Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 7294 |
| ensemblid | ENSG00000074966.11 |
| hgncid | 12434 |
| symbol | TXK |
| name | TXK tyrosine kinase |
| refseq_nuc | NM_003328.3 |
| refseq_prot | NP_003319.2 |
| ensembl_nuc | ENST00000264316.9 |
| ensembl_prot | ENSP00000264316.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 48066393 |
| end | 48134250 |
| strand | - |
| ver | v1.2 |
| region | chr4:48066393-48134250 |
| region5000 | chr4:48061393-48139250 |
| regionname0 | TXK_chr4_48066393_48134250 |
| regionname5000 | TXK_chr4_48061393_48139250 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 527 | 299 | 89 | 38 | 132 | 4 | 34 | 99 | TXK_chr4_48061393_48139250 | TXK | MILSS others(522): Show |
chr4 | 48061393 | 48139250 |
| a0002 | 0/0 | 527 | 49 | 3 | 20 | 14 | 5 | 7 | 9 | TXK_chr4_48061393_48139250 | TXK | MILSS others(522): Show |
chr4 | 48061393 | 48139250 |
| a0003 | 0/0 | 527 | 11 | 0 | 6 | 0 | 4 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | MILSS others(522): Show |
chr4 | 48061393 | 48139250 |
| a0004 | 0/0 | 527 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | TXK_chr4_48061393_48139250 | TXK | MILSS others(522): Show |
chr4 | 48061393 | 48139250 |
| a0005 | 0/0 | 527 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | MILSS others(522): Show |
chr4 | 48061393 | 48139250 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1581 | 169 | 41 | 24 | 78 | 2 | 22 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0001c0002 | 0/0 | 1581 | 97 | 22 | 12 | 50 | 2 | 11 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0001c0005 | 0/0 | 1581 | 8 | 8 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0001c0006 | 0/0 | 1581 | 7 | 7 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0001c0007 | 0/0 | 1581 | 6 | 4 | 1 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0001c0008 | 0/0 | 1581 | 4 | 4 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0001c0009 | 0/0 | 1581 | 4 | 0 | 0 | 4 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0001c0010 | 0/0 | 1581 | 2 | 2 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0001c0014 | 0/0 | 1581 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0001c0015 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0002c0003 | 0/0 | 1581 | 47 | 3 | 19 | 13 | 5 | 7 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0002c0012 | 0/0 | 1581 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0002c0013 | 0/0 | 1581 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0003c0004 | 0/0 | 1581 | 11 | 0 | 6 | 0 | 4 | 1 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0004c0011 | 0/0 | 1581 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 | ||
| a0005c0016 | 0/0 | 1581 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | ATGAT others(1576): Show |
chr4 | 48061393 | 48139250 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2908 | 60 | 6 | 6 | 43 | 1 | 3 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0001t0002 | 0/0 | 2908 | 62 | 1 | 17 | 35 | 1 | 8 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0001t0003 | 0/0 | 2908 | 20 | 10 | 0 | 0 | 0 | 10 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0001t0004 | 1/0 | 2908 | 19 | 17 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0001t0005 | 0/0 | 2908 | 5 | 5 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0001t0006 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0001t0007 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0001t0009 | 0/0 | 2908 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0002t0001 | 0/0 | 2908 | 96 | 22 | 12 | 49 | 2 | 11 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0002t0008 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0005t0001 | 0/0 | 2908 | 8 | 8 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0006t0001 | 0/0 | 2908 | 7 | 7 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0007t0001 | 0/0 | 2908 | 6 | 4 | 1 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0008t0003 | 0/0 | 2908 | 3 | 3 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0008t0006 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0009t0001 | 0/0 | 2908 | 4 | 0 | 0 | 4 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0010t0001 | 0/0 | 2908 | 2 | 2 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0014t0001 | 0/0 | 2908 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0001c0015t0001 | 0/0 | 2908 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0002c0003t0001 | 0/0 | 2908 | 47 | 3 | 19 | 13 | 5 | 7 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0002c0012t0002 | 0/0 | 2908 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0002c0013t0001 | 0/0 | 2908 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0003c0004t0003 | 0/0 | 2908 | 11 | 0 | 6 | 0 | 4 | 1 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0004c0011t0001 | 0/0 | 2908 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| a0005c0016t0001 | 0/0 | 2908 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | AGTTG others(2903): Show |
chr4 | 48061393 | 48139250 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0167 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0023 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0004g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0005g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0005g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0005g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0006g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0007g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0001t0009g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0001 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0008 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0012 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0017 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0002t0008g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0006 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0005t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0006t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0007t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0008t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0008t0003g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0008t0003g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0008t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0009t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0010t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0010t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0014t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0001c0015t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0005 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0009 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0003t0001g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0012t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0002c0013t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0002 | 0/0 | 4 | 0 | 3 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0111 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0003c0004t0003g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0004c0011t0001g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| a0005c0016t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0140 | EUR | GBR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00140 | hp2 | a0002 | c0003 | t0001 | g0005 | EUR | GBR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | FIN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00280 | hp2 | a0002 | c0003 | t0001 | g0243 | EUR | FIN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00323 | hp1 | a0003 | c0004 | t0003 | g0118 | EUR | FIN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00323 | hp2 | a0001 | c0002 | t0001 | g0101 | EUR | FIN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0315 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00438 | hp1 | a0001 | c0002 | t0001 | g0274 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0069 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00597 | hp1 | a0001 | c0002 | t0001 | g0045 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00597 | hp2 | a0001 | c0001 | t0002 | g0303 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00609 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00621 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00639 | hp1 | a0002 | c0003 | t0001 | g0009 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00639 | hp2 | a0003 | c0004 | t0003 | g0139 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00642 | hp1 | a0002 | c0012 | t0002 | g0247 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0265 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0295 | EAS | CHS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0195 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00733 | hp2 | a0002 | c0003 | t0001 | g0009 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00735 | hp1 | a0002 | c0003 | t0001 | g0250 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00735 | hp2 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG00738 | hp2 | a0002 | c0003 | t0001 | g0009 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01071 | hp1 | a0002 | c0003 | t0001 | g0259 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0001 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0085 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01109 | hp1 | a0003 | c0004 | t0003 | g0002 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0233 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01167 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01168 | hp1 | a0001 | c0001 | t0002 | g0196 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01168 | hp2 | a0002 | c0003 | t0001 | g0261 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01169 | hp2 | a0002 | c0003 | t0001 | g0249 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0224 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01175 | hp2 | a0002 | c0003 | t0001 | g0235 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01192 | hp1 | a0002 | c0003 | t0001 | g0318 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01192 | hp2 | a0002 | c0003 | t0001 | g0232 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01243 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01243 | hp2 | a0001 | c0015 | t0001 | g0040 | AMR | PUR | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01255 | hp1 | a0001 | c0007 | t0001 | g0109 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01255 | hp2 | a0001 | c0001 | t0004 | g0096 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01256 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0049 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0093 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01346 | hp2 | a0001 | c0002 | t0001 | g0226 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01358 | hp1 | a0002 | c0003 | t0001 | g0054 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01358 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01361 | hp2 | a0003 | c0004 | t0003 | g0002 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0092 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01496 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01515 | hp1 | a0002 | c0003 | t0001 | g0011 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01515 | hp2 | a0005 | c0016 | t0001 | g0175 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01516 | hp1 | a0003 | c0004 | t0003 | g0111 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01516 | hp2 | a0002 | c0003 | t0001 | g0246 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01517 | hp1 | a0002 | c0003 | t0001 | g0011 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01517 | hp2 | a0003 | c0004 | t0003 | g0002 | EUR | IBS | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01884 | hp1 | a0001 | c0006 | t0001 | g0127 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01884 | hp2 | a0001 | c0001 | t0005 | g0321 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0311 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0254 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0001 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01928 | hp2 | a0002 | c0003 | t0001 | g0238 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0094 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01943 | hp2 | a0002 | c0003 | t0001 | g0089 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01952 | hp1 | a0002 | c0003 | t0001 | g0241 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01978 | hp1 | a0002 | c0003 | t0001 | g0050 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01978 | hp2 | a0002 | c0003 | t0001 | g0005 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01993 | hp2 | a0002 | c0003 | t0001 | g0248 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02004 | hp1 | a0002 | c0003 | t0001 | g0005 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02004 | hp2 | a0001 | c0001 | t0002 | g0203 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0291 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02027 | hp2 | a0002 | c0003 | t0001 | g0060 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02040 | hp1 | a0001 | c0002 | t0001 | g0206 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02040 | hp2 | a0002 | c0003 | t0001 | g0061 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0234 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02055 | hp2 | a0002 | c0003 | t0001 | g0320 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02056 | hp2 | a0002 | c0003 | t0001 | g0240 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02071 | hp1 | a0002 | c0003 | t0001 | g0063 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0098 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02132 | hp2 | a0002 | c0003 | t0001 | g0172 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02145 | hp1 | a0001 | c0007 | t0001 | g0124 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0037 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02148 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02155 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | CDX | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CDX | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02257 | hp1 | a0001 | c0014 | t0001 | g0032 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0191 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02258 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02273 | hp2 | a0001 | c0002 | t0001 | g0091 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02280 | hp1 | a0001 | c0002 | t0001 | g0270 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0209 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02300 | hp1 | a0001 | c0001 | t0002 | g0266 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02300 | hp2 | a0003 | c0004 | t0003 | g0112 | AMR | PEL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02451 | hp1 | a0001 | c0006 | t0001 | g0036 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02451 | hp2 | a0001 | c0001 | t0004 | g0253 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02523 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02523 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | KHV | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02572 | hp1 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02572 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0071 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02615 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02615 | hp2 | a0001 | c0002 | t0001 | g0264 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0188 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0252 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02630 | hp2 | a0001 | c0001 | t0005 | g0025 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02647 | hp2 | a0001 | c0005 | t0001 | g0030 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02698 | hp1 | a0001 | c0001 | t0009 | g0217 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02698 | hp2 | a0002 | c0003 | t0001 | g0237 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0256 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02717 | hp2 | a0001 | c0010 | t0001 | g0119 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0312 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0077 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02738 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02738 | hp2 | a0002 | c0003 | t0001 | g0095 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02809 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02809 | hp2 | a0001 | c0002 | t0001 | g0231 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0184 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02818 | hp2 | a0001 | c0005 | t0001 | g0033 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0081 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02886 | hp2 | a0001 | c0008 | t0006 | g0229 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02895 | hp1 | a0001 | c0002 | t0001 | g0099 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02895 | hp2 | a0001 | c0006 | t0001 | g0283 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02897 | hp1 | a0001 | c0008 | t0003 | g0227 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02897 | hp2 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02922 | hp1 | a0001 | c0010 | t0001 | g0214 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02965 | hp1 | a0001 | c0001 | t0004 | g0181 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02965 | hp2 | a0001 | c0001 | t0005 | g0046 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02970 | hp2 | a0001 | c0001 | t0004 | g0185 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0245 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0257 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0110 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03017 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03041 | hp1 | a0001 | c0001 | t0004 | g0192 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0282 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03098 | hp1 | a0001 | c0006 | t0001 | g0035 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03098 | hp2 | a0001 | c0006 | t0001 | g0097 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03130 | hp1 | a0001 | c0005 | t0001 | g0031 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03130 | hp2 | a0001 | c0001 | t0005 | g0322 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03139 | hp1 | a0001 | c0005 | t0001 | g0029 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03139 | hp2 | a0001 | c0006 | t0001 | g0038 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0183 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0279 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03225 | hp1 | a0001 | c0002 | t0001 | g0263 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03225 | hp2 | a0001 | c0001 | t0004 | g0187 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03239 | hp1 | a0003 | c0004 | t0003 | g0114 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03239 | hp2 | a0001 | c0007 | t0001 | g0165 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0273 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03486 | hp2 | a0001 | c0001 | t0004 | g0126 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03491 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0065 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03492 | hp1 | a0002 | c0003 | t0001 | g0319 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0066 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03516 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03516 | hp2 | a0001 | c0001 | t0004 | g0190 | AFR | ESN | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0079 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03540 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0078 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0269 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0104 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03654 | hp2 | a0001 | c0001 | t0003 | g0107 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03669 | hp1 | a0001 | c0002 | t0001 | g0012 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0026 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03710 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03710 | hp2 | a0001 | c0001 | t0002 | g0204 | SAS | PJL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03831 | hp2 | a0002 | c0003 | t0001 | g0242 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03834 | hp1 | a0001 | c0001 | t0003 | g0105 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03834 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03942 | hp1 | a0001 | c0001 | t0003 | g0106 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03942 | hp2 | a0001 | c0002 | t0001 | g0012 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0059 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04184 | hp2 | a0001 | c0001 | t0002 | g0215 | SAS | BEB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04199 | hp1 | a0002 | c0003 | t0001 | g0262 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04199 | hp2 | a0001 | c0002 | t0001 | g0044 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0113 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04204 | hp2 | a0002 | c0003 | t0001 | g0239 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04228 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG04228 | hp2 | a0001 | c0001 | t0003 | g0138 | SAS | STU | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18612 | hp2 | a0001 | c0002 | t0001 | g0169 | EAS | CHB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0199 | EAS | CHB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0176 | EAS | CHB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0258 | AFR | YRI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0189 | AFR | YRI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18939 | hp2 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18940 | hp2 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18942 | hp1 | a0004 | c0011 | t0001 | g0016 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0086 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18944 | hp1 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18945 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18945 | hp2 | a0001 | c0002 | t0001 | g0307 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18949 | hp1 | a0002 | c0013 | t0001 | g0052 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18957 | hp1 | a0001 | c0009 | t0001 | g0004 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18957 | hp2 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18960 | hp1 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18960 | hp2 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0102 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18965 | hp1 | a0001 | c0002 | t0001 | g0100 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18967 | hp1 | a0002 | c0003 | t0001 | g0043 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18969 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18969 | hp2 | a0004 | c0011 | t0001 | g0016 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18970 | hp2 | a0001 | c0009 | t0001 | g0004 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18971 | hp2 | a0001 | c0002 | t0001 | g0027 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18973 | hp1 | a0001 | c0001 | t0002 | g0290 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18973 | hp2 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18974 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18974 | hp2 | a0001 | c0002 | t0001 | g0041 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18977 | hp1 | a0001 | c0002 | t0001 | g0133 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18979 | hp1 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18979 | hp2 | a0001 | c0001 | t0002 | g0278 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18981 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0276 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18982 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18984 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18985 | hp1 | a0001 | c0002 | t0001 | g0268 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18989 | hp2 | a0001 | c0002 | t0001 | g0008 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18992 | hp1 | a0001 | c0002 | t0001 | g0024 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18993 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18994 | hp2 | a0001 | c0002 | t0001 | g0202 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18997 | hp1 | a0001 | c0002 | t0001 | g0308 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19001 | hp1 | a0002 | c0003 | t0001 | g0057 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0084 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0090 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19003 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19004 | hp1 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19005 | hp1 | a0001 | c0002 | t0008 | g0048 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19006 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19006 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19007 | hp1 | a0001 | c0002 | t0001 | g0200 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0304 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19011 | hp1 | a0001 | c0009 | t0001 | g0004 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19030 | hp1 | a0001 | c0001 | t0004 | g0186 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19030 | hp2 | a0001 | c0007 | t0001 | g0039 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19043 | hp1 | a0001 | c0001 | t0007 | g0121 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19043 | hp2 | a0001 | c0001 | t0003 | g0309 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19054 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19056 | hp1 | a0001 | c0002 | t0001 | g0072 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19057 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19062 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19063 | hp2 | a0002 | c0003 | t0001 | g0087 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19064 | hp1 | a0002 | c0003 | t0001 | g0010 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19065 | hp2 | a0001 | c0002 | t0001 | g0007 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19075 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19075 | hp2 | a0002 | c0003 | t0001 | g0062 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19078 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19079 | hp1 | a0001 | c0009 | t0001 | g0004 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19079 | hp2 | a0001 | c0002 | t0001 | g0001 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0201 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19080 | hp2 | a0002 | c0003 | t0001 | g0056 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19082 | hp1 | a0002 | c0003 | t0001 | g0058 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19082 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19083 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19087 | hp2 | a0001 | c0002 | t0001 | g0013 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19088 | hp1 | a0001 | c0002 | t0001 | g0267 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19088 | hp2 | a0001 | c0001 | t0002 | g0288 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19090 | hp2 | a0001 | c0002 | t0001 | g0277 | EAS | JPT | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19240 | hp1 | a0001 | c0005 | t0001 | g0006 | AFR | YRI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA19240 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | YRI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20129 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ASW | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ASW | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0017 | EUR | TSI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20752 | hp2 | a0003 | c0004 | t0003 | g0108 | EUR | TSI | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0115 | SAS | GIH | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0017 | SAS | GIH | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01123 | hp1 | a0003 | c0004 | t0003 | g0236 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG01123 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | CLM | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02109 | hp1 | a0001 | c0001 | t0004 | g0179 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02109 | hp2 | a0001 | c0007 | t0001 | g0125 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0260 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02486 | hp2 | a0001 | c0005 | t0001 | g0034 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02559 | hp1 | a0001 | c0008 | t0003 | g0218 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG02559 | hp2 | a0001 | c0001 | t0003 | g0313 | AFR | ACB | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03471 | hp1 | a0001 | c0001 | t0004 | g0180 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG03471 | hp2 | a0001 | c0005 | t0001 | g0006 | AFR | MSL | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG06807 | hp1 | a0001 | c0001 | t0006 | g0244 | AFR | USA | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| HG06807 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | USA | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20300 | hp1 | a0002 | c0003 | t0001 | g0005 | AFR | USA | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA20300 | hp2 | a0001 | c0008 | t0003 | g0228 | AFR | USA | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA21309 | hp1 | a0002 | c0003 | t0001 | g0251 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| NA21309 | hp2 | a0001 | c0007 | t0001 | g0120 | AFR | LWK | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0167 | REF | REF | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0004 | g0223 | REF | REF | TXK_chr4_48061393_48139250 | TXK | chr4 | 48061393 | 48139250 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48080078 | C | T | 1 | a0003 | 11 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(8): Show |
missense_variant | MODERATE | c.1007G>A | p.Arg336Gln | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/15 | 1087/2908 | 1007/1584 | 336/527 | chr4 | 48080078 | |||
| chr4:48094151 | T | C | 1 | a0004 | 2 | NA18942.hp1 NA18969.hp2 |
missense_variant | MODERATE | c.635A>G | p.Gln212Arg | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/15 | 715/2908 | 635/1584 | 212/527 | chr4 | 48094151 | |||
| chr4:48112500 | G | A | 1 | a0005 | 1 | HG01515.hp2 | missense_variant | MODERATE | c.187C>T | p.Arg63Cys | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/15 | 267/2908 | 187/1584 | 63/527 | chr4 | 48112500 | |||
| chr4:48113247 | C | T | 1 | a0002 | 49 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(46): Show |
missense_variant | MODERATE | c.134G>A | p.Arg45His | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/15 | 214/2908 | 134/1584 | 45/527 | chr4 | 48113247 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48067658 | T | A | 1 | a0002c0013 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.1563A>T | p.Thr521Thr | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1643/2908 | 1563/1584 | 521/527 | chr4 | 48067658 | |||
| chr4:48067667 | C | A | 1 | a0002c0013 | 1 | NA18949.hp1 | synonymous_variant | LOW | c.1554G>T | p.Arg518Arg | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1634/2908 | 1554/1584 | 518/527 | chr4 | 48067667 | |||
| chr4:48067679 | G | C | 5 | a0001c0002 a0001c0010 a0001c0014 others(2): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
synonymous_variant | LOW | c.1542C>G | p.Ala514Ala | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1622/2908 | 1542/1584 | 514/527 | chr4 | 48067679 | |||
| chr4:48089751 | G | A | 1 | a0001c0007 | 6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
splice_region_variant&synonymous_variant | LOW | c.783C>T | p.Tyr261Tyr | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/15 | 863/2908 | 783/1584 | 261/527 | chr4 | 48089751 | |||
| chr4:48094084 | A | G | 3 | a0001c0005 a0001c0006 a0001c0014 |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
synonymous_variant | LOW | c.702T>C | p.Asn234Asn | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/15 | 782/2908 | 702/1584 | 234/527 | chr4 | 48094084 | |||
| chr4:48095163 | G | A | 1 | a0001c0015 | 1 | HG01243.hp2 | synonymous_variant | LOW | c.561C>T | p.Ser187Ser | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/15 | 641/2908 | 561/1584 | 187/527 | chr4 | 48095163 | |||
| chr4:48095163 | G | T | 2 | a0001c0008 a0001c0010 |
6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
synonymous_variant | LOW | c.561C>A | p.Ser187Ser | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/15 | 641/2908 | 561/1584 | 187/527 | chr4 | 48095163 | |||
| chr4:48110594 | G | A | 1 | a0001c0009 | 4 | NA18957.hp1 NA18970.hp2 NA19011.hp1 others(1): Show |
synonymous_variant | LOW | c.390C>T | p.Gly130Gly | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/15 | 470/2908 | 390/1584 | 130/527 | chr4 | 48110594 | |||
| chr4:48112489 | C | T | 2 | a0001c0005 a0001c0014 |
9 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
synonymous_variant | LOW | c.198G>A | p.Pro66Pro | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/15 | 278/2908 | 198/1584 | 66/527 | chr4 | 48112489 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48066429 | T | C | 1 | a0001c0002t0008 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1208A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1208 | chr4 | 48066429 | ||||||
| chr4:48066608 | T | C | 24 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(21): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
3_prime_UTR_variant | MODIFIER | c.*1029A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1029 | chr4 | 48066608 | ||||||
| chr4:48066610 | A | T | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(15): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*1027T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 1027 | chr4 | 48066610 | ||||||
| chr4:48066766 | G | A | 3 | a0001c0001t0002 a0001c0001t0009 a0002c0012t0002 |
64 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*871C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 871 | chr4 | 48066766 | ||||||
| chr4:48067270 | T | A | 18 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0007 others(15): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
3_prime_UTR_variant | MODIFIER | c.*367A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 367 | chr4 | 48067270 | ||||||
| chr4:48067275 | C | T | 1 | a0001c0001t0007 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*362G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 362 | chr4 | 48067275 | ||||||
| chr4:48067304 | T | C | 1 | a0001c0001t0005 | 5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*333A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 333 | chr4 | 48067304 | ||||||
| chr4:48067371 | G | A | 1 | a0001c0001t0009 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*266C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 266 | chr4 | 48067371 | ||||||
| chr4:48067445 | A | G | 2 | a0001c0001t0006 a0001c0008t0006 |
2 | HG02886.hp2 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*192T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 15/15 | 192 | chr4 | 48067445 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr4:48067708 | G | A | 128 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(125): Show |
148 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(145): Show |
splice_region_variant&intron_variant | LOW | c.1516-3C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48067708 | |||||||
| chr4:48067720 | T | G | 1 | a0001c0001t0005g0322 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1516-15A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48067720 | |||||||
| chr4:48067883 | C | G | 1 | a0002c0003t0001g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1516-178G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48067883 | |||||||
| chr4:48067936 | A | T | 1 | a0002c0013t0001g0052 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1516-231T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48067936 | |||||||
| chr4:48068056 | C | T | 1 | a0002c0003t0001g0172 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1516-351G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068056 | |||||||
| chr4:48068213 | C | T | 1 | a0001c0001t0003g0312 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1516-508G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068213 | |||||||
| chr4:48068838 | G | A | 302 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(299): Show |
342 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.1516-1133C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068838 | |||||||
| chr4:48068913 | G | GCTCTGTG others(130): Show |
75 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(72): Show |
87 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1516-1209_1516-120 others(141): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068913 | |||||||
| chr4:48068934 | T | C | 44 | a0001c0002t0001g0017 a0001c0002t0001g0092 a0001c0002t0001g0226 others(41): Show |
52 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.1516-1229A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068934 | |||||||
| chr4:48068936 | C | T | 265 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1516-1231G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48068936 | |||||||
| chr4:48069173 | A | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1516-1468T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069173 | |||||||
| chr4:48069218 | C | T | 265 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.1516-1513G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069218 | |||||||
| chr4:48069321 | C | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1616G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069321 | |||||||
| chr4:48069322 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1617A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069322 | |||||||
| chr4:48069323 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1618A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069323 | |||||||
| chr4:48069324 | T | G | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1619A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069324 | |||||||
| chr4:48069325 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1620A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069325 | |||||||
| chr4:48069326 | C | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1621G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069326 | |||||||
| chr4:48069326 | C | CTT | 15 | a0001c0001t0003g0269 a0001c0001t0003g0273 a0001c0001t0003g0279 others(12): Show |
15 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1516-1623_1516-162 others(6): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069326 | |||||||
| chr4:48069327 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1622A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069327 | |||||||
| chr4:48069327 | T | TTTTC | 49 | a0001c0002t0001g0017 a0001c0002t0001g0092 a0001c0002t0001g0199 others(46): Show |
57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1516-1623_1516-162 others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069327 | |||||||
| chr4:48069328 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1623A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069328 | |||||||
| chr4:48069328 | T | TTTC | 211 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(208): Show |
239 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(236): Show |
intron_variant | MODIFIER | c.1516-1624_1516-162 others(7): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069328 | |||||||
| chr4:48069329 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1624A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069329 | |||||||
| chr4:48069330 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1625A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069330 | |||||||
| chr4:48069331 | T | G | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1626A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069331 | |||||||
| chr4:48069332 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1627A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069332 | |||||||
| chr4:48069332 | T | C | 49 | a0001c0002t0001g0017 a0001c0002t0001g0092 a0001c0002t0001g0199 others(46): Show |
57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1516-1627A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069332 | |||||||
| chr4:48069333 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(210): Show |
241 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(238): Show |
intron_variant | MODIFIER | c.1516-1628A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069333 | |||||||
| chr4:48069335 | T | G | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1630A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069335 | |||||||
| chr4:48069336 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1631A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069336 | |||||||
| chr4:48069340 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1635A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069340 | |||||||
| chr4:48069356 | G | T | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1651C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069356 | |||||||
| chr4:48069365 | A | T | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1660T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069365 | |||||||
| chr4:48069374 | G | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1669C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069374 | |||||||
| chr4:48069375 | G | C | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1670C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069375 | |||||||
| chr4:48069385 | G | T | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1680C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069385 | |||||||
| chr4:48069386 | T | G | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1681A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069386 | |||||||
| chr4:48069388 | G | C | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1683C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069388 | |||||||
| chr4:48069389 | G | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1684C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069389 | |||||||
| chr4:48069393 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1688A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069393 | |||||||
| chr4:48069406 | A | G | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1701T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069406 | |||||||
| chr4:48069419 | A | T | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1714T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069419 | |||||||
| chr4:48069422 | T | G | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1717A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069422 | |||||||
| chr4:48069424 | C | T | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1719G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069424 | |||||||
| chr4:48069426 | A | C | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1721T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069426 | |||||||
| chr4:48069432 | T | C | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1727A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069432 | |||||||
| chr4:48069434 | T | G | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1729A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069434 | |||||||
| chr4:48069437 | T | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1732A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069437 | |||||||
| chr4:48069453 | G | A | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1748C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069453 | |||||||
| chr4:48069463 | T | C | 1 | a0001c0001t0002g0302 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.1516-1758A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069463 | |||||||
| chr4:48069562 | G | A | 1 | a0001c0002t0001g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1516-1857C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069562 | |||||||
| chr4:48069569 | G | A | 19 | a0001c0001t0003g0269 a0001c0001t0003g0273 a0001c0001t0003g0279 others(16): Show |
20 | HG01884.hp2 HG01891.hp1 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1516-1864C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069569 | |||||||
| chr4:48069578 | A | G | 264 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(261): Show |
300 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(297): Show |
intron_variant | MODIFIER | c.1516-1873T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069578 | |||||||
| chr4:48069621 | C | T | 1 | a0001c0001t0001g0055 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1515+1896G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48069621 | |||||||
| chr4:48070143 | TC | T | 85 | a0001c0001t0001g0103 a0001c0001t0001g0117 a0001c0001t0001g0122 others(82): Show |
93 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(90): Show |
intron_variant | MODIFIER | c.1515+1373delG | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070143 | |||||||
| chr4:48070188 | C | G | 284 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(281): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1515+1329G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070188 | |||||||
| chr4:48070225 | G | T | 1 | a0001c0001t0002g0215 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1515+1292C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070225 | |||||||
| chr4:48070264 | GA | G | 4 | a0001c0002t0001g0231 a0001c0002t0001g0264 a0001c0010t0001g0119 others(1): Show |
4 | HG02615.hp2 HG02717.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1515+1252delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070264 | |||||||
| chr4:48070349 | T | A | 18 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 others(15): Show |
21 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.1515+1168A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070349 | |||||||
| chr4:48070429 | C | T | 1 | a0001c0002t0001g0226 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1515+1088G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070429 | |||||||
| chr4:48070590 | A | T | 73 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(70): Show |
85 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1515+927T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070590 | |||||||
| chr4:48070623 | G | C | 1 | a0001c0002t0001g0206 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1515+894C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070623 | |||||||
| chr4:48070639 | C | T | 269 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(266): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1515+878G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070639 | |||||||
| chr4:48070696 | C | A | 284 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(281): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.1515+821G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070696 | |||||||
| chr4:48070796 | C | G | 35 | a0001c0001t0002g0020 a0001c0001t0002g0021 a0001c0001t0002g0022 others(32): Show |
39 | HG00438.hp2 HG00597.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1515+721G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070796 | |||||||
| chr4:48070831 | G | A | 1 | a0001c0001t0002g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1515+686C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070831 | |||||||
| chr4:48070859 | G | A | 1 | a0001c0002t0001g0075 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1515+658C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070859 | |||||||
| chr4:48070893 | C | CT | 9 | a0001c0001t0002g0208 a0001c0001t0002g0221 a0001c0001t0002g0302 others(6): Show |
9 | HG00735.hp2 HG01123.hp1 HG01175.hp2 others(6): Show |
intron_variant | MODIFIER | c.1515+623dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070893 | |||||||
| chr4:48070893 | CT | C | 93 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(90): Show |
104 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(101): Show |
intron_variant | MODIFIER | c.1515+623delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070893 | |||||||
| chr4:48070893 | CTT | C | 5 | a0001c0001t0001g0122 a0001c0001t0003g0313 a0001c0001t0005g0025 others(2): Show |
6 | HG01884.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1515+622_1515+623d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48070893 | |||||||
| chr4:48071056 | C | T | 59 | a0001c0001t0002g0018 a0001c0001t0002g0020 a0001c0001t0002g0021 others(56): Show |
64 | HG00140.hp1 HG00438.hp2 HG00597.hp2 others(61): Show |
intron_variant | MODIFIER | c.1515+461G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071056 | |||||||
| chr4:48071283 | G | C | 213 | a0001c0001t0001g0103 a0001c0001t0001g0117 a0001c0001t0001g0122 others(210): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1515+234C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071283 | |||||||
| chr4:48071284 | A | G | 1 | a0001c0001t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1515+233T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071284 | |||||||
| chr4:48071297 | A | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.1515+220T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071297 | |||||||
| chr4:48071339 | A | T | 75 | a0001c0002t0001g0001 a0001c0002t0001g0007 a0001c0002t0001g0008 others(72): Show |
87 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.1515+178T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071339 | |||||||
| chr4:48071356 | T | C | 8 | a0001c0001t0003g0269 a0001c0001t0003g0273 a0001c0001t0003g0279 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.1515+161A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071356 | |||||||
| chr4:48071484 | G | T | 269 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(266): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1515+33C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 14/14 | chr4 | 48071484 | |||||||
| chr4:48071919 | C | T | 15 | a0001c0001t0003g0269 a0001c0001t0003g0273 a0001c0001t0003g0279 others(12): Show |
15 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1358-245G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48071919 | |||||||
| chr4:48071920 | T | C | 213 | a0001c0001t0001g0103 a0001c0001t0001g0117 a0001c0001t0001g0122 others(210): Show |
241 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(238): Show |
intron_variant | MODIFIER | c.1358-246A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48071920 | |||||||
| chr4:48071956 | C | CT | 211 | a0001c0001t0001g0103 a0001c0001t0001g0117 a0001c0001t0001g0122 others(208): Show |
239 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(236): Show |
intron_variant | MODIFIER | c.1358-283dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48071956 | |||||||
| chr4:48071984 | C | T | 1 | a0001c0001t0003g0281 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1358-310G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48071984 | |||||||
| chr4:48072118 | T | G | 1 | a0002c0003t0001g0238 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1358-444A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48072118 | |||||||
| chr4:48072155 | C | G | 1 | a0001c0001t0003g0105 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1358-481G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48072155 | |||||||
| chr4:48072669 | T | C | 2 | a0001c0001t0006g0244 a0001c0008t0006g0229 |
2 | HG02886.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.1358-995A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48072669 | |||||||
| chr4:48072702 | T | C | 1 | a0001c0001t0003g0269 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1358-1028A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48072702 | |||||||
| chr4:48073010 | A | T | 1 | a0001c0002t0001g0084 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1357+925T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073010 | |||||||
| chr4:48073091 | A | AT | 161 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(158): Show |
179 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(176): Show |
intron_variant | MODIFIER | c.1357+843dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073091 | |||||||
| chr4:48073091 | A | ATT | 57 | a0001c0001t0001g0157 a0001c0001t0002g0204 a0001c0001t0002g0278 others(54): Show |
65 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(62): Show |
intron_variant | MODIFIER | c.1357+842_1357+843d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073091 | |||||||
| chr4:48073091 | A | ATTT | 73 | a0001c0001t0002g0068 a0001c0002t0001g0001 a0001c0002t0001g0007 others(70): Show |
85 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(82): Show |
intron_variant | MODIFIER | c.1357+841_1357+843d others(5): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073091 | |||||||
| chr4:48073117 | G | T | 2 | a0001c0002t0001g0071 a0001c0002t0001g0077 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.1357+818C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073117 | |||||||
| chr4:48073582 | T | C | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1357+353A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073582 | |||||||
| chr4:48073814 | A | G | 1 | a0001c0007t0001g0125 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1357+121T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 13/14 | chr4 | 48073814 | |||||||
| chr4:48074074 | G | A | 20 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0003g0104 others(17): Show |
23 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1239-21C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074074 | |||||||
| chr4:48074106 | T | C | 1 | a0001c0001t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1239-53A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074106 | |||||||
| chr4:48074231 | A | G | 80 | a0001c0001t0001g0103 a0001c0001t0001g0177 a0001c0001t0002g0018 others(77): Show |
88 | HG00140.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1239-178T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074231 | |||||||
| chr4:48074300 | C | T | 1 | a0001c0002t0001g0082 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1239-247G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074300 | |||||||
| chr4:48074376 | TA | T | 3 | a0001c0002t0001g0012 a0001c0002t0001g0042 a0001c0002t0001g0044 |
4 | HG03669.hp1 HG03834.hp2 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-324delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074376 | |||||||
| chr4:48074468 | C | T | 6 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.1239-415G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074468 | |||||||
| chr4:48074469 | G | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
63 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1239-416C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074469 | |||||||
| chr4:48074545 | T | A | 132 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(129): Show |
149 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(146): Show |
intron_variant | MODIFIER | c.1239-492A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074545 | |||||||
| chr4:48074689 | TGAG | T | 4 | a0001c0001t0001g0177 a0001c0006t0001g0097 a0001c0006t0001g0127 others(1): Show |
4 | HG01884.hp1 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239-639_1239-637d others(5): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074689 | |||||||
| chr4:48074707 | A | G | 25 | a0001c0001t0003g0269 a0001c0001t0003g0273 a0001c0001t0003g0279 others(22): Show |
27 | HG01891.hp1 HG02258.hp1 HG02486.hp2 others(24): Show |
intron_variant | MODIFIER | c.1239-654T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074707 | |||||||
| chr4:48074976 | G | A | 1 | a0001c0001t0004g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1239-923C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48074976 | |||||||
| chr4:48075070 | C | T | 1 | a0002c0003t0001g0172 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1239-1017G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075070 | |||||||
| chr4:48075089 | G | A | 54 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(51): Show |
63 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.1239-1036C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075089 | |||||||
| chr4:48075121 | A | G | 1 | a0001c0001t0004g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1239-1068T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075121 | |||||||
| chr4:48075247 | C | T | 47 | a0001c0001t0002g0271 a0001c0002t0001g0017 a0001c0002t0001g0092 others(44): Show |
55 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.1238+1155G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075247 | |||||||
| chr4:48075300 | T | C | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1238+1102A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075300 | |||||||
| chr4:48075312 | T | C | 52 | a0001c0001t0001g0103 a0001c0001t0003g0309 a0001c0002t0001g0017 others(49): Show |
60 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.1238+1090A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075312 | |||||||
| chr4:48075367 | C | T | 4 | a0003c0004t0003g0002 a0003c0004t0003g0111 a0003c0004t0003g0112 others(1): Show |
7 | HG00323.hp1 HG01109.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.1238+1035G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075367 | |||||||
| chr4:48075676 | A | G | 1 | a0001c0001t0003g0106 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1238+726T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075676 | |||||||
| chr4:48075805 | A | C | 289 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(286): Show |
328 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(325): Show |
intron_variant | MODIFIER | c.1238+597T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075805 | |||||||
| chr4:48075827 | G | A | 1 | a0001c0001t0003g0279 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1238+575C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075827 | |||||||
| chr4:48075875 | C | A | 1 | a0001c0001t0001g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1238+527G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075875 | |||||||
| chr4:48075945 | G | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1238+457C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 12/14 | chr4 | 48075945 | |||||||
| chr4:48076576 | C | A | 216 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(213): Show |
245 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(242): Show |
intron_variant | MODIFIER | c.1174-110G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48076576 | |||||||
| chr4:48076968 | A | G | 15 | a0001c0001t0001g0177 a0001c0005t0001g0006 a0001c0005t0001g0029 others(12): Show |
17 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1174-502T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48076968 | |||||||
| chr4:48077271 | A | C | 8 | a0001c0002t0001g0045 a0001c0002t0001g0065 a0001c0002t0001g0066 others(5): Show |
8 | HG00558.hp2 HG00597.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.1174-805T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48077271 | |||||||
| chr4:48077273 | G | GTAAAC | 297 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(294): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1174-808_1174-807i others(7): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48077273 | |||||||
| chr4:48077519 | G | GA | 297 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(294): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1174-1054dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48077519 | |||||||
| chr4:48077579 | G | A | 2 | a0001c0001t0004g0126 a0001c0001t0004g0182 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1174-1113C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48077579 | |||||||
| chr4:48077907 | G | A | 297 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(294): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.1174-1441C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48077907 | |||||||
| chr4:48078102 | G | A | 9 | a0001c0001t0001g0014 a0001c0001t0001g0128 a0001c0001t0001g0142 others(6): Show |
13 | NA18940.hp1 NA18949.hp2 NA18957.hp1 others(10): Show |
intron_variant | MODIFIER | c.1174-1636C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078102 | |||||||
| chr4:48078178 | G | A | 3 | a0001c0001t0001g0088 a0001c0002t0001g0084 a0001c0002t0001g0098 |
3 | HG02129.hp1 NA19001.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1174-1712C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078178 | |||||||
| chr4:48078204 | T | C | 50 | a0001c0001t0002g0224 a0001c0001t0006g0244 a0001c0002t0001g0017 others(47): Show |
58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.1173+1708A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078204 | |||||||
| chr4:48078223 | A | G | 1 | a0001c0001t0003g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1173+1689T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078223 | |||||||
| chr4:48078445 | G | A | 1 | a0001c0002t0001g0201 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.1173+1467C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078445 | |||||||
| chr4:48078472 | C | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1173+1440G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078472 | |||||||
| chr4:48078519 | A | C | 275 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(272): Show |
312 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(309): Show |
intron_variant | MODIFIER | c.1173+1393T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078519 | |||||||
| chr4:48078556 | C | T | 49 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(46): Show |
57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.1173+1356G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078556 | |||||||
| chr4:48078590 | A | G | 1 | a0001c0002t0001g0206 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1173+1322T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078590 | |||||||
| chr4:48078632 | G | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(52): Show |
64 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.1173+1280C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48078632 | |||||||
| chr4:48079099 | C | A | 8 | a0001c0001t0001g0129 a0001c0001t0001g0149 a0001c0001t0001g0151 others(5): Show |
8 | HG01515.hp2 HG01952.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.1173+813G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079099 | |||||||
| chr4:48079301 | G | A | 5 | a0001c0001t0006g0244 a0001c0002t0001g0252 a0001c0002t0001g0263 others(2): Show |
5 | HG00642.hp2 HG02615.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.1173+611C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079301 | |||||||
| chr4:48079385 | C | T | 1 | a0001c0001t0001g0028 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1173+527G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079385 | |||||||
| chr4:48079454 | G | A | 1 | a0001c0002t0001g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1173+458C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079454 | |||||||
| chr4:48079528 | T | C | 276 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(273): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1173+384A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079528 | |||||||
| chr4:48079879 | CA | C | 119 | a0001c0001t0001g0289 a0001c0001t0002g0018 a0001c0001t0002g0020 others(116): Show |
132 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(129): Show |
intron_variant | MODIFIER | c.1173+32delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 11/14 | chr4 | 48079879 | |||||||
| chr4:48080191 | T | C | 297 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(294): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.957-63A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080191 | |||||||
| chr4:48080357 | A | G | 297 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(294): Show |
336 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(333): Show |
intron_variant | MODIFIER | c.957-229T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080357 | |||||||
| chr4:48080662 | T | TCA | 10 | a0001c0001t0001g0145 a0001c0001t0007g0121 a0001c0002t0001g0026 others(7): Show |
10 | HG00280.hp1 HG01099.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.957-536_957-535dup others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | |||||||
| chr4:48080662 | T | TCACA | 61 | a0001c0001t0001g0088 a0001c0001t0001g0177 a0001c0001t0002g0020 others(58): Show |
74 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(71): Show |
intron_variant | MODIFIER | c.957-538_957-535dup others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | |||||||
| chr4:48080662 | T | TCACACA | 47 | a0001c0001t0001g0117 a0001c0001t0001g0289 a0001c0001t0002g0018 others(44): Show |
55 | HG00323.hp1 HG00544.hp1 HG00558.hp2 others(52): Show |
intron_variant | MODIFIER | c.957-540_957-535dup others(6): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | |||||||
| chr4:48080662 | T | TCACACAC others(1): Show |
25 | a0001c0001t0002g0023 a0001c0001t0002g0140 a0001c0001t0002g0195 others(22): Show |
26 | HG00140.hp1 HG00733.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.957-542_957-535dup others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | |||||||
| chr4:48080662 | T | TCACACAC others(3): Show |
20 | a0001c0001t0002g0210 a0001c0001t0002g0284 a0001c0001t0002g0285 others(17): Show |
20 | HG00438.hp2 HG00597.hp2 HG00673.hp2 others(17): Show |
intron_variant | MODIFIER | c.957-544_957-535dup others(10): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | |||||||
| chr4:48080662 | T | TCACACAC others(5): Show |
5 | a0001c0001t0001g0122 a0001c0001t0002g0207 a0001c0001t0002g0292 others(2): Show |
5 | HG01099.hp2 HG03041.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.957-546_957-535dup others(12): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | |||||||
| chr4:48080662 | T | TCACACAC others(7): Show |
1 | a0001c0001t0003g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.957-548_957-535dup others(14): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | |||||||
| chr4:48080662 | TCA | T | 20 | a0001c0001t0001g0015 a0001c0001t0001g0147 a0001c0001t0001g0148 others(17): Show |
21 | HG00558.hp1 HG00642.hp2 HG00673.hp1 others(18): Show |
intron_variant | MODIFIER | c.957-536_957-535del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | |||||||
| chr4:48080662 | TCACA | T | 54 | a0001c0001t0001g0055 a0001c0001t0001g0144 a0001c0001t0001g0154 others(51): Show |
62 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.957-538_957-535del others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | |||||||
| chr4:48080662 | TCACACAC others(1): Show |
T | 6 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.957-542_957-535del others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080662 | |||||||
| chr4:48080664 | A | T | 2 | a0002c0003t0001g0239 a0002c0003t0001g0242 |
2 | HG03831.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.957-536T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080664 | |||||||
| chr4:48080666 | A | T | 5 | a0001c0002t0001g0265 a0002c0003t0001g0054 a0002c0003t0001g0089 others(2): Show |
5 | HG00642.hp2 HG00735.hp1 HG01358.hp1 others(2): Show |
intron_variant | MODIFIER | c.957-538T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080666 | |||||||
| chr4:48080668 | A | T | 44 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(41): Show |
52 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.957-540T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080668 | |||||||
| chr4:48080704 | A | AC | 3 | a0001c0001t0001g0129 a0001c0001t0001g0134 a0001c0001t0001g0162 |
3 | HG03831.hp1 NA18993.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.957-577_957-576ins others(1): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080704 | |||||||
| chr4:48080785 | G | A | 1 | a0001c0007t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.957-657C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080785 | |||||||
| chr4:48080864 | T | C | 1 | a0003c0004t0003g0114 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.957-736A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080864 | |||||||
| chr4:48080931 | C | G | 4 | a0001c0001t0001g0177 a0001c0006t0001g0097 a0001c0006t0001g0127 others(1): Show |
4 | HG01884.hp1 HG02895.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.957-803G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080931 | |||||||
| chr4:48080997 | T | G | 1 | a0002c0003t0001g0235 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.957-869A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48080997 | |||||||
| chr4:48081004 | G | A | 52 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(49): Show |
61 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(58): Show |
intron_variant | MODIFIER | c.957-876C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081004 | |||||||
| chr4:48081112 | T | C | 1 | a0001c0001t0001g0150 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.957-984A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081112 | |||||||
| chr4:48081277 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.957-1149C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081277 | |||||||
| chr4:48081379 | C | T | 18 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0003g0104 others(15): Show |
21 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.957-1251G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081379 | |||||||
| chr4:48081408 | A | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.957-1280T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081408 | |||||||
| chr4:48081637 | G | A | 1 | a0001c0001t0004g0181 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.957-1509C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081637 | |||||||
| chr4:48081715 | T | C | 5 | a0001c0001t0003g0269 a0001c0001t0003g0273 a0001c0001t0003g0279 others(2): Show |
5 | HG02258.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.957-1587A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081715 | |||||||
| chr4:48081868 | C | T | 49 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(46): Show |
57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.957-1740G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081868 | |||||||
| chr4:48081929 | G | A | 1 | a0002c0003t0001g0246 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.957-1801C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081929 | |||||||
| chr4:48081971 | T | G | 1 | a0001c0001t0003g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.957-1843A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48081971 | |||||||
| chr4:48082011 | A | G | 1 | a0001c0001t0003g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.957-1883T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082011 | |||||||
| chr4:48082321 | C | A | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.957-2193G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082321 | |||||||
| chr4:48082322 | T | A | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.957-2194A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082322 | |||||||
| chr4:48082343 | T | C | 1 | a0001c0001t0006g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.957-2215A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082343 | |||||||
| chr4:48082345 | T | A | 1 | a0001c0001t0004g0126 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.957-2217A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082345 | |||||||
| chr4:48082365 | T | C | 1 | a0001c0002t0001g0090 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.957-2237A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082365 | |||||||
| chr4:48082607 | T | A | 1 | a0001c0008t0006g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.957-2479A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082607 | |||||||
| chr4:48082718 | C | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.957-2590G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082718 | |||||||
| chr4:48082733 | A | G | 1 | a0001c0002t0001g0072 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.957-2605T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082733 | |||||||
| chr4:48082735 | C | T | 1 | a0002c0003t0001g0050 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.957-2607G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082735 | |||||||
| chr4:48082736 | G | A | 1 | a0001c0002t0001g0102 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.957-2608C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082736 | |||||||
| chr4:48082776 | C | T | 44 | a0001c0002t0001g0017 a0001c0002t0001g0092 a0001c0002t0001g0245 others(41): Show |
52 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.957-2648G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082776 | |||||||
| chr4:48082820 | C | T | 6 | a0001c0007t0001g0039 a0001c0007t0001g0109 a0001c0007t0001g0120 others(3): Show |
6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.957-2692G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48082820 | |||||||
| chr4:48083206 | C | T | 1 | a0001c0006t0001g0038 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.957-3078G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48083206 | |||||||
| chr4:48083456 | G | A | 1 | a0001c0001t0001g0159 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.956+3010C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48083456 | |||||||
| chr4:48083467 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.956+2999C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48083467 | |||||||
| chr4:48084110 | G | T | 19 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0003g0104 others(16): Show |
22 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.956+2356C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084110 | |||||||
| chr4:48084232 | G | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(152): Show |
179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.956+2234C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084232 | |||||||
| chr4:48084287 | T | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.956+2179A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084287 | |||||||
| chr4:48084290 | C | T | 1 | a0001c0002t0001g0304 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.956+2176G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084290 | |||||||
| chr4:48084341 | A | G | 2 | a0001c0010t0001g0119 a0001c0010t0001g0214 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.956+2125T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084341 | |||||||
| chr4:48084687 | G | A | 19 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0003g0104 others(16): Show |
22 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.956+1779C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084687 | |||||||
| chr4:48084737 | T | C | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.956+1729A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084737 | |||||||
| chr4:48084819 | C | T | 1 | a0001c0001t0001g0143 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.956+1647G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084819 | |||||||
| chr4:48084823 | A | AGAGAATG others(13): Show |
11 | a0001c0001t0001g0194 a0001c0001t0001g0219 a0001c0001t0002g0196 others(8): Show |
11 | HG01168.hp1 HG02015.hp2 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.956+1623_956+1642d others(22): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084823 | |||||||
| chr4:48084823 | A | AGAGAATG others(33): Show |
51 | a0001c0001t0002g0018 a0001c0001t0002g0195 a0001c0001t0002g0197 others(48): Show |
60 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.956+1603_956+1642d others(42): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084823 | |||||||
| chr4:48084823 | A | AGAGAATG others(53): Show |
67 | a0001c0001t0001g0289 a0001c0001t0002g0020 a0001c0001t0002g0021 others(64): Show |
71 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.956+1583_956+1642d others(62): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084823 | |||||||
| chr4:48084823 | AGAGAATG others(13): Show |
A | 55 | a0001c0001t0001g0088 a0001c0001t0001g0151 a0001c0001t0002g0068 others(52): Show |
66 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(63): Show |
intron_variant | MODIFIER | c.956+1623_956+1642d others(22): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084823 | |||||||
| chr4:48084842 | T | TCGAGAAT others(33): Show |
1 | a0002c0003t0001g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.956+1623_956+1624i others(42): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084842 | |||||||
| chr4:48084844 | G | GAGAATGG others(33): Show |
15 | a0001c0001t0001g0177 a0001c0005t0001g0006 a0001c0005t0001g0029 others(12): Show |
17 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.956+1621_956+1622i others(42): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084844 | |||||||
| chr4:48084942 | C | T | 2 | a0001c0008t0003g0227 a0001c0008t0003g0228 |
2 | HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.956+1524G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084942 | |||||||
| chr4:48084989 | C | T | 1 | a0001c0002t0001g0245 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.956+1477G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48084989 | |||||||
| chr4:48085203 | C | T | 2 | a0001c0007t0001g0109 a0001c0007t0001g0165 |
2 | HG01255.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.956+1263G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085203 | |||||||
| chr4:48085231 | T | C | 277 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(274): Show |
314 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(311): Show |
intron_variant | MODIFIER | c.956+1235A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085231 | |||||||
| chr4:48085407 | G | GA | 9 | a0001c0001t0001g0132 a0001c0001t0001g0134 a0001c0001t0001g0135 others(6): Show |
9 | HG02602.hp2 HG02735.hp1 HG03491.hp2 others(6): Show |
intron_variant | MODIFIER | c.956+1058dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085407 | |||||||
| chr4:48085678 | CAG | C | 49 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(46): Show |
57 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.956+786_956+787del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085678 | |||||||
| chr4:48085705 | A | G | 3 | a0002c0003t0001g0246 a0002c0003t0001g0248 a0002c0012t0002g0247 |
3 | HG00642.hp1 HG01516.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.956+761T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085705 | |||||||
| chr4:48085763 | C | G | 6 | a0003c0004t0003g0002 a0003c0004t0003g0108 a0003c0004t0003g0111 others(3): Show |
9 | HG00323.hp1 HG01109.hp1 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.956+703G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085763 | |||||||
| chr4:48085838 | G | A | 276 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(273): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.956+628C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085838 | |||||||
| chr4:48085950 | G | A | 1 | a0002c0003t0001g0050 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.956+516C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48085950 | |||||||
| chr4:48086052 | C | T | 276 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(273): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.956+414G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086052 | |||||||
| chr4:48086105 | C | T | 2 | a0001c0002t0001g0042 a0001c0002t0001g0044 |
2 | HG03834.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.956+361G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086105 | |||||||
| chr4:48086163 | A | G | 298 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(295): Show |
337 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(334): Show |
intron_variant | MODIFIER | c.956+303T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086163 | |||||||
| chr4:48086310 | C | T | 1 | a0001c0002t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.956+156G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086310 | |||||||
| chr4:48086402 | C | T | 154 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(151): Show |
178 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.956+64G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086402 | |||||||
| chr4:48086405 | A | G | 15 | a0001c0001t0001g0177 a0001c0005t0001g0006 a0001c0005t0001g0029 others(12): Show |
17 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.956+61T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086405 | |||||||
| chr4:48086429 | A | G | 276 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(273): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.956+37T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 10/14 | chr4 | 48086429 | |||||||
| chr4:48086799 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0001g0174 |
2 | HG00558.hp1 HG00673.hp1 |
intron_variant | MODIFIER | c.785-162G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48086799 | |||||||
| chr4:48086874 | C | T | 1 | a0001c0002t0001g0133 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.785-237G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48086874 | |||||||
| chr4:48086985 | G | GT | 228 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(225): Show |
257 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.785-349dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48086985 | |||||||
| chr4:48087075 | C | T | 2 | a0001c0010t0001g0119 a0001c0010t0001g0214 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.785-438G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087075 | |||||||
| chr4:48087092 | T | C | 1 | a0002c0003t0001g0259 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.785-455A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087092 | |||||||
| chr4:48087241 | CTG | C | 72 | a0001c0001t0001g0289 a0001c0001t0002g0018 a0001c0001t0002g0020 others(69): Show |
77 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.785-606_785-605del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087241 | |||||||
| chr4:48087359 | A | G | 6 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.785-722T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087359 | |||||||
| chr4:48087438 | A | T | 2 | a0001c0001t0002g0287 a0001c0015t0001g0040 |
2 | HG01243.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.785-801T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087438 | |||||||
| chr4:48087441 | A | T | 80 | a0001c0001t0001g0220 a0001c0001t0001g0289 a0001c0001t0002g0018 others(77): Show |
87 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.785-804T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087441 | |||||||
| chr4:48087444 | T | A | 48 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(45): Show |
56 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.785-807A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087444 | |||||||
| chr4:48087750 | A | C | 14 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(11): Show |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.785-1113T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087750 | |||||||
| chr4:48087843 | A | G | 9 | a0001c0001t0003g0269 a0001c0001t0003g0273 a0001c0001t0003g0279 others(6): Show |
9 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.785-1206T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48087843 | |||||||
| chr4:48088023 | T | C | 53 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(50): Show |
62 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.785-1386A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088023 | |||||||
| chr4:48088118 | C | T | 228 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(225): Show |
257 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.785-1481G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088118 | |||||||
| chr4:48088135 | T | A | 1 | a0001c0010t0001g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.785-1498A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088135 | |||||||
| chr4:48088152 | C | A | 6 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.785-1515G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088152 | |||||||
| chr4:48088425 | G | GC | 6 | a0001c0001t0001g0015 a0001c0001t0001g0152 a0001c0001t0001g0155 others(3): Show |
7 | HG00408.hp1 HG02071.hp2 NA18747.hp2 others(4): Show |
intron_variant | MODIFIER | c.784+1324dupG | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088425 | |||||||
| chr4:48088537 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.784+1213C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088537 | |||||||
| chr4:48088630 | T | C | 1 | a0001c0001t0005g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.784+1120A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088630 | |||||||
| chr4:48088807 | C | T | 2 | a0003c0004t0003g0139 a0003c0004t0003g0236 |
2 | HG00639.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.784+943G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088807 | |||||||
| chr4:48088811 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.784+939G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088811 | |||||||
| chr4:48088857 | C | T | 4 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.784+893G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48088857 | |||||||
| chr4:48089289 | C | T | 2 | a0001c0002t0001g0071 a0001c0002t0001g0077 |
2 | HG02602.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.784+461G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48089289 | |||||||
| chr4:48089385 | C | CT | 52 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(49): Show |
60 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.784+364dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48089385 | |||||||
| chr4:48089399 | C | CT | 6 | a0001c0007t0001g0039 a0001c0007t0001g0109 a0001c0007t0001g0120 others(3): Show |
6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.784+350dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48089399 | |||||||
| chr4:48089416 | A | G | 1 | a0002c0003t0001g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.784+334T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48089416 | |||||||
| chr4:48089550 | C | G | 1 | a0001c0002t0001g0070 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.784+200G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 9/14 | chr4 | 48089550 | |||||||
| chr4:48089841 | A | G | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.710-17T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48089841 | |||||||
| chr4:48089960 | C | T | 2 | a0001c0002t0001g0008 a0001c0002t0001g0200 |
4 | NA18969.hp1 NA18979.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.710-136G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48089960 | |||||||
| chr4:48089988 | AT | A | 72 | a0001c0001t0001g0289 a0001c0001t0002g0018 a0001c0001t0002g0020 others(69): Show |
77 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.710-165delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48089988 | |||||||
| chr4:48090215 | T | C | 2 | a0001c0001t0004g0126 a0001c0001t0004g0182 |
2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.710-391A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090215 | |||||||
| chr4:48090277 | A | G | 1 | a0001c0001t0001g0132 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.710-453T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090277 | |||||||
| chr4:48090280 | T | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0083 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.710-456A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090280 | |||||||
| chr4:48090463 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.710-639A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090463 | |||||||
| chr4:48090659 | T | C | 1 | a0001c0002t0001g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.710-835A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090659 | |||||||
| chr4:48090772 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.710-948C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48090772 | |||||||
| chr4:48091380 | A | G | 1 | a0001c0002t0001g0101 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.710-1556T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091380 | |||||||
| chr4:48091415 | C | T | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.710-1591G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091415 | |||||||
| chr4:48091510 | CT | C | 25 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(22): Show |
26 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.710-1687delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091510 | |||||||
| chr4:48091565 | G | A | 50 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(47): Show |
58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.710-1741C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091565 | |||||||
| chr4:48091749 | C | G | 1 | a0001c0002t0001g0084 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.710-1925G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091749 | |||||||
| chr4:48091751 | C | A | 16 | a0001c0002t0001g0019 a0001c0002t0001g0067 a0001c0002t0001g0078 others(13): Show |
17 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.710-1927G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091751 | |||||||
| chr4:48091756 | T | C | 1 | a0001c0001t0004g0180 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.710-1932A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091756 | |||||||
| chr4:48091787 | G | A | 1 | a0001c0001t0002g0314 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.710-1963C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48091787 | |||||||
| chr4:48092009 | G | A | 1 | a0002c0003t0001g0087 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.709+2068C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092009 | |||||||
| chr4:48092088 | T | C | 18 | a0001c0001t0001g0117 a0001c0001t0003g0104 a0001c0001t0003g0105 others(15): Show |
21 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.709+1989A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092088 | |||||||
| chr4:48092144 | C | A | 6 | a0001c0007t0001g0039 a0001c0007t0001g0109 a0001c0007t0001g0120 others(3): Show |
6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+1933G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092144 | |||||||
| chr4:48092258 | C | T | 70 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(67): Show |
80 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.709+1819G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092258 | |||||||
| chr4:48092517 | A | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
172 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.709+1560T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092517 | |||||||
| chr4:48092517 | A | T | 1 | a0001c0001t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.709+1560T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092517 | |||||||
| chr4:48092553 | TGGACACA others(60): Show |
T | 56 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(53): Show |
64 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(61): Show |
intron_variant | MODIFIER | c.709+1457_709+1523d others(69): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092553 | |||||||
| chr4:48092573 | T | C | 22 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(19): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.709+1504A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092573 | |||||||
| chr4:48092640 | T | C | 44 | a0001c0002t0001g0017 a0001c0002t0001g0092 a0002c0003t0001g0005 others(41): Show |
52 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(49): Show |
intron_variant | MODIFIER | c.709+1437A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092640 | |||||||
| chr4:48092690 | G | A | 1 | a0001c0007t0001g0124 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.709+1387C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092690 | |||||||
| chr4:48092790 | T | C | 3 | a0001c0002t0001g0234 a0001c0002t0001g0254 a0001c0002t0001g0256 |
3 | HG01891.hp2 HG02055.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.709+1287A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48092790 | |||||||
| chr4:48093110 | T | C | 18 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(15): Show |
18 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.709+967A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48093110 | |||||||
| chr4:48093394 | G | A | 1 | a0001c0001t0003g0116 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.709+683C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48093394 | |||||||
| chr4:48093592 | C | T | 6 | a0001c0007t0001g0039 a0001c0007t0001g0109 a0001c0007t0001g0120 others(3): Show |
6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.709+485G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48093592 | |||||||
| chr4:48093732 | A | G | 1 | a0002c0003t0001g0058 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.709+345T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48093732 | |||||||
| chr4:48093971 | T | C | 6 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.709+106A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 8/14 | chr4 | 48093971 | |||||||
| chr4:48094284 | C | A | 1 | a0001c0001t0001g0153 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.582-80G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094284 | |||||||
| chr4:48094588 | A | G | 3 | a0001c0001t0001g0088 a0001c0002t0001g0084 a0001c0002t0001g0098 |
3 | HG02129.hp1 NA19001.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.582-384T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094588 | |||||||
| chr4:48094764 | T | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.581+379A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094764 | |||||||
| chr4:48094772 | G | A | 1 | a0001c0001t0002g0022 | 2 | NA18950.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.581+371C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094772 | |||||||
| chr4:48094777 | G | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.581+366C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094777 | |||||||
| chr4:48094963 | G | A | 75 | a0001c0001t0001g0088 a0001c0001t0002g0068 a0001c0002t0001g0001 others(72): Show |
87 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.581+180C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 7/14 | chr4 | 48094963 | |||||||
| chr4:48095383 | T | A | 50 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(47): Show |
58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.502-161A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095383 | |||||||
| chr4:48095463 | A | G | 155 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(152): Show |
179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.502-241T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095463 | |||||||
| chr4:48095596 | G | A | 1 | a0001c0008t0006g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-374C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095596 | |||||||
| chr4:48095817 | T | C | 1 | a0001c0002t0001g0092 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.502-595A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095817 | |||||||
| chr4:48095829 | G | A | 1 | a0003c0004t0003g0108 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.502-607C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095829 | |||||||
| chr4:48095869 | T | C | 1 | a0001c0001t0001g0130 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.502-647A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095869 | |||||||
| chr4:48095876 | C | T | 1 | a0001c0008t0003g0218 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.502-654G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095876 | |||||||
| chr4:48095922 | A | C | 1 | a0001c0007t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.502-700T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48095922 | |||||||
| chr4:48096060 | G | A | 1 | a0001c0008t0006g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.502-838C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096060 | |||||||
| chr4:48096353 | T | C | 50 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(47): Show |
58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.502-1131A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096353 | |||||||
| chr4:48096370 | G | T | 1 | a0001c0005t0001g0029 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.502-1148C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096370 | |||||||
| chr4:48096557 | G | A | 155 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(152): Show |
179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.502-1335C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096557 | |||||||
| chr4:48096573 | T | C | 1 | a0001c0002t0001g0047 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.502-1351A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096573 | |||||||
| chr4:48096582 | A | G | 1 | a0001c0001t0003g0281 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.502-1360T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096582 | |||||||
| chr4:48096590 | G | A | 6 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-1368C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096590 | |||||||
| chr4:48096607 | A | C | 5 | a0001c0002t0001g0092 a0002c0003t0001g0005 a0002c0003t0001g0049 others(2): Show |
8 | HG00140.hp2 HG01256.hp2 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.502-1385T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096607 | |||||||
| chr4:48096825 | G | A | 1 | a0001c0006t0001g0283 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.502-1603C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096825 | |||||||
| chr4:48096873 | C | T | 4 | a0001c0006t0001g0097 a0001c0006t0001g0127 a0001c0006t0001g0283 others(1): Show |
4 | HG01243.hp2 HG01884.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.502-1651G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096873 | |||||||
| chr4:48096883 | C | A | 1 | a0001c0001t0003g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.502-1661G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096883 | |||||||
| chr4:48096925 | A | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-1703T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096925 | |||||||
| chr4:48096952 | T | C | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.502-1730A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096952 | |||||||
| chr4:48096960 | T | A | 22 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(19): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.502-1738A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48096960 | |||||||
| chr4:48097056 | A | C | 2 | a0001c0002t0001g0080 a0001c0002t0001g0099 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.502-1834T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097056 | |||||||
| chr4:48097208 | C | A | 2 | a0001c0010t0001g0119 a0001c0010t0001g0214 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.502-1986G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097208 | |||||||
| chr4:48097343 | A | G | 22 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(19): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.502-2121T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097343 | |||||||
| chr4:48097422 | C | CT | 31 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(28): Show |
32 | HG01255.hp2 HG01516.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.502-2201dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097422 | |||||||
| chr4:48097422 | C | CTT | 145 | a0001c0001t0001g0088 a0001c0001t0001g0117 a0001c0001t0001g0122 others(142): Show |
168 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.502-2202_502-2201d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097422 | |||||||
| chr4:48097422 | C | CTTT | 69 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(66): Show |
80 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.502-2203_502-2201d others(5): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097422 | |||||||
| chr4:48097627 | A | G | 234 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.502-2405T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097627 | |||||||
| chr4:48097640 | G | A | 2 | a0001c0001t0006g0244 a0001c0002t0001g0245 |
2 | HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.502-2418C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097640 | |||||||
| chr4:48097748 | A | AT | 11 | a0001c0001t0001g0128 a0001c0001t0001g0220 a0001c0001t0002g0205 others(8): Show |
11 | HG00738.hp1 HG01243.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.502-2527dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097748 | |||||||
| chr4:48097748 | A | G | 1 | a0001c0002t0001g0076 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.502-2526T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097748 | |||||||
| chr4:48097748 | AT | A | 26 | a0001c0001t0001g0122 a0001c0001t0005g0025 a0001c0001t0005g0046 others(23): Show |
29 | HG01884.hp1 HG01884.hp2 HG02145.hp2 others(26): Show |
intron_variant | MODIFIER | c.502-2527delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097748 | |||||||
| chr4:48097894 | C | A | 6 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-2672G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097894 | |||||||
| chr4:48097991 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.502-2769G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48097991 | |||||||
| chr4:48098433 | C | G | 1 | a0001c0006t0001g0038 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.502-3211G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098433 | |||||||
| chr4:48098469 | T | C | 1 | a0003c0004t0003g0114 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.502-3247A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098469 | |||||||
| chr4:48098480 | A | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(174): Show |
202 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.502-3258T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098480 | |||||||
| chr4:48098556 | T | TTTTTTTT others(453): Show |
1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3335_502-3334i others(462): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098556 | |||||||
| chr4:48098559 | A | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3337T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098559 | |||||||
| chr4:48098561 | A | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3339T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098561 | |||||||
| chr4:48098563 | T | C | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3341A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098563 | |||||||
| chr4:48098565 | T | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3343A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098565 | |||||||
| chr4:48098576 | G | C | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3354C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098576 | |||||||
| chr4:48098578 | A | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3356T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098578 | |||||||
| chr4:48098579 | A | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3357T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098579 | |||||||
| chr4:48098583 | G | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3361C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098583 | |||||||
| chr4:48098589 | A | C | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3367T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098589 | |||||||
| chr4:48098590 | C | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3368G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098590 | |||||||
| chr4:48098593 | C | T | 3 | a0002c0003t0001g0318 a0002c0003t0001g0319 a0002c0003t0001g0320 |
3 | HG01192.hp1 HG02055.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.502-3371G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098593 | |||||||
| chr4:48098595 | T | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3373A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098595 | |||||||
| chr4:48098598 | A | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3376T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098598 | |||||||
| chr4:48098601 | C | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3379G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098601 | |||||||
| chr4:48098602 | A | C | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3380T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098602 | |||||||
| chr4:48098603 | A | ATGATTTA others(968): Show |
1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3382_502-3381i others(977): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098603 | |||||||
| chr4:48098607 | C | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3385G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098607 | |||||||
| chr4:48098609 | C | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.502-3387G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098609 | |||||||
| chr4:48098640 | T | G | 22 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(19): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.502-3418A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098640 | |||||||
| chr4:48098716 | C | CT | 50 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(47): Show |
58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.502-3495dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098716 | |||||||
| chr4:48098858 | G | A | 1 | a0001c0001t0001g0028 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.502-3636C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098858 | |||||||
| chr4:48098923 | A | G | 1 | a0001c0006t0001g0038 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.502-3701T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098923 | |||||||
| chr4:48098945 | A | G | 1 | a0001c0001t0002g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.502-3723T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098945 | |||||||
| chr4:48098947 | CA | C | 233 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(230): Show |
266 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(263): Show |
intron_variant | MODIFIER | c.502-3726delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098947 | |||||||
| chr4:48098957 | A | T | 1 | a0002c0003t0001g0057 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-3735T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098957 | |||||||
| chr4:48098958 | T | G | 1 | a0002c0003t0001g0057 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-3736A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098958 | |||||||
| chr4:48098961 | G | A | 1 | a0002c0003t0001g0057 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-3739C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098961 | |||||||
| chr4:48098971 | A | G | 6 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.502-3749T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48098971 | |||||||
| chr4:48099204 | G | A | 5 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 others(2): Show |
5 | HG02559.hp1 HG02717.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-3982C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099204 | |||||||
| chr4:48099343 | C | T | 1 | a0001c0001t0005g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.502-4121G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099343 | |||||||
| chr4:48099549 | G | A | 1 | a0002c0003t0001g0057 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-4327C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099549 | |||||||
| chr4:48099550 | A | AT | 5 | a0001c0007t0001g0039 a0001c0007t0001g0109 a0001c0007t0001g0124 others(2): Show |
5 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.502-4329dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099550 | |||||||
| chr4:48099550 | A | G | 1 | a0002c0003t0001g0057 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-4328T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099550 | |||||||
| chr4:48099551 | T | A | 1 | a0002c0003t0001g0057 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.502-4329A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48099551 | |||||||
| chr4:48100025 | A | G | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.502-4803T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100025 | |||||||
| chr4:48100077 | C | T | 6 | a0001c0007t0001g0039 a0001c0007t0001g0109 a0001c0007t0001g0120 others(3): Show |
6 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+4824G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100077 | |||||||
| chr4:48100089 | G | A | 3 | a0001c0006t0001g0097 a0001c0006t0001g0127 a0001c0006t0001g0283 |
3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.501+4812C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100089 | |||||||
| chr4:48100158 | A | C | 234 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(231): Show |
267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.501+4743T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100158 | |||||||
| chr4:48100171 | C | CA | 42 | a0001c0001t0001g0117 a0001c0001t0003g0104 a0001c0001t0003g0105 others(39): Show |
48 | HG00323.hp1 HG00621.hp2 HG00639.hp2 others(45): Show |
intron_variant | MODIFIER | c.501+4729dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | |||||||
| chr4:48100171 | C | CAA | 21 | a0001c0001t0003g0115 a0001c0001t0003g0116 a0001c0001t0004g0179 others(18): Show |
21 | HG02055.hp1 HG02109.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.501+4728_501+4729d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | |||||||
| chr4:48100171 | C | CAAA | 28 | a0001c0001t0001g0122 a0001c0001t0004g0096 a0001c0001t0004g0126 others(25): Show |
36 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.501+4727_501+4729d others(5): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | |||||||
| chr4:48100171 | C | CAAAA | 16 | a0001c0001t0006g0244 a0001c0002t0001g0092 a0001c0002t0001g0245 others(13): Show |
16 | HG00280.hp2 HG00642.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.501+4726_501+4729d others(6): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | |||||||
| chr4:48100171 | CA | C | 96 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(93): Show |
109 | HG00280.hp1 HG00408.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.501+4729delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | |||||||
| chr4:48100171 | CAA | C | 8 | a0001c0001t0002g0020 a0001c0001t0002g0203 a0001c0001t0002g0266 others(5): Show |
9 | HG02004.hp2 HG02258.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.501+4728_501+4729d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100171 | |||||||
| chr4:48100397 | T | C | 1 | a0001c0001t0002g0317 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.501+4504A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100397 | |||||||
| chr4:48100496 | A | C | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+4405T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100496 | |||||||
| chr4:48100506 | G | A | 1 | a0002c0003t0001g0050 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.501+4395C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100506 | |||||||
| chr4:48100635 | C | T | 50 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(47): Show |
58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.501+4266G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100635 | |||||||
| chr4:48100717 | G | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+4184C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100717 | |||||||
| chr4:48100874 | T | A | 1 | a0001c0002t0001g0077 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.501+4027A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100874 | |||||||
| chr4:48100923 | T | A | 3 | a0001c0001t0004g0192 a0002c0003t0001g0250 a0002c0003t0001g0251 |
3 | HG00735.hp1 HG03041.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.501+3978A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48100923 | |||||||
| chr4:48101056 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.501+3845A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101056 | |||||||
| chr4:48101082 | A | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+3819T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101082 | |||||||
| chr4:48101113 | C | T | 2 | a0001c0002t0001g0082 a0001c0002t0001g0083 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.501+3788G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101113 | |||||||
| chr4:48101202 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.501+3699A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101202 | |||||||
| chr4:48101600 | A | G | 3 | a0001c0002t0001g0252 a0001c0002t0001g0263 a0001c0002t0001g0265 |
3 | HG00642.hp2 HG02622.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.501+3301T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101600 | |||||||
| chr4:48101657 | T | G | 1 | a0001c0001t0003g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.501+3244A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101657 | |||||||
| chr4:48101662 | T | A | 1 | a0001c0001t0004g0253 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.501+3239A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101662 | |||||||
| chr4:48101815 | A | T | 14 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(11): Show |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+3086T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101815 | |||||||
| chr4:48101924 | A | C | 2 | a0001c0001t0001g0145 a0001c0001t0001g0146 |
2 | HG00280.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.501+2977T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48101924 | |||||||
| chr4:48102186 | C | A | 1 | a0002c0003t0001g0235 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.501+2715G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102186 | |||||||
| chr4:48102235 | T | C | 45 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(42): Show |
53 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.501+2666A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102235 | |||||||
| chr4:48102239 | G | A | 248 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(245): Show |
283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.501+2662C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102239 | |||||||
| chr4:48102274 | C | A | 1 | a0003c0004t0003g0108 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.501+2627G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102274 | |||||||
| chr4:48102290 | A | C | 1 | a0001c0001t0002g0068 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.501+2611T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102290 | |||||||
| chr4:48102293 | T | C | 22 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(19): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.501+2608A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102293 | |||||||
| chr4:48102493 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.501+2408G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102493 | |||||||
| chr4:48102635 | C | G | 155 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(152): Show |
179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.501+2266G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102635 | |||||||
| chr4:48102811 | G | A | 1 | a0001c0002t0001g0307 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.501+2090C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48102811 | |||||||
| chr4:48103204 | C | T | 50 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(47): Show |
58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.501+1697G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103204 | |||||||
| chr4:48103244 | A | G | 6 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+1657T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103244 | |||||||
| chr4:48103346 | G | A | 1 | a0001c0001t0002g0171 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.501+1555C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103346 | |||||||
| chr4:48103358 | G | A | 2 | a0001c0002t0001g0080 a0001c0002t0001g0099 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.501+1543C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103358 | |||||||
| chr4:48103455 | C | T | 1 | a0001c0002t0001g0100 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.501+1446G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103455 | |||||||
| chr4:48103478 | A | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+1423T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103478 | |||||||
| chr4:48103974 | G | A | 51 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(48): Show |
59 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.501+927C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48103974 | |||||||
| chr4:48104115 | T | C | 1 | a0001c0002t0001g0086 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.501+786A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104115 | |||||||
| chr4:48104205 | AAT | A | 224 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(221): Show |
258 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(255): Show |
intron_variant | MODIFIER | c.501+694_501+695del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104205 | |||||||
| chr4:48104212 | A | ATATATAT others(30): Show |
1 | a0001c0008t0003g0227 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.501+688_501+689ins others(37): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104212 | |||||||
| chr4:48104214 | ATATATAT others(7): Show |
A | 22 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(19): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.501+673_501+686del others(14): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104214 | |||||||
| chr4:48104222 | T | A | 1 | a0001c0008t0003g0227 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.501+679A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104222 | |||||||
| chr4:48104223 | A | T | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.501+678T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104223 | |||||||
| chr4:48104229 | T | A | 225 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(222): Show |
259 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(256): Show |
intron_variant | MODIFIER | c.501+672A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104229 | |||||||
| chr4:48104234 | T | A | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.501+667A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104234 | |||||||
| chr4:48104234 | TATATATA others(20): Show |
T | 14 | a0001c0001t0001g0289 a0001c0001t0002g0171 a0001c0001t0002g0198 others(11): Show |
14 | HG00544.hp1 HG00597.hp2 HG02015.hp1 others(11): Show |
intron_variant | MODIFIER | c.501+640_501+666del others(27): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104234 | |||||||
| chr4:48104234 | TATATATA others(48): Show |
T | 4 | a0001c0001t0002g0021 a0001c0001t0002g0022 a0001c0001t0002g0286 others(1): Show |
6 | HG00609.hp2 NA18950.hp1 NA18997.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+612_501+666del others(55): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104234 | |||||||
| chr4:48104241 | A | T | 22 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(19): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.501+660T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104241 | |||||||
| chr4:48104243 | T | A | 1 | a0001c0002t0001g0042 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.501+658A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104243 | |||||||
| chr4:48104245 | T | C | 1 | a0001c0001t0004g0180 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.501+656A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104245 | |||||||
| chr4:48104245 | T | TA | 17 | a0001c0001t0002g0053 a0001c0001t0002g0278 a0001c0001t0002g0284 others(14): Show |
17 | HG00438.hp2 HG00673.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.501+655dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104245 | |||||||
| chr4:48104248 | ATTTTATA others(286): Show |
A | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.501+360_501+652del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104248 | |||||||
| chr4:48104250 | T | A | 17 | a0001c0001t0002g0053 a0001c0001t0002g0278 a0001c0001t0002g0284 others(14): Show |
17 | HG00438.hp2 HG00673.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.501+651A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104250 | |||||||
| chr4:48104250 | TTTATATA others(245): Show |
T | 7 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 others(4): Show |
7 | HG01884.hp1 HG02145.hp2 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+399_501+650del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104250 | |||||||
| chr4:48104252 | T | A | 17 | a0001c0001t0002g0053 a0001c0001t0002g0278 a0001c0001t0002g0284 others(14): Show |
17 | HG00438.hp2 HG00673.hp2 HG02523.hp2 others(14): Show |
intron_variant | MODIFIER | c.501+649A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104252 | |||||||
| chr4:48104252 | T | TATATATA others(21): Show |
1 | a0001c0001t0002g0140 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.501+621_501+648dup others(28): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104252 | |||||||
| chr4:48104252 | T | TATATATA others(84): Show |
1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.501+648_501+649ins others(91): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104252 | |||||||
| chr4:48104252 | TATATATA others(21): Show |
T | 4 | a0001c0001t0002g0020 a0001c0001t0002g0023 a0001c0001t0002g0197 others(1): Show |
5 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(2): Show |
intron_variant | MODIFIER | c.501+621_501+648del others(28): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104252 | |||||||
| chr4:48104261 | A | T | 1 | a0001c0008t0006g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.501+640T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104261 | |||||||
| chr4:48104261 | AATATATA others(117): Show |
A | 1 | a0002c0003t0001g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.501+516_501+639del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104261 | |||||||
| chr4:48104268 | AATATAAT others(259): Show |
A | 4 | a0001c0001t0001g0157 a0001c0001t0001g0158 a0001c0001t0001g0159 others(1): Show |
4 | HG01952.hp2 HG01981.hp1 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+367_501+632del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104268 | |||||||
| chr4:48104270 | T | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(146): Show |
172 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.501+631A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104270 | |||||||
| chr4:48104270 | TATAATAT others(115): Show |
T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+509_501+630del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104270 | |||||||
| chr4:48104271 | ATAATATA others(225): Show |
A | 1 | a0002c0003t0001g0237 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.501+398_501+629del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104271 | |||||||
| chr4:48104272 | TA | T | 145 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(142): Show |
169 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.501+628delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | |||||||
| chr4:48104272 | TAATATAT others(1): Show |
T | 41 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(38): Show |
48 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.501+621_501+628del others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | |||||||
| chr4:48104272 | TAATATAT others(85): Show |
T | 1 | a0002c0003t0001g0087 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.501+537_501+628del others(92): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | |||||||
| chr4:48104272 | TAATATAT others(113): Show |
T | 4 | a0001c0002t0001g0252 a0001c0002t0001g0263 a0001c0002t0001g0264 others(1): Show |
4 | HG00642.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+509_501+628del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | |||||||
| chr4:48104272 | TAATATAT others(141): Show |
T | 2 | a0002c0003t0001g0248 a0002c0003t0001g0320 |
2 | HG01993.hp2 HG02055.hp2 |
intron_variant | MODIFIER | c.501+481_501+628del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | |||||||
| chr4:48104272 | TAATATAT others(178): Show |
T | 4 | a0001c0001t0001g0161 a0001c0002t0001g0202 a0001c0007t0001g0124 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+444_501+628del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104272 | |||||||
| chr4:48104273 | A | T | 35 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(32): Show |
38 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(35): Show |
intron_variant | MODIFIER | c.501+628T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104273 | |||||||
| chr4:48104273 | AATATATA others(142): Show |
A | 1 | a0002c0003t0001g0005 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.501+479_501+627del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104273 | |||||||
| chr4:48104280 | A | AATATATA others(4): Show |
2 | a0001c0008t0003g0218 a0001c0008t0003g0228 |
2 | HG02559.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.501+620_501+621ins others(11): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104280 | |||||||
| chr4:48104280 | A | T | 1 | a0001c0001t0001g0151 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.501+621T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104280 | |||||||
| chr4:48104283 | ATATATAA others(122): Show |
A | 12 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(9): Show |
12 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+489_501+617del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104283 | |||||||
| chr4:48104283 | ATATATAA others(206): Show |
A | 7 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(4): Show |
9 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.501+405_501+617del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104283 | |||||||
| chr4:48104284 | TATATAAT others(10): Show |
T | 1 | a0001c0001t0004g0190 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+600_501+616del others(17): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104284 | |||||||
| chr4:48104284 | TATATAAT others(66): Show |
T | 3 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 |
3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+544_501+616del others(73): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104284 | |||||||
| chr4:48104289 | A | AATATATA others(77): Show |
1 | a0001c0010t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.501+611_501+612ins others(84): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104289 | |||||||
| chr4:48104289 | A | T | 192 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(189): Show |
224 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(221): Show |
intron_variant | MODIFIER | c.501+612T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104289 | |||||||
| chr4:48104290 | A | T | 150 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(147): Show |
175 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.501+611T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104290 | |||||||
| chr4:48104295 | TA | T | 149 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(146): Show |
174 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.501+605delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104295 | |||||||
| chr4:48104296 | AATATAAT others(231): Show |
A | 1 | a0001c0001t0001g0151 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.501+367_501+604del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104296 | |||||||
| chr4:48104301 | A | T | 47 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(44): Show |
54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.501+600T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104301 | |||||||
| chr4:48104306 | A | T | 1 | a0001c0001t0004g0190 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+595T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104306 | |||||||
| chr4:48104308 | A | T | 1 | a0001c0001t0004g0190 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+593T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104308 | |||||||
| chr4:48104308 | AATATATA others(53): Show |
A | 1 | a0001c0001t0004g0189 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.501+533_501+592del others(60): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104308 | |||||||
| chr4:48104309 | A | T | 4 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+592T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104309 | |||||||
| chr4:48104315 | ATAATATA others(219): Show |
A | 139 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
162 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.501+360_501+585del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104315 | |||||||
| chr4:48104316 | TAATATAT others(239): Show |
T | 1 | a0001c0002t0001g0081 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.501+339_501+584del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104316 | |||||||
| chr4:48104317 | A | T | 49 | a0001c0001t0001g0103 a0001c0001t0004g0185 a0001c0001t0005g0046 others(46): Show |
56 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(53): Show |
intron_variant | MODIFIER | c.501+584T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104317 | |||||||
| chr4:48104318 | A | T | 1 | a0001c0001t0004g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.501+583T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104318 | |||||||
| chr4:48104318 | ATATATAA others(171): Show |
A | 1 | a0001c0001t0005g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.501+405_501+582del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104318 | |||||||
| chr4:48104321 | TATA | T | 6 | a0001c0001t0001g0103 a0001c0002t0001g0007 a0001c0002t0001g0072 others(3): Show |
6 | NA18965.hp1 NA18973.hp2 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.501+577_501+579del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104321 | |||||||
| chr4:48104325 | A | T | 3 | a0001c0001t0005g0025 a0001c0001t0005g0321 a0001c0001t0005g0322 |
4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+576T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104325 | |||||||
| chr4:48104327 | A | T | 3 | a0001c0001t0005g0025 a0001c0001t0005g0321 a0001c0001t0005g0322 |
4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+574T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104327 | |||||||
| chr4:48104329 | A | AT | 3 | a0001c0001t0005g0025 a0001c0001t0005g0321 a0001c0001t0005g0322 |
4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+571_501+572ins others(1): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104329 | |||||||
| chr4:48104329 | A | T | 48 | a0001c0001t0004g0190 a0001c0001t0006g0244 a0001c0002t0001g0017 others(45): Show |
55 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.501+572T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104329 | |||||||
| chr4:48104337 | ATATATAT others(124): Show |
A | 41 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(38): Show |
48 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.501+433_501+563del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104337 | |||||||
| chr4:48104342 | TATAATAT others(136): Show |
T | 1 | a0001c0001t0004g0185 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.501+416_501+558del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104342 | |||||||
| chr4:48104343 | ATAATATA others(128): Show |
A | 3 | a0001c0001t0005g0025 a0001c0001t0005g0321 a0001c0001t0005g0322 |
4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+423_501+557del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104343 | |||||||
| chr4:48104343 | ATAATATA others(191): Show |
A | 4 | a0001c0002t0001g0007 a0001c0002t0001g0072 a0001c0002t0001g0074 others(1): Show |
4 | NA18973.hp2 NA19056.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+360_501+557del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104343 | |||||||
| chr4:48104345 | A | T | 3 | a0001c0001t0001g0103 a0001c0001t0004g0190 a0001c0002t0001g0100 |
3 | HG03516.hp2 NA18965.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.501+556T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104345 | |||||||
| chr4:48104346 | A | T | 1 | a0001c0001t0004g0190 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+555T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104346 | |||||||
| chr4:48104349 | TATA | T | 4 | a0001c0001t0001g0103 a0001c0001t0002g0053 a0001c0001t0002g0294 others(1): Show |
4 | NA18965.hp1 NA19006.hp1 NA19087.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+549_501+551del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104349 | |||||||
| chr4:48104357 | A | AATATATA others(161): Show |
1 | a0001c0001t0003g0279 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.501+543_501+544ins others(168): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | |||||||
| chr4:48104357 | A | AATATATA others(77): Show |
1 | a0001c0001t0003g0312 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.501+460_501+543dup others(84): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | |||||||
| chr4:48104357 | A | AATATATA others(105): Show |
2 | a0001c0001t0003g0280 a0001c0001t0003g0313 |
2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.501+432_501+543dup others(112): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | |||||||
| chr4:48104357 | A | AATATATA others(133): Show |
3 | a0001c0001t0003g0269 a0001c0001t0003g0282 a0001c0001t0003g0311 |
3 | HG01891.hp1 HG03041.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.501+543_501+544ins others(140): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | |||||||
| chr4:48104357 | A | T | 12 | a0001c0001t0002g0053 a0001c0001t0002g0216 a0001c0001t0002g0294 others(9): Show |
12 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+544T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | |||||||
| chr4:48104357 | AATATATA others(21): Show |
A | 1 | a0001c0001t0002g0204 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.501+516_501+543del others(28): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104357 | |||||||
| chr4:48104362 | A | T | 3 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 |
3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+539T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104362 | |||||||
| chr4:48104364 | A | T | 3 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 |
3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+537T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104364 | |||||||
| chr4:48104371 | ATAATATA others(163): Show |
A | 1 | a0001c0002t0001g0100 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.501+360_501+529del | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104371 | |||||||
| chr4:48104373 | A | T | 3 | a0001c0001t0004g0189 a0001c0010t0001g0214 a0002c0003t0001g0087 |
3 | HG02922.hp1 NA18906.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.501+528T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104373 | |||||||
| chr4:48104377 | TATA | T | 4 | a0001c0001t0002g0053 a0001c0001t0002g0294 a0001c0001t0002g0310 others(1): Show |
4 | NA19003.hp2 NA19006.hp1 NA19010.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+521_501+523del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104377 | |||||||
| chr4:48104380 | A | AATATTAT others(18): Show |
1 | a0001c0002t0001g0304 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.501+496_501+520dup others(25): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104380 | |||||||
| chr4:48104380 | A | AATATTAT others(102): Show |
1 | a0001c0001t0003g0281 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.501+520_501+521ins others(109): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104380 | |||||||
| chr4:48104385 | T | A | 4 | a0001c0001t0002g0021 a0001c0001t0002g0284 a0001c0001t0002g0286 others(1): Show |
4 | HG00438.hp2 HG00673.hp2 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+516A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104385 | |||||||
| chr4:48104390 | A | T | 2 | a0001c0001t0004g0189 a0001c0001t0004g0190 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501+511T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104390 | |||||||
| chr4:48104392 | A | T | 3 | a0001c0001t0001g0103 a0001c0001t0004g0189 a0001c0001t0004g0190 |
3 | HG03516.hp2 NA18906.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.501+509T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104392 | |||||||
| chr4:48104401 | A | T | 10 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 others(7): Show |
10 | HG00642.hp2 HG01243.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.501+500T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104401 | |||||||
| chr4:48104402 | A | T | 3 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 |
3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+499T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104402 | |||||||
| chr4:48104405 | TATA | T | 28 | a0001c0001t0001g0289 a0001c0001t0002g0021 a0001c0001t0002g0022 others(25): Show |
30 | HG00544.hp1 HG00597.hp2 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.501+493_501+495del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104405 | |||||||
| chr4:48104407 | TA | T | 3 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 |
3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+493delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104407 | |||||||
| chr4:48104408 | A | AATATTAT others(18): Show |
2 | a0001c0001t0002g0284 a0001c0001t0002g0295 |
2 | HG00438.hp2 HG00673.hp2 |
intron_variant | MODIFIER | c.501+468_501+492dup others(25): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104408 | |||||||
| chr4:48104413 | T | A | 3 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 |
3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+488A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104413 | |||||||
| chr4:48104418 | A | T | 12 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(9): Show |
12 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+483T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104418 | |||||||
| chr4:48104419 | T | A | 1 | a0001c0001t0002g0287 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.501+482A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104419 | |||||||
| chr4:48104420 | A | T | 14 | a0001c0001t0001g0103 a0001c0001t0002g0287 a0001c0001t0004g0096 others(11): Show |
14 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.501+481T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104420 | |||||||
| chr4:48104426 | TATA | T | 3 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 |
3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+472_501+474del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104426 | |||||||
| chr4:48104429 | A | T | 13 | a0001c0001t0002g0287 a0001c0001t0004g0189 a0001c0001t0004g0190 others(10): Show |
13 | HG00642.hp2 HG01993.hp2 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.501+472T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104429 | |||||||
| chr4:48104430 | A | T | 2 | a0001c0001t0004g0189 a0001c0001t0004g0190 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501+471T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104430 | |||||||
| chr4:48104439 | AT | A | 4 | a0001c0001t0002g0287 a0001c0001t0004g0188 a0001c0001t0004g0193 others(1): Show |
4 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+461delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104439 | |||||||
| chr4:48104441 | T | A | 2 | a0001c0001t0004g0189 a0001c0001t0004g0190 |
2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.501+460A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104441 | |||||||
| chr4:48104446 | A | T | 3 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 |
3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+455T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104446 | |||||||
| chr4:48104448 | A | T | 7 | a0001c0001t0002g0213 a0001c0001t0002g0294 a0001c0001t0002g0316 others(4): Show |
7 | HG02451.hp2 HG02622.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+453T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104448 | |||||||
| chr4:48104449 | A | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+452T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104449 | |||||||
| chr4:48104449 | ATATATAT others(12): Show |
A | 2 | a0002c0003t0001g0087 a0002c0003t0001g0251 |
2 | NA19063.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.501+433_501+451del others(19): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104449 | |||||||
| chr4:48104449 | ATATATAT others(40): Show |
A | 1 | a0001c0001t0001g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.501+405_501+451del others(47): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104449 | |||||||
| chr4:48104457 | A | T | 19 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(16): Show |
19 | HG00642.hp2 HG01255.hp2 HG01993.hp2 others(16): Show |
intron_variant | MODIFIER | c.501+444T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104457 | |||||||
| chr4:48104458 | A | T | 16 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(13): Show |
16 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+443T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104458 | |||||||
| chr4:48104463 | TA | T | 12 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(9): Show |
12 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+437delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104463 | |||||||
| chr4:48104464 | AATAT | A | 4 | a0001c0002t0001g0252 a0001c0002t0001g0263 a0001c0002t0001g0264 others(1): Show |
4 | HG00642.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+433_501+436del others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104464 | |||||||
| chr4:48104467 | AT | A | 7 | a0001c0001t0001g0161 a0001c0001t0002g0293 a0001c0001t0004g0189 others(4): Show |
7 | HG02109.hp2 HG02145.hp1 HG02155.hp2 others(4): Show |
intron_variant | MODIFIER | c.501+433delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104467 | |||||||
| chr4:48104467 | ATTATATA others(1): Show |
A | 4 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 others(1): Show |
4 | HG01243.hp2 HG02451.hp2 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+426_501+433del others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104467 | |||||||
| chr4:48104469 | T | A | 12 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(9): Show |
12 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.501+432A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104469 | |||||||
| chr4:48104474 | A | T | 6 | a0001c0001t0001g0161 a0001c0001t0004g0189 a0001c0001t0004g0190 others(3): Show |
6 | HG02109.hp2 HG02145.hp1 HG02155.hp2 others(3): Show |
intron_variant | MODIFIER | c.501+427T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104474 | |||||||
| chr4:48104476 | T | A | 34 | a0001c0001t0003g0212 a0001c0001t0003g0269 a0001c0001t0003g0273 others(31): Show |
34 | HG00642.hp2 HG01255.hp2 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.501+425A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104476 | |||||||
| chr4:48104477 | A | T | 43 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(40): Show |
50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.501+424T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104477 | |||||||
| chr4:48104479 | A | ATATATAA others(49): Show |
1 | a0001c0001t0003g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.501+421_501+422ins others(56): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104479 | |||||||
| chr4:48104482 | TATA | T | 16 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(13): Show |
16 | HG00642.hp2 HG01255.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+416_501+418del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104482 | |||||||
| chr4:48104483 | A | T | 1 | a0002c0003t0001g0248 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.501+418T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104483 | |||||||
| chr4:48104484 | T | A | 2 | a0001c0008t0003g0218 a0001c0008t0003g0227 |
2 | HG02559.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.501+417A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104484 | |||||||
| chr4:48104484 | TA | T | 3 | a0001c0001t0005g0025 a0001c0001t0005g0321 a0001c0001t0005g0322 |
4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+416delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104484 | |||||||
| chr4:48104485 | A | T | 7 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0006g0229 others(4): Show |
7 | HG01993.hp2 HG02055.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.501+416T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104485 | |||||||
| chr4:48104486 | A | T | 2 | a0002c0003t0001g0005 a0002c0003t0001g0320 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.501+415T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104486 | |||||||
| chr4:48104486 | ATATATAA others(3): Show |
A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.501+405_501+414del others(10): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104486 | |||||||
| chr4:48104488 | ATATAATA others(1): Show |
A | 3 | a0001c0001t0004g0188 a0001c0001t0004g0193 a0001c0001t0004g0253 |
3 | HG02451.hp2 HG02622.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.501+405_501+412del others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104488 | |||||||
| chr4:48104493 | ATAT | A | 8 | a0001c0001t0001g0161 a0001c0002t0001g0202 a0001c0002t0001g0252 others(5): Show |
8 | HG00642.hp2 HG02109.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.501+405_501+407del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104493 | |||||||
| chr4:48104495 | AT | A | 17 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(14): Show |
18 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.501+405delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104495 | |||||||
| chr4:48104495 | ATTATATA others(1): Show |
A | 43 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(40): Show |
50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.501+398_501+405del others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104495 | |||||||
| chr4:48104495 | ATTATATA others(40): Show |
A | 1 | a0001c0001t0004g0190 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+359_501+405del others(47): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104495 | |||||||
| chr4:48104496 | T | A | 2 | a0002c0003t0001g0005 a0002c0003t0001g0320 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.501+405A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104496 | |||||||
| chr4:48104497 | T | A | 1 | a0002c0003t0001g0248 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.501+404A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104497 | |||||||
| chr4:48104502 | A | T | 28 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(25): Show |
31 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(28): Show |
intron_variant | MODIFIER | c.501+399T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104502 | |||||||
| chr4:48104503 | T | A | 2 | a0002c0003t0001g0005 a0002c0003t0001g0320 |
2 | HG02055.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.501+398A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104503 | |||||||
| chr4:48104503 | T | TAATATAT others(22): Show |
1 | a0001c0001t0002g0316 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.501+397_501+398ins others(29): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104503 | |||||||
| chr4:48104504 | T | A | 16 | a0001c0001t0002g0213 a0001c0001t0003g0269 a0001c0001t0003g0273 others(13): Show |
16 | HG01891.hp1 HG02258.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.501+397A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104504 | |||||||
| chr4:48104504 | T | TATATATA others(21): Show |
3 | a0001c0001t0002g0203 a0001c0001t0002g0207 a0001c0001t0002g0210 |
3 | HG01099.hp2 HG01496.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.501+396_501+397ins others(28): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104504 | |||||||
| chr4:48104505 | A | T | 5 | a0001c0002t0001g0252 a0001c0002t0001g0263 a0001c0002t0001g0264 others(2): Show |
5 | HG00642.hp2 HG01243.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+396T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104505 | |||||||
| chr4:48104513 | A | AATATATA others(68): Show |
1 | a0001c0008t0003g0228 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.501+387_501+388ins others(75): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104513 | |||||||
| chr4:48104513 | A | T | 2 | a0001c0008t0006g0229 a0001c0010t0001g0119 |
2 | HG02717.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.501+388T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104513 | |||||||
| chr4:48104519 | TA | T | 45 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(42): Show |
53 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.501+381delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104519 | |||||||
| chr4:48104521 | A | T | 2 | a0001c0007t0001g0124 a0001c0007t0001g0125 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.501+380T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104521 | |||||||
| chr4:48104523 | A | T | 46 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(43): Show |
54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.501+378T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104523 | |||||||
| chr4:48104523 | AT | A | 4 | a0001c0001t0001g0103 a0001c0001t0001g0161 a0001c0007t0001g0125 others(1): Show |
4 | HG01243.hp2 HG02109.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.501+377delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104523 | |||||||
| chr4:48104524 | T | TA | 27 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(24): Show |
28 | HG00642.hp2 HG01255.hp2 HG01884.hp2 others(25): Show |
intron_variant | MODIFIER | c.501+376_501+377ins others(1): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104524 | |||||||
| chr4:48104532 | T | A | 156 | a0001c0001t0001g0103 a0001c0001t0001g0161 a0001c0001t0001g0289 others(153): Show |
171 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.501+369A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104532 | |||||||
| chr4:48104532 | T | TATATATA others(12): Show |
2 | a0001c0008t0003g0218 a0001c0008t0003g0227 |
2 | HG02559.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.501+368_501+369ins others(19): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104532 | |||||||
| chr4:48104532 | T | TATATATA others(21): Show |
1 | a0001c0001t0002g0196 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.501+368_501+369ins others(28): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104532 | |||||||
| chr4:48104532 | T | TATATATA others(49): Show |
2 | a0001c0001t0002g0205 a0001c0001t0002g0209 |
2 | HG00738.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.501+368_501+369ins others(56): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104532 | |||||||
| chr4:48104539 | ATT | A | 5 | a0001c0001t0001g0103 a0001c0001t0001g0161 a0001c0002t0001g0202 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+360_501+361del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104539 | |||||||
| chr4:48104540 | T | TAATATAT others(14): Show |
1 | a0001c0001t0003g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.501+360_501+361ins others(21): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104540 | |||||||
| chr4:48104541 | T | A | 9 | a0001c0001t0001g0151 a0001c0001t0001g0157 a0001c0001t0001g0158 others(6): Show |
9 | HG00642.hp2 HG01952.hp2 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.501+360A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104541 | |||||||
| chr4:48104542 | T | A | 3 | a0001c0001t0003g0212 a0001c0008t0006g0229 a0001c0010t0001g0214 |
3 | HG02886.hp2 HG02922.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.501+359A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104542 | |||||||
| chr4:48104545 | TATATATA | T | 50 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(47): Show |
58 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(55): Show |
intron_variant | MODIFIER | c.501+349_501+355del others(7): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104545 | |||||||
| chr4:48104547 | T | TAATATTA others(107): Show |
1 | a0001c0010t0001g0214 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.501+353_501+354ins others(114): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104547 | |||||||
| chr4:48104552 | A | T | 5 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0006g0229 others(2): Show |
5 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.501+349T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104552 | |||||||
| chr4:48104559 | AAT | A | 38 | a0001c0001t0001g0289 a0001c0001t0002g0021 a0001c0001t0002g0022 others(35): Show |
41 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.501+340_501+341del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104559 | |||||||
| chr4:48104560 | A | T | 2 | a0001c0001t0004g0190 a0001c0008t0003g0228 |
2 | HG03516.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.501+341T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104560 | |||||||
| chr4:48104562 | A | T | 1 | a0001c0001t0004g0190 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.501+339T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104562 | |||||||
| chr4:48104570 | ATAAT | A | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG01884.hp1 HG02257.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.501+327_501+330del others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104570 | |||||||
| chr4:48104572 | AAT | A | 196 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(193): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.501+327_501+328del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104572 | |||||||
| chr4:48104573 | A | T | 2 | a0001c0001t0004g0190 a0003c0004t0003g0139 |
2 | HG00639.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.501+328T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104573 | |||||||
| chr4:48104574 | T | A | 2 | a0001c0001t0004g0190 a0003c0004t0003g0139 |
2 | HG00639.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.501+327A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104574 | |||||||
| chr4:48104581 | A | T | 35 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(32): Show |
36 | HG00642.hp1 HG01192.hp1 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.501+320T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104581 | |||||||
| chr4:48104584 | A | T | 64 | a0001c0001t0004g0181 a0001c0001t0004g0190 a0001c0001t0006g0244 others(61): Show |
74 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(71): Show |
intron_variant | MODIFIER | c.501+317T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104584 | |||||||
| chr4:48104586 | A | T | 43 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(40): Show |
51 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.501+315T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104586 | |||||||
| chr4:48104591 | T | G | 1 | a0001c0001t0003g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.501+310A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104591 | |||||||
| chr4:48104591 | TATATAG | T | 4 | a0002c0003t0001g0262 a0002c0003t0001g0318 a0002c0003t0001g0319 others(1): Show |
4 | HG01192.hp1 HG02055.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.501+304_501+309del others(6): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104591 | |||||||
| chr4:48104593 | T | G | 24 | a0001c0001t0001g0131 a0001c0001t0001g0147 a0001c0001t0001g0150 others(21): Show |
24 | HG00673.hp1 HG00738.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.501+308A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104593 | |||||||
| chr4:48104595 | T | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(175): Show |
199 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(196): Show |
intron_variant | MODIFIER | c.501+306A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104595 | |||||||
| chr4:48104595 | TAG | T | 24 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(21): Show |
25 | HG00642.hp1 HG01243.hp2 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.501+304_501+305del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104595 | |||||||
| chr4:48104597 | G | T | 40 | a0001c0001t0002g0020 a0001c0001t0002g0222 a0001c0001t0002g0225 others(37): Show |
46 | HG00323.hp1 HG00408.hp2 HG00639.hp2 others(43): Show |
intron_variant | MODIFIER | c.501+304C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104597 | |||||||
| chr4:48104599 | G | T | 27 | a0001c0001t0002g0222 a0001c0001t0002g0266 a0001c0001t0003g0281 others(24): Show |
32 | HG01109.hp1 HG01123.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.501+302C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104599 | |||||||
| chr4:48104601 | G | T | 3 | a0001c0006t0001g0036 a0001c0006t0001g0037 a0001c0006t0001g0038 |
3 | HG02145.hp2 HG02451.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.501+300C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104601 | |||||||
| chr4:48104679 | CT | C | 22 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(19): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.501+221delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104679 | |||||||
| chr4:48104797 | T | C | 1 | a0001c0001t0002g0305 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.501+104A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 6/14 | chr4 | 48104797 | |||||||
| chr4:48104957 | T | G | 1 | a0001c0001t0005g0046 | 1 | HG02965.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.447-2A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48104957 | |||||||
| chr4:48105070 | G | C | 4 | a0001c0002t0001g0252 a0001c0002t0001g0263 a0001c0002t0001g0264 others(1): Show |
4 | HG00642.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.447-115C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105070 | |||||||
| chr4:48105079 | T | A | 51 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(48): Show |
59 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.447-124A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105079 | |||||||
| chr4:48105080 | A | T | 1 | a0001c0001t0002g0305 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-125T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105080 | |||||||
| chr4:48105109 | T | C | 76 | a0001c0001t0001g0088 a0001c0001t0001g0103 a0001c0001t0002g0068 others(73): Show |
88 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(85): Show |
intron_variant | MODIFIER | c.447-154A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105109 | |||||||
| chr4:48105287 | C | G | 46 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(43): Show |
54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.447-332G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105287 | |||||||
| chr4:48105293 | G | A | 242 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(239): Show |
277 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(274): Show |
intron_variant | MODIFIER | c.447-338C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105293 | |||||||
| chr4:48105478 | G | T | 14 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(11): Show |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.447-523C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105478 | |||||||
| chr4:48105547 | G | A | 14 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(11): Show |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.447-592C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105547 | |||||||
| chr4:48105572 | G | C | 19 | a0001c0001t0001g0117 a0001c0001t0001g0122 a0001c0001t0003g0104 others(16): Show |
22 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.447-617C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105572 | |||||||
| chr4:48105588 | A | G | 22 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(19): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.447-633T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105588 | |||||||
| chr4:48105620 | C | T | 1 | a0001c0001t0003g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.447-665G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105620 | |||||||
| chr4:48105624 | C | T | 14 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(11): Show |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.447-669G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105624 | |||||||
| chr4:48105663 | G | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.447-708C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105663 | |||||||
| chr4:48105694 | A | T | 1 | a0001c0001t0005g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.447-739T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105694 | |||||||
| chr4:48105702 | A | G | 14 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(11): Show |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.447-747T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105702 | |||||||
| chr4:48105741 | C | T | 22 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(19): Show |
23 | HG01255.hp2 HG01884.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.447-786G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48105741 | |||||||
| chr4:48106041 | A | G | 1 | a0002c0003t0001g0172 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.447-1086T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106041 | |||||||
| chr4:48106121 | C | T | 2 | a0001c0001t0004g0096 a0001c0001t0004g0188 |
2 | HG01255.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.447-1166G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106121 | |||||||
| chr4:48106185 | G | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.447-1230C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106185 | |||||||
| chr4:48106210 | A | C | 205 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(202): Show |
237 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.447-1255T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106210 | |||||||
| chr4:48106388 | G | GT | 124 | a0001c0001t0001g0088 a0001c0001t0001g0103 a0001c0001t0001g0131 others(121): Show |
139 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.447-1434dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106388 | |||||||
| chr4:48106392 | T | G | 1 | a0001c0002t0001g0308 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.447-1437A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106392 | |||||||
| chr4:48106548 | G | C | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18992.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.447-1593C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106548 | |||||||
| chr4:48106598 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.447-1643T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106598 | |||||||
| chr4:48106642 | T | C | 1 | a0001c0001t0003g0280 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.447-1687A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106642 | |||||||
| chr4:48106805 | A | G | 12 | a0001c0007t0001g0039 a0001c0007t0001g0109 a0001c0007t0001g0120 others(9): Show |
12 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.447-1850T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106805 | |||||||
| chr4:48106901 | T | A | 16 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 others(13): Show |
19 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.447-1946A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106901 | |||||||
| chr4:48106914 | A | G | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.447-1959T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106914 | |||||||
| chr4:48106960 | A | C | 1 | a0002c0003t0001g0319 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.447-2005T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48106960 | |||||||
| chr4:48107303 | C | A | 16 | a0001c0002t0001g0019 a0001c0002t0001g0067 a0001c0002t0001g0078 others(13): Show |
17 | HG01167.hp1 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.447-2348G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107303 | |||||||
| chr4:48107373 | A | T | 1 | a0001c0001t0002g0305 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-2418T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107373 | |||||||
| chr4:48107386 | C | G | 1 | a0001c0001t0002g0305 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-2431G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107386 | |||||||
| chr4:48107387 | T | C | 1 | a0001c0001t0002g0305 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-2432A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107387 | |||||||
| chr4:48107388 | C | T | 1 | a0001c0001t0002g0305 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.447-2433G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107388 | |||||||
| chr4:48107393 | C | G | 1 | a0001c0001t0009g0217 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.447-2438G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107393 | |||||||
| chr4:48107438 | C | T | 46 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(43): Show |
54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.447-2483G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107438 | |||||||
| chr4:48107574 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0163 |
2 | NA18992.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.447-2619C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107574 | |||||||
| chr4:48107723 | A | C | 248 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(245): Show |
283 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(280): Show |
intron_variant | MODIFIER | c.447-2768T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107723 | |||||||
| chr4:48107753 | C | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.446+2785G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107753 | |||||||
| chr4:48107758 | C | A | 3 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 |
3 | HG02559.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.446+2780G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107758 | |||||||
| chr4:48107800 | C | T | 1 | a0001c0001t0003g0104 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.446+2738G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107800 | |||||||
| chr4:48107838 | G | A | 1 | a0002c0003t0001g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.446+2700C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107838 | |||||||
| chr4:48107899 | T | TA | 32 | a0001c0001t0002g0197 a0001c0001t0002g0210 a0001c0001t0002g0211 others(29): Show |
33 | HG00597.hp2 HG00735.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.446+2638dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107899 | |||||||
| chr4:48107899 | T | TAA | 6 | a0001c0001t0002g0305 a0001c0001t0003g0281 a0001c0007t0001g0039 others(3): Show |
6 | HG01255.hp1 HG02145.hp1 HG03516.hp1 others(3): Show |
intron_variant | MODIFIER | c.446+2637_446+2638d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107899 | |||||||
| chr4:48107899 | TA | T | 8 | a0001c0005t0001g0029 a0001c0005t0001g0030 a0001c0005t0001g0031 others(5): Show |
8 | HG01884.hp1 HG02257.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.446+2638delT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107899 | |||||||
| chr4:48107899 | TAAAAAAA others(5): Show |
T | 4 | a0001c0001t0001g0164 a0001c0001t0001g0168 a0001c0001t0001g0177 others(1): Show |
4 | HG02258.hp2 HG02922.hp2 NA18967.hp1 others(1): Show |
intron_variant | MODIFIER | c.446+2627_446+2638d others(14): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107899 | |||||||
| chr4:48107899 | TAAAAAAA others(6): Show |
T | 195 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(192): Show |
227 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(224): Show |
intron_variant | MODIFIER | c.446+2626_446+2638d others(15): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107899 | |||||||
| chr4:48107939 | C | T | 1 | a0001c0001t0004g0181 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.446+2599G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107939 | |||||||
| chr4:48107945 | C | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(196): Show |
231 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(228): Show |
intron_variant | MODIFIER | c.446+2593G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107945 | |||||||
| chr4:48107965 | G | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.446+2573C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48107965 | |||||||
| chr4:48108072 | AAAAT | A | 12 | a0001c0007t0001g0039 a0001c0007t0001g0109 a0001c0007t0001g0120 others(9): Show |
12 | HG01255.hp1 HG02109.hp2 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.446+2462_446+2465d others(6): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108072 | |||||||
| chr4:48108199 | G | T | 1 | a0001c0002t0001g0084 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.446+2339C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108199 | |||||||
| chr4:48108227 | A | T | 1 | a0002c0003t0001g0232 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.446+2311T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108227 | |||||||
| chr4:48108280 | T | C | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.446+2258A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108280 | |||||||
| chr4:48108323 | TTTCATAG others(6): Show |
T | 1 | a0001c0002t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.446+2202_446+2214d others(15): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108323 | |||||||
| chr4:48108324 | T | G | 75 | a0001c0001t0001g0088 a0001c0001t0001g0103 a0001c0001t0002g0068 others(72): Show |
87 | HG00323.hp2 HG00408.hp2 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.446+2214A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108324 | |||||||
| chr4:48108337 | A | C | 1 | a0001c0002t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.446+2201T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108337 | |||||||
| chr4:48108338 | A | C | 1 | a0001c0002t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.446+2200T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108338 | |||||||
| chr4:48108381 | C | T | 236 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(233): Show |
271 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(268): Show |
intron_variant | MODIFIER | c.446+2157G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108381 | |||||||
| chr4:48108394 | T | C | 1 | a0001c0006t0001g0283 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.446+2144A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108394 | |||||||
| chr4:48108404 | T | C | 14 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(11): Show |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.446+2134A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108404 | |||||||
| chr4:48108832 | C | T | 14 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(11): Show |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.446+1706G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48108832 | |||||||
| chr4:48109148 | G | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.446+1390C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109148 | |||||||
| chr4:48109181 | C | CT | 138 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(135): Show |
159 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.446+1356dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109181 | |||||||
| chr4:48109181 | C | CTT | 10 | a0001c0001t0001g0028 a0001c0001t0001g0055 a0001c0001t0001g0130 others(7): Show |
10 | HG02129.hp2 NA18612.hp1 NA18949.hp1 others(7): Show |
intron_variant | MODIFIER | c.446+1355_446+1356d others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109181 | |||||||
| chr4:48109181 | CT | C | 15 | a0001c0002t0001g0083 a0001c0005t0001g0006 a0001c0005t0001g0029 others(12): Show |
17 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.446+1356delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109181 | |||||||
| chr4:48109200 | C | CT | 14 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(11): Show |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.446+1337dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109200 | |||||||
| chr4:48109216 | A | C | 1 | a0001c0001t0001g0014 | 2 | NA18949.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.446+1322T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109216 | |||||||
| chr4:48109401 | C | T | 45 | a0001c0001t0006g0244 a0001c0002t0001g0017 a0001c0002t0001g0092 others(42): Show |
53 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.446+1137G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109401 | |||||||
| chr4:48109402 | G | A | 14 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(11): Show |
16 | HG01884.hp1 HG02145.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.446+1136C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109402 | |||||||
| chr4:48109506 | T | C | 1 | a0002c0003t0001g0061 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.446+1032A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109506 | |||||||
| chr4:48109670 | A | C | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.446+868T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109670 | |||||||
| chr4:48109874 | G | C | 5 | a0002c0003t0001g0243 a0002c0003t0001g0262 a0002c0003t0001g0318 others(2): Show |
5 | HG00280.hp2 HG01192.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.446+664C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48109874 | |||||||
| chr4:48110057 | A | G | 1 | a0001c0007t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.446+481T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110057 | |||||||
| chr4:48110088 | C | T | 1 | a0001c0001t0006g0244 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.446+450G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110088 | |||||||
| chr4:48110219 | C | A | 19 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(16): Show |
19 | HG01255.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.446+319G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110219 | |||||||
| chr4:48110274 | A | T | 187 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(184): Show |
211 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(208): Show |
intron_variant | MODIFIER | c.446+264T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110274 | |||||||
| chr4:48110365 | A | T | 225 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(222): Show |
252 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.446+173T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110365 | |||||||
| chr4:48110442 | CT | C | 7 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(4): Show |
9 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.446+95delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 5/14 | chr4 | 48110442 | |||||||
| chr4:48110619 | A | G | 3 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 |
3 | HG02145.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.381-16T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48110619 | |||||||
| chr4:48110931 | A | G | 1 | a0001c0001t0003g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.381-328T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48110931 | |||||||
| chr4:48111070 | G | A | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.381-467C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111070 | |||||||
| chr4:48111128 | T | C | 1 | a0001c0001t0003g0212 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.381-525A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111128 | |||||||
| chr4:48111202 | C | G | 55 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(52): Show |
64 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.381-599G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111202 | |||||||
| chr4:48111374 | T | C | 48 | a0001c0001t0006g0244 a0001c0002t0001g0245 a0001c0002t0001g0252 others(45): Show |
55 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.381-771A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111374 | |||||||
| chr4:48111724 | T | C | 55 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(52): Show |
64 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.380+583A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111724 | |||||||
| chr4:48111792 | G | C | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.380+515C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111792 | |||||||
| chr4:48111803 | C | G | 30 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(27): Show |
32 | HG01255.hp2 HG02055.hp1 HG02109.hp1 others(29): Show |
intron_variant | MODIFIER | c.380+504G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111803 | |||||||
| chr4:48111806 | T | C | 1 | a0001c0001t0001g0137 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.380+501A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111806 | |||||||
| chr4:48111821 | T | C | 3 | a0001c0006t0001g0097 a0001c0006t0001g0127 a0001c0006t0001g0283 |
3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.380+486A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111821 | |||||||
| chr4:48111841 | G | A | 5 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(2): Show |
6 | HG01243.hp2 HG01884.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.380+466C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111841 | |||||||
| chr4:48111913 | C | T | 1 | a0001c0002t0001g0091 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.380+394G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48111913 | |||||||
| chr4:48112010 | C | G | 139 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(136): Show |
156 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.380+297G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48112010 | |||||||
| chr4:48112193 | G | A | 1 | a0001c0001t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.380+114C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 4/14 | chr4 | 48112193 | |||||||
| chr4:48112677 | C | T | 60 | a0001c0001t0001g0088 a0001c0001t0001g0103 a0001c0001t0002g0068 others(57): Show |
65 | HG00323.hp2 HG00544.hp2 HG00558.hp2 others(62): Show |
intron_variant | MODIFIER | c.175-165G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/14 | chr4 | 48112677 | |||||||
| chr4:48112685 | T | G | 6 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 others(3): Show |
6 | HG02559.hp1 HG02717.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-173A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/14 | chr4 | 48112685 | |||||||
| chr4:48112821 | A | AT | 5 | a0001c0001t0003g0269 a0001c0001t0005g0025 a0001c0001t0005g0046 others(2): Show |
6 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.175-310dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/14 | chr4 | 48112821 | |||||||
| chr4:48112858 | T | C | 3 | a0001c0006t0001g0097 a0001c0006t0001g0127 a0001c0006t0001g0283 |
3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.175-346A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/14 | chr4 | 48112858 | |||||||
| chr4:48112869 | G | C | 1 | a0001c0001t0002g0213 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.174+338C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 3/14 | chr4 | 48112869 | |||||||
| chr4:48113486 | T | C | 1 | a0001c0002t0001g0264 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.72-177A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48113486 | |||||||
| chr4:48113495 | C | T | 3 | a0001c0002t0001g0024 a0001c0002t0001g0306 a0001c0002t0001g0307 |
4 | NA18940.hp2 NA18945.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.72-186G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48113495 | |||||||
| chr4:48113656 | C | T | 16 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 others(13): Show |
19 | HG00323.hp1 HG00639.hp2 HG01109.hp1 others(16): Show |
intron_variant | MODIFIER | c.72-347G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48113656 | |||||||
| chr4:48113717 | A | T | 225 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(222): Show |
252 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(249): Show |
intron_variant | MODIFIER | c.72-408T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48113717 | |||||||
| chr4:48113976 | G | T | 1 | a0001c0001t0003g0105 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.71+372C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48113976 | |||||||
| chr4:48114046 | A | G | 1 | a0001c0001t0001g0117 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.71+302T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48114046 | |||||||
| chr4:48114118 | G | A | 3 | a0001c0006t0001g0097 a0001c0006t0001g0127 a0001c0006t0001g0283 |
3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.71+230C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48114118 | |||||||
| chr4:48114261 | G | A | 1 | a0001c0001t0002g0266 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.71+87C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 2/14 | chr4 | 48114261 | |||||||
| chr4:48114664 | G | A | 1 | a0001c0001t0001g0166 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.17-262C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114664 | |||||||
| chr4:48114700 | G | A | 1 | a0001c0001t0003g0312 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.17-298C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114700 | |||||||
| chr4:48114835 | C | T | 4 | a0001c0002t0001g0252 a0001c0002t0001g0263 a0001c0002t0001g0264 others(1): Show |
4 | HG00642.hp2 HG02615.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-433G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114835 | |||||||
| chr4:48114865 | T | G | 1 | a0001c0007t0001g0039 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.17-463A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114865 | |||||||
| chr4:48114869 | G | T | 177 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(174): Show |
197 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.17-467C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114869 | |||||||
| chr4:48114976 | A | G | 1 | a0001c0001t0003g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.17-574T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114976 | |||||||
| chr4:48114992 | A | T | 7 | a0001c0002t0001g0234 a0001c0002t0001g0254 a0001c0002t0001g0255 others(4): Show |
7 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.17-590T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48114992 | |||||||
| chr4:48115033 | CT | C | 177 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(174): Show |
197 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.17-632delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115033 | |||||||
| chr4:48115070 | A | G | 1 | a0002c0003t0001g0172 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.17-668T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115070 | |||||||
| chr4:48115385 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.17-983G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115385 | |||||||
| chr4:48115436 | T | C | 1 | a0001c0002t0001g0081 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.17-1034A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115436 | |||||||
| chr4:48115478 | A | G | 1 | a0001c0001t0004g0182 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.17-1076T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115478 | |||||||
| chr4:48115601 | C | T | 3 | a0001c0006t0001g0097 a0001c0006t0001g0127 a0001c0006t0001g0283 |
3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.17-1199G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115601 | |||||||
| chr4:48115612 | C | T | 1 | a0001c0001t0001g0142 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.17-1210G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115612 | |||||||
| chr4:48115639 | G | A | 4 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-1237C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115639 | |||||||
| chr4:48115683 | C | T | 1 | a0001c0001t0001g0275 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.17-1281G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115683 | |||||||
| chr4:48115724 | G | C | 2 | a0001c0002t0001g0257 a0001c0002t0001g0258 |
2 | HG02976.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.17-1322C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115724 | |||||||
| chr4:48115749 | G | T | 1 | a0001c0006t0001g0283 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.17-1347C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115749 | |||||||
| chr4:48115960 | G | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-1558C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48115960 | |||||||
| chr4:48116185 | T | C | 240 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(237): Show |
267 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(264): Show |
intron_variant | MODIFIER | c.17-1783A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48116185 | |||||||
| chr4:48116257 | C | T | 1 | a0001c0010t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.17-1855G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48116257 | |||||||
| chr4:48116583 | C | T | 4 | a0001c0007t0001g0039 a0001c0007t0001g0120 a0001c0007t0001g0124 others(1): Show |
4 | HG02109.hp2 HG02145.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-2181G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48116583 | |||||||
| chr4:48116794 | A | G | 18 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(15): Show |
18 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-2392T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48116794 | |||||||
| chr4:48116878 | T | C | 1 | a0001c0001t0003g0281 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.17-2476A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48116878 | |||||||
| chr4:48117003 | A | G | 1 | a0002c0003t0001g0237 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.17-2601T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117003 | |||||||
| chr4:48117177 | C | T | 46 | a0001c0001t0006g0244 a0001c0002t0001g0245 a0001c0006t0001g0097 others(43): Show |
53 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(50): Show |
intron_variant | MODIFIER | c.17-2775G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117177 | |||||||
| chr4:48117178 | G | A | 141 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(138): Show |
158 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(155): Show |
intron_variant | MODIFIER | c.17-2776C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117178 | |||||||
| chr4:48117258 | C | T | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.17-2856G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117258 | |||||||
| chr4:48117494 | C | T | 1 | a0001c0001t0003g0110 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.17-3092G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117494 | |||||||
| chr4:48117646 | C | G | 4 | a0001c0002t0001g0026 a0001c0002t0001g0027 a0001c0002t0001g0047 others(1): Show |
4 | HG03688.hp2 NA18612.hp2 NA18944.hp1 others(1): Show |
intron_variant | MODIFIER | c.17-3244G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117646 | |||||||
| chr4:48117960 | A | G | 2 | a0001c0002t0001g0065 a0001c0002t0001g0066 |
2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.17-3558T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48117960 | |||||||
| chr4:48118002 | T | C | 3 | a0001c0001t0005g0025 a0001c0001t0005g0321 a0001c0001t0005g0322 |
4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-3600A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118002 | |||||||
| chr4:48118005 | C | A | 2 | a0001c0002t0001g0082 a0001c0002t0001g0083 |
2 | HG02615.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.17-3603G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118005 | |||||||
| chr4:48118109 | T | C | 2 | a0001c0010t0001g0119 a0001c0010t0001g0214 |
2 | HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.17-3707A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118109 | |||||||
| chr4:48118185 | T | G | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.17-3783A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118185 | |||||||
| chr4:48118210 | A | G | 2 | a0002c0003t0001g0043 a0002c0003t0001g0056 |
2 | NA18967.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.17-3808T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118210 | |||||||
| chr4:48118767 | T | C | 3 | a0001c0006t0001g0035 a0001c0006t0001g0036 a0001c0006t0001g0037 |
3 | HG02145.hp2 HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.17-4365A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118767 | |||||||
| chr4:48118801 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.17-4399G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118801 | |||||||
| chr4:48118854 | G | A | 8 | a0001c0001t0003g0269 a0001c0001t0003g0273 a0001c0001t0003g0279 others(5): Show |
8 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.17-4452C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48118854 | |||||||
| chr4:48119166 | A | G | 5 | a0001c0001t0003g0269 a0001c0001t0003g0273 a0001c0001t0003g0279 others(2): Show |
5 | HG02258.hp1 HG02559.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-4764T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119166 | |||||||
| chr4:48119210 | G | A | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.17-4808C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119210 | |||||||
| chr4:48119296 | A | G | 1 | a0002c0003t0001g0087 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.17-4894T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119296 | |||||||
| chr4:48119300 | T | C | 3 | a0001c0006t0001g0097 a0001c0006t0001g0127 a0001c0006t0001g0283 |
3 | HG01884.hp1 HG02895.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.17-4898A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119300 | |||||||
| chr4:48119873 | T | G | 1 | a0002c0003t0001g0063 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.17-5471A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119873 | |||||||
| chr4:48119905 | A | G | 19 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(16): Show |
19 | HG01255.hp2 HG02055.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.17-5503T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119905 | |||||||
| chr4:48119924 | T | C | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.17-5522A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48119924 | |||||||
| chr4:48120078 | TAC | T | 314 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(311): Show |
354 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(351): Show |
intron_variant | MODIFIER | c.17-5678_17-5677del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120078 | |||||||
| chr4:48120107 | G | A | 18 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(15): Show |
18 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-5705C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120107 | |||||||
| chr4:48120112 | C | CAT | 4 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-5712_17-5711dup others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120112 | |||||||
| chr4:48120116 | C | T | 1 | a0001c0001t0004g0181 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.17-5714G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120116 | |||||||
| chr4:48120126 | T | C | 272 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(269): Show |
303 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(300): Show |
intron_variant | MODIFIER | c.17-5724A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120126 | |||||||
| chr4:48120157 | A | ATATGTAT others(1): Show |
238 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(235): Show |
262 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.17-5756_17-5755ins others(8): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120157 | |||||||
| chr4:48120161 | A | G | 34 | a0002c0003t0001g0005 a0002c0003t0001g0009 a0002c0003t0001g0010 others(31): Show |
41 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(38): Show |
intron_variant | MODIFIER | c.17-5759T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120161 | |||||||
| chr4:48120164 | TGTATATA others(55): Show |
T | 33 | a0002c0003t0001g0005 a0002c0003t0001g0009 a0002c0003t0001g0010 others(30): Show |
40 | HG00140.hp2 HG00639.hp1 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.17-5824_17-5763del others(62): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120164 | |||||||
| chr4:48120168 | T | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(159): Show |
179 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(176): Show |
intron_variant | MODIFIER | c.17-5766A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120168 | |||||||
| chr4:48120172 | C | T | 1 | a0002c0003t0001g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.17-5770G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120172 | |||||||
| chr4:48120179 | G | A | 1 | a0002c0003t0001g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.17-5777C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120179 | |||||||
| chr4:48120180 | T | C | 1 | a0002c0003t0001g0243 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.17-5778A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120180 | |||||||
| chr4:48120188 | T | C | 4 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-5786A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120188 | |||||||
| chr4:48120196 | CACATATA others(13): Show |
C | 1 | a0001c0001t0001g0132 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.17-5814_17-5795del others(20): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120196 | |||||||
| chr4:48120242 | C | T | 1 | a0001c0001t0005g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.17-5840G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120242 | |||||||
| chr4:48120328 | G | A | 47 | a0001c0001t0006g0244 a0001c0002t0001g0245 a0001c0002t0001g0252 others(44): Show |
54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.17-5926C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120328 | |||||||
| chr4:48120382 | C | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-5980G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120382 | |||||||
| chr4:48120428 | C | T | 1 | a0001c0001t0003g0313 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.17-6026G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120428 | |||||||
| chr4:48120456 | GCTCT | G | 3 | a0002c0003t0001g0246 a0002c0003t0001g0248 a0002c0012t0002g0247 |
3 | HG00642.hp1 HG01516.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.17-6058_17-6055del others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120456 | |||||||
| chr4:48120522 | G | A | 158 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(155): Show |
175 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(172): Show |
intron_variant | MODIFIER | c.17-6120C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120522 | |||||||
| chr4:48120533 | G | A | 18 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(15): Show |
18 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-6131C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120533 | |||||||
| chr4:48120569 | C | T | 1 | a0001c0006t0001g0035 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.17-6167G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120569 | |||||||
| chr4:48120658 | T | A | 4 | a0002c0003t0001g0249 a0002c0003t0001g0250 a0002c0003t0001g0251 others(1): Show |
4 | HG00735.hp1 HG01168.hp2 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.17-6256A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120658 | |||||||
| chr4:48120677 | G | A | 1 | a0001c0001t0005g0046 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.17-6275C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120677 | |||||||
| chr4:48120818 | T | A | 2 | a0001c0002t0001g0252 a0001c0002t0001g0265 |
2 | HG00642.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.17-6416A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120818 | |||||||
| chr4:48120834 | C | T | 5 | a0001c0001t0001g0103 a0001c0006t0001g0097 a0001c0006t0001g0127 others(2): Show |
5 | HG01243.hp2 HG01884.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-6432G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120834 | |||||||
| chr4:48120869 | G | GA | 167 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(164): Show |
185 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.17-6468dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120869 | |||||||
| chr4:48120926 | T | C | 1 | a0001c0001t0009g0217 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.17-6524A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120926 | |||||||
| chr4:48120931 | C | T | 159 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(156): Show |
176 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(173): Show |
intron_variant | MODIFIER | c.17-6529G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48120931 | |||||||
| chr4:48121069 | C | T | 1 | a0001c0002t0001g0064 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.17-6667G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121069 | |||||||
| chr4:48121397 | T | G | 1 | a0001c0002t0001g0084 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.17-6995A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121397 | |||||||
| chr4:48121398 | C | T | 18 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(15): Show |
18 | HG01255.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.17-6996G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121398 | |||||||
| chr4:48121558 | A | G | 1 | a0001c0001t0001g0219 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.17-7156T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121558 | |||||||
| chr4:48121583 | C | T | 53 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(50): Show |
62 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(59): Show |
intron_variant | MODIFIER | c.17-7181G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121583 | |||||||
| chr4:48121705 | A | G | 8 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(5): Show |
9 | HG01884.hp1 HG01884.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.17-7303T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121705 | |||||||
| chr4:48121906 | C | G | 9 | a0001c0001t0003g0269 a0001c0001t0003g0273 a0001c0001t0003g0279 others(6): Show |
9 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.17-7504G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48121906 | |||||||
| chr4:48122003 | A | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-7601T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122003 | |||||||
| chr4:48122004 | T | C | 3 | a0001c0008t0003g0218 a0001c0008t0003g0227 a0001c0008t0003g0228 |
3 | HG02559.hp1 HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.17-7602A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122004 | |||||||
| chr4:48122040 | C | T | 47 | a0001c0001t0006g0244 a0001c0002t0001g0245 a0001c0002t0001g0252 others(44): Show |
54 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(51): Show |
intron_variant | MODIFIER | c.17-7638G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122040 | |||||||
| chr4:48122183 | C | A | 1 | a0001c0001t0001g0122 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.17-7781G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122183 | |||||||
| chr4:48122205 | A | T | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.17-7803T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122205 | |||||||
| chr4:48122389 | C | T | 1 | a0001c0002t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.17-7987G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122389 | |||||||
| chr4:48122571 | T | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-8169A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122571 | |||||||
| chr4:48122821 | C | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(52): Show |
64 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.17-8419G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122821 | |||||||
| chr4:48122829 | T | G | 1 | a0001c0002t0001g0085 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.17-8427A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122829 | |||||||
| chr4:48122932 | G | A | 4 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(1): Show |
5 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.17-8530C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48122932 | |||||||
| chr4:48123278 | C | T | 1 | a0001c0008t0006g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.17-8876G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48123278 | |||||||
| chr4:48123442 | C | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-9040G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48123442 | |||||||
| chr4:48123630 | G | C | 1 | a0002c0003t0001g0320 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.17-9228C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48123630 | |||||||
| chr4:48123785 | G | T | 55 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(52): Show |
64 | HG00280.hp1 HG00408.hp1 HG00558.hp1 others(61): Show |
intron_variant | MODIFIER | c.17-9383C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48123785 | |||||||
| chr4:48123849 | A | G | 268 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(265): Show |
299 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.17-9447T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48123849 | |||||||
| chr4:48124060 | G | T | 1 | a0003c0004t0003g0108 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.17-9658C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124060 | |||||||
| chr4:48124069 | T | C | 268 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(265): Show |
299 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(296): Show |
intron_variant | MODIFIER | c.17-9667A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124069 | |||||||
| chr4:48124232 | C | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.17-9830G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124232 | |||||||
| chr4:48124374 | C | T | 1 | a0001c0001t0004g0180 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.16+9781G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124374 | |||||||
| chr4:48124384 | T | C | 1 | a0001c0007t0001g0120 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.16+9771A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124384 | |||||||
| chr4:48124420 | C | CT | 7 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(4): Show |
9 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.16+9734dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124420 | |||||||
| chr4:48124522 | C | T | 1 | a0003c0004t0003g0139 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.16+9633G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124522 | |||||||
| chr4:48124560 | C | CT | 6 | a0001c0001t0001g0122 a0001c0001t0005g0025 a0001c0001t0005g0046 others(3): Show |
7 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.16+9594dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124560 | |||||||
| chr4:48124563 | C | T | 212 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(209): Show |
237 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(234): Show |
intron_variant | MODIFIER | c.16+9592G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124563 | |||||||
| chr4:48124577 | A | G | 21 | a0001c0001t0004g0096 a0001c0001t0004g0126 a0001c0001t0004g0179 others(18): Show |
21 | HG01255.hp2 HG02109.hp1 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.16+9578T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124577 | |||||||
| chr4:48124639 | G | A | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16+9516C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124639 | |||||||
| chr4:48124662 | G | A | 48 | a0001c0001t0001g0289 a0001c0001t0002g0020 a0001c0001t0002g0021 others(45): Show |
52 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(49): Show |
intron_variant | MODIFIER | c.16+9493C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124662 | |||||||
| chr4:48124715 | A | G | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+9440T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124715 | |||||||
| chr4:48124884 | G | A | 1 | a0002c0003t0001g0259 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.16+9271C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124884 | |||||||
| chr4:48124980 | T | C | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+9175A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48124980 | |||||||
| chr4:48125107 | C | A | 2 | a0001c0008t0003g0227 a0001c0008t0003g0228 |
2 | HG02897.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.16+9048G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125107 | |||||||
| chr4:48125245 | A | G | 43 | a0001c0001t0002g0266 a0001c0001t0004g0253 a0001c0001t0006g0244 others(40): Show |
49 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(46): Show |
intron_variant | MODIFIER | c.16+8910T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125245 | |||||||
| chr4:48125520 | C | T | 1 | a0001c0001t0002g0198 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.16+8635G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125520 | |||||||
| chr4:48125521 | G | A | 4 | a0001c0002t0001g0024 a0001c0002t0001g0306 a0001c0002t0001g0307 others(1): Show |
5 | NA18940.hp2 NA18945.hp2 NA18992.hp1 others(2): Show |
intron_variant | MODIFIER | c.16+8634C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125521 | |||||||
| chr4:48125584 | A | G | 3 | a0001c0001t0002g0195 a0001c0001t0002g0196 a0001c0001t0002g0197 |
3 | HG00733.hp1 HG01168.hp1 HG01243.hp1 |
intron_variant | MODIFIER | c.16+8571T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125584 | |||||||
| chr4:48125684 | C | T | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+8471G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125684 | |||||||
| chr4:48125794 | T | C | 7 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(4): Show |
9 | HG02257.hp1 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.16+8361A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125794 | |||||||
| chr4:48125959 | G | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+8196C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48125959 | |||||||
| chr4:48126162 | CCT | C | 60 | a0001c0001t0002g0020 a0001c0001t0002g0266 a0001c0001t0003g0104 others(57): Show |
70 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(67): Show |
intron_variant | MODIFIER | c.16+7991_16+7992del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126162 | |||||||
| chr4:48126174 | CT | C | 125 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(122): Show |
140 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.16+7980delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126174 | |||||||
| chr4:48126265 | A | G | 1 | a0001c0001t0001g0194 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.16+7890T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126265 | |||||||
| chr4:48126281 | T | G | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+7874A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126281 | |||||||
| chr4:48126288 | T | C | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+7867A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126288 | |||||||
| chr4:48126368 | C | A | 4 | a0001c0001t0003g0104 a0001c0001t0003g0105 a0001c0001t0003g0106 others(1): Show |
4 | HG03654.hp1 HG03654.hp2 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+7787G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126368 | |||||||
| chr4:48126395 | C | G | 5 | a0001c0007t0001g0039 a0001c0007t0001g0120 a0001c0007t0001g0124 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+7760G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126395 | |||||||
| chr4:48126535 | C | G | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+7620G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126535 | |||||||
| chr4:48126550 | G | T | 2 | a0002c0003t0001g0010 a0002c0013t0001g0052 |
3 | NA18949.hp1 NA18960.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.16+7605C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126550 | |||||||
| chr4:48126667 | A | AT | 98 | a0001c0001t0001g0275 a0001c0001t0001g0289 a0001c0001t0002g0020 others(95): Show |
113 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.16+7487dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126667 | |||||||
| chr4:48126723 | C | T | 1 | a0001c0002t0001g0274 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.16+7432G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126723 | |||||||
| chr4:48126833 | T | G | 259 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(256): Show |
294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.16+7322A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126833 | |||||||
| chr4:48126887 | C | T | 1 | a0002c0003t0001g0235 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.16+7268G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48126887 | |||||||
| chr4:48127071 | A | G | 1 | a0001c0001t0003g0138 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.16+7084T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127071 | |||||||
| chr4:48127095 | T | A | 258 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(255): Show |
293 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(290): Show |
intron_variant | MODIFIER | c.16+7060A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127095 | |||||||
| chr4:48127171 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
166 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.16+6984G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127171 | |||||||
| chr4:48127207 | T | G | 99 | a0001c0001t0001g0275 a0001c0001t0001g0289 a0001c0001t0002g0020 others(96): Show |
114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.16+6948A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127207 | |||||||
| chr4:48127298 | C | A | 1 | a0001c0001t0003g0309 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.16+6857G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127298 | |||||||
| chr4:48127523 | G | T | 5 | a0001c0001t0001g0122 a0001c0001t0005g0025 a0001c0001t0005g0046 others(2): Show |
6 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+6632C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127523 | |||||||
| chr4:48127746 | C | T | 3 | a0001c0002t0001g0051 a0002c0003t0001g0049 a0002c0003t0001g0050 |
3 | HG01256.hp2 HG01978.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.16+6409G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127746 | |||||||
| chr4:48127763 | G | A | 1 | a0001c0001t0001g0088 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.16+6392C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127763 | |||||||
| chr4:48127784 | A | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.16+6371T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127784 | |||||||
| chr4:48127795 | G | A | 1 | a0001c0001t0002g0020 | 2 | HG02602.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.16+6360C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127795 | |||||||
| chr4:48127898 | C | T | 56 | a0001c0001t0001g0275 a0001c0001t0001g0289 a0001c0001t0002g0021 others(53): Show |
64 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.16+6257G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48127898 | |||||||
| chr4:48128116 | A | C | 4 | a0001c0001t0001g0134 a0001c0001t0001g0135 a0001c0001t0001g0136 others(1): Show |
4 | NA18985.hp2 NA19005.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+6039T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128116 | |||||||
| chr4:48128165 | G | A | 1 | a0001c0001t0003g0273 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.16+5990C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128165 | |||||||
| chr4:48128168 | T | C | 148 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
166 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.16+5987A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128168 | |||||||
| chr4:48128308 | T | C | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16+5847A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128308 | |||||||
| chr4:48128373 | T | G | 3 | a0001c0001t0001g0173 a0001c0001t0001g0178 a0001c0009t0001g0004 |
6 | NA18940.hp1 NA18957.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+5782A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128373 | |||||||
| chr4:48128483 | T | A | 1 | a0001c0001t0002g0310 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.16+5672A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128483 | |||||||
| chr4:48128520 | A | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(145): Show |
166 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(163): Show |
intron_variant | MODIFIER | c.16+5635T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128520 | |||||||
| chr4:48128529 | A | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.16+5626T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128529 | |||||||
| chr4:48128561 | C | CT | 117 | a0001c0001t0001g0055 a0001c0001t0001g0088 a0001c0001t0001g0103 others(114): Show |
130 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.16+5593dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128561 | |||||||
| chr4:48128561 | C | CTT | 58 | a0001c0001t0001g0275 a0001c0001t0001g0289 a0001c0001t0002g0021 others(55): Show |
68 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.16+5592_16+5593dup others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128561 | |||||||
| chr4:48128561 | C | CTTT | 7 | a0001c0001t0002g0271 a0001c0001t0002g0272 a0001c0001t0003g0269 others(4): Show |
7 | HG02280.hp1 HG02559.hp2 HG03486.hp1 others(4): Show |
intron_variant | MODIFIER | c.16+5591_16+5593dup others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128561 | |||||||
| chr4:48128561 | CT | C | 11 | a0001c0001t0001g0122 a0001c0001t0001g0174 a0001c0001t0004g0192 others(8): Show |
11 | HG00323.hp1 HG00558.hp1 HG01515.hp2 others(8): Show |
intron_variant | MODIFIER | c.16+5593delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128561 | |||||||
| chr4:48128666 | G | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+5489C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128666 | |||||||
| chr4:48128757 | C | T | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16+5398G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128757 | |||||||
| chr4:48128846 | C | T | 1 | a0001c0001t0007g0121 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.16+5309G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128846 | |||||||
| chr4:48128858 | C | T | 1 | a0001c0002t0001g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.16+5297G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48128858 | |||||||
| chr4:48129013 | G | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+5142C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129013 | |||||||
| chr4:48129091 | T | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
161 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.16+5064A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129091 | |||||||
| chr4:48129125 | T | C | 5 | a0001c0001t0001g0122 a0001c0001t0005g0025 a0001c0001t0005g0046 others(2): Show |
6 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.16+5030A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129125 | |||||||
| chr4:48129162 | T | A | 4 | a0001c0002t0001g0091 a0001c0002t0001g0092 a0001c0002t0001g0093 others(1): Show |
4 | HG01346.hp1 HG01496.hp1 HG01943.hp1 others(1): Show |
intron_variant | MODIFIER | c.16+4993A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129162 | |||||||
| chr4:48129222 | T | A | 1 | a0001c0008t0006g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.16+4933A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129222 | |||||||
| chr4:48129364 | G | T | 6 | a0001c0001t0001g0122 a0001c0001t0005g0025 a0001c0001t0005g0046 others(3): Show |
7 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.16+4791C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129364 | |||||||
| chr4:48129374 | AAAG | A | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+4778_16+4780del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129374 | |||||||
| chr4:48129412 | G | A | 265 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.16+4743C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129412 | |||||||
| chr4:48129474 | T | C | 1 | a0002c0003t0001g0095 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.16+4681A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129474 | |||||||
| chr4:48129548 | T | A | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+4607A>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129548 | |||||||
| chr4:48129679 | C | G | 1 | a0001c0001t0003g0104 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.16+4476G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129679 | |||||||
| chr4:48129785 | C | T | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+4370G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129785 | |||||||
| chr4:48129840 | A | G | 1 | a0001c0001t0001g0128 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.16+4315T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129840 | |||||||
| chr4:48129862 | C | G | 71 | a0001c0001t0001g0055 a0001c0001t0001g0088 a0001c0001t0001g0103 others(68): Show |
77 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.16+4293G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129862 | |||||||
| chr4:48129928 | G | A | 17 | a0001c0001t0003g0313 a0001c0001t0004g0126 a0001c0001t0004g0179 others(14): Show |
17 | HG02109.hp1 HG02257.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.16+4227C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48129928 | |||||||
| chr4:48130153 | C | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
161 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.16+4002G>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130153 | |||||||
| chr4:48130172 | A | G | 43 | a0001c0001t0002g0020 a0001c0001t0002g0266 a0001c0001t0004g0253 others(40): Show |
50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.16+3983T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130172 | |||||||
| chr4:48130321 | G | A | 1 | a0001c0001t0002g0314 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.16+3834C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130321 | |||||||
| chr4:48130330 | T | C | 265 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.16+3825A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130330 | |||||||
| chr4:48130376 | C | G | 99 | a0001c0001t0001g0275 a0001c0001t0001g0289 a0001c0001t0002g0020 others(96): Show |
114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.16+3779G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130376 | |||||||
| chr4:48130437 | G | A | 1 | a0001c0002t0001g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.16+3718C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130437 | |||||||
| chr4:48130454 | C | T | 67 | a0001c0001t0001g0055 a0001c0001t0001g0088 a0001c0001t0002g0053 others(64): Show |
73 | HG00323.hp2 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.16+3701G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130454 | |||||||
| chr4:48130536 | A | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+3619T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130536 | |||||||
| chr4:48130541 | T | C | 143 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
161 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.16+3614A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130541 | |||||||
| chr4:48130602 | A | T | 1 | a0001c0002t0001g0017 | 2 | NA20752.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.16+3553T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130602 | |||||||
| chr4:48130669 | A | G | 99 | a0001c0001t0001g0275 a0001c0001t0001g0289 a0001c0001t0002g0020 others(96): Show |
114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.16+3486T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130669 | |||||||
| chr4:48130682 | C | G | 5 | a0001c0007t0001g0039 a0001c0007t0001g0120 a0001c0007t0001g0124 others(2): Show |
5 | HG02109.hp2 HG02145.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.16+3473G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130682 | |||||||
| chr4:48130812 | G | T | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+3343C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130812 | |||||||
| chr4:48130874 | G | A | 143 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
161 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.16+3281C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130874 | |||||||
| chr4:48130923 | C | T | 1 | a0001c0002t0001g0101 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.16+3232G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48130923 | |||||||
| chr4:48131317 | CT | C | 23 | a0001c0001t0001g0122 a0001c0001t0001g0129 a0001c0001t0002g0316 others(20): Show |
26 | HG00408.hp2 HG01168.hp2 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.16+2837delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131317 | |||||||
| chr4:48131317 | CTT | C | 135 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(132): Show |
153 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(150): Show |
intron_variant | MODIFIER | c.16+2836_16+2837del others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131317 | |||||||
| chr4:48131317 | CTTT | C | 6 | a0001c0001t0001g0176 a0001c0001t0001g0177 a0001c0001t0001g0178 others(3): Show |
6 | HG00323.hp1 HG02129.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.16+2835_16+2837del others(3): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131317 | |||||||
| chr4:48131443 | TTTTG | T | 143 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(140): Show |
161 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.16+2708_16+2711del others(4): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131443 | |||||||
| chr4:48131452 | T | G | 1 | a0001c0002t0001g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.16+2703A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131452 | |||||||
| chr4:48131632 | C | T | 2 | a0001c0002t0001g0027 a0001c0002t0001g0047 |
2 | NA18944.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.16+2523G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131632 | |||||||
| chr4:48131680 | C | T | 43 | a0001c0001t0002g0020 a0001c0001t0002g0266 a0001c0001t0004g0253 others(40): Show |
50 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.16+2475G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131680 | |||||||
| chr4:48131681 | G | A | 1 | a0001c0002t0001g0100 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.16+2474C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131681 | |||||||
| chr4:48131713 | A | G | 265 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(262): Show |
301 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(298): Show |
intron_variant | MODIFIER | c.16+2442T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131713 | |||||||
| chr4:48131903 | G | A | 2 | a0001c0007t0001g0124 a0001c0007t0001g0125 |
2 | HG02109.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.16+2252C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131903 | |||||||
| chr4:48131924 | C | T | 1 | a0001c0002t0001g0267 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.16+2231G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131924 | |||||||
| chr4:48131972 | G | C | 1 | a0001c0008t0006g0229 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.16+2183C>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48131972 | |||||||
| chr4:48132040 | A | AT | 63 | a0001c0001t0001g0055 a0001c0001t0001g0088 a0001c0001t0001g0128 others(60): Show |
69 | HG00558.hp2 HG00621.hp2 HG01099.hp1 others(66): Show |
intron_variant | MODIFIER | c.16+2114dupA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132040 | |||||||
| chr4:48132040 | A | ATT | 9 | a0001c0001t0005g0025 a0001c0001t0005g0046 a0001c0001t0005g0321 others(6): Show |
10 | HG00597.hp1 HG01884.hp2 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.16+2113_16+2114dup others(2): Show |
TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132040 | |||||||
| chr4:48132040 | AT | A | 18 | a0001c0001t0002g0317 a0001c0001t0004g0126 a0001c0001t0004g0179 others(15): Show |
18 | HG02109.hp1 HG02257.hp2 HG02622.hp1 others(15): Show |
intron_variant | MODIFIER | c.16+2114delA | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132040 | |||||||
| chr4:48132075 | A | G | 38 | a0001c0001t0004g0253 a0001c0001t0006g0244 a0001c0002t0001g0019 others(35): Show |
44 | HG00140.hp2 HG00280.hp2 HG00639.hp1 others(41): Show |
intron_variant | MODIFIER | c.16+2080T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132075 | |||||||
| chr4:48132092 | G | A | 1 | a0001c0006t0001g0127 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.16+2063C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132092 | |||||||
| chr4:48132101 | G | A | 56 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(53): Show |
65 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(62): Show |
intron_variant | MODIFIER | c.16+2054C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132101 | |||||||
| chr4:48132186 | A | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+1969T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132186 | |||||||
| chr4:48132310 | C | G | 1 | a0001c0015t0001g0040 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.16+1845G>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132310 | |||||||
| chr4:48132425 | T | C | 1 | a0001c0001t0002g0230 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.16+1730A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132425 | |||||||
| chr4:48132698 | C | T | 1 | a0001c0007t0001g0039 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.16+1457G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132698 | |||||||
| chr4:48132944 | T | TA | 15 | a0001c0001t0004g0179 a0001c0001t0004g0180 a0001c0001t0004g0181 others(12): Show |
15 | HG02109.hp1 HG02257.hp2 HG02622.hp1 others(12): Show |
intron_variant | MODIFIER | c.16+1210dupT | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48132944 | |||||||
| chr4:48133164 | A | C | 99 | a0001c0001t0001g0275 a0001c0001t0001g0289 a0001c0001t0002g0020 others(96): Show |
114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.16+991T>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133164 | |||||||
| chr4:48133204 | A | G | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+951T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133204 | |||||||
| chr4:48133224 | TG | T | 214 | a0001c0001t0001g0003 a0001c0001t0001g0014 a0001c0001t0001g0015 others(211): Show |
240 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.16+930delC | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133224 | |||||||
| chr4:48133225 | GGT | G | 56 | a0001c0001t0001g0275 a0001c0001t0001g0289 a0001c0001t0002g0021 others(53): Show |
64 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(61): Show |
intron_variant | MODIFIER | c.16+928_16+929delAC | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133225 | |||||||
| chr4:48133226 | G | T | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+929C>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133226 | |||||||
| chr4:48133316 | G | A | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+839C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133316 | |||||||
| chr4:48133591 | C | T | 11 | a0001c0005t0001g0006 a0001c0005t0001g0029 a0001c0005t0001g0030 others(8): Show |
13 | HG02145.hp2 HG02257.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.16+564G>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133591 | |||||||
| chr4:48133661 | G | A | 3 | a0002c0003t0001g0318 a0002c0003t0001g0319 a0002c0003t0001g0320 |
3 | HG01192.hp1 HG02055.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.16+494C>T | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133661 | |||||||
| chr4:48133695 | A | T | 1 | a0001c0001t0001g0028 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.16+460T>A | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133695 | |||||||
| chr4:48133766 | T | G | 99 | a0001c0001t0001g0275 a0001c0001t0001g0289 a0001c0001t0002g0020 others(96): Show |
114 | HG00140.hp2 HG00280.hp2 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.16+389A>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133766 | |||||||
| chr4:48133769 | A | G | 1 | a0001c0002t0001g0027 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.16+386T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133769 | |||||||
| chr4:48133887 | T | C | 3 | a0001c0001t0005g0025 a0001c0001t0005g0321 a0001c0001t0005g0322 |
4 | HG01884.hp2 HG02572.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.16+268A>G | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48133887 | |||||||
| chr4:48134112 | A | G | 1 | a0001c0002t0001g0026 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.16+43T>C | TXK | ENSG00000074966.11 | transcript | ENST00000264316.9 | protein_coding | 1/14 | chr4 | 48134112 |