | C | T | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(83): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-19+4699C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867052 | |||||||
| chr3:136867053 | T | C | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(83): Show |
91 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.-19+4700T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867053 | |||||||
| chr3:136867071 | T | G | 3 | a0001c0001t0001g0031 a0001c0001t0001g0049 a0001c0001t0001g0127 |
3 | HG03195.hp1 HG03491.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-19+4718T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867071 | |||||||
| chr3:136867073 | T | TC | 3 | a0001c0001t0001g0031 a0001c0001t0001g0049 a0001c0001t0001g0127 |
3 | HG03195.hp1 HG03491.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.-19+4720_-19+4721i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867073 | |||||||
| chr3:136867075 | T | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0029 others(10): Show |
13 | HG00609.hp1 HG01891.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+4722T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867075 | |||||||
| chr3:136867077 | T | TC | 13 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0029 others(10): Show |
13 | HG00609.hp1 HG01891.hp2 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+4724_-19+4725i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867077 | |||||||
| chr3:136867077 | TTTCTTTC others(57): Show |
T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+4728_-19+4791d others(66): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867077 | ||||||
| chr3:136867079 | T | G | 8 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0056 others(5): Show |
8 | HG00140.hp2 HG01070.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+4726T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867079 | |||||||
| chr3:136867081 | T | TC | 8 | a0001c0001t0001g0015 a0001c0001t0001g0038 a0001c0001t0001g0056 others(5): Show |
8 | HG00140.hp2 HG01070.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+4728_-19+4729i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867081 | |||||||
| chr3:136867083 | T | G | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG01361.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-19+4730T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867083 | |||||||
| chr3:136867085 | T | TC | 3 | a0001c0001t0001g0058 a0001c0001t0001g0059 a0001c0001t0001g0060 |
3 | HG01361.hp2 NA19240.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-19+4732_-19+4733i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867085 | |||||||
| chr3:136867085 | TTTCTTTC others(41): Show |
T | 1 | a0002c0002t0002g0178 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+4736_-19+4783d others(50): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867085 | ||||||
| chr3:136867087 | T | G | 4 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0034 others(1): Show |
4 | HG00544.hp1 HG01256.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+4734T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867087 | |||||||
| chr3:136867088 | CTTTCTTT others(25): Show |
C | 1 | a0001c0001t0002g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+4748_-19+4779d others(34): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867088 | ||||||
| chr3:136867089 | T | TC | 4 | a0001c0001t0001g0016 a0001c0001t0001g0033 a0001c0001t0001g0034 others(1): Show |
4 | HG00544.hp1 HG01256.hp1 HG02015.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+4736_-19+4737i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867089 | |||||||
| chr3:136867089 | TTTCTTTC others(37): Show |
T | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+4740_-19+4783d others(46): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867089 | ||||||
| chr3:136867089 | TTTCTTTC others(41): Show |
T | 2 | a0001c0001t0003g0209 a0001c0001t0003g0218 |
2 | HG00544.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.-19+4740_-19+4787d others(50): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867089 | ||||||
| chr3:136867091 | T | G | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-19+4738T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867091 | |||||||
| chr3:136867092 | CTTTCTTT others(21): Show |
C | 3 | a0001c0001t0002g0150 a0001c0001t0005g0188 a0001c0001t0005g0189 |
3 | HG01167.hp1 HG01169.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-19+4752_-19+4779d others(30): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867092 | ||||||
| chr3:136867093 | TTTCTTTC others(33): Show |
T | 1 | a0002c0002t0006g0193 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-19+4744_-19+4783d others(42): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867093 | ||||||
| chr3:136867093 | TTTCTTTC others(37): Show |
T | 5 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0069 others(2): Show |
5 | HG02965.hp2 HG04115.hp1 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4744_-19+4787d others(46): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867093 | ||||||
| chr3:136867093 | TTTCTTTC others(49): Show |
T | 2 | a0001c0001t0001g0062 a0001c0001t0001g0121 |
2 | NA18994.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-19+4744_-19+4799d others(58): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867093 | ||||||
| chr3:136867096 | CTTTCTTT others(17): Show |
C | 1 | a0001c0001t0002g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+4756_-19+4779d others(26): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867096 | ||||||
| chr3:136867097 | TTTCTTTC others(29): Show |
T | 7 | a0001c0001t0001g0087 a0001c0001t0001g0096 a0001c0001t0001g0103 others(4): Show |
7 | HG00099.hp1 HG01496.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+4748_-19+4783d others(38): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867097 | ||||||
| chr3:136867097 | TTTCTTTC others(33): Show |
T | 11 | a0001c0001t0001g0070 a0001c0001t0001g0072 a0001c0001t0001g0092 others(8): Show |
11 | HG00621.hp1 HG01433.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+4748_-19+4787d others(42): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867097 | ||||||
| chr3:136867097 | TTTCTTTC others(37): Show |
T | 2 | a0001c0001t0001g0002 a0001c0001t0007g0005 |
3 | HG01074.hp1 HG01346.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+4748_-19+4791d others(46): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867097 | ||||||
| chr3:136867100 | CTTTCTTT others(13): Show |
C | 3 | a0001c0001t0002g0143 a0001c0001t0002g0164 a0001c0001t0005g0198 |
3 | HG03654.hp1 HG03669.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-19+4760_-19+4779d others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867100 | ||||||
| chr3:136867101 | T | C | 1 | a0001c0001t0001g0039 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.-19+4748T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867101 | |||||||
| chr3:136867101 | TTTCTTTC others(25): Show |
T | 12 | a0001c0001t0001g0010 a0001c0001t0001g0091 a0001c0001t0001g0098 others(9): Show |
12 | HG00140.hp1 HG01106.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+4752_-19+4783d others(34): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867101 | ||||||
| chr3:136867101 | TTTCTTTC others(29): Show |
T | 16 | a0001c0001t0001g0116 a0001c0001t0001g0223 a0001c0001t0002g0138 others(13): Show |
16 | HG00408.hp2 HG01070.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+4752_-19+4787d others(38): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867101 | ||||||
| chr3:136867101 | TTTCTTTC others(33): Show |
T | 14 | a0001c0001t0001g0002 a0001c0001t0001g0022 a0001c0001t0001g0042 others(11): Show |
14 | HG01243.hp2 HG01257.hp2 HG02976.hp2 others(11): Show |
intron_variant | MODIFIER | c.-19+4752_-19+4791d others(42): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867101 | ||||||
| chr3:136867104 | CTTTCTTT others(9): Show |
C | 8 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0040 others(5): Show |
8 | HG02129.hp1 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+4764_-19+4779d others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867104 | ||||||
| chr3:136867105 | TTTCTTTC others(21): Show |
T | 10 | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0021 others(7): Show |
10 | HG00408.hp1 HG01167.hp2 HG01346.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+4756_-19+4783d others(30): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867105 | ||||||
| chr3:136867105 | TTTCTTTC others(25): Show |
T | 16 | a0001c0001t0001g0001 a0001c0001t0001g0043 a0001c0001t0001g0099 others(13): Show |
17 | HG00280.hp1 HG00738.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19+4756_-19+4787d others(34): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867105 | ||||||
| chr3:136867105 | TTTCTTTC others(29): Show |
T | 12 | a0001c0001t0001g0044 a0001c0001t0001g0065 a0001c0001t0001g0078 others(9): Show |
12 | HG01099.hp2 HG02109.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-19+4756_-19+4791d others(38): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867105 | ||||||
| chr3:136867105 | TTTCTTTC others(33): Show |
T | 1 | a0001c0001t0002g0003 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-19+4756_-19+4795d others(42): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867105 | ||||||
| chr3:136867105 | TTTCTTTC others(37): Show |
T | 2 | a0001c0001t0001g0011 a0001c0001t0001g0120 |
2 | NA18955.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.-19+4756_-19+4799d others(46): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867105 | ||||||
| chr3:136867108 | CTTTCTTT others(5): Show |
C | 2 | a0001c0001t0001g0132 a0001c0001t0013g0131 |
2 | HG01433.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.-19+4767_-19+4778d others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867108 | ||||||
| chr3:136867109 | TTTCTTTC others(17): Show |
T | 10 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0085 others(7): Show |
10 | HG00639.hp1 HG01109.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+4760_-19+4783d others(26): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867109 | ||||||
| chr3:136867109 | TTTCTTTC others(21): Show |
T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0067 a0001c0001t0001g0105 others(10): Show |
13 | HG00609.hp2 HG01106.hp1 HG01361.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+4760_-19+4787d others(30): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867109 | ||||||
| chr3:136867109 | TTTCTTTC others(25): Show |
T | 8 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0066 others(5): Show |
8 | HG00741.hp1 HG01109.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+4760_-19+4791d others(34): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867109 | ||||||
| chr3:136867109 | TTTCTTTC others(29): Show |
T | 2 | a0001c0001t0003g0216 a0002c0002t0002g0197 |
2 | HG02818.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-19+4760_-19+4795d others(38): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867109 | ||||||
| chr3:136867112 | CTTTCTTT others(10): Show |
C | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19+4762_-19+4778d others(19): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867112 | ||||||
| chr3:136867113 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-19+4760T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867113 | |||||||
| chr3:136867113 | TTTCTTTG others(13): Show |
T | 5 | a0001c0001t0001g0081 a0001c0001t0001g0101 a0001c0001t0001g0113 others(2): Show |
5 | HG02965.hp1 HG03139.hp2 NA18612.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4764_-19+4783d others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867113 | ||||||
| chr3:136867113 | TTTCTTTG others(17): Show |
T | 6 | a0001c0001t0001g0001 a0001c0001t0001g0019 a0001c0001t0003g0206 others(3): Show |
6 | HG00099.hp2 HG00280.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+4764_-19+4787d others(26): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867113 | ||||||
| chr3:136867113 | TTTCTTTG others(21): Show |
T | 4 | a0001c0001t0001g0027 a0001c0001t0002g0165 a0001c0001t0002g0182 others(1): Show |
4 | HG00639.hp2 HG02109.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+4764_-19+4791d others(30): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867113 | ||||||
| chr3:136867115 | TCTTTGTT others(10): Show |
T | 1 | a0001c0001t0001g0094 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-19+4766_-19+4782d others(19): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867115 | ||||||
| chr3:136867115 | TCTTTGTT others(14): Show |
T | 1 | a0001c0001t0002g0151 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-19+4766_-19+4786d others(23): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867115 | ||||||
| chr3:136867117 | TTTGTTTC others(9): Show |
T | 2 | a0001c0001t0001g0114 a0001c0001t0001g0119 |
2 | HG01099.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.-19+4767_-19+4782d others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867117 | ||||||
| chr3:136867117 | TTTGTTTC others(13): Show |
T | 1 | a0001c0001t0003g0213 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-19+4767_-19+4786d others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867117 | ||||||
| chr3:136867117 | TTTGTTTC others(17): Show |
T | 5 | a0001c0001t0001g0077 a0001c0001t0002g0146 a0001c0001t0002g0169 others(2): Show |
5 | HG00423.hp1 HG00738.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+4767_-19+4790d others(26): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867117 | ||||||
| chr3:136867120 | G | C | 33 | a0001c0001t0001g0006 a0001c0001t0001g0014 a0001c0001t0001g0015 others(30): Show |
33 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.-19+4767G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867120 | |||||||
| chr3:136867121 | T | C | 6 | a0001c0001t0001g0037 a0001c0001t0001g0039 a0001c0001t0001g0040 others(3): Show |
6 | HG02486.hp1 HG02615.hp2 NA18906.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+4768T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867121 | |||||||
| chr3:136867125 | T | C | 12 | a0001c0001t0001g0006 a0001c0001t0001g0031 a0001c0001t0001g0037 others(9): Show |
12 | HG01433.hp1 HG02486.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+4772T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867125 | |||||||
| chr3:136867125 | TTTCTTTC others(13): Show |
T | 1 | a0001c0001t0002g0144 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-19+4776_-19+4795d others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867125 | ||||||
| chr3:136867129 | T | C | 20 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(17): Show |
20 | HG00609.hp1 HG01433.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.-19+4776T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867129 | |||||||
| chr3:136867178 | TTC | T | 127 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(124): Show |
132 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.-19+4827_-19+4828d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867178 | ||||||
| chr3:136867181 | T | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0056 others(7): Show |
11 | HG00423.hp1 HG01256.hp1 HG03710.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+4828T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867181 | |||||||
| chr3:136867183 | TC | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0056 others(2): Show |
5 | HG01256.hp1 HG03710.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4831delC | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867183 | |||||||
| chr3:136867185 | TTTC | T | 62 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(59): Show |
62 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(59): Show |
intron_variant | MODIFIER | c.-19+4835_-19+4837d others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867185 | ||||||
| chr3:136867187 | T | C | 5 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0056 others(2): Show |
5 | HG01256.hp1 HG03710.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4834T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867187 | |||||||
| chr3:136867188 | C | T | 5 | a0001c0001t0001g0016 a0001c0001t0001g0050 a0001c0001t0001g0056 others(2): Show |
5 | HG01256.hp1 HG03710.hp1 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+4835C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867188 | |||||||
| chr3:136867202 | CCCTT | C | 141 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(138): Show |
146 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(143): Show |
intron_variant | MODIFIER | c.-19+4868_-19+4871d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867202 | ||||||
| chr3:136867253 | G | GTC | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): Show |
156 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(153): Show |
intron_variant | MODIFIER | c.-19+4912_-19+4913d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867253 | ||||||
| chr3:136867253 | G | GTCTC | 2 | a0001c0001t0001g0051 a0001c0001t0001g0123 |
2 | HG01891.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.-19+4910_-19+4913d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867253 | ||||||
| chr3:136867305 | C | G | 1 | a0001c0001t0001g0031 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19+4952C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867305 | |||||||
| chr3:136867312 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-19+4959T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867312 | |||||||
| chr3:136867405 | A | AT | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(9): Show |
13 | HG01257.hp2 HG02055.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+5073dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867405 | ||||||
| chr3:136867405 | A | ATT | 97 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(94): Show |
102 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(99): Show |
intron_variant | MODIFIER | c.-19+5072_-19+5073d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867405 | ||||||
| chr3:136867405 | A | ATTT | 25 | a0001c0001t0001g0008 a0001c0001t0001g0013 a0001c0001t0001g0029 others(22): Show |
25 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(22): Show |
intron_variant | MODIFIER | c.-19+5071_-19+5073d others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867405 | ||||||
| chr3:136867405 | A | ATTTT | 5 | a0001c0001t0001g0006 a0001c0001t0001g0030 a0001c0001t0001g0038 others(2): Show |
5 | HG01261.hp1 HG02738.hp2 NA18968.hp1 others(2): Show |
intron_variant | MODIFIER | c.-19+5070_-19+5073d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867405 | ||||||
| chr3:136867664 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-19+5311C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867664 | |||||||
| chr3:136867776 | G | A | 67 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(64): Show |
67 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(64): Show |
intron_variant | MODIFIER | c.-19+5423G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867776 | |||||||
| chr3:136867865 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-19+5512G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136867865 | |||||||
| chr3:136867921 | AT | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+5581delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136867921 | ||||||
| chr3:136868011 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+5658G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868011 | |||||||
| chr3:136868056 | C | T | 1 | a0001c0001t0001g0081 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-19+5703C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868056 | |||||||
| chr3:136868213 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.-19+5860G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868213 | |||||||
| chr3:136868275 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(156): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-19+5922A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868275 | |||||||
| chr3:136868350 | C | T | 1 | a0001c0001t0001g0006 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-19+5997C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868350 | |||||||
| chr3:136868481 | C | T | 1 | a0001c0001t0001g0119 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-19+6128C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868481 | |||||||
| chr3:136868592 | T | G | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+6239T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136868592 | |||||||
| chr3:136869082 | A | T | 13 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(10): Show |
13 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+6729A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136869082 | |||||||
| chr3:136869321 | C | T | 3 | a0001c0001t0001g0116 a0001c0001t0002g0192 a0001c0001t0002g0194 |
3 | HG01891.hp1 HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-19+6968C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136869321 | |||||||
| chr3:136869664 | A | G | 3 | a0002c0002t0002g0195 a0002c0002t0002g0196 a0002c0002t0002g0197 |
3 | HG02280.hp1 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19+7311A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136869664 | |||||||
| chr3:136869675 | C | G | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 |
3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+7322C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136869675 | |||||||
| chr3:136870014 | G | A | 2 | a0001c0001t0001g0086 a0001c0001t0001g0087 |
2 | HG03831.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.-19+7661G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870014 | |||||||
| chr3:136870028 | G | GT | 7 | a0001c0001t0002g0143 a0001c0001t0002g0168 a0001c0001t0002g0169 others(4): Show |
7 | HG00140.hp1 HG01106.hp1 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+7697dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870028 | ||||||
| chr3:136870028 | G | GTT | 17 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0016 others(14): Show |
17 | HG00639.hp1 HG01169.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.-19+7696_-19+7697d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870028 | ||||||
| chr3:136870028 | G | GTTT | 85 | a0001c0001t0001g0010 a0001c0001t0001g0012 a0001c0001t0001g0014 others(82): Show |
85 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.-19+7695_-19+7697d others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870028 | ||||||
| chr3:136870028 | G | GTTTT | 17 | a0001c0001t0001g0006 a0001c0001t0001g0011 a0001c0001t0001g0013 others(14): Show |
17 | HG01070.hp2 HG01106.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19+7694_-19+7697d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870028 | ||||||
| chr3:136870028 | GT | G | 7 | a0001c0001t0002g0142 a0001c0001t0002g0149 a0001c0001t0002g0173 others(4): Show |
8 | HG00099.hp2 HG00280.hp1 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+7697delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870028 | ||||||
| chr3:136870044 | TTTTTTTA | T | 13 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0062 others(10): Show |
18 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19+7692_-19+7698d others(9): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870044 | |||||||
| chr3:136870050 | T | A | 1 | a0002c0002t0002g0195 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-19+7697T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870050 | |||||||
| chr3:136870051 | A | T | 120 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(117): Show |
120 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.-19+7698A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870051 | |||||||
| chr3:136870084 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-19+7731T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870084 | |||||||
| chr3:136870341 | C | CA | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+8001dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870341 | ||||||
| chr3:136870360 | CCTTTT | C | 17 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(14): Show |
17 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19+8011_-19+8015d others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870360 | ||||||
| chr3:136870478 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+8125C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870478 | |||||||
| chr3:136870511 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-19+8158G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870511 | |||||||
| chr3:136870687 | TA | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-19+8354delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870687 | ||||||
| chr3:136870687 | TAA | T | 6 | a0001c0001t0001g0013 a0001c0001t0001g0031 a0001c0001t0001g0051 others(3): Show |
6 | HG01257.hp2 HG01891.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+8353_-19+8354d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870687 | ||||||
| chr3:136870687 | TAAAAAAA others(4): Show |
T | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+8344_-19+8354d others(13): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136870687 | ||||||
| chr3:136870707 | A | T | 29 | a0001c0001t0002g0003 a0001c0001t0002g0144 a0001c0001t0002g0145 others(26): Show |
30 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(27): Show |
intron_variant | MODIFIER | c.-19+8354A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870707 | |||||||
| chr3:136870824 | G | C | 1 | a0001c0001t0010g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-19+8471G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136870824 | |||||||
| chr3:136871063 | T | G | 7 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+8710T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871063 | |||||||
| chr3:136871092 | A | AT | 6 | a0001c0001t0003g0202 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01243.hp1 HG02897.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+8748dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136871092 | ||||||
| chr3:136871223 | C | T | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19+8870C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871223 | |||||||
| chr3:136871282 | C | T | 1 | a0001c0001t0001g0032 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-19+8929C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871282 | |||||||
| chr3:136871304 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+8951G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871304 | |||||||
| chr3:136871354 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+9001C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871354 | |||||||
| chr3:136871409 | A | G | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-19+9056A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871409 | |||||||
| chr3:136871460 | C | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-19+9107C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871460 | |||||||
| chr3:136871569 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+9216C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871569 | |||||||
| chr3:136871628 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-19+9275C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871628 | |||||||
| chr3:136871714 | C | T | 1 | a0001c0001t0001g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19+9361C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871714 | |||||||
| chr3:136871735 | G | A | 1 | a0001c0001t0002g0172 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-19+9382G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871735 | |||||||
| chr3:136871751 | G | A | 4 | a0001c0001t0002g0144 a0001c0001t0002g0151 a0001c0001t0002g0152 others(1): Show |
4 | HG00099.hp2 HG01074.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+9398G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871751 | |||||||
| chr3:136871823 | C | T | 7 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+9470C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871823 | |||||||
| chr3:136871882 | T | C | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-19+9529T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136871882 | |||||||
| chr3:136872018 | G | T | 5 | a0001c0001t0002g0003 a0001c0001t0002g0145 a0001c0001t0002g0146 others(2): Show |
6 | HG00423.hp1 NA18963.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+9665G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872018 | |||||||
| chr3:136872266 | G | A | 1 | a0001c0001t0002g0192 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-19+9913G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872266 | |||||||
| chr3:136872306 | C | A | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+9953C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872306 | |||||||
| chr3:136872449 | A | C | 1 | a0001c0001t0001g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-19+10096A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872449 | |||||||
| chr3:136872673 | G | A | 7 | a0002c0002t0002g0178 a0002c0002t0002g0195 a0002c0002t0002g0196 others(4): Show |
7 | HG02280.hp1 HG02818.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+10320G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872673 | |||||||
| chr3:136872741 | A | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+10388A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872741 | |||||||
| chr3:136872780 | C | T | 1 | a0001c0001t0004g0020 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+10427C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136872780 | |||||||
| chr3:136873345 | A | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+10992A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136873345 | |||||||
| chr3:136873375 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+11022G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136873375 | |||||||
| chr3:136873960 | T | C | 1 | a0001c0001t0001g0052 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-19+11607T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136873960 | |||||||
| chr3:136873990 | A | G | 2 | a0001c0001t0001g0019 a0001c0001t0014g0023 |
2 | HG01496.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-19+11637A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136873990 | |||||||
| chr3:136874057 | GTGATAGT others(11): Show |
G | 5 | a0001c0001t0002g0003 a0001c0001t0002g0145 a0001c0001t0002g0146 others(2): Show |
6 | HG00423.hp1 NA18963.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+11705_-19+1172 others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874057 | |||||||
| chr3:136874074 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-19+11721T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874074 | |||||||
| chr3:136874077 | G | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0145 a0001c0001t0002g0146 others(2): Show |
6 | HG00423.hp1 NA18963.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.-19+11724G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874077 | |||||||
| chr3:136874114 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+11761A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874114 | |||||||
| chr3:136874251 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 |
3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+11898C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874251 | |||||||
| chr3:136874290 | C | G | 1 | a0001c0001t0001g0044 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-19+11937C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874290 | |||||||
| chr3:136874402 | AGTCCTGA others(6): Show |
A | 2 | a0001c0001t0001g0069 a0001c0001t0001g0070 |
2 | HG04115.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-19+12052_-19+1206 others(17): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136874402 | ||||||
| chr3:136874422 | C | A | 8 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0003g0202 others(5): Show |
8 | HG01243.hp1 HG02897.hp1 HG03486.hp2 others(5): Show |
intron_variant | MODIFIER | c.-19+12069C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874422 | |||||||
| chr3:136874475 | C | T | 2 | a0001c0001t0002g0192 a0001c0001t0002g0194 |
2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-19+12122C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874475 | |||||||
| chr3:136874606 | A | G | 1 | a0002c0002t0006g0191 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-19+12253A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874606 | |||||||
| chr3:136874809 | CTT | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-19+12462_-19+1246 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136874809 | ||||||
| chr3:136874825 | T | C | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-19+12472T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874825 | |||||||
| chr3:136874942 | G | C | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+12589G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136874942 | |||||||
| chr3:136875505 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+13152A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136875505 | |||||||
| chr3:136875668 | C | T | 1 | a0001c0001t0002g0144 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-19+13315C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136875668 | |||||||
| chr3:136875798 | T | G | 1 | a0001c0001t0001g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-19+13445T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136875798 | |||||||
| chr3:136876087 | G | A | 3 | a0001c0001t0001g0038 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | NA18952.hp1 NA18967.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.-19+13734G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876087 | |||||||
| chr3:136876123 | A | G | 1 | a0001c0001t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+13770A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876123 | |||||||
| chr3:136876126 | C | G | 1 | a0001c0001t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-19+13773C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876126 | |||||||
| chr3:136876177 | A | C | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+13824A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876177 | |||||||
| chr3:136876381 | G | A | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
4 | HG01243.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+14028G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876381 | |||||||
| chr3:136876513 | C | G | 1 | a0001c0001t0002g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+14160C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876513 | |||||||
| chr3:136876540 | C | T | 1 | a0002c0002t0002g0197 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-19+14187C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876540 | |||||||
| chr3:136876768 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+14415G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876768 | |||||||
| chr3:136876786 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+14433G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876786 | |||||||
| chr3:136876909 | T | A | 1 | a0001c0001t0001g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19+14556T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136876909 | |||||||
| chr3:136877157 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-19+14804G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877157 | |||||||
| chr3:136877226 | T | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 |
3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+14873T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877226 | |||||||
| chr3:136877269 | A | G | 1 | a0001c0001t0003g0211 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19+14916A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877269 | |||||||
| chr3:136877280 | C | A | 1 | a0001c0001t0001g0094 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-19+14927C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877280 | |||||||
| chr3:136877693 | A | G | 1 | a0001c0001t0011g0109 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-19+15340A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877693 | |||||||
| chr3:136877832 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-19+15479G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136877832 | |||||||
| chr3:136878129 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 |
3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-19+15776C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878129 | |||||||
| chr3:136878131 | G | A | 3 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 |
3 | HG00544.hp1 HG00621.hp2 HG02015.hp2 |
intron_variant | MODIFIER | c.-19+15778G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878131 | |||||||
| chr3:136878278 | A | G | 124 | a0001c0001t0001g0006 a0001c0001t0001g0008 a0001c0001t0001g0009 others(121): Show |
124 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(121): Show |
intron_variant | MODIFIER | c.-19+15925A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878278 | |||||||
| chr3:136878702 | TA | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+16352delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136878702 | ||||||
| chr3:136878707 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+16354C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878707 | |||||||
| chr3:136878710 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+16357T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878710 | |||||||
| chr3:136878711 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+16358T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878711 | |||||||
| chr3:136878712 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+16359T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878712 | |||||||
| chr3:136878713 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+16360T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878713 | |||||||
| chr3:136878714 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+16361T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878714 | |||||||
| chr3:136878716 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+16363T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878716 | |||||||
| chr3:136878847 | A | G | 4 | a0002c0002t0002g0178 a0002c0002t0006g0191 a0002c0002t0006g0193 others(1): Show |
4 | HG03139.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+16494A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878847 | |||||||
| chr3:136878848 | A | C | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(1): Show |
4 | HG02300.hp2 NA18939.hp2 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+16495A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136878848 | |||||||
| chr3:136879081 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-19+16728A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136879081 | |||||||
| chr3:136879131 | C | CA | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-19+16787dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136879131 | ||||||
| chr3:136879133 | A | AC | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+16780_-19+1678 others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136879133 | |||||||
| chr3:136879586 | A | G | 1 | a0001c0001t0001g0115 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-19+17233A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136879586 | |||||||
| chr3:136879810 | G | A | 1 | a0001c0001t0002g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-19+17457G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136879810 | |||||||
| chr3:136879821 | A | T | 1 | a0001c0001t0001g0105 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-19+17468A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136879821 | |||||||
| chr3:136879864 | G | GATAGCAT others(64): Show |
1 | a0001c0001t0001g0021 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-19+17513_-19+1758 others(75): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136879864 | ||||||
| chr3:136879989 | T | TAAAAAAA others(3): Show |
119 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(116): Show |
124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.-19+17640_-19+1764 others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136879989 | ||||||
| chr3:136879989 | T | TAAAAAAA others(4): Show |
11 | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0051 others(8): Show |
11 | HG01261.hp1 HG01358.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+17639_-19+1764 others(15): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136879989 | ||||||
| chr3:136879989 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-19+17638_-19+1764 others(16): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136879989 | ||||||
| chr3:136880003 | G | T | 1 | a0001c0001t0001g0090 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-19+17650G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880003 | |||||||
| chr3:136880006 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+17653T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880006 | |||||||
| chr3:136880017 | G | T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+17664G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880017 | |||||||
| chr3:136880181 | A | G | 6 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 others(3): Show |
6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.-19+17828A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880181 | |||||||
| chr3:136880210 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+17857G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880210 | |||||||
| chr3:136880237 | A | G | 10 | a0001c0001t0003g0004 a0001c0001t0003g0201 a0001c0001t0003g0203 others(7): Show |
11 | HG00544.hp2 HG02135.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+17884A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880237 | |||||||
| chr3:136880321 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+17968G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880321 | |||||||
| chr3:136880321 | G | T | 1 | a0001c0001t0001g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-19+17968G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880321 | |||||||
| chr3:136880370 | C | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-19+18017C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880370 | |||||||
| chr3:136880972 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+18619T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136880972 | |||||||
| chr3:136881011 | A | G | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+18658A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881011 | |||||||
| chr3:136881206 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+18853C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881206 | |||||||
| chr3:136881241 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+18888A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881241 | |||||||
| chr3:136881373 | C | G | 1 | a0001c0001t0001g0055 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-19+19020C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881373 | |||||||
| chr3:136881467 | C | T | 2 | a0001c0001t0001g0089 a0001c0001t0001g0105 |
2 | HG00609.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-19+19114C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881467 | |||||||
| chr3:136881710 | C | G | 1 | a0001c0001t0001g0029 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19+19357C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881710 | |||||||
| chr3:136881825 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+19472G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881825 | |||||||
| chr3:136881990 | G | T | 2 | a0002c0002t0002g0195 a0002c0002t0002g0196 |
2 | HG02280.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19+19637G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136881990 | |||||||
| chr3:136882103 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+19750A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882103 | |||||||
| chr3:136882149 | T | G | 1 | a0001c0001t0001g0029 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-19+19796T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882149 | |||||||
| chr3:136882204 | T | A | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-19+19851T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882204 | |||||||
| chr3:136882394 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+20041A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882394 | |||||||
| chr3:136882547 | C | CTG | 41 | a0001c0001t0001g0013 a0001c0001t0001g0019 a0001c0001t0001g0022 others(38): Show |
41 | HG00140.hp2 HG00544.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.-19+20236_-19+2023 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | ||||||
| chr3:136882547 | C | CTGTG | 25 | a0001c0001t0001g0035 a0001c0001t0001g0051 a0001c0001t0001g0060 others(22): Show |
26 | HG00140.hp1 HG01070.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.-19+20234_-19+2023 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | ||||||
| chr3:136882547 | C | CTGTGTG | 3 | a0001c0001t0003g0205 a0001c0001t0003g0219 a0001c0001t0007g0005 |
4 | HG01433.hp2 HG01517.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+20232_-19+2023 others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | ||||||
| chr3:136882547 | C | CTGTGTGT others(3): Show |
1 | a0001c0001t0003g0204 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-19+20228_-19+2023 others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | ||||||
| chr3:136882547 | CTG | C | 45 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(42): Show |
45 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(42): Show |
intron_variant | MODIFIER | c.-19+20236_-19+2023 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | ||||||
| chr3:136882547 | CTGTG | C | 9 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0068 others(6): Show |
9 | HG00621.hp2 HG00741.hp2 HG02015.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+20234_-19+2023 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | ||||||
| chr3:136882547 | CTGTGTG | C | 4 | a0001c0001t0001g0027 a0001c0001t0002g0185 a0001c0001t0002g0186 others(1): Show |
4 | HG02055.hp2 HG02572.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+20232_-19+2023 others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136882547 | ||||||
| chr3:136882720 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+20367T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882720 | |||||||
| chr3:136882803 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+20450G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136882803 | |||||||
| chr3:136883300 | G | A | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+20947G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136883300 | |||||||
| chr3:136883319 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+20966C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136883319 | |||||||
| chr3:136883606 | G | A | 1 | a0001c0001t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-19+21253G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136883606 | |||||||
| chr3:136883997 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+21644A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136883997 | |||||||
| chr3:136884601 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+22248C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136884601 | |||||||
| chr3:136884718 | C | CT | 165 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(162): Show |
172 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(169): Show |
intron_variant | MODIFIER | c.-19+22377dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136884718 | ||||||
| chr3:136884757 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-19+22404G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136884757 | |||||||
| chr3:136884928 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-19+22575T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136884928 | |||||||
| chr3:136884963 | T | G | 1 | a0001c0001t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-19+22610T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136884963 | |||||||
| chr3:136885198 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-19+22845T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136885198 | |||||||
| chr3:136885461 | T | G | 13 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(10): Show |
13 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.-19+23108T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136885461 | |||||||
| chr3:136885855 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+23502T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136885855 | |||||||
| chr3:136885963 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19+23610G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136885963 | |||||||
| chr3:136886128 | A | T | 1 | a0001c0001t0001g0014 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-19+23775A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886128 | |||||||
| chr3:136886305 | A | G | 2 | a0001c0001t0002g0141 a0001c0001t0002g0150 |
2 | NA19043.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-19+23952A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886305 | |||||||
| chr3:136886544 | T | C | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-19+24191T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886544 | |||||||
| chr3:136886567 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+24214C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886567 | |||||||
| chr3:136886787 | T | G | 1 | a0001c0001t0002g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+24434T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886787 | |||||||
| chr3:136886817 | CTTT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(128): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.-19+24480_-19+2448 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136886817 | ||||||
| chr3:136886955 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+24602T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136886955 | |||||||
| chr3:136887009 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-19+24656A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887009 | |||||||
| chr3:136887319 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0012g0073 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-19+24966C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887319 | |||||||
| chr3:136887429 | T | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-19+25076T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887429 | |||||||
| chr3:136887636 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+25283C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887636 | |||||||
| chr3:136887724 | AG | A | 10 | a0001c0001t0003g0004 a0001c0001t0003g0201 a0001c0001t0003g0203 others(7): Show |
11 | HG00544.hp2 HG02135.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.-19+25372delG | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887724 | |||||||
| chr3:136887902 | A | G | 1 | a0001c0001t0002g0161 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-19+25549A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887902 | |||||||
| chr3:136887923 | TTTTC | T | 34 | a0001c0001t0001g0059 a0001c0001t0002g0138 a0001c0001t0002g0139 others(31): Show |
35 | HG00140.hp1 HG00544.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.-19+25590_-19+2559 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136887923 | ||||||
| chr3:136887975 | G | A | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | HG03491.hp1 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-19+25622G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887975 | |||||||
| chr3:136887992 | T | C | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+25639T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136887992 | |||||||
| chr3:136888232 | C | T | 1 | a0001c0001t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-19+25879C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888232 | |||||||
| chr3:136888265 | C | T | 1 | a0001c0001t0003g0220 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-19+25912C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888265 | |||||||
| chr3:136888356 | A | G | 14 | a0001c0001t0003g0200 a0001c0001t0003g0202 a0001c0001t0003g0204 others(11): Show |
14 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.-19+26003A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888356 | |||||||
| chr3:136888482 | A | C | 1 | a0003c0003t0001g0026 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-19+26129A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888482 | |||||||
| chr3:136888505 | T | C | 1 | a0001c0001t0003g0209 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-19+26152T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888505 | |||||||
| chr3:136888656 | C | A | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+26303C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136888656 | |||||||
| chr3:136889044 | A | AT | 19 | a0001c0001t0002g0143 a0001c0001t0002g0144 a0001c0001t0002g0147 others(16): Show |
19 | HG00639.hp2 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19+26721dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | ||||||
| chr3:136889044 | AT | A | 7 | a0001c0001t0002g0151 a0001c0001t0003g0201 a0001c0001t0003g0210 others(4): Show |
7 | HG01106.hp1 HG01256.hp2 HG02135.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+26721delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | ||||||
| chr3:136889044 | ATT | A | 17 | a0001c0001t0003g0004 a0001c0001t0003g0202 a0001c0001t0003g0203 others(14): Show |
18 | HG00544.hp2 HG00738.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-19+26720_-19+2672 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | ||||||
| chr3:136889044 | ATTTTT | A | 24 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0009 others(21): Show |
27 | HG00280.hp2 HG01081.hp1 HG01109.hp2 others(24): Show |
intron_variant | MODIFIER | c.-19+26717_-19+2672 others(9): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | ||||||
| chr3:136889044 | ATTTTTT | A | 79 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0012 others(76): Show |
79 | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.-19+26716_-19+2672 others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | ||||||
| chr3:136889044 | ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0003g0200 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-19+26712_-19+2672 others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | ||||||
| chr3:136889044 | ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0002g0145 a0001c0001t0007g0005 |
3 | HG03139.hp1 HG03195.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.-19+26711_-19+2672 others(15): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | ||||||
| chr3:136889044 | ATTTTTTT others(6): Show |
A | 18 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19+26709_-19+2672 others(17): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | ||||||
| chr3:136889044 | ATTTTTTT others(7): Show |
A | 7 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(4): Show |
9 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.-19+26708_-19+2672 others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136889044 | ||||||
| chr3:136889140 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+26787T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889140 | |||||||
| chr3:136889289 | G | A | 1 | a0001c0001t0001g0031 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19+26936G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889289 | |||||||
| chr3:136889300 | C | T | 1 | a0001c0001t0002g0142 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-19+26947C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889300 | |||||||
| chr3:136889419 | C | T | 1 | a0001c0001t0002g0169 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-19+27066C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889419 | |||||||
| chr3:136889526 | T | C | 18 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-19+27173T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889526 | |||||||
| chr3:136889540 | C | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-19+27187C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889540 | |||||||
| chr3:136889603 | A | G | 49 | a0001c0001t0002g0003 a0001c0001t0002g0138 a0001c0001t0002g0139 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.-19+27250A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889603 | |||||||
| chr3:136889635 | T | G | 12 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(9): Show |
12 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.-19+27282T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889635 | |||||||
| chr3:136889764 | C | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+27411C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889764 | |||||||
| chr3:136889807 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+27454G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889807 | |||||||
| chr3:136889836 | C | T | 17 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(14): Show |
17 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.-19+27483C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889836 | |||||||
| chr3:136889924 | C | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+27571C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889924 | |||||||
| chr3:136889951 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-19+27598G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889951 | |||||||
| chr3:136889999 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.-19+27646C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136889999 | |||||||
| chr3:136890036 | C | T | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+27683C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890036 | |||||||
| chr3:136890057 | C | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.-19+27704C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890057 | |||||||
| chr3:136890130 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+27777C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890130 | |||||||
| chr3:136890175 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-19+27822G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890175 | |||||||
| chr3:136890184 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0117 |
2 | HG03831.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-19+27831G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890184 | |||||||
| chr3:136890253 | C | A | 1 | a0001c0001t0001g0016 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-19+27900C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890253 | |||||||
| chr3:136890353 | C | T | 4 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(1): Show |
4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+28000C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890353 | |||||||
| chr3:136890397 | C | G | 1 | a0001c0001t0001g0037 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-19+28044C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890397 | |||||||
| chr3:136890448 | A | G | 1 | a0001c0001t0014g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-19+28095A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890448 | |||||||
| chr3:136890676 | C | G | 1 | a0001c0001t0003g0209 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-19+28323C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890676 | |||||||
| chr3:136890676 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-19+28323C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890676 | |||||||
| chr3:136890778 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-19+28425C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890778 | |||||||
| chr3:136890960 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-19+28607C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890960 | |||||||
| chr3:136890996 | T | C | 44 | a0001c0001t0002g0003 a0001c0001t0002g0138 a0001c0001t0002g0139 others(41): Show |
45 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(42): Show |
intron_variant | MODIFIER | c.-19+28643T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136890996 | |||||||
| chr3:136891064 | A | G | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+28711A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891064 | |||||||
| chr3:136891087 | G | A | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+28734G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891087 | |||||||
| chr3:136891183 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-19+28830G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891183 | |||||||
| chr3:136891217 | C | T | 1 | a0001c0001t0001g0097 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-19+28864C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891217 | |||||||
| chr3:136891788 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+29435G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891788 | |||||||
| chr3:136891791 | A | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+29438A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891791 | |||||||
| chr3:136891989 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+29636A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136891989 | |||||||
| chr3:136892033 | T | G | 1 | a0001c0001t0003g0219 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-19+29680T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892033 | |||||||
| chr3:136892103 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+29750G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892103 | |||||||
| chr3:136892154 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+29801T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892154 | |||||||
| chr3:136892309 | G | A | 1 | a0001c0001t0002g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+29956G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892309 | |||||||
| chr3:136892314 | A | G | 7 | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0032 others(4): Show |
7 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.-19+29961A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892314 | |||||||
| chr3:136892382 | C | A | 1 | a0001c0001t0005g0180 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-19+30029C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892382 | |||||||
| chr3:136892388 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+30035G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892388 | |||||||
| chr3:136892441 | A | G | 1 | a0001c0001t0001g0068 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-19+30088A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892441 | |||||||
| chr3:136892505 | TTGA | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+30158_-19+3016 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136892505 | ||||||
| chr3:136892734 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-19+30381T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892734 | |||||||
| chr3:136892928 | C | G | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+30575C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136892928 | |||||||
| chr3:136893130 | G | A | 4 | a0001c0001t0002g0144 a0001c0001t0002g0151 a0001c0001t0002g0152 others(1): Show |
4 | HG00099.hp2 HG01074.hp2 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+30777G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893130 | |||||||
| chr3:136893147 | A | AGT | 86 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(83): Show |
92 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(89): Show |
intron_variant | MODIFIER | c.-19+30825_-19+3082 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | ||||||
| chr3:136893147 | A | AGTGT | 34 | a0001c0001t0001g0011 a0001c0001t0001g0021 a0001c0001t0001g0046 others(31): Show |
34 | HG00423.hp2 HG00621.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.-19+30823_-19+3082 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | ||||||
| chr3:136893147 | A | AGTGTGT | 24 | a0001c0001t0001g0033 a0001c0001t0001g0045 a0001c0001t0001g0049 others(21): Show |
24 | HG00544.hp1 HG00544.hp2 HG01070.hp2 others(21): Show |
intron_variant | MODIFIER | c.-19+30821_-19+3082 others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | ||||||
| chr3:136893147 | A | AGTGTGTG others(1): Show |
21 | a0001c0001t0001g0006 a0001c0001t0001g0013 a0001c0001t0001g0022 others(18): Show |
22 | HG00099.hp2 HG00280.hp1 HG00423.hp1 others(19): Show |
intron_variant | MODIFIER | c.-19+30819_-19+3082 others(12): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | ||||||
| chr3:136893147 | A | AGTGTGTG others(3): Show |
23 | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0032 others(20): Show |
23 | HG00609.hp1 HG00621.hp2 HG01261.hp2 others(20): Show |
intron_variant | MODIFIER | c.-19+30817_-19+3082 others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | ||||||
| chr3:136893147 | A | AGTGTGTG others(5): Show |
2 | a0001c0001t0001g0105 a0001c0001t0002g0160 |
2 | HG00408.hp2 HG00609.hp2 |
intron_variant | MODIFIER | c.-19+30815_-19+3082 others(16): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | ||||||
| chr3:136893147 | A | AGTGTGTG others(7): Show |
2 | a0001c0001t0001g0044 a0001c0001t0002g0161 |
2 | NA18522.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-19+30813_-19+3082 others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893147 | ||||||
| chr3:136893155 | T | TGC | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+30803_-19+3080 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893155 | ||||||
| chr3:136893167 | T | TGTGTGTG others(29): Show |
3 | a0002c0002t0002g0195 a0002c0002t0002g0196 a0002c0002t0002g0197 |
3 | HG02280.hp1 HG02818.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.-19+30826_-19+3082 others(40): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893167 | ||||||
| chr3:136893178 | G | A | 1 | a0001c0001t0001g0014 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-19+30825G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893178 | |||||||
| chr3:136893178 | G | GTA | 2 | a0001c0001t0002g0192 a0001c0001t0002g0194 |
2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-19+30838_-19+3083 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893178 | ||||||
| chr3:136893178 | G | GTGTGTGT others(7): Show |
1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-19+30826_-19+3082 others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893178 | ||||||
| chr3:136893178 | G | GTGTGTGT others(11): Show |
1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-19+30826_-19+3082 others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893178 | ||||||
| chr3:136893180 | A | G | 150 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(147): Show |
157 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.-19+30827A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893180 | |||||||
| chr3:136893182 | A | G | 81 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(78): Show |
88 | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.-19+30829A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893182 | |||||||
| chr3:136893184 | A | G | 29 | a0001c0001t0001g0006 a0001c0001t0001g0061 a0001c0001t0001g0064 others(26): Show |
31 | HG00544.hp2 HG00738.hp1 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.-19+30831A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893184 | |||||||
| chr3:136893186 | A | G | 2 | a0001c0001t0001g0078 a0001c0001t0007g0005 |
3 | HG03139.hp1 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-19+30833A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893186 | |||||||
| chr3:136893189 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-19+30836T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893189 | |||||||
| chr3:136893191 | T | C | 9 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(6): Show |
9 | HG00099.hp1 HG00408.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+30838T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893191 | |||||||
| chr3:136893196 | A | ACACACAC others(107): Show |
1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(118): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | ||||||
| chr3:136893196 | A | ACACACAC others(103): Show |
11 | a0001c0001t0001g0011 a0001c0001t0001g0046 a0001c0001t0001g0047 others(8): Show |
11 | HG00621.hp1 HG02135.hp2 NA18939.hp1 others(8): Show |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(114): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | ||||||
| chr3:136893196 | A | ACACACAC others(101): Show |
52 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 others(49): Show |
52 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(112): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | ||||||
| chr3:136893196 | A | ACACACAC others(99): Show |
66 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(63): Show |
71 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(68): Show |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(110): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | ||||||
| chr3:136893196 | A | ACACACAC others(97): Show |
1 | a0003c0003t0001g0024 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-19+30845_-19+3084 others(108): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | ||||||
| chr3:136893196 | A | ACACACAC others(95): Show |
2 | a0001c0001t0001g0014 a0001c0001t0001g0031 |
2 | HG02738.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(106): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | ||||||
| chr3:136893196 | A | ACACACAC others(93): Show |
2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-19+30845_-19+3084 others(104): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893196 | ||||||
| chr3:136893217 | G | A | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-19+30864G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893217 | |||||||
| chr3:136893307 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+30954T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893307 | |||||||
| chr3:136893354 | TA | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+31003delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136893354 | ||||||
| chr3:136893360 | G | A | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-19+31007G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893360 | |||||||
| chr3:136893408 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.-19+31055T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893408 | |||||||
| chr3:136893563 | G | A | 1 | a0001c0001t0001g0038 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-19+31210G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893563 | |||||||
| chr3:136893919 | C | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+31566C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136893919 | |||||||
| chr3:136894076 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.-19+31723G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894076 | |||||||
| chr3:136894429 | C | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-19+32076C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894429 | |||||||
| chr3:136894632 | T | C | 1 | a0001c0001t0003g0211 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-19+32279T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894632 | |||||||
| chr3:136894642 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-19+32289G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894642 | |||||||
| chr3:136894883 | T | TG | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+32530_-19+3253 others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894883 | |||||||
| chr3:136894884 | T | G | 2 | a0001c0001t0002g0143 a0001c0001t0007g0005 |
3 | HG03139.hp1 HG03195.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-19+32531T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894884 | |||||||
| chr3:136894944 | C | T | 7 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-19+32591C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894944 | |||||||
| chr3:136894945 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-19+32592G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136894945 | |||||||
| chr3:136895012 | A | G | 1 | a0001c0001t0001g0015 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-19+32659A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895012 | |||||||
| chr3:136895183 | T | A | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18-32801T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895183 | |||||||
| chr3:136895321 | T | TTA | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-32651_-18-3265 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136895321 | ||||||
| chr3:136895397 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-32587C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895397 | |||||||
| chr3:136895705 | C | T | 1 | a0001c0001t0001g0031 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-18-32279C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895705 | |||||||
| chr3:136895765 | A | G | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-32219A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136895765 | |||||||
| chr3:136896384 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-31600C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896384 | |||||||
| chr3:136896426 | G | A | 68 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(65): Show |
68 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(65): Show |
intron_variant | MODIFIER | c.-18-31558G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896426 | |||||||
| chr3:136896429 | A | T | 1 | a0001c0001t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-18-31555A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896429 | |||||||
| chr3:136896471 | T | C | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-18-31513T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896471 | |||||||
| chr3:136896602 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-31382A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896602 | |||||||
| chr3:136896657 | G | A | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-31327G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896657 | |||||||
| chr3:136896797 | C | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(1): Show |
4 | HG01243.hp2 HG02818.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-31187C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136896797 | |||||||
| chr3:136897053 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-18-30931A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136897053 | |||||||
| chr3:136897114 | T | C | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-30870T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136897114 | |||||||
| chr3:136897232 | G | T | 1 | a0001c0001t0002g0194 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-18-30752G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136897232 | |||||||
| chr3:136897738 | C | T | 1 | a0001c0001t0001g0015 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-18-30246C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136897738 | |||||||
| chr3:136898120 | G | T | 3 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0012 |
3 | NA18939.hp2 NA18959.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.-18-29864G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136898120 | |||||||
| chr3:136898385 | C | CA | 20 | a0001c0001t0001g0019 a0001c0001t0001g0029 a0001c0001t0001g0030 others(17): Show |
20 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.-18-29580dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136898385 | ||||||
| chr3:136898385 | CA | C | 15 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0062 others(12): Show |
20 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18-29580delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136898385 | ||||||
| chr3:136898432 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-29552G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136898432 | |||||||
| chr3:136898461 | A | G | 2 | a0001c0001t0001g0035 a0001c0001t0001g0037 |
2 | NA18964.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.-18-29523A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136898461 | |||||||
| chr3:136898512 | A | T | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-29472A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136898512 | |||||||
| chr3:136899023 | T | G | 1 | a0001c0001t0009g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18-28961T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899023 | |||||||
| chr3:136899132 | G | C | 1 | a0001c0001t0001g0006 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-18-28852G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899132 | |||||||
| chr3:136899156 | A | T | 21 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0030 others(18): Show |
21 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-28828A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899156 | |||||||
| chr3:136899372 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-28612G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899372 | |||||||
| chr3:136899419 | C | CT | 142 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(139): Show |
148 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(145): Show |
intron_variant | MODIFIER | c.-18-28551dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136899419 | ||||||
| chr3:136899433 | T | A | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-18-28551T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899433 | |||||||
| chr3:136899433 | T | TA | 10 | a0001c0001t0001g0086 a0001c0001t0001g0087 a0001c0001t0001g0094 others(7): Show |
10 | HG00408.hp1 HG00423.hp2 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18-28548dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136899433 | ||||||
| chr3:136899434 | A | T | 2 | a0001c0001t0001g0019 a0001c0001t0014g0023 |
2 | HG01496.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.-18-28550A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899434 | |||||||
| chr3:136899586 | T | C | 1 | a0001c0001t0001g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-18-28398T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899586 | |||||||
| chr3:136899600 | C | T | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-28384C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899600 | |||||||
| chr3:136899718 | C | T | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-28266C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899718 | |||||||
| chr3:136899868 | CT | C | 6 | a0001c0001t0002g0144 a0001c0001t0002g0151 a0001c0001t0002g0152 others(3): Show |
6 | HG00099.hp2 HG01074.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-28106delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136899868 | ||||||
| chr3:136899878 | T | A | 1 | a0001c0001t0002g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-18-28106T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899878 | |||||||
| chr3:136899962 | A | G | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-28022A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136899962 | |||||||
| chr3:136900067 | G | C | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0062 others(11): Show |
19 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18-27917G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136900067 | |||||||
| chr3:136900724 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-27260A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136900724 | |||||||
| chr3:136901267 | A | AT | 26 | a0001c0001t0001g0027 a0001c0001t0001g0124 a0001c0001t0003g0004 others(23): Show |
27 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(24): Show |
intron_variant | MODIFIER | c.-18-26704dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136901267 | ||||||
| chr3:136901272 | T | A | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-26712T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901272 | |||||||
| chr3:136901305 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-18-26679G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901305 | |||||||
| chr3:136901363 | C | CT | 5 | a0001c0001t0001g0119 a0001c0001t0005g0180 a0001c0001t0005g0189 others(2): Show |
5 | HG01099.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-26610dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136901363 | ||||||
| chr3:136901374 | T | A | 2 | a0001c0001t0001g0027 a0001c0001t0015g0007 |
2 | HG03516.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-26610T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901374 | |||||||
| chr3:136901374 | T | TA | 24 | a0001c0001t0003g0004 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-26607dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136901374 | ||||||
| chr3:136901621 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-18-26363A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901621 | |||||||
| chr3:136901842 | C | G | 1 | a0001c0001t0001g0106 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-18-26142C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901842 | |||||||
| chr3:136901857 | G | A | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-26127G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901857 | |||||||
| chr3:136901973 | T | C | 1 | a0001c0001t0003g0219 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-18-26011T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136901973 | |||||||
| chr3:136902040 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-18-25944C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902040 | |||||||
| chr3:136902113 | G | T | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18-25871G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902113 | |||||||
| chr3:136902165 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-25819G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902165 | |||||||
| chr3:136902193 | T | TTTG | 6 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(3): Show |
6 | HG01358.hp1 HG02572.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.-18-25789_-18-2578 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136902193 | ||||||
| chr3:136902194 | T | TTTG | 6 | a0001c0001t0001g0046 a0001c0001t0001g0072 a0001c0001t0001g0074 others(3): Show |
6 | HG00741.hp2 HG02135.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-25788_-18-2578 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136902194 | ||||||
| chr3:136902197 | T | G | 33 | a0001c0001t0002g0145 a0001c0001t0003g0004 a0001c0001t0003g0200 others(30): Show |
35 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(32): Show |
intron_variant | MODIFIER | c.-18-25787T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902197 | |||||||
| chr3:136902198 | T | G | 12 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(9): Show |
12 | HG00741.hp2 HG01358.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.-18-25786T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902198 | |||||||
| chr3:136902198 | T | TTTG | 115 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(112): Show |
120 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(117): Show |
intron_variant | MODIFIER | c.-18-25784_-18-2578 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136902198 | ||||||
| chr3:136902198 | T | TTTTG | 6 | a0001c0001t0001g0029 a0001c0001t0001g0035 a0001c0001t0001g0037 others(3): Show |
6 | HG00639.hp1 HG02523.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.-18-25783_-18-2578 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136902198 | ||||||
| chr3:136902199 | T | G | 1 | a0001c0001t0002g0165 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-18-25785T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902199 | |||||||
| chr3:136902203 | G | T | 2 | a0001c0001t0002g0164 a0001c0001t0002g0166 |
2 | HG01261.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-18-25781G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902203 | |||||||
| chr3:136902346 | T | C | 166 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(163): Show |
173 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.-18-25638T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902346 | |||||||
| chr3:136902483 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-25501T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902483 | |||||||
| chr3:136902496 | A | G | 14 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0062 others(11): Show |
19 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18-25488A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902496 | |||||||
| chr3:136902596 | T | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-25388T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902596 | |||||||
| chr3:136902627 | G | A | 2 | a0001c0001t0001g0064 a0001c0001t0001g0067 |
2 | HG01167.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.-18-25357G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902627 | |||||||
| chr3:136902683 | T | C | 1 | a0001c0001t0002g0157 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-18-25301T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902683 | |||||||
| chr3:136902776 | C | T | 24 | a0001c0001t0003g0004 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-25208C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902776 | |||||||
| chr3:136902875 | A | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-25109A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136902875 | |||||||
| chr3:136903084 | C | T | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-24900C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903084 | |||||||
| chr3:136903166 | C | A | 24 | a0001c0001t0003g0004 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-24818C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903166 | |||||||
| chr3:136903368 | G | A | 10 | a0001c0001t0003g0004 a0001c0001t0003g0201 a0001c0001t0003g0203 others(7): Show |
11 | HG00544.hp2 HG02135.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-24616G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903368 | |||||||
| chr3:136903400 | T | A | 4 | a0002c0002t0002g0178 a0002c0002t0006g0191 a0002c0002t0006g0193 others(1): Show |
4 | HG03139.hp2 HG03486.hp1 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-24584T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903400 | |||||||
| chr3:136903419 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-18-24565G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903419 | |||||||
| chr3:136903624 | C | T | 7 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0088 others(4): Show |
7 | HG01346.hp2 HG01361.hp2 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.-18-24360C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903624 | |||||||
| chr3:136903718 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-18-24266C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903718 | |||||||
| chr3:136903773 | CAG | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-18-24208_-18-2420 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136903773 | ||||||
| chr3:136903835 | G | C | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-24149G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903835 | |||||||
| chr3:136903842 | A | G | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-18-24142A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136903842 | |||||||
| chr3:136904184 | G | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-23800G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136904184 | |||||||
| chr3:136904481 | C | T | 7 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(4): Show |
7 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.-18-23503C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136904481 | |||||||
| chr3:136904834 | A | AT | 121 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(118): Show |
123 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.-18-23137dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136904834 | ||||||
| chr3:136904834 | A | ATT | 8 | a0001c0001t0001g0056 a0001c0001t0001g0060 a0001c0001t0001g0088 others(5): Show |
8 | HG01346.hp2 HG01361.hp2 HG01517.hp2 others(5): Show |
intron_variant | MODIFIER | c.-18-23138_-18-2313 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136904834 | ||||||
| chr3:136904900 | C | G | 1 | a0001c0001t0014g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-18-23084C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136904900 | |||||||
| chr3:136904949 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-23035C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136904949 | |||||||
| chr3:136905007 | C | CT | 24 | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0082 others(21): Show |
27 | HG00280.hp2 HG00544.hp2 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.-18-22960dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136905007 | ||||||
| chr3:136905007 | C | CTT | 4 | a0001c0001t0001g0083 a0001c0001t0003g0004 a0001c0001t0003g0201 others(1): Show |
5 | HG01109.hp2 NA18959.hp2 NA18973.hp1 others(2): Show |
intron_variant | MODIFIER | c.-18-22961_-18-2296 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136905007 | ||||||
| chr3:136905007 | CTTTTTTT others(1): Show |
C | 14 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(11): Show |
16 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.-18-22967_-18-2296 others(12): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136905007 | ||||||
| chr3:136905183 | G | C | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 |
3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-22801G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905183 | |||||||
| chr3:136905202 | T | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-22782T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905202 | |||||||
| chr3:136905224 | G | A | 2 | a0001c0001t0002g0173 a0001c0001t0002g0174 |
2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-18-22760G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905224 | |||||||
| chr3:136905280 | C | T | 2 | a0001c0001t0002g0149 a0001c0001t0002g0165 |
2 | HG00639.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.-18-22704C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905280 | |||||||
| chr3:136905641 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-22343C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905641 | |||||||
| chr3:136905952 | C | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-22032C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136905952 | |||||||
| chr3:136905984 | AT | A | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-21997delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136905984 | ||||||
| chr3:136906161 | A | G | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-21823A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906161 | |||||||
| chr3:136906312 | G | C | 18 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0044 others(15): Show |
18 | HG00738.hp1 HG01109.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18-21672G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906312 | |||||||
| chr3:136906427 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0083 others(14): Show |
20 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.-18-21557G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906427 | |||||||
| chr3:136906448 | G | T | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-21536G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906448 | |||||||
| chr3:136906468 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-21516G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906468 | |||||||
| chr3:136906497 | C | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-21487C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906497 | |||||||
| chr3:136906594 | G | A | 129 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(126): Show |
131 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.-18-21390G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906594 | |||||||
| chr3:136906652 | G | A | 3 | a0001c0001t0003g0210 a0001c0001t0003g0221 a0001c0001t0003g0222 |
3 | NA18987.hp1 NA19012.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-18-21332G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906652 | |||||||
| chr3:136906813 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.-18-21171G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906813 | |||||||
| chr3:136906831 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-18-21153G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136906831 | |||||||
| chr3:136907060 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-20924C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907060 | |||||||
| chr3:136907128 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 |
3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-20856C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907128 | |||||||
| chr3:136907320 | G | A | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | HG03491.hp1 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-18-20664G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907320 | |||||||
| chr3:136907373 | A | G | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-20611A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907373 | |||||||
| chr3:136907855 | G | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-20129G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907855 | |||||||
| chr3:136907888 | G | A | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-20096G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907888 | |||||||
| chr3:136907934 | C | T | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-20050C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136907934 | |||||||
| chr3:136908624 | T | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(199): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-18-19360T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136908624 | |||||||
| chr3:136908916 | G | A | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-19068G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136908916 | |||||||
| chr3:136910178 | A | G | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | HG03491.hp1 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.-18-17806A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910178 | |||||||
| chr3:136910344 | C | T | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-17640C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910344 | |||||||
| chr3:136910365 | C | T | 10 | a0001c0001t0003g0004 a0001c0001t0003g0201 a0001c0001t0003g0203 others(7): Show |
11 | HG00544.hp2 HG02135.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-17619C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910365 | |||||||
| chr3:136910427 | C | T | 11 | a0001c0001t0002g0153 a0001c0001t0002g0154 a0001c0001t0002g0155 others(8): Show |
11 | HG00408.hp2 HG01070.hp1 HG01081.hp2 others(8): Show |
intron_variant | MODIFIER | c.-18-17557C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910427 | |||||||
| chr3:136910648 | G | A | 132 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(129): Show |
135 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.-18-17336G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910648 | |||||||
| chr3:136910692 | A | G | 3 | a0001c0001t0003g0004 a0001c0001t0003g0201 a0001c0001t0003g0203 |
4 | NA18959.hp2 NA18973.hp1 NA18994.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-17292A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136910692 | |||||||
| chr3:136911144 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-16840A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136911144 | |||||||
| chr3:136911288 | C | A | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-16696C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136911288 | |||||||
| chr3:136911470 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-18-16514T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136911470 | |||||||
| chr3:136912162 | C | CT | 68 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 others(65): Show |
71 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(68): Show |
intron_variant | MODIFIER | c.-18-15804dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912162 | ||||||
| chr3:136912162 | C | CTT | 16 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0083 others(13): Show |
19 | HG00280.hp2 HG00738.hp2 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.-18-15805_-18-1580 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912162 | ||||||
| chr3:136912162 | C | CTTT | 9 | a0001c0001t0002g0181 a0001c0001t0002g0182 a0001c0001t0002g0183 others(6): Show |
9 | HG02015.hp1 HG02055.hp2 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-15806_-18-1580 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912162 | ||||||
| chr3:136912162 | CT | C | 21 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0031 others(18): Show |
21 | HG00544.hp1 HG00621.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.-18-15804delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912162 | ||||||
| chr3:136912162 | CTTTTTTT others(2): Show |
C | 48 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0014 others(45): Show |
48 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.-18-15812_-18-1580 others(13): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912162 | ||||||
| chr3:136912187 | G | A | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-15797G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912187 | |||||||
| chr3:136912188 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-18-15796A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912188 | |||||||
| chr3:136912230 | T | C | 1 | a0001c0001t0001g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-18-15754T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912230 | |||||||
| chr3:136912360 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-15624G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912360 | |||||||
| chr3:136912413 | C | A | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18-15571C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912413 | |||||||
| chr3:136912433 | C | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-15551C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912433 | |||||||
| chr3:136912492 | CTT | C | 130 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(127): Show |
132 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-18-15479_-18-1547 others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912492 | ||||||
| chr3:136912763 | C | G | 1 | a0001c0001t0001g0129 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-18-15221C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912763 | |||||||
| chr3:136912800 | C | T | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-18-15184C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136912800 | |||||||
| chr3:136912864 | CTGGTCT | C | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-15111_-18-1510 others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136912864 | ||||||
| chr3:136913280 | C | T | 3 | a0003c0003t0001g0024 a0003c0003t0001g0025 a0003c0003t0001g0026 |
3 | HG01070.hp2 HG01261.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.-18-14704C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913280 | |||||||
| chr3:136913298 | T | C | 1 | a0001c0001t0001g0014 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-18-14686T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913298 | |||||||
| chr3:136913413 | T | C | 2 | a0001c0001t0002g0192 a0001c0001t0002g0194 |
2 | HG01891.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.-18-14571T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913413 | |||||||
| chr3:136913435 | A | G | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-14549A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913435 | |||||||
| chr3:136913635 | G | A | 1 | a0001c0001t0001g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-18-14349G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913635 | |||||||
| chr3:136913695 | A | G | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(155): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-18-14289A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913695 | |||||||
| chr3:136913911 | T | TC | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-14073_-18-1407 others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136913911 | |||||||
| chr3:136914094 | C | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(127): Show |
132 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-18-13890C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914094 | |||||||
| chr3:136914165 | T | C | 1 | a0001c0001t0002g0141 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-18-13819T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914165 | |||||||
| chr3:136914245 | G | T | 1 | a0001c0001t0001g0107 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18-13739G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914245 | |||||||
| chr3:136914488 | C | T | 1 | a0001c0001t0001g0102 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-18-13496C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914488 | |||||||
| chr3:136914729 | A | T | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-13255A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914729 | |||||||
| chr3:136914752 | C | T | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-13232C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136914752 | |||||||
| chr3:136915151 | C | T | 1 | a0001c0001t0002g0184 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-18-12833C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915151 | |||||||
| chr3:136915197 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.-18-12787C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915197 | |||||||
| chr3:136915198 | A | G | 131 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0008 others(128): Show |
133 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.-18-12786A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915198 | |||||||
| chr3:136915604 | T | A | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-18-12380T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915604 | |||||||
| chr3:136915704 | T | C | 16 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(13): Show |
18 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(15): Show |
intron_variant | MODIFIER | c.-18-12280T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915704 | |||||||
| chr3:136915730 | G | T | 1 | a0001c0001t0002g0150 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-12254G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915730 | |||||||
| chr3:136915959 | C | T | 1 | a0001c0001t0001g0126 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-18-12025C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136915959 | |||||||
| chr3:136916179 | G | T | 1 | a0001c0001t0001g0022 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-18-11805G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916179 | |||||||
| chr3:136916329 | A | G | 49 | a0001c0001t0002g0003 a0001c0001t0002g0138 a0001c0001t0002g0139 others(46): Show |
50 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18-11655A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916329 | |||||||
| chr3:136916451 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-18-11533T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916451 | |||||||
| chr3:136916553 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.-18-11431A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916553 | |||||||
| chr3:136916587 | T | C | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-11397T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916587 | |||||||
| chr3:136916747 | C | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0006 a0001c0001t0001g0009 others(127): Show |
132 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-18-11237C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916747 | |||||||
| chr3:136916747 | CAGTT | C | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-11236_-18-1123 others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136916747 | |||||||
| chr3:136917232 | C | CT | 88 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0083 others(85): Show |
93 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(90): Show |
intron_variant | MODIFIER | c.-18-10737dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136917232 | ||||||
| chr3:136917232 | C | CTTT | 9 | a0001c0001t0001g0032 a0001c0001t0001g0049 a0001c0001t0001g0057 others(6): Show |
10 | HG00609.hp1 HG00609.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18-10739_-18-1073 others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136917232 | ||||||
| chr3:136917520 | C | T | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-10464C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136917520 | |||||||
| chr3:136917741 | C | A | 27 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0083 others(24): Show |
31 | HG00280.hp2 HG00544.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18-10243C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136917741 | |||||||
| chr3:136917792 | C | T | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-10192C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136917792 | |||||||
| chr3:136917843 | T | C | 11 | a0001c0001t0001g0002 a0001c0001t0001g0062 a0001c0001t0001g0063 others(8): Show |
13 | HG00741.hp1 HG01074.hp1 HG01099.hp2 others(10): Show |
intron_variant | MODIFIER | c.-18-10141T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136917843 | |||||||
| chr3:136917970 | G | C | 2 | a0001c0001t0001g0049 a0001c0001t0012g0073 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-18-10014G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136917970 | |||||||
| chr3:136918342 | G | GA | 27 | a0001c0001t0001g0001 a0001c0001t0001g0082 a0001c0001t0001g0083 others(24): Show |
31 | HG00280.hp2 HG00544.hp2 HG00738.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18-9633dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136918342 | ||||||
| chr3:136918882 | A | T | 1 | a0001c0001t0012g0073 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-18-9102A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136918882 | |||||||
| chr3:136919011 | A | G | 2 | a0001c0001t0002g0173 a0001c0001t0002g0174 |
2 | HG00280.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.-18-8973A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136919011 | |||||||
| chr3:136919920 | T | C | 1 | a0001c0001t0005g0189 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.-18-8064T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136919920 | |||||||
| chr3:136920133 | A | G | 19 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0062 others(16): Show |
24 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(21): Show |
intron_variant | MODIFIER | c.-18-7851A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920133 | |||||||
| chr3:136920234 | T | C | 1 | a0001c0001t0001g0050 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-18-7750T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920234 | |||||||
| chr3:136920257 | A | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
140 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.-18-7727A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920257 | |||||||
| chr3:136920333 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-7651A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920333 | |||||||
| chr3:136920395 | T | G | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-18-7589T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920395 | |||||||
| chr3:136920459 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 |
3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-7525G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920459 | |||||||
| chr3:136920607 | C | A | 1 | a0001c0001t0001g0121 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-18-7377C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920607 | |||||||
| chr3:136920652 | C | G | 1 | a0001c0001t0005g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18-7332C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920652 | |||||||
| chr3:136920673 | A | G | 24 | a0001c0001t0003g0004 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-7311A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920673 | |||||||
| chr3:136920962 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-18-7022A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136920962 | |||||||
| chr3:136921329 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0015g0007 |
2 | HG03516.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-18-6655C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136921329 | |||||||
| chr3:136921468 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-18-6516A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136921468 | |||||||
| chr3:136921849 | T | A | 1 | a0001c0001t0001g0116 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.-18-6135T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136921849 | |||||||
| chr3:136921991 | G | T | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-5993G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136921991 | |||||||
| chr3:136922003 | T | A | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.-18-5981T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922003 | |||||||
| chr3:136922234 | C | T | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-5750C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922234 | |||||||
| chr3:136922358 | G | C | 1 | a0001c0001t0002g0155 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-18-5626G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922358 | |||||||
| chr3:136922388 | G | A | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-5596G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922388 | |||||||
| chr3:136922604 | A | C | 1 | a0001c0001t0001g0112 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-18-5380A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136922604 | |||||||
| chr3:136923071 | A | G | 1 | a0001c0001t0003g0218 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-18-4913A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923071 | |||||||
| chr3:136923105 | A | ATG | 16 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0062 others(13): Show |
21 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18-4864_-18-4863d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923105 | ||||||
| chr3:136923228 | T | A | 1 | a0002c0002t0002g0196 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18-4756T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923228 | |||||||
| chr3:136923269 | G | C | 1 | a0001c0001t0001g0047 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-18-4715G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923269 | |||||||
| chr3:136923316 | G | GA | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-18-4667dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923316 | ||||||
| chr3:136923330 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0012g0073 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-18-4654C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923330 | |||||||
| chr3:136923555 | G | A | 1 | a0001c0001t0001g0108 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-18-4429G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923555 | |||||||
| chr3:136923559 | C | CAAAT | 13 | a0001c0001t0001g0016 a0001c0001t0001g0019 a0001c0001t0001g0063 others(10): Show |
13 | HG00140.hp2 HG01099.hp2 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-4392_-18-4389d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | ||||||
| chr3:136923559 | C | CAAATAAA others(1): Show |
21 | a0001c0001t0001g0013 a0001c0001t0001g0051 a0001c0001t0002g0138 others(18): Show |
22 | HG00099.hp2 HG00140.hp1 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.-18-4396_-18-4389d others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | ||||||
| chr3:136923559 | C | CAAATAAA others(5): Show |
49 | a0001c0001t0002g0003 a0001c0001t0002g0139 a0001c0001t0002g0141 others(46): Show |
51 | HG00280.hp1 HG00408.hp2 HG00423.hp1 others(48): Show |
intron_variant | MODIFIER | c.-18-4400_-18-4389d others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | ||||||
| chr3:136923559 | C | CAAATAAA others(9): Show |
17 | a0001c0001t0002g0175 a0001c0001t0002g0182 a0001c0001t0002g0184 others(14): Show |
17 | HG01167.hp1 HG01169.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.-18-4404_-18-4389d others(18): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | ||||||
| chr3:136923559 | C | CAAATAAA others(13): Show |
1 | a0001c0001t0005g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-18-4408_-18-4389d others(22): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | ||||||
| chr3:136923559 | C | CAAATAAA others(17): Show |
1 | a0001c0001t0002g0181 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-18-4412_-18-4389d others(26): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923559 | ||||||
| chr3:136923571 | TA | T | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0132 |
3 | HG01433.hp1 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-18-4410delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923571 | ||||||
| chr3:136923881 | ACT | A | 2 | a0001c0001t0002g0138 a0001c0001t0002g0140 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-18-4100_-18-4099d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | INFO_REALIGN_3_PRIME | chr3 | 136923881 | ||||||
| chr3:136923981 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-4003C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136923981 | |||||||
| chr3:136924160 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0051 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.-18-3824A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924160 | |||||||
| chr3:136924203 | A | G | 1 | a0001c0001t0001g0066 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18-3781A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924203 | |||||||
| chr3:136924239 | G | A | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-18-3745G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924239 | |||||||
| chr3:136924434 | A | G | 1 | a0001c0001t0001g0107 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-18-3550A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924434 | |||||||
| chr3:136924729 | T | A | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(155): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.-18-3255T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924729 | |||||||
| chr3:136924791 | C | T | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-3193C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924791 | |||||||
| chr3:136924892 | A | G | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(156): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.-18-3092A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136924892 | |||||||
| chr3:136925017 | C | T | 1 | a0001c0001t0002g0187 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-18-2967C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925017 | |||||||
| chr3:136925335 | T | A | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.-18-2649T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925335 | |||||||
| chr3:136925436 | A | G | 24 | a0001c0001t0003g0004 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-2548A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925436 | |||||||
| chr3:136925535 | C | T | 1 | a0001c0001t0001g0106 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.-18-2449C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925535 | |||||||
| chr3:136925558 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-18-2426C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925558 | |||||||
| chr3:136925693 | A | G | 1 | a0001c0001t0002g0175 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-18-2291A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136925693 | |||||||
| chr3:136926045 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-1939G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926045 | |||||||
| chr3:136926240 | C | G | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-1744C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926240 | |||||||
| chr3:136926369 | G | T | 2 | a0001c0001t0002g0175 a0001c0001t0002g0176 |
2 | HG02572.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-18-1615G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926369 | |||||||
| chr3:136926401 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-18-1583A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926401 | |||||||
| chr3:136926462 | A | G | 1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-18-1522A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926462 | |||||||
| chr3:136926571 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-1413G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926571 | |||||||
| chr3:136926575 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-1409A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926575 | |||||||
| chr3:136926967 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-1017G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926967 | |||||||
| chr3:136926985 | T | G | 9 | a0001c0001t0001g0046 a0001c0001t0001g0047 a0001c0001t0001g0092 others(6): Show |
9 | HG00621.hp1 HG02135.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-999T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136926985 | |||||||
| chr3:136927117 | G | A | 1 | a0001c0001t0009g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-18-867G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927117 | |||||||
| chr3:136927226 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-758C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927226 | |||||||
| chr3:136927320 | C | T | 3 | a0001c0001t0001g0021 a0001c0001t0001g0022 a0001c0001t0001g0027 |
3 | HG03209.hp2 HG03471.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-664C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927320 | |||||||
| chr3:136927358 | C | T | 1 | a0001c0001t0010g0093 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-18-626C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927358 | |||||||
| chr3:136927434 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-18-550C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927434 | |||||||
| chr3:136927545 | C | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-18-439C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927545 | |||||||
| chr3:136927797 | G | A | 1 | a0001c0001t0002g0166 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-18-187G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927797 | |||||||
| chr3:136927894 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-18-90T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927894 | |||||||
| chr3:136927963 | A | G | 1 | a0001c0001t0001g0030 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-18-21A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 1/3 | chr3 | 136927963 | |||||||
| chr3:136928316 | T | C | 1 | a0001c0001t0014g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.226+89T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928316 | |||||||
| chr3:136928404 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+177A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928404 | |||||||
| chr3:136928639 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.226+412G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928639 | |||||||
| chr3:136928787 | G | GGCCCTAA others(1): Show |
6 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 others(3): Show |
6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+561_226+562ins others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136928787 | ||||||
| chr3:136928789 | A | G | 6 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 others(3): Show |
6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+562A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928789 | |||||||
| chr3:136928790 | G | A | 6 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 others(3): Show |
6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+563G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928790 | |||||||
| chr3:136928795 | C | A | 6 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 others(3): Show |
6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+568C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928795 | |||||||
| chr3:136928796 | T | G | 6 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 others(3): Show |
6 | HG00140.hp1 HG03491.hp1 HG03492.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+569T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928796 | |||||||
| chr3:136928807 | C | T | 1 | a0001c0001t0001g0043 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.226+580C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928807 | |||||||
| chr3:136928858 | C | CT | 6 | a0001c0001t0002g0141 a0001c0001t0002g0182 a0001c0001t0002g0183 others(3): Show |
6 | HG02055.hp2 HG02109.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.226+634dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136928858 | ||||||
| chr3:136928861 | T | TA | 11 | a0001c0001t0001g0006 a0001c0001t0001g0022 a0001c0001t0001g0055 others(8): Show |
11 | HG00423.hp1 HG01358.hp2 HG01433.hp2 others(8): Show |
intron_variant | MODIFIER | c.226+658dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136928861 | ||||||
| chr3:136928861 | TA | T | 15 | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0029 others(12): Show |
15 | HG00140.hp2 HG01074.hp2 HG01256.hp1 others(12): Show |
intron_variant | MODIFIER | c.226+658delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136928861 | ||||||
| chr3:136928943 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.226+716G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928943 | |||||||
| chr3:136928965 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+738C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136928965 | |||||||
| chr3:136929062 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+835T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136929062 | |||||||
| chr3:136929063 | G | A | 1 | a0001c0001t0003g0200 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.226+836G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136929063 | |||||||
| chr3:136929765 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+1538T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136929765 | |||||||
| chr3:136929801 | T | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(156): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.226+1574T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136929801 | |||||||
| chr3:136929851 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+1624G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136929851 | |||||||
| chr3:136930015 | C | G | 1 | a0001c0001t0001g0054 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.226+1788C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136930015 | |||||||
| chr3:136930216 | T | TGAAAGTT others(6103): Show |
1 | a0001c0001t0002g0224 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.226+2004_226+2005i others(6112): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136930216 | ||||||
| chr3:136930231 | A | G | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.226+2004A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136930231 | |||||||
| chr3:136930621 | C | T | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.226+2394C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136930621 | |||||||
| chr3:136930768 | C | T | 10 | a0001c0001t0003g0004 a0001c0001t0003g0201 a0001c0001t0003g0203 others(7): Show |
11 | HG00544.hp2 HG02135.hp1 NA18954.hp2 others(8): Show |
intron_variant | MODIFIER | c.226+2541C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136930768 | |||||||
| chr3:136930812 | A | G | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.226+2585A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136930812 | |||||||
| chr3:136930980 | CT | C | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.226+2765delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136930980 | ||||||
| chr3:136931004 | G | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.226+2777G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931004 | |||||||
| chr3:136931017 | T | A | 1 | a0001c0001t0001g0014 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.226+2790T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931017 | |||||||
| chr3:136931022 | G | A | 2 | a0001c0001t0001g0136 a0001c0001t0001g0137 |
2 | HG02055.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.226+2795G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931022 | |||||||
| chr3:136931394 | A | G | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.226+3167A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931394 | |||||||
| chr3:136931568 | AT | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+3346delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136931568 | ||||||
| chr3:136931858 | G | A | 1 | a0001c0001t0001g0041 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.226+3631G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931858 | |||||||
| chr3:136931929 | G | C | 1 | a0001c0001t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.226+3702G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136931929 | |||||||
| chr3:136932085 | T | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(155): Show |
164 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(161): Show |
intron_variant | MODIFIER | c.226+3858T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932085 | |||||||
| chr3:136932118 | C | CA | 12 | a0001c0001t0001g0029 a0001c0001t0001g0129 a0001c0001t0003g0004 others(9): Show |
13 | HG00544.hp2 HG02135.hp1 HG02523.hp2 others(10): Show |
intron_variant | MODIFIER | c.226+3910dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136932118 | ||||||
| chr3:136932118 | CA | C | 11 | a0001c0001t0001g0008 a0001c0001t0001g0022 a0001c0001t0001g0027 others(8): Show |
11 | HG00408.hp2 HG01256.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.226+3910delA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136932118 | ||||||
| chr3:136932133 | A | AG | 13 | a0001c0001t0003g0200 a0001c0001t0003g0202 a0001c0001t0003g0204 others(10): Show |
13 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.226+3906_226+3907i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932133 | |||||||
| chr3:136932133 | A | G | 1 | a0001c0001t0003g0206 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.226+3906A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932133 | |||||||
| chr3:136932311 | A | G | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.226+4084A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932311 | |||||||
| chr3:136932597 | C | G | 5 | a0001c0001t0002g0003 a0001c0001t0002g0145 a0001c0001t0002g0146 others(2): Show |
6 | HG00423.hp1 NA18963.hp2 NA18964.hp2 others(3): Show |
intron_variant | MODIFIER | c.226+4370C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932597 | |||||||
| chr3:136932675 | G | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+4448G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932675 | |||||||
| chr3:136932757 | T | G | 1 | a0001c0001t0014g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.226+4530T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932757 | |||||||
| chr3:136932780 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.226+4553C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932780 | |||||||
| chr3:136932827 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.226+4600A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136932827 | |||||||
| chr3:136933122 | A | C | 129 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(126): Show |
134 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(131): Show |
intron_variant | MODIFIER | c.226+4895A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136933122 | |||||||
| chr3:136933292 | A | G | 24 | a0001c0001t0003g0004 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.226+5065A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136933292 | |||||||
| chr3:136933355 | C | T | 2 | a0001c0001t0001g0049 a0001c0001t0012g0073 |
2 | HG02572.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.226+5128C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136933355 | |||||||
| chr3:136933710 | CT | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.226+5494delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136933710 | ||||||
| chr3:136934039 | T | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+5812T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136934039 | |||||||
| chr3:136934615 | A | G | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.226+6388A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136934615 | |||||||
| chr3:136934829 | A | T | 1 | a0001c0001t0001g0015 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.226+6602A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136934829 | |||||||
| chr3:136934841 | G | A | 159 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(156): Show |
166 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.226+6614G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136934841 | |||||||
| chr3:136935086 | C | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+6859C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136935086 | |||||||
| chr3:136935225 | A | G | 1 | a0001c0001t0005g0198 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.226+6998A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136935225 | |||||||
| chr3:136935842 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+7615C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136935842 | |||||||
| chr3:136936004 | A | C | 1 | a0001c0001t0001g0012 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.226+7777A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936004 | |||||||
| chr3:136936038 | CT | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0008 others(102): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(107): Show |
intron_variant | MODIFIER | c.226+7829delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136936038 | ||||||
| chr3:136936038 | CTT | C | 25 | a0001c0001t0001g0006 a0001c0001t0001g0019 a0001c0001t0001g0029 others(22): Show |
25 | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.226+7828_226+7829d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136936038 | ||||||
| chr3:136936102 | G | A | 3 | a0001c0001t0001g0029 a0001c0001t0001g0041 a0001c0001t0001g0053 |
3 | HG02523.hp2 NA18971.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.226+7875G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936102 | |||||||
| chr3:136936110 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+7883A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936110 | |||||||
| chr3:136936304 | G | A | 2 | a0001c0001t0001g0134 a0001c0001t0001g0135 |
2 | HG02129.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.226+8077G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936304 | |||||||
| chr3:136936443 | C | T | 5 | a0001c0001t0005g0180 a0001c0001t0005g0188 a0001c0001t0005g0189 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.226+8216C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936443 | |||||||
| chr3:136936471 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.226+8244T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936471 | |||||||
| chr3:136936570 | A | G | 1 | a0001c0001t0003g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.226+8343A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936570 | |||||||
| chr3:136936774 | C | T | 4 | a0001c0001t0004g0017 a0001c0001t0004g0018 a0001c0001t0004g0020 others(1): Show |
4 | HG02630.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.226+8547C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936774 | |||||||
| chr3:136936830 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.226+8603T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936830 | |||||||
| chr3:136936899 | A | G | 3 | a0001c0001t0002g0138 a0001c0001t0002g0139 a0001c0001t0002g0140 |
3 | HG03491.hp1 HG03492.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.226+8672A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136936899 | |||||||
| chr3:136937088 | G | A | 3 | a0001c0001t0001g0050 a0001c0001t0001g0052 a0001c0001t0001g0057 |
3 | HG03239.hp1 HG03834.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.227-8495G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937088 | |||||||
| chr3:136937092 | T | C | 1 | a0001c0001t0001g0013 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.227-8491T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937092 | |||||||
| chr3:136937122 | C | T | 2 | a0001c0001t0001g0096 a0001c0001t0002g0162 |
2 | HG02135.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.227-8461C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937122 | |||||||
| chr3:136937187 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.227-8396A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937187 | |||||||
| chr3:136937300 | C | T | 2 | a0001c0001t0001g0035 a0001c0001t0001g0037 |
2 | NA18964.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.227-8283C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937300 | |||||||
| chr3:136937571 | C | T | 5 | a0001c0001t0005g0180 a0001c0001t0005g0188 a0001c0001t0005g0189 others(2): Show |
5 | HG01167.hp1 HG01169.hp2 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-8012C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937571 | |||||||
| chr3:136937751 | C | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0062 others(9): Show |
17 | HG00280.hp2 HG00741.hp1 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.227-7832C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937751 | |||||||
| chr3:136937894 | C | T | 1 | a0001c0001t0002g0143 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.227-7689C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136937894 | |||||||
| chr3:136937952 | AG | A | 135 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(132): Show |
141 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(138): Show |
intron_variant | MODIFIER | c.227-7629delG | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136937952 | ||||||
| chr3:136938110 | T | A | 1 | a0001c0001t0002g0147 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.227-7473T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938110 | |||||||
| chr3:136938428 | TCTGATGT others(3): Show |
T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.227-7153_227-7144d others(12): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136938428 | ||||||
| chr3:136938439 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0123 |
2 | HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.227-7144C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938439 | |||||||
| chr3:136938517 | T | C | 4 | a0001c0001t0001g0014 a0001c0001t0001g0015 a0001c0001t0001g0016 others(1): Show |
4 | HG00099.hp1 HG01256.hp1 HG02738.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-7066T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938517 | |||||||
| chr3:136938578 | A | G | 1 | a0001c0001t0001g0058 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.227-7005A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938578 | |||||||
| chr3:136938765 | A | C | 1 | a0001c0001t0001g0089 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.227-6818A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136938765 | |||||||
| chr3:136939701 | C | T | 1 | a0001c0001t0003g0207 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.227-5882C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939701 | |||||||
| chr3:136939839 | C | CT | 51 | a0001c0001t0002g0003 a0001c0001t0002g0138 a0001c0001t0002g0139 others(48): Show |
52 | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(49): Show |
intron_variant | MODIFIER | c.227-5721dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136939839 | ||||||
| chr3:136939839 | C | CTT | 7 | a0001c0001t0002g0144 a0001c0001t0002g0146 a0001c0001t0002g0151 others(4): Show |
7 | HG00099.hp2 HG00423.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.227-5722_227-5721d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136939839 | ||||||
| chr3:136939846 | T | G | 3 | a0001c0001t0001g0074 a0001c0001t0001g0075 a0001c0001t0001g0081 |
3 | HG02451.hp2 HG02965.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.227-5737T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939846 | |||||||
| chr3:136939858 | TTTTTA | T | 5 | a0001c0001t0001g0047 a0001c0001t0001g0058 a0001c0001t0001g0092 others(2): Show |
5 | HG02615.hp1 HG02897.hp2 NA18939.hp1 others(2): Show |
intron_variant | MODIFIER | c.227-5724_227-5720d others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939858 | |||||||
| chr3:136939859 | TTTTA | T | 121 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(118): Show |
126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.227-5723_227-5720d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939859 | |||||||
| chr3:136939860 | TTTA | T | 8 | a0001c0001t0001g0008 a0001c0001t0001g0039 a0001c0001t0001g0041 others(5): Show |
8 | HG02055.hp1 HG02109.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-5722_227-5720d others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939860 | |||||||
| chr3:136939863 | A | T | 87 | a0001c0001t0002g0003 a0001c0001t0002g0138 a0001c0001t0002g0139 others(84): Show |
90 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.227-5720A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939863 | |||||||
| chr3:136939925 | A | G | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.227-5658A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136939925 | |||||||
| chr3:136940074 | G | C | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-5509G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940074 | |||||||
| chr3:136940126 | G | A | 4 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(1): Show |
4 | NA18939.hp2 NA18955.hp1 NA18959.hp1 others(1): Show |
intron_variant | MODIFIER | c.227-5457G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940126 | |||||||
| chr3:136940270 | T | G | 1 | a0001c0001t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.227-5313T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940270 | |||||||
| chr3:136940320 | A | G | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-5263A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940320 | |||||||
| chr3:136940499 | C | G | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.227-5084C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940499 | |||||||
| chr3:136940810 | G | T | 1 | a0001c0001t0001g0016 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.227-4773G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940810 | |||||||
| chr3:136940882 | C | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.227-4701C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940882 | |||||||
| chr3:136940937 | G | T | 37 | a0001c0001t0002g0003 a0001c0001t0002g0141 a0001c0001t0002g0142 others(34): Show |
38 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(35): Show |
intron_variant | MODIFIER | c.227-4646G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940937 | |||||||
| chr3:136940999 | A | G | 14 | a0001c0001t0003g0200 a0001c0001t0003g0202 a0001c0001t0003g0204 others(11): Show |
14 | HG00738.hp2 HG01106.hp1 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.227-4584A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136940999 | |||||||
| chr3:136941116 | CT | C | 57 | a0001c0001t0001g0069 a0001c0001t0001g0086 a0001c0001t0002g0138 others(54): Show |
59 | HG00140.hp1 HG00544.hp2 HG00738.hp2 others(56): Show |
intron_variant | MODIFIER | c.227-4449delT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136941116 | ||||||
| chr3:136941116 | CTT | C | 131 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(128): Show |
136 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(133): Show |
intron_variant | MODIFIER | c.227-4450_227-4449d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136941116 | ||||||
| chr3:136941318 | C | T | 1 | a0001c0001t0001g0033 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.227-4265C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136941318 | |||||||
| chr3:136941381 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.227-4202T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136941381 | |||||||
| chr3:136941623 | C | A | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-3960C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136941623 | |||||||
| chr3:136941713 | C | CA | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.227-3861dupA | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136941713 | ||||||
| chr3:136941943 | A | G | 1 | a0001c0001t0009g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.227-3640A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136941943 | |||||||
| chr3:136942088 | G | T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.227-3495G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942088 | |||||||
| chr3:136942237 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.227-3346G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942237 | |||||||
| chr3:136942505 | A | G | 1 | a0001c0001t0001g0223 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.227-3078A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942505 | |||||||
| chr3:136942741 | T | A | 1 | a0001c0001t0002g0161 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.227-2842T>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942741 | |||||||
| chr3:136942901 | A | C | 1 | a0001c0001t0002g0147 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.227-2682A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942901 | |||||||
| chr3:136942955 | C | T | 1 | a0001c0001t0001g0085 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.227-2628C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136942955 | |||||||
| chr3:136943220 | G | A | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.227-2363G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943220 | |||||||
| chr3:136943492 | G | GAACCTTC others(8): Show |
1 | a0005c0005t0008g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-2088_227-2074d others(17): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136943492 | ||||||
| chr3:136943687 | C | T | 24 | a0001c0001t0003g0004 a0001c0001t0003g0200 a0001c0001t0003g0201 others(21): Show |
25 | HG00544.hp2 HG00738.hp2 HG01106.hp1 others(22): Show |
intron_variant | MODIFIER | c.227-1896C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943687 | |||||||
| chr3:136943761 | G | A | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.227-1822G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943761 | |||||||
| chr3:136943766 | C | A | 1 | a0005c0005t0008g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-1817C>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943766 | |||||||
| chr3:136943767 | A | C | 1 | a0005c0005t0008g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-1816A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136943767 | |||||||
| chr3:136944015 | A | T | 1 | a0005c0005t0008g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-1568A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944015 | |||||||
| chr3:136944110 | AC | A | 33 | a0001c0001t0001g0069 a0001c0001t0002g0003 a0001c0001t0002g0144 others(30): Show |
34 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(31): Show |
intron_variant | MODIFIER | c.227-1471delC | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | INFO_REALIGN_3_PRIME | chr3 | 136944110 | ||||||
| chr3:136944111 | C | CT | 6 | a0001c0001t0002g0169 a0001c0001t0002g0185 a0001c0001t0002g0224 others(3): Show |
6 | HG02055.hp2 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(3): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | C | CTTTTTT | 5 | a0001c0001t0001g0002 a0001c0001t0001g0027 a0001c0001t0001g0068 others(2): Show |
6 | HG01074.hp1 HG01346.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | C | CTTTTTTT | 10 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0022 others(7): Show |
13 | HG00280.hp2 HG00741.hp1 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(9): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | C | CTTTTTTT others(1): Show |
7 | a0001c0001t0001g0019 a0001c0001t0001g0042 a0001c0001t0001g0049 others(4): Show |
7 | HG01109.hp2 HG01496.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(10): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0051 a0001c0001t0001g0058 a0001c0001t0001g0059 others(3): Show |
6 | HG01109.hp1 HG01891.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(11): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | C | CTTTTTTT others(3): Show |
10 | a0001c0001t0001g0029 a0001c0001t0001g0038 a0001c0001t0001g0077 others(7): Show |
10 | HG00609.hp2 HG00738.hp1 HG01070.hp2 others(7): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(12): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | C | CTTTTTTT others(4): Show |
11 | a0001c0001t0001g0006 a0001c0001t0001g0033 a0001c0001t0001g0037 others(8): Show |
11 | HG00544.hp1 HG01261.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(13): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | C | CTTTTTTT others(5): Show |
8 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0035 others(5): Show |
8 | HG00621.hp2 HG01167.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-1472_227-1471i others(14): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | CCT | C | 16 | a0001c0001t0001g0067 a0001c0001t0003g0004 a0001c0001t0003g0201 others(13): Show |
17 | HG00738.hp2 HG01106.hp1 HG01433.hp2 others(14): Show |
intron_variant | MODIFIER | c.227-1471_227-1470d others(4): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | CCTT | C | 6 | a0001c0001t0003g0202 a0001c0001t0003g0212 a0001c0001t0003g0213 others(3): Show |
6 | HG01243.hp1 HG02897.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.227-1471_227-1469d others(5): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | CCTTT | C | 8 | a0001c0001t0001g0057 a0001c0001t0001g0086 a0001c0001t0001g0088 others(5): Show |
8 | HG00408.hp1 HG00741.hp2 HG01346.hp2 others(5): Show |
intron_variant | MODIFIER | c.227-1471_227-1468d others(6): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | CCTTTT | C | 58 | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0011 others(55): Show |
58 | HG00099.hp1 HG00140.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.227-1471_227-1467d others(7): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | CCTTTTT | C | 3 | a0001c0001t0001g0054 a0001c0001t0001g0090 a0001c0001t0001g0103 |
3 | HG01169.hp1 NA19060.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.227-1471_227-1466d others(8): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | CCTTTTTT others(7): Show |
C | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-1471_227-1458d others(16): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944111 | CCTTTTTT others(8): Show |
C | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.227-1471_227-1457d others(17): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944111 | |||||||
| chr3:136944112 | C | T | 95 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(92): Show |
100 | HG00140.hp1 HG00280.hp2 HG00544.hp1 others(97): Show |
intron_variant | MODIFIER | c.227-1471C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944112 | |||||||
| chr3:136944199 | A | G | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.227-1384A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944199 | |||||||
| chr3:136944428 | A | G | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-1155A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944428 | |||||||
| chr3:136944448 | G | A | 1 | a0001c0001t0001g0019 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.227-1135G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944448 | |||||||
| chr3:136944457 | A | G | 2 | a0001c0001t0001g0013 a0001c0001t0001g0051 |
2 | HG01891.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.227-1126A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944457 | |||||||
| chr3:136944561 | A | T | 1 | a0005c0005t0008g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-1022A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944561 | |||||||
| chr3:136944642 | A | T | 1 | a0005c0005t0008g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.227-941A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944642 | |||||||
| chr3:136944793 | C | T | 17 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0031 others(14): Show |
17 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.227-790C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136944793 | |||||||
| chr3:136945054 | G | T | 1 | a0001c0001t0002g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.227-529G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945054 | |||||||
| chr3:136945055 | C | T | 1 | a0001c0001t0002g0177 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.227-528C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945055 | |||||||
| chr3:136945216 | G | A | 1 | a0001c0001t0007g0005 | 2 | HG03139.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.227-367G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945216 | |||||||
| chr3:136945285 | A | G | 1 | a0001c0001t0001g0008 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.227-298A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945285 | |||||||
| chr3:136945313 | T | G | 1 | a0001c0001t0001g0064 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.227-270T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945313 | |||||||
| chr3:136945561 | T | C | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.227-22T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 2/3 | chr3 | 136945561 | |||||||
| chr3:136946349 | A | G | 1 | a0001c0001t0009g0179 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.939+54A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946349 | |||||||
| chr3:136946436 | A | G | 2 | a0001c0001t0003g0209 a0001c0001t0003g0220 |
2 | HG00544.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.939+141A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946436 | |||||||
| chr3:136946666 | TTGGATGC others(9): Show |
T | 134 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(131): Show |
139 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.939+372_939+387del others(16): Show |
NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946666 | |||||||
| chr3:136946684 | A | G | 1 | a0005c0005t0008g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.939+389A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946684 | |||||||
| chr3:136946711 | T | C | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.939+416T>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946711 | |||||||
| chr3:136946799 | A | T | 1 | a0001c0001t0002g0192 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.939+504A>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136946799 | |||||||
| chr3:136946981 | C | CT | 19 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0031 others(16): Show |
19 | HG00544.hp1 HG00609.hp2 HG00621.hp2 others(16): Show |
intron_variant | MODIFIER | c.939+689dupT | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | INFO_REALIGN_3_PRIME | chr3 | 136946981 | ||||||
| chr3:136947055 | G | A | 1 | a0001c0001t0014g0023 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.939+760G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947055 | |||||||
| chr3:136947153 | G | C | 1 | a0001c0001t0001g0047 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.939+858G>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947153 | |||||||
| chr3:136947204 | T | G | 1 | a0001c0001t0015g0007 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.939+909T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947204 | |||||||
| chr3:136947467 | G | A | 3 | a0001c0001t0001g0122 a0001c0001t0001g0123 a0001c0001t0001g0132 |
3 | HG01433.hp1 HG02723.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.940-792G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947467 | |||||||
| chr3:136947525 | T | G | 1 | a0005c0005t0008g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.940-734T>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947525 | |||||||
| chr3:136947527 | G | T | 1 | a0005c0005t0008g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.940-732G>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947527 | |||||||
| chr3:136947528 | C | G | 1 | a0005c0005t0008g0128 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.940-731C>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947528 | |||||||
| chr3:136947612 | C | T | 132 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(129): Show |
137 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.940-647C>T | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947612 | |||||||
| chr3:136947757 | A | G | 133 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0006 others(130): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(135): Show |
intron_variant | MODIFIER | c.940-502A>G | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136947757 | |||||||
| chr3:136948042 | G | A | 2 | a0001c0001t0003g0209 a0001c0001t0003g0220 |
2 | HG00544.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.940-217G>A | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136948042 | |||||||
| chr3:136948194 | A | C | 1 | a0002c0002t0002g0196 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.940-65A>C | NCK1 | ENSG00000158092.7 | transcript | ENST00000481752.6 | protein_coding | 3/3 | chr3 | 136948194 |