Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 63917 |
| ensemblid | ENSG00000178234.13 |
| hgncid | 19875 |
| symbol | GALNT11 |
| name | polypeptide N-acetylgalactosaminyltransferase 11 |
| refseq_nuc | NM_022087.4 |
| refseq_prot | NP_071370.2 |
| ensembl_nuc | ENST00000430044.7 |
| ensembl_prot | ENSP00000395122.2 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 152025674 |
| end | 152122340 |
| strand | + |
| ver | v1.2 |
| region | chr7:152025674-152122340 |
| region5000 | chr7:152020674-152127340 |
| regionname0 | GALNT11_chr7_152025674_152122340 |
| regionname5000 | GALNT11_chr7_152020674_152127340 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 608 | 264 | 77 | 50 | 103 | 8 | 24 | 67 | GALNT11_chr7_152020674_152127340 | GALNT11 | MGSVT others(603): Show |
chr7 | 152020674 | 152127340 |
| a0002 | 0/0 | 608 | 8 | 6 | 2 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | MGSVT others(603): Show |
chr7 | 152020674 | 152127340 |
| a0003 | 0/0 | 608 | 8 | 0 | 0 | 8 | 0 | 0 | 8 | GALNT11_chr7_152020674_152127340 | GALNT11 | MGSVT others(603): Show |
chr7 | 152020674 | 152127340 |
| a0004 | 0/0 | 608 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | MGSVT others(603): Show |
chr7 | 152020674 | 152127340 |
| a0005 | 0/0 | 608 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | MGSVT others(603): Show |
chr7 | 152020674 | 152127340 |
| a0006 | 0/0 | 608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | MGSVT others(603): Show |
chr7 | 152020674 | 152127340 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1824 | 260 | 76 | 49 | 101 | 8 | 24 | GALNT11_chr7_152020674_152127340 | GALNT11 | ATGGG others(1819): Show |
chr7 | 152020674 | 152127340 | ||
| a0001c0004 | 0/0 | 1824 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | ATGGG others(1819): Show |
chr7 | 152020674 | 152127340 | ||
| a0001c0007 | 0/0 | 1824 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | ATGGG others(1819): Show |
chr7 | 152020674 | 152127340 | ||
| a0001c0008 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | ATGGG others(1819): Show |
chr7 | 152020674 | 152127340 | ||
| a0002c0003 | 0/0 | 1824 | 8 | 6 | 2 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | ATGGG others(1819): Show |
chr7 | 152020674 | 152127340 | ||
| a0003c0002 | 0/0 | 1824 | 8 | 0 | 0 | 8 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | ATGGG others(1819): Show |
chr7 | 152020674 | 152127340 | ||
| a0004c0005 | 0/0 | 1824 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | ATGGG others(1819): Show |
chr7 | 152020674 | 152127340 | ||
| a0005c0009 | 0/0 | 1824 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | ATGGG others(1819): Show |
chr7 | 152020674 | 152127340 | ||
| a0006c0006 | 0/0 | 1824 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | ATGGG others(1819): Show |
chr7 | 152020674 | 152127340 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 2739 | 160 | 33 | 38 | 60 | 8 | 20 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0002 | 0/0 | 2740 | 46 | 7 | 6 | 29 | 0 | 4 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2735): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0003 | 0/0 | 2739 | 27 | 26 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0004 | 0/0 | 2738 | 7 | 7 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2733): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0005 | 0/0 | 2739 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0006 | 0/0 | 2740 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2735): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0007 | 0/0 | 2758 | 3 | 0 | 0 | 3 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2753): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0008 | 0/0 | 2739 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0009 | 0/0 | 2739 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0010 | 1/0 | 2739 | 2 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0011 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0012 | 0/0 | 2740 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2735): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0013 | 0/0 | 2738 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2733): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0014 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0015 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0001c0001t0016 | 0/0 | 2759 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2754): Show |
chr7 | 152020674 | 152127340 |
| a0001c0004t0002 | 0/0 | 2740 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2735): Show |
chr7 | 152020674 | 152127340 |
| a0001c0007t0001 | 0/0 | 2739 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0001c0008t0002 | 0/0 | 2740 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2735): Show |
chr7 | 152020674 | 152127340 |
| a0002c0003t0003 | 0/0 | 2739 | 8 | 6 | 2 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0003c0002t0001 | 0/0 | 2739 | 8 | 0 | 0 | 8 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0004c0005t0005 | 0/0 | 2739 | 2 | 2 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0005c0009t0001 | 0/0 | 2739 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| a0006c0006t0001 | 0/0 | 2739 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | GCGGA others(2734): Show |
chr7 | 152020674 | 152127340 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0238 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0001 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0004g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0004g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0004g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0004g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0004g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0004g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0005g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0005g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0006g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0006g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0007g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0007g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0007g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0008g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0008g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0009g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0010g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0010g0279 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0011g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0012g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0013g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0014g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0015g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0001t0016g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0004t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0004t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0007t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0001c0008t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0002c0003t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0002c0003t0003g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0002c0003t0003g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0002c0003t0003g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0002c0003t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0002c0003t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0002c0003t0003g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0002c0003t0003g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0003c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0003c0002t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0003c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0003c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0003c0002t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0003c0002t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0003c0002t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0003c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0004c0005t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0004c0005t0005g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0005c0009t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| a0006c0006t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0149 | EUR | GBR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0128 | EUR | GBR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0192 | EUR | GBR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0122 | EUR | GBR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0253 | EUR | FIN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0183 | EUR | FIN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00544 | hp1 | a0001 | c0001 | t0007 | g0125 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0247 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00639 | hp2 | a0002 | c0003 | t0003 | g0009 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0079 | EAS | CHS | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00735 | hp2 | a0002 | c0003 | t0003 | g0013 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01069 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01109 | hp1 | a0001 | c0001 | t0011 | g0162 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01169 | hp2 | a0001 | c0001 | t0013 | g0145 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01175 | hp2 | a0001 | c0007 | t0001 | g0148 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0218 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0001 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0278 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01256 | hp2 | a0001 | c0001 | t0010 | g0202 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0260 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0237 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01361 | hp2 | a0001 | c0001 | t0008 | g0029 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0069 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01884 | hp2 | a0002 | c0003 | t0003 | g0011 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01891 | hp1 | a0001 | c0001 | t0003 | g0022 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01891 | hp2 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0139 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0048 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02055 | hp1 | a0001 | c0001 | t0003 | g0040 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0277 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02071 | hp2 | a0001 | c0001 | t0016 | g0077 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02083 | hp1 | a0001 | c0001 | t0006 | g0091 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02135 | hp1 | a0001 | c0001 | t0006 | g0092 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0049 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | CDX | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02293 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | PEL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0043 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02451 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02572 | hp1 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02572 | hp2 | a0005 | c0009 | t0001 | g0178 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02615 | hp1 | a0001 | c0001 | t0004 | g0095 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02615 | hp2 | a0001 | c0001 | t0003 | g0019 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02622 | hp1 | a0001 | c0001 | t0004 | g0036 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0267 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02647 | hp1 | a0001 | c0008 | t0002 | g0094 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02647 | hp2 | a0001 | c0001 | t0004 | g0034 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0254 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02717 | hp2 | a0002 | c0003 | t0003 | g0006 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0031 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02818 | hp1 | a0001 | c0001 | t0003 | g0014 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02886 | hp2 | a0001 | c0001 | t0002 | g0082 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02895 | hp1 | a0004 | c0005 | t0005 | g0257 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02897 | hp2 | a0004 | c0005 | t0005 | g0256 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02922 | hp2 | a0001 | c0001 | t0005 | g0258 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02965 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02965 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0026 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03041 | hp1 | a0002 | c0003 | t0003 | g0010 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03098 | hp2 | a0001 | c0001 | t0004 | g0096 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03139 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03209 | hp1 | a0001 | c0001 | t0004 | g0035 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03209 | hp2 | a0001 | c0001 | t0003 | g0276 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0165 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03453 | hp1 | a0001 | c0001 | t0003 | g0275 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03453 | hp2 | a0001 | c0001 | t0003 | g0042 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03486 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03490 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03492 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03540 | hp1 | a0001 | c0001 | t0004 | g0032 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0021 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0262 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0268 | SAS | BEB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | BEB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | BEB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | STU | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG04199 | hp2 | a0001 | c0001 | t0002 | g0090 | SAS | STU | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | STU | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | STU | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18522 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | YRI | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18522 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | YRI | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18906 | hp1 | a0001 | c0001 | t0003 | g0041 | AFR | YRI | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | YRI | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18942 | hp1 | a0003 | c0002 | t0001 | g0164 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18947 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18951 | hp1 | a0003 | c0002 | t0001 | g0211 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18960 | hp2 | a0001 | c0001 | t0006 | g0093 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18962 | hp2 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18963 | hp1 | a0001 | c0001 | t0002 | g0066 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18963 | hp2 | a0001 | c0001 | t0009 | g0130 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18965 | hp2 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18968 | hp1 | a0001 | c0001 | t0009 | g0129 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18972 | hp2 | a0001 | c0001 | t0015 | g0144 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18981 | hp2 | a0001 | c0001 | t0002 | g0085 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0078 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18984 | hp1 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18984 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18985 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18987 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18989 | hp1 | a0001 | c0001 | t0007 | g0124 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18989 | hp2 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18990 | hp1 | a0003 | c0002 | t0001 | g0212 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18990 | hp2 | a0001 | c0001 | t0012 | g0062 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18994 | hp2 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA18999 | hp2 | a0003 | c0002 | t0001 | g0210 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19001 | hp1 | a0001 | c0001 | t0002 | g0088 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19004 | hp1 | a0003 | c0002 | t0001 | g0099 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19004 | hp2 | a0001 | c0004 | t0002 | g0071 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19007 | hp1 | a0003 | c0002 | t0001 | g0214 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19010 | hp1 | a0006 | c0006 | t0001 | g0227 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0076 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19030 | hp2 | a0001 | c0001 | t0005 | g0259 | AFR | LWK | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | LWK | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19043 | hp2 | a0002 | c0003 | t0003 | g0012 | AFR | LWK | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19058 | hp1 | a0003 | c0002 | t0001 | g0243 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19058 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19060 | hp2 | a0001 | c0001 | t0014 | g0272 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0084 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19066 | hp1 | a0001 | c0001 | t0007 | g0132 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19066 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19068 | hp1 | a0001 | c0004 | t0002 | g0073 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19072 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19087 | hp1 | a0003 | c0002 | t0001 | g0245 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0080 | EAS | JPT | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA19240 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | YRI | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0044 | AFR | ASW | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ASW | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0239 | EUR | TSI | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0097 | EUR | TSI | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | GIH | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | GIH | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02109 | hp1 | a0002 | c0003 | t0003 | g0007 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02109 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02486 | hp2 | a0001 | c0001 | t0004 | g0033 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG06807 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | USA | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| HG06807 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | USA | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | USA | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | USA | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA21309 | hp1 | a0002 | c0003 | t0003 | g0008 | AFR | LWK | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | LWK | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0238 | REF | REF | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0010 | g0279 | REF | REF | GALNT11_chr7_152020674_152127340 | GALNT11 | chr7 | 152020674 | 152127340 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:152094376 | C | T | 1 | a0005 | 1 | HG02572.hp2 | missense_variant | MODERATE | c.149C>T | p.Pro50Leu | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/12 | 398/2739 | 149/1827 | 50/608 | chr7 | 152094376 | |||
| chr7:152100816 | G | A | 1 | a0006 | 1 | NA19010.hp1 | missense_variant | MODERATE | c.314G>A | p.Arg105His | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/12 | 563/2739 | 314/1827 | 105/608 | chr7 | 152100816 | |||
| chr7:152103143 | C | T | 1 | a0002 | 8 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(5): Show |
missense_variant | MODERATE | c.451C>T | p.Pro151Ser | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/12 | 700/2739 | 451/1827 | 151/608 | chr7 | 152103143 | |||
| chr7:152105247 | G | T | 1 | a0003 | 8 | NA18942.hp1 NA18951.hp1 NA18990.hp1 others(5): Show |
missense_variant&splice_region_variant | MODERATE | c.589G>T | p.Asp197Tyr | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/12 | 838/2739 | 589/1827 | 197/608 | chr7 | 152105247 | |||
| chr7:152121639 | G | A | 1 | a0004 | 2 | HG02895.hp1 HG02897.hp2 |
missense_variant | MODERATE | c.1789G>A | p.Asp597Asn | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 2038/2739 | 1789/1827 | 597/608 | chr7 | 152121639 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:152094281 | G | A | 1 | a0001c0004 | 2 | NA19004.hp2 NA19068.hp1 |
synonymous_variant | LOW | c.54G>A | p.Ala18Ala | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/12 | 303/2739 | 54/1827 | 18/608 | chr7 | 152094281 | |||
| chr7:152108264 | G | A | 1 | a0001c0007 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.939G>A | p.Ala313Ala | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/12 | 1188/2739 | 939/1827 | 313/608 | chr7 | 152108264 | |||
| chr7:152120902 | C | A | 1 | a0001c0008 | 1 | HG02647.hp1 | synonymous_variant | LOW | c.1629C>A | p.Arg543Arg | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 11/12 | 1878/2739 | 1629/1827 | 543/608 | chr7 | 152120902 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:152025694 | A | ACTGGGCG others(12): Show |
2 | a0001c0001t0007 a0001c0001t0016 |
4 | HG00544.hp1 HG02071.hp2 NA18989.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-225_-207dupGGCGAG others(13): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/12 | 68511 | INFO_REALIGN_3_PRIME | chr7 | 152025694 | |||||
| chr7:152025748 | T | A | 1 | a0001c0001t0008 | 2 | HG01361.hp2 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-175T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/12 | 68480 | chr7 | 152025748 | ||||||
| chr7:152121692 | T | C | 23 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(20): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
3_prime_UTR_variant | MODIFIER | c.*15T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 15 | chr7 | 152121692 | ||||||
| chr7:152121698 | C | T | 1 | a0001c0001t0006 | 3 | HG02083.hp1 HG02135.hp1 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*21C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 21 | chr7 | 152121698 | ||||||
| chr7:152121796 | C | T | 1 | a0001c0001t0015 | 1 | NA18972.hp2 | 3_prime_UTR_variant | MODIFIER | c.*119C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 119 | chr7 | 152121796 | ||||||
| chr7:152121879 | A | G | 1 | a0001c0001t0014 | 1 | NA19060.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 202 | chr7 | 152121879 | ||||||
| chr7:152121937 | G | T | 11 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(8): Show |
101 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(98): Show |
3_prime_UTR_variant | MODIFIER | c.*260G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 260 | chr7 | 152121937 | ||||||
| chr7:152122022 | A | G | 2 | a0001c0001t0005 a0004c0005t0005 |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*345A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 345 | chr7 | 152122022 | ||||||
| chr7:152122062 | T | G | 1 | a0001c0001t0011 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*385T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 385 | chr7 | 152122062 | ||||||
| chr7:152122122 | A | G | 1 | a0001c0001t0009 | 2 | NA18963.hp2 NA18968.hp1 |
3_prime_UTR_variant | MODIFIER | c.*445A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 445 | chr7 | 152122122 | ||||||
| chr7:152122160 | T | TA | 6 | a0001c0001t0002 a0001c0001t0006 a0001c0001t0012 others(3): Show |
54 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*497dupA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 498 | INFO_REALIGN_3_PRIME | chr7 | 152122160 | |||||
| chr7:152122160 | TA | T | 2 | a0001c0001t0004 a0001c0001t0013 |
8 | HG01169.hp2 HG02486.hp2 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*497delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 12/12 | 497 | INFO_REALIGN_3_PRIME | chr7 | 152122160 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:152025912 | C | T | 1 | a0001c0001t0003g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-39+28C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152025912 | |||||||
| chr7:152025937 | TGCG | T | 276 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(273): Show |
279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-39+66_-39+68delGC others(1): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152025937 | ||||||
| chr7:152025946 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-39+62G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152025946 | |||||||
| chr7:152026658 | T | C | 11 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 others(8): Show |
11 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39+774T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152026658 | |||||||
| chr7:152026896 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-39+1012T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152026896 | |||||||
| chr7:152026907 | G | C | 1 | a0001c0001t0001g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-39+1023G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152026907 | |||||||
| chr7:152027065 | C | T | 2 | a0001c0001t0003g0014 a0001c0001t0003g0281 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-39+1181C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027065 | |||||||
| chr7:152027073 | T | C | 93 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(90): Show |
95 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(92): Show |
intron_variant | MODIFIER | c.-39+1189T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027073 | |||||||
| chr7:152027118 | A | G | 95 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(92): Show |
97 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.-39+1234A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027118 | |||||||
| chr7:152027122 | G | A | 1 | a0001c0001t0003g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-39+1238G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027122 | |||||||
| chr7:152027221 | C | G | 1 | a0001c0001t0001g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-39+1337C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027221 | |||||||
| chr7:152027236 | G | A | 13 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0014 others(10): Show |
14 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39+1352G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027236 | |||||||
| chr7:152027299 | A | G | 2 | a0001c0001t0004g0095 a0001c0001t0004g0096 |
2 | HG02615.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.-39+1415A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027299 | |||||||
| chr7:152027306 | C | T | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-39+1422C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027306 | |||||||
| chr7:152027307 | A | G | 51 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(48): Show |
52 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.-39+1423A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027307 | |||||||
| chr7:152027458 | G | A | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+1574G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027458 | |||||||
| chr7:152027470 | T | C | 2 | a0001c0001t0001g0097 a0001c0001t0001g0098 |
2 | HG02559.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.-39+1586T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027470 | |||||||
| chr7:152027639 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+1755C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027639 | |||||||
| chr7:152027651 | C | T | 5 | a0001c0001t0001g0269 a0001c0001t0001g0270 a0001c0001t0001g0271 others(2): Show |
5 | HG02040.hp1 HG02135.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+1767C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027651 | |||||||
| chr7:152027655 | A | C | 27 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(24): Show |
27 | HG00639.hp2 HG00735.hp2 HG01361.hp2 others(24): Show |
intron_variant | MODIFIER | c.-39+1771A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027655 | |||||||
| chr7:152027706 | A | G | 1 | a0001c0001t0001g0268 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-39+1822A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027706 | |||||||
| chr7:152027715 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-39+1831C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027715 | |||||||
| chr7:152027750 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-39+1866C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027750 | |||||||
| chr7:152027809 | C | T | 1 | a0001c0001t0001g0265 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-39+1925C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027809 | |||||||
| chr7:152027839 | G | A | 1 | a0003c0002t0001g0099 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-39+1955G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027839 | |||||||
| chr7:152027907 | GGGTTCAT others(16): Show |
G | 88 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(85): Show |
90 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-39+2026_-39+2048d others(25): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152027907 | ||||||
| chr7:152027986 | C | T | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+2102C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152027986 | |||||||
| chr7:152028080 | T | A | 1 | a0001c0001t0001g0100 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-39+2196T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028080 | |||||||
| chr7:152028110 | A | G | 40 | a0001c0001t0001g0037 a0001c0001t0003g0001 a0001c0001t0003g0005 others(37): Show |
41 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-39+2226A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028110 | |||||||
| chr7:152028160 | G | T | 1 | a0001c0001t0001g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-39+2276G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028160 | |||||||
| chr7:152028164 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+2280C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028164 | |||||||
| chr7:152028169 | A | G | 92 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(89): Show |
94 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-39+2285A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028169 | |||||||
| chr7:152028181 | C | A | 5 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(2): Show |
5 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+2297C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028181 | |||||||
| chr7:152028363 | G | A | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-39+2479G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028363 | |||||||
| chr7:152028534 | T | C | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-39+2650T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028534 | |||||||
| chr7:152028646 | G | A | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-39+2762G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028646 | |||||||
| chr7:152028753 | G | A | 13 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0014 others(10): Show |
14 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39+2869G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028753 | |||||||
| chr7:152028839 | A | G | 1 | a0001c0001t0001g0263 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-39+2955A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028839 | |||||||
| chr7:152028961 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-39+3077G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152028961 | |||||||
| chr7:152029104 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-39+3220C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152029104 | |||||||
| chr7:152029777 | C | T | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01261.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-39+3893C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152029777 | |||||||
| chr7:152029905 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-39+4021T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152029905 | |||||||
| chr7:152029908 | C | T | 41 | a0001c0001t0002g0002 a0001c0001t0002g0052 a0001c0001t0002g0053 others(38): Show |
42 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.-39+4024C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152029908 | |||||||
| chr7:152029929 | G | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+4045G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152029929 | |||||||
| chr7:152030092 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-39+4208C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152030092 | |||||||
| chr7:152030153 | A | G | 89 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0052 others(86): Show |
91 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.-39+4269A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152030153 | |||||||
| chr7:152030266 | G | A | 2 | a0001c0001t0003g0014 a0001c0001t0003g0281 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-39+4382G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152030266 | |||||||
| chr7:152030269 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-39+4385G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152030269 | |||||||
| chr7:152030278 | A | C | 1 | a0001c0001t0002g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-39+4394A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152030278 | |||||||
| chr7:152030700 | G | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+4816G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152030700 | |||||||
| chr7:152030968 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+5084C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152030968 | |||||||
| chr7:152031008 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-39+5124G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031008 | |||||||
| chr7:152031013 | A | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+5129A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031013 | |||||||
| chr7:152031241 | T | C | 1 | a0001c0001t0001g0104 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-39+5357T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031241 | |||||||
| chr7:152031397 | G | A | 1 | a0001c0001t0001g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-39+5513G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031397 | |||||||
| chr7:152031432 | G | A | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | NA18951.hp2 NA18987.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-39+5548G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031432 | |||||||
| chr7:152031573 | G | C | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-39+5689G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031573 | |||||||
| chr7:152031616 | T | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+5732T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031616 | |||||||
| chr7:152031642 | G | A | 274 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): Show |
intron_variant | MODIFIER | c.-39+5758G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031642 | |||||||
| chr7:152031677 | A | G | 67 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(64): Show |
68 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-39+5793A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031677 | |||||||
| chr7:152031885 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-39+6001G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031885 | |||||||
| chr7:152031991 | G | C | 1 | a0001c0001t0001g0111 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-39+6107G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152031991 | |||||||
| chr7:152032085 | C | G | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+6201C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032085 | |||||||
| chr7:152032097 | A | G | 2 | a0001c0001t0003g0027 a0001c0001t0003g0041 |
2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-39+6213A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032097 | |||||||
| chr7:152032239 | A | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+6355A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032239 | |||||||
| chr7:152032438 | A | G | 3 | a0001c0001t0003g0001 a0001c0001t0003g0025 a0001c0001t0003g0026 |
4 | HG01243.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+6554A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032438 | |||||||
| chr7:152032465 | C | T | 89 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0052 others(86): Show |
91 | HG00438.hp2 HG00621.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.-39+6581C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032465 | |||||||
| chr7:152032540 | G | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+6656G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032540 | |||||||
| chr7:152032574 | T | G | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+6690T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032574 | |||||||
| chr7:152032668 | G | C | 1 | a0001c0001t0002g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-39+6784G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032668 | |||||||
| chr7:152032788 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-39+6904G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032788 | |||||||
| chr7:152032851 | C | T | 1 | a0001c0001t0001g0251 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-39+6967C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032851 | |||||||
| chr7:152032943 | C | T | 75 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0102 others(72): Show |
76 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(73): Show |
intron_variant | MODIFIER | c.-39+7059C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032943 | |||||||
| chr7:152032976 | C | T | 2 | a0001c0001t0003g0014 a0001c0001t0003g0281 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-39+7092C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032976 | |||||||
| chr7:152032977 | G | A | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+7093G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152032977 | |||||||
| chr7:152033007 | G | A | 1 | a0001c0001t0001g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-39+7123G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033007 | |||||||
| chr7:152033043 | A | C | 10 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(7): Show |
10 | HG00140.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+7159A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033043 | |||||||
| chr7:152033059 | C | T | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+7175C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033059 | |||||||
| chr7:152033115 | C | G | 60 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0052 others(57): Show |
61 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.-39+7231C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033115 | |||||||
| chr7:152033160 | T | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+7276T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033160 | |||||||
| chr7:152033169 | C | T | 3 | a0001c0001t0001g0100 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG00280.hp2 HG01978.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.-39+7285C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033169 | |||||||
| chr7:152033218 | A | G | 1 | a0001c0001t0001g0250 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-39+7334A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033218 | |||||||
| chr7:152033236 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-39+7352C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033236 | |||||||
| chr7:152033293 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG02897.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-39+7409G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033293 | |||||||
| chr7:152033362 | C | G | 60 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0052 others(57): Show |
61 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(58): Show |
intron_variant | MODIFIER | c.-39+7478C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033362 | |||||||
| chr7:152033434 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+7550C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033434 | |||||||
| chr7:152033525 | G | T | 1 | a0001c0001t0001g0249 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.-39+7641G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033525 | |||||||
| chr7:152033894 | C | T | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-39+8010C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152033894 | |||||||
| chr7:152034017 | C | T | 10 | a0001c0001t0001g0112 a0001c0001t0001g0241 a0001c0001t0001g0242 others(7): Show |
10 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+8133C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034017 | |||||||
| chr7:152034020 | A | C | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-39+8136A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034020 | |||||||
| chr7:152034101 | A | G | 40 | a0001c0001t0001g0037 a0001c0001t0003g0001 a0001c0001t0003g0005 others(37): Show |
41 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.-39+8217A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034101 | |||||||
| chr7:152034246 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-39+8362G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034246 | |||||||
| chr7:152034266 | A | G | 1 | a0001c0001t0001g0179 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-39+8382A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034266 | |||||||
| chr7:152034309 | T | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+8425T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034309 | |||||||
| chr7:152034464 | C | T | 1 | a0001c0001t0001g0268 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-39+8580C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034464 | |||||||
| chr7:152034618 | G | C | 5 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(2): Show |
5 | HG02015.hp2 HG02071.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.-39+8734G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034618 | |||||||
| chr7:152034670 | C | A | 41 | a0001c0001t0002g0002 a0001c0001t0002g0052 a0001c0001t0002g0053 others(38): Show |
42 | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.-39+8786C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034670 | |||||||
| chr7:152034732 | T | C | 1 | a0001c0001t0001g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-39+8848T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034732 | |||||||
| chr7:152034739 | G | C | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-39+8855G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034739 | |||||||
| chr7:152034760 | C | T | 1 | a0001c0001t0003g0005 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-39+8876C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034760 | |||||||
| chr7:152034826 | G | A | 23 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0014 others(20): Show |
24 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.-39+8942G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034826 | |||||||
| chr7:152034940 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-39+9056G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034940 | |||||||
| chr7:152034972 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+9088G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034972 | |||||||
| chr7:152034990 | T | C | 4 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0023 others(1): Show |
4 | HG01891.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+9106T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152034990 | |||||||
| chr7:152035057 | T | A | 2 | a0004c0005t0005g0256 a0004c0005t0005g0257 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-39+9173T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035057 | |||||||
| chr7:152035082 | G | T | 92 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(89): Show |
94 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-39+9198G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035082 | |||||||
| chr7:152035235 | C | T | 21 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0014 others(18): Show |
22 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-39+9351C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035235 | |||||||
| chr7:152035253 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-39+9369C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035253 | |||||||
| chr7:152035292 | A | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+9408A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035292 | |||||||
| chr7:152035344 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-39+9460G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035344 | |||||||
| chr7:152035439 | G | T | 1 | a0005c0009t0001g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-39+9555G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035439 | |||||||
| chr7:152035510 | CTTG | C | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+9631_-39+9633d others(5): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152035510 | ||||||
| chr7:152035526 | C | T | 1 | a0001c0001t0001g0177 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-39+9642C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035526 | |||||||
| chr7:152035569 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-39+9685C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035569 | |||||||
| chr7:152035625 | G | C | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-39+9741G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035625 | |||||||
| chr7:152035657 | C | T | 7 | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(4): Show |
7 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39+9773C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035657 | |||||||
| chr7:152035834 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-39+9950G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035834 | |||||||
| chr7:152035875 | C | G | 1 | a0001c0001t0002g0089 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-39+9991C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035875 | |||||||
| chr7:152035949 | G | C | 4 | a0001c0001t0002g0052 a0001c0001t0002g0053 a0001c0001t0002g0054 others(1): Show |
4 | HG03098.hp1 NA18522.hp2 NA19240.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+10065G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035949 | |||||||
| chr7:152035950 | G | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+10066G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035950 | |||||||
| chr7:152035960 | C | G | 92 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(89): Show |
94 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-39+10076C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152035960 | |||||||
| chr7:152036255 | T | C | 67 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(64): Show |
68 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-39+10371T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152036255 | |||||||
| chr7:152036333 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-39+10449G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152036333 | |||||||
| chr7:152036350 | T | C | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+10466T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152036350 | |||||||
| chr7:152036459 | A | G | 1 | a0001c0001t0001g0280 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-39+10575A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152036459 | |||||||
| chr7:152036482 | C | T | 2 | a0001c0001t0003g0019 a0001c0001t0003g0020 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+10598C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152036482 | |||||||
| chr7:152036486 | C | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+10602C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152036486 | |||||||
| chr7:152036519 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-39+10635T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152036519 | |||||||
| chr7:152036656 | T | A | 67 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(64): Show |
68 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(65): Show |
intron_variant | MODIFIER | c.-39+10772T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152036656 | |||||||
| chr7:152036874 | T | C | 1 | a0002c0003t0003g0006 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-39+10990T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152036874 | |||||||
| chr7:152036903 | C | T | 1 | a0001c0001t0001g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-39+11019C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152036903 | |||||||
| chr7:152037093 | C | T | 2 | a0001c0001t0003g0019 a0001c0001t0003g0020 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+11209C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037093 | |||||||
| chr7:152037167 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+11283C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037167 | |||||||
| chr7:152037260 | A | C | 4 | a0001c0001t0001g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(1): Show |
4 | HG02055.hp1 HG02257.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+11376A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037260 | |||||||
| chr7:152037327 | C | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0169 a0001c0001t0001g0251 |
3 | HG02809.hp2 HG02970.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-39+11443C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037327 | |||||||
| chr7:152037350 | C | T | 7 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
7 | HG01433.hp2 HG02559.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39+11466C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037350 | |||||||
| chr7:152037496 | G | A | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-39+11612G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037496 | |||||||
| chr7:152037602 | A | AT | 6 | a0001c0001t0001g0037 a0001c0001t0001g0120 a0001c0001t0002g0088 others(3): Show |
6 | HG02055.hp1 HG02257.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39+11728dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152037602 | ||||||
| chr7:152037754 | C | T | 4 | a0001c0001t0001g0239 a0001c0001t0003g0018 a0001c0001t0003g0019 others(1): Show |
4 | HG02572.hp1 HG02615.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.-39+11870C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037754 | |||||||
| chr7:152037768 | A | AT | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+11894dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152037768 | ||||||
| chr7:152037790 | A | G | 1 | a0001c0001t0003g0005 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-39+11906A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037790 | |||||||
| chr7:152037931 | G | T | 1 | a0001c0001t0002g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-39+12047G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037931 | |||||||
| chr7:152037967 | T | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+12083T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037967 | |||||||
| chr7:152037967 | T | G | 90 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(87): Show |
92 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(89): Show |
intron_variant | MODIFIER | c.-39+12083T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152037967 | |||||||
| chr7:152038061 | T | C | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-39+12177T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038061 | |||||||
| chr7:152038165 | C | T | 1 | a0001c0001t0003g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-39+12281C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038165 | |||||||
| chr7:152038202 | T | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+12318T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038202 | |||||||
| chr7:152038228 | C | T | 88 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(85): Show |
90 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(87): Show |
intron_variant | MODIFIER | c.-39+12344C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038228 | |||||||
| chr7:152038453 | C | A | 1 | a0001c0001t0002g0052 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-39+12569C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038453 | |||||||
| chr7:152038490 | G | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+12606G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038490 | |||||||
| chr7:152038517 | G | A | 9 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(6): Show |
10 | HG00544.hp1 HG01243.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-39+12633G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038517 | |||||||
| chr7:152038566 | G | T | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-39+12682G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038566 | |||||||
| chr7:152038640 | A | C | 5 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(2): Show |
5 | HG00639.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+12756A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038640 | |||||||
| chr7:152038849 | A | G | 7 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(4): Show |
7 | HG00558.hp2 HG01069.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39+12965A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038849 | |||||||
| chr7:152038856 | G | C | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-39+12972G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038856 | |||||||
| chr7:152038888 | T | A | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-39+13004T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152038888 | |||||||
| chr7:152039165 | C | T | 1 | a0003c0002t0001g0164 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-39+13281C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152039165 | |||||||
| chr7:152039377 | C | G | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+13493C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152039377 | |||||||
| chr7:152039516 | C | T | 6 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0190 others(3): Show |
6 | HG00140.hp1 HG01106.hp2 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.-39+13632C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152039516 | |||||||
| chr7:152039597 | G | A | 21 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0014 others(18): Show |
22 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-39+13713G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152039597 | |||||||
| chr7:152039614 | ACAGTTGG | A | 21 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0014 others(18): Show |
22 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-39+13733_-39+1373 others(11): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152039614 | ||||||
| chr7:152039751 | A | G | 1 | a0001c0001t0001g0103 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-39+13867A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152039751 | |||||||
| chr7:152039966 | G | A | 1 | a0001c0001t0001g0101 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-39+14082G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152039966 | |||||||
| chr7:152040011 | C | T | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-39+14127C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152040011 | |||||||
| chr7:152040120 | G | A | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.-39+14236G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152040120 | |||||||
| chr7:152040130 | G | T | 21 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0014 others(18): Show |
22 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-39+14246G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152040130 | |||||||
| chr7:152040278 | T | G | 1 | a0001c0001t0003g0005 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-39+14394T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152040278 | |||||||
| chr7:152040520 | A | G | 1 | a0001c0001t0001g0237 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-39+14636A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152040520 | |||||||
| chr7:152040640 | TA | T | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-39+14759delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152040640 | ||||||
| chr7:152040726 | A | G | 1 | a0001c0001t0001g0119 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-39+14842A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152040726 | |||||||
| chr7:152041103 | C | T | 3 | a0001c0001t0006g0091 a0001c0001t0006g0092 a0001c0001t0006g0093 |
3 | HG02083.hp1 HG02135.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.-39+15219C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152041103 | |||||||
| chr7:152041104 | G | A | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+15220G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152041104 | |||||||
| chr7:152041385 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.-39+15501T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152041385 | |||||||
| chr7:152041417 | T | G | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00140.hp1 HG00738.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39+15533T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152041417 | |||||||
| chr7:152041834 | G | T | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-39+15950G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152041834 | |||||||
| chr7:152042043 | A | C | 1 | a0001c0001t0001g0192 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-39+16159A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042043 | |||||||
| chr7:152042155 | A | G | 92 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(89): Show |
94 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-39+16271A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042155 | |||||||
| chr7:152042180 | A | G | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-39+16296A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042180 | |||||||
| chr7:152042212 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-39+16328G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042212 | |||||||
| chr7:152042257 | A | G | 1 | a0001c0001t0001g0261 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-39+16373A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042257 | |||||||
| chr7:152042298 | A | ATGTCCCC others(6): Show |
11 | a0001c0001t0001g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(8): Show |
11 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39+16418_-39+1643 others(17): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152042298 | ||||||
| chr7:152042319 | C | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+16435C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042319 | |||||||
| chr7:152042515 | TA | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+16633delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152042515 | ||||||
| chr7:152042535 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+16651G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042535 | |||||||
| chr7:152042628 | T | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+16744T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042628 | |||||||
| chr7:152042860 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-39+16976G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042860 | |||||||
| chr7:152042868 | A | G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+16984A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042868 | |||||||
| chr7:152042889 | G | A | 1 | a0001c0001t0001g0128 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-39+17005G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042889 | |||||||
| chr7:152042960 | C | A | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+17076C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152042960 | |||||||
| chr7:152043122 | G | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+17238G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152043122 | |||||||
| chr7:152043298 | C | T | 1 | a0001c0001t0001g0277 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-39+17414C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152043298 | |||||||
| chr7:152043332 | A | C | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-39+17448A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152043332 | |||||||
| chr7:152043382 | C | T | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+17498C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152043382 | |||||||
| chr7:152043460 | C | T | 13 | a0001c0001t0001g0097 a0001c0001t0001g0098 a0001c0001t0003g0005 others(10): Show |
13 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.-39+17576C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152043460 | |||||||
| chr7:152043705 | G | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+17821G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152043705 | |||||||
| chr7:152043772 | C | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | NA18962.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-39+17888C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152043772 | |||||||
| chr7:152043792 | T | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+17908T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152043792 | |||||||
| chr7:152043941 | C | G | 14 | a0001c0001t0001g0112 a0001c0001t0001g0163 a0001c0001t0001g0241 others(11): Show |
14 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39+18057C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152043941 | |||||||
| chr7:152043954 | C | T | 1 | a0001c0001t0001g0254 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-39+18070C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152043954 | |||||||
| chr7:152044031 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-39+18147G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152044031 | |||||||
| chr7:152044123 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+18239G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152044123 | |||||||
| chr7:152044302 | G | A | 1 | a0001c0001t0002g0090 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-39+18418G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152044302 | |||||||
| chr7:152044416 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-39+18532G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152044416 | |||||||
| chr7:152044465 | T | C | 7 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(4): Show |
7 | HG00140.hp1 HG00738.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39+18581T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152044465 | |||||||
| chr7:152044669 | A | C | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+18785A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152044669 | |||||||
| chr7:152045115 | T | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+19231T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152045115 | |||||||
| chr7:152045212 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-39+19328A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152045212 | |||||||
| chr7:152045260 | G | A | 1 | a0001c0001t0002g0180 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-39+19376G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152045260 | |||||||
| chr7:152045294 | G | A | 1 | a0001c0001t0001g0100 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-39+19410G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152045294 | |||||||
| chr7:152045325 | C | T | 1 | a0001c0001t0001g0273 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-39+19441C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152045325 | |||||||
| chr7:152045811 | T | C | 1 | a0001c0001t0001g0185 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-39+19927T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152045811 | |||||||
| chr7:152045835 | TCTTG | T | 14 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0018 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39+19955_-39+1995 others(8): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152045835 | ||||||
| chr7:152045876 | T | C | 2 | a0001c0001t0003g0019 a0001c0001t0003g0020 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+19992T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152045876 | |||||||
| chr7:152046046 | C | T | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-39+20162C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152046046 | |||||||
| chr7:152046432 | A | C | 1 | a0001c0001t0001g0191 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-39+20548A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152046432 | |||||||
| chr7:152046600 | T | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+20716T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152046600 | |||||||
| chr7:152046936 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-39+21052G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152046936 | |||||||
| chr7:152047199 | G | C | 14 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0018 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39+21315G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152047199 | |||||||
| chr7:152047236 | C | T | 3 | a0001c0001t0002g0083 a0001c0001t0002g0084 a0001c0001t0002g0085 |
3 | NA18964.hp1 NA18981.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-39+21352C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152047236 | |||||||
| chr7:152047237 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-39+21353G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152047237 | |||||||
| chr7:152047465 | AAAAC | A | 3 | a0001c0001t0003g0275 a0001c0001t0003g0276 a0001c0008t0002g0094 |
3 | HG02647.hp1 HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+21601_-39+2160 others(8): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152047465 | ||||||
| chr7:152047509 | A | T | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-39+21625A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152047509 | |||||||
| chr7:152047687 | C | CGT | 4 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0002c0003t0003g0012 others(1): Show |
4 | HG00735.hp2 NA18972.hp1 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+21825_-39+2182 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152047687 | ||||||
| chr7:152047687 | C | CGTGT | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+21823_-39+2182 others(8): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152047687 | ||||||
| chr7:152047687 | C | CGTGTGT | 3 | a0001c0001t0005g0258 a0004c0005t0005g0256 a0004c0005t0005g0257 |
3 | HG02895.hp1 HG02897.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-39+21821_-39+2182 others(10): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152047687 | ||||||
| chr7:152047687 | C | CGTGTGTG others(1): Show |
3 | a0001c0001t0003g0275 a0001c0001t0003g0276 a0001c0001t0005g0259 |
3 | HG03209.hp2 HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-39+21819_-39+2182 others(12): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152047687 | ||||||
| chr7:152047687 | C | CGTGTGTG others(15): Show |
1 | a0001c0001t0003g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-39+21805_-39+2182 others(26): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152047687 | ||||||
| chr7:152047687 | CGT | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+21825_-39+2182 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152047687 | ||||||
| chr7:152047688 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-39+21804G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152047688 | |||||||
| chr7:152047689 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-39+21805T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152047689 | |||||||
| chr7:152047709 | T | C | 6 | a0001c0001t0001g0015 a0001c0001t0001g0170 a0001c0001t0001g0171 others(3): Show |
6 | HG01167.hp1 HG01169.hp1 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.-39+21825T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152047709 | |||||||
| chr7:152047709 | T | TGTGTGTG others(5): Show |
2 | a0001c0001t0003g0019 a0001c0001t0003g0020 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+21826_-39+2182 others(16): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152047709 | ||||||
| chr7:152047764 | T | C | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-39+21880T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152047764 | |||||||
| chr7:152047845 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-39+21961T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152047845 | |||||||
| chr7:152047920 | C | G | 8 | a0001c0001t0001g0102 a0001c0001t0001g0228 a0001c0001t0001g0229 others(5): Show |
8 | HG00408.hp2 HG00639.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-39+22036C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152047920 | |||||||
| chr7:152048226 | C | G | 4 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0023 others(1): Show |
4 | HG01891.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+22342C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152048226 | |||||||
| chr7:152048592 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-39+22708C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152048592 | |||||||
| chr7:152048703 | T | C | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-39+22819T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152048703 | |||||||
| chr7:152048866 | A | G | 1 | a0002c0003t0003g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-39+22982A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152048866 | |||||||
| chr7:152048953 | C | T | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-39+23069C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152048953 | |||||||
| chr7:152049161 | G | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+23277G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049161 | |||||||
| chr7:152049169 | C | G | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-39+23285C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049169 | |||||||
| chr7:152049387 | T | C | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-39+23503T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049387 | |||||||
| chr7:152049477 | C | G | 1 | a0001c0001t0002g0082 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-39+23593C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049477 | |||||||
| chr7:152049571 | C | T | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-39+23687C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049571 | |||||||
| chr7:152049597 | G | T | 1 | a0001c0001t0001g0108 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-39+23713G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049597 | |||||||
| chr7:152049603 | A | G | 11 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 others(8): Show |
11 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39+23719A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049603 | |||||||
| chr7:152049811 | G | A | 1 | a0001c0001t0001g0191 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-39+23927G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049811 | |||||||
| chr7:152049813 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-39+23929G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049813 | |||||||
| chr7:152049914 | G | C | 2 | a0001c0001t0003g0019 a0001c0001t0003g0020 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+24030G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049914 | |||||||
| chr7:152049936 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-39+24052T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152049936 | |||||||
| chr7:152050140 | G | A | 47 | a0001c0001t0001g0003 a0001c0001t0001g0102 a0001c0001t0001g0103 others(44): Show |
48 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.-39+24256G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152050140 | |||||||
| chr7:152050342 | T | A | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-39+24458T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152050342 | |||||||
| chr7:152051011 | C | A | 1 | a0001c0001t0001g0105 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-39+25127C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051011 | |||||||
| chr7:152051199 | G | GT | 27 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0101 others(24): Show |
27 | HG00544.hp2 HG00673.hp1 HG00735.hp1 others(24): Show |
intron_variant | MODIFIER | c.-39+25342dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152051199 | ||||||
| chr7:152051199 | GT | G | 10 | a0001c0001t0001g0037 a0001c0001t0001g0133 a0001c0001t0001g0143 others(7): Show |
10 | HG01978.hp1 HG02155.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+25342delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152051199 | ||||||
| chr7:152051199 | GTTT | G | 50 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(47): Show |
52 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.-39+25340_-39+2534 others(7): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152051199 | ||||||
| chr7:152051199 | GTTTT | G | 32 | a0001c0001t0001g0108 a0001c0001t0002g0056 a0001c0001t0002g0063 others(29): Show |
32 | HG00639.hp2 HG00735.hp2 HG01361.hp2 others(29): Show |
intron_variant | MODIFIER | c.-39+25339_-39+2534 others(8): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152051199 | ||||||
| chr7:152051204 | T | G | 1 | a0001c0001t0003g0275 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-39+25320T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051204 | |||||||
| chr7:152051206 | T | G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+25322T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051206 | |||||||
| chr7:152051210 | T | G | 18 | a0001c0001t0001g0193 a0001c0001t0001g0194 a0001c0001t0001g0195 others(15): Show |
18 | HG00597.hp1 HG01069.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.-39+25326T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051210 | |||||||
| chr7:152051353 | T | G | 1 | a0001c0001t0001g0108 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-39+25469T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051353 | |||||||
| chr7:152051652 | G | T | 33 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.-39+25768G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051652 | |||||||
| chr7:152051665 | T | C | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-39+25781T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051665 | |||||||
| chr7:152051746 | A | G | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+25862A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051746 | |||||||
| chr7:152051751 | GA | G | 14 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0018 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39+25872delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152051751 | ||||||
| chr7:152051768 | G | C | 33 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.-39+25884G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051768 | |||||||
| chr7:152051784 | T | C | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-39+25900T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051784 | |||||||
| chr7:152051815 | G | C | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+25931G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152051815 | |||||||
| chr7:152052005 | A | C | 1 | a0001c0001t0001g0108 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-39+26121A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152052005 | |||||||
| chr7:152052056 | T | G | 1 | a0001c0001t0001g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-39+26172T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152052056 | |||||||
| chr7:152052534 | C | T | 14 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0018 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39+26650C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152052534 | |||||||
| chr7:152052613 | C | T | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-39+26729C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152052613 | |||||||
| chr7:152052637 | T | C | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+26753T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152052637 | |||||||
| chr7:152052656 | A | G | 33 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.-39+26772A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152052656 | |||||||
| chr7:152052863 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01433.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-39+26979A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152052863 | |||||||
| chr7:152052984 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-39+27100T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152052984 | |||||||
| chr7:152053060 | T | C | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-39+27176T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152053060 | |||||||
| chr7:152053120 | T | C | 1 | a0001c0001t0001g0228 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.-39+27236T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152053120 | |||||||
| chr7:152053335 | A | C | 1 | a0001c0001t0003g0005 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-39+27451A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152053335 | |||||||
| chr7:152053614 | C | T | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-39+27730C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152053614 | |||||||
| chr7:152053655 | G | C | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+27771G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152053655 | |||||||
| chr7:152053785 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-39+27901G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152053785 | |||||||
| chr7:152053824 | C | A | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-39+27940C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152053824 | |||||||
| chr7:152053872 | A | G | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG02897.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-39+27988A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152053872 | |||||||
| chr7:152053983 | TTA | T | 91 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(88): Show |
93 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(90): Show |
intron_variant | MODIFIER | c.-39+28103_-39+2810 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152053983 | ||||||
| chr7:152054049 | A | T | 95 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(92): Show |
97 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(94): Show |
intron_variant | MODIFIER | c.-39+28165A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152054049 | |||||||
| chr7:152054111 | A | G | 4 | a0001c0001t0001g0224 a0001c0001t0006g0091 a0001c0001t0006g0092 others(1): Show |
4 | HG02083.hp1 HG02135.hp1 NA18960.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+28227A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152054111 | |||||||
| chr7:152054154 | C | G | 14 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0018 others(11): Show |
14 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.-39+28270C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152054154 | |||||||
| chr7:152054503 | C | CT | 7 | a0001c0001t0001g0186 a0001c0001t0001g0223 a0001c0001t0002g0049 others(4): Show |
7 | HG00738.hp1 HG01069.hp1 HG01928.hp2 others(4): Show |
intron_variant | MODIFIER | c.-39+28641dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152054503 | ||||||
| chr7:152054503 | CT | C | 22 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(19): Show |
23 | HG01069.hp2 HG01074.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.-39+28641delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152054503 | ||||||
| chr7:152054503 | CTT | C | 7 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0034 others(4): Show |
7 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39+28640_-39+2864 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152054503 | ||||||
| chr7:152054633 | C | T | 11 | a0001c0001t0001g0116 a0001c0001t0001g0117 a0001c0001t0001g0118 others(8): Show |
11 | HG00597.hp2 HG02015.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.-39+28749C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152054633 | |||||||
| chr7:152054678 | AT | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+28807delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152054678 | ||||||
| chr7:152054728 | A | T | 1 | a0001c0001t0001g0115 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-39+28844A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152054728 | |||||||
| chr7:152054774 | C | T | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+28890C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152054774 | |||||||
| chr7:152054804 | C | T | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-39+28920C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152054804 | |||||||
| chr7:152055387 | C | T | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-39+29503C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152055387 | |||||||
| chr7:152055520 | C | CGT | 3 | a0001c0001t0001g0158 a0001c0001t0001g0246 a0003c0002t0001g0245 |
3 | HG00408.hp1 HG00621.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.-39+29683_-39+2968 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055520 | ||||||
| chr7:152055520 | C | CGTGT | 3 | a0001c0001t0001g0122 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG00140.hp2 HG00544.hp2 HG02074.hp2 |
intron_variant | MODIFIER | c.-39+29681_-39+2968 others(8): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055520 | ||||||
| chr7:152055520 | CGT | C | 41 | a0001c0001t0001g0003 a0001c0001t0001g0098 a0001c0001t0001g0100 others(38): Show |
42 | HG00280.hp1 HG00280.hp2 HG00639.hp1 others(39): Show |
intron_variant | MODIFIER | c.-39+29683_-39+2968 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055520 | ||||||
| chr7:152055520 | CGTGT | C | 42 | a0001c0001t0001g0097 a0001c0001t0001g0105 a0001c0001t0001g0109 others(39): Show |
43 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.-39+29681_-39+2968 others(8): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055520 | ||||||
| chr7:152055520 | CGTGTGT | C | 63 | a0001c0001t0001g0004 a0001c0001t0001g0119 a0001c0001t0001g0123 others(60): Show |
63 | HG00099.hp2 HG00438.hp2 HG00558.hp2 others(60): Show |
intron_variant | MODIFIER | c.-39+29679_-39+2968 others(10): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055520 | ||||||
| chr7:152055520 | CGTGTGTG others(1): Show |
C | 45 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0101 others(42): Show |
45 | HG00544.hp1 HG00558.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.-39+29677_-39+2968 others(12): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055520 | ||||||
| chr7:152055520 | CGTGTGTG others(3): Show |
C | 23 | a0001c0001t0001g0113 a0001c0001t0001g0120 a0001c0001t0001g0133 others(20): Show |
24 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.-39+29675_-39+2968 others(14): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055520 | ||||||
| chr7:152055520 | CGTGTGTG others(5): Show |
C | 9 | a0001c0001t0001g0037 a0001c0001t0001g0115 a0002c0003t0003g0006 others(6): Show |
9 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.-39+29673_-39+2968 others(16): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055520 | ||||||
| chr7:152055520 | CGTGTGTG others(7): Show |
C | 12 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(9): Show |
12 | HG02486.hp2 HG02572.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.-39+29671_-39+2968 others(18): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055520 | ||||||
| chr7:152055520 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-39+29667_-39+2968 others(22): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055520 | ||||||
| chr7:152055563 | G | A | 1 | a0001c0001t0002g0089 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-39+29679G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152055563 | |||||||
| chr7:152055565 | G | A | 56 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0184 others(53): Show |
57 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-39+29681G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152055565 | |||||||
| chr7:152055565 | GTGTA | G | 10 | a0001c0001t0001g0155 a0001c0001t0001g0208 a0001c0001t0001g0209 others(7): Show |
10 | HG00597.hp1 HG02818.hp2 NA18942.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+29683_-39+2968 others(8): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055565 | ||||||
| chr7:152055567 | G | A | 104 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0101 others(101): Show |
105 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.-39+29683G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152055567 | |||||||
| chr7:152055574 | T | C | 5 | a0001c0001t0002g0089 a0001c0001t0005g0258 a0001c0001t0005g0259 others(2): Show |
5 | HG02040.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+29690T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152055574 | |||||||
| chr7:152055576 | C | T | 5 | a0001c0001t0002g0089 a0001c0001t0005g0258 a0001c0001t0005g0259 others(2): Show |
5 | HG02040.hp2 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-39+29692C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152055576 | |||||||
| chr7:152055624 | A | G | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+29740A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152055624 | |||||||
| chr7:152055661 | T | G | 33 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(30): Show |
33 | HG00639.hp2 HG00735.hp2 HG01361.hp2 others(30): Show |
intron_variant | MODIFIER | c.-39+29777T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152055661 | |||||||
| chr7:152055798 | ATTC | A | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-39+29920_-39+2992 others(7): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152055798 | ||||||
| chr7:152055845 | T | C | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-39+29961T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152055845 | |||||||
| chr7:152056165 | G | A | 1 | a0001c0001t0001g0269 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-39+30281G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152056165 | |||||||
| chr7:152056521 | C | G | 1 | a0001c0001t0015g0144 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-39+30637C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152056521 | |||||||
| chr7:152057004 | AT | A | 184 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(181): Show |
186 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(183): Show |
intron_variant | MODIFIER | c.-39+31143delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152057004 | ||||||
| chr7:152057004 | ATT | A | 27 | a0001c0001t0001g0105 a0001c0001t0001g0170 a0001c0001t0001g0182 others(24): Show |
27 | HG00558.hp2 HG00673.hp2 HG01069.hp1 others(24): Show |
intron_variant | MODIFIER | c.-39+31142_-39+3114 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152057004 | ||||||
| chr7:152057210 | G | T | 1 | a0001c0001t0002g0082 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-39+31326G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152057210 | |||||||
| chr7:152057238 | AT | A | 36 | a0001c0001t0001g0037 a0001c0001t0001g0159 a0001c0001t0002g0053 others(33): Show |
36 | HG00639.hp2 HG00735.hp2 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.-39+31364delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152057238 | ||||||
| chr7:152057310 | CT | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+31440delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152057310 | ||||||
| chr7:152057639 | C | CG | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+31755_-39+3175 others(5): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152057639 | |||||||
| chr7:152057754 | CCT | C | 55 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(52): Show |
57 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-39+31871_-39+3187 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152057754 | |||||||
| chr7:152057922 | G | A | 89 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(86): Show |
91 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(88): Show |
intron_variant | MODIFIER | c.-39+32038G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152057922 | |||||||
| chr7:152057924 | G | A | 1 | a0001c0001t0004g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-39+32040G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152057924 | |||||||
| chr7:152057958 | T | C | 1 | a0001c0001t0001g0260 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-39+32074T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152057958 | |||||||
| chr7:152058011 | T | C | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+32127T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058011 | |||||||
| chr7:152058032 | G | A | 2 | a0001c0001t0003g0019 a0001c0001t0003g0020 |
2 | HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-39+32148G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058032 | |||||||
| chr7:152058095 | T | A | 2 | a0001c0001t0002g0061 a0001c0001t0002g0080 |
2 | NA18950.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.-39+32211T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058095 | |||||||
| chr7:152058098 | A | G | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+32214A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058098 | |||||||
| chr7:152058162 | A | G | 1 | a0001c0001t0001g0101 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-39+32278A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058162 | |||||||
| chr7:152058175 | G | A | 13 | a0001c0001t0001g0147 a0001c0001t0001g0262 a0001c0001t0003g0043 others(10): Show |
13 | HG00639.hp2 HG00735.hp2 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.-39+32291G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058175 | |||||||
| chr7:152058330 | TTTTTG | T | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-39+32471_-39+3247 others(9): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152058330 | ||||||
| chr7:152058353 | T | G | 1 | a0001c0001t0007g0132 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-39+32469T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058353 | |||||||
| chr7:152058375 | T | C | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-39+32491T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058375 | |||||||
| chr7:152058437 | G | A | 1 | a0002c0003t0003g0013 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-39+32553G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058437 | |||||||
| chr7:152058459 | G | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+32575G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058459 | |||||||
| chr7:152058616 | G | A | 1 | a0001c0001t0001g0219 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-39+32732G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058616 | |||||||
| chr7:152058655 | G | T | 7 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0034 others(4): Show |
7 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-39+32771G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058655 | |||||||
| chr7:152058675 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-39+32791G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058675 | |||||||
| chr7:152058693 | G | C | 55 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(52): Show |
57 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.-39+32809G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058693 | |||||||
| chr7:152058701 | T | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-39+32817T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058701 | |||||||
| chr7:152058758 | T | A | 25 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(22): Show |
25 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-39+32874T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058758 | |||||||
| chr7:152058953 | G | T | 186 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0037 others(183): Show |
188 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(185): Show |
intron_variant | MODIFIER | c.-39+33069G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152058953 | |||||||
| chr7:152058983 | C | CATCTGTG | 25 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(22): Show |
25 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-39+33100_-39+3310 others(11): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152058983 | ||||||
| chr7:152059013 | C | T | 1 | a0001c0001t0002g0078 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-39+33129C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059013 | |||||||
| chr7:152059287 | C | T | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.-39+33403C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059287 | |||||||
| chr7:152059300 | C | T | 25 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(22): Show |
25 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-39+33416C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059300 | |||||||
| chr7:152059336 | A | C | 2 | a0001c0001t0001g0100 a0001c0001t0001g0183 |
2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-39+33452A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059336 | |||||||
| chr7:152059466 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-39+33582A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059466 | |||||||
| chr7:152059511 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.-39+33627C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059511 | |||||||
| chr7:152059588 | G | C | 2 | a0001c0001t0009g0129 a0001c0001t0009g0130 |
2 | NA18963.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.-39+33704G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059588 | |||||||
| chr7:152059610 | T | G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-39+33726T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059610 | |||||||
| chr7:152059690 | C | A | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | NA18981.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.-39+33806C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059690 | |||||||
| chr7:152059857 | T | C | 1 | a0001c0001t0001g0165 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-39+33973T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059857 | |||||||
| chr7:152059943 | A | G | 4 | a0001c0001t0001g0197 a0001c0001t0001g0216 a0001c0001t0001g0218 others(1): Show |
4 | HG01192.hp2 HG01346.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-39+34059A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152059943 | |||||||
| chr7:152060250 | A | G | 92 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(89): Show |
94 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-38-33940A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060250 | |||||||
| chr7:152060272 | A | G | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-33918A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060272 | |||||||
| chr7:152060343 | C | T | 1 | a0001c0001t0002g0079 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-38-33847C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060343 | |||||||
| chr7:152060400 | G | C | 8 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-33790G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060400 | |||||||
| chr7:152060464 | T | C | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-33726T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060464 | |||||||
| chr7:152060482 | T | A | 1 | a0001c0001t0001g0203 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-38-33708T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060482 | |||||||
| chr7:152060558 | G | A | 1 | a0001c0001t0001g0165 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-38-33632G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060558 | |||||||
| chr7:152060564 | G | A | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG00280.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.-38-33626G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060564 | |||||||
| chr7:152060573 | T | C | 1 | a0001c0001t0002g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-38-33617T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060573 | |||||||
| chr7:152060611 | G | T | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38-33579G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060611 | |||||||
| chr7:152060625 | C | A | 25 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(22): Show |
25 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38-33565C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060625 | |||||||
| chr7:152060626 | C | G | 1 | a0001c0001t0002g0074 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-38-33564C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060626 | |||||||
| chr7:152060798 | T | G | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-38-33392T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060798 | |||||||
| chr7:152060892 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-38-33298G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060892 | |||||||
| chr7:152060897 | A | C | 25 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(22): Show |
25 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38-33293A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060897 | |||||||
| chr7:152060926 | A | G | 7 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0018 others(4): Show |
7 | HG02071.hp2 HG02572.hp1 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38-33264A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152060926 | |||||||
| chr7:152061044 | A | G | 1 | a0003c0002t0001g0099 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-38-33146A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061044 | |||||||
| chr7:152061156 | G | A | 3 | a0001c0001t0001g0135 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG00099.hp1 HG00738.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.-38-33034G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061156 | |||||||
| chr7:152061310 | T | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-32880T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061310 | |||||||
| chr7:152061571 | T | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0023 others(1): Show |
4 | HG01891.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-32619T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061571 | |||||||
| chr7:152061572 | T | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0023 others(1): Show |
4 | HG01891.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-32618T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061572 | |||||||
| chr7:152061598 | A | G | 1 | a0001c0001t0001g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-38-32592A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061598 | |||||||
| chr7:152061694 | GC | G | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-38-32495delC | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061694 | |||||||
| chr7:152061708 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-38-32482C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061708 | |||||||
| chr7:152061775 | A | G | 1 | a0001c0001t0003g0020 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-38-32415A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061775 | |||||||
| chr7:152061812 | T | C | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-32378T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061812 | |||||||
| chr7:152061824 | A | C | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-32366A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061824 | |||||||
| chr7:152061845 | G | T | 1 | a0001c0001t0001g0265 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-38-32345G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061845 | |||||||
| chr7:152061938 | G | A | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-32252G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152061938 | |||||||
| chr7:152062270 | T | C | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-31920T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152062270 | |||||||
| chr7:152062477 | C | T | 2 | a0001c0001t0001g0169 a0001c0001t0001g0251 |
2 | HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-38-31713C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152062477 | |||||||
| chr7:152062483 | C | T | 1 | a0001c0001t0004g0096 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-38-31707C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152062483 | |||||||
| chr7:152062754 | T | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-31436T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152062754 | |||||||
| chr7:152062793 | C | G | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-31397C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152062793 | |||||||
| chr7:152062804 | A | G | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-38-31386A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152062804 | |||||||
| chr7:152063024 | A | C | 27 | a0001c0001t0001g0037 a0001c0001t0001g0166 a0001c0001t0001g0167 others(24): Show |
27 | HG01361.hp2 HG01433.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-38-31166A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152063024 | |||||||
| chr7:152063376 | C | T | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-38-30814C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152063376 | |||||||
| chr7:152063466 | G | A | 1 | a0001c0001t0002g0082 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-38-30724G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152063466 | |||||||
| chr7:152063908 | T | C | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-30282T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152063908 | |||||||
| chr7:152063968 | A | G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0281 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-38-30222A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152063968 | |||||||
| chr7:152063976 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-38-30214C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152063976 | |||||||
| chr7:152063999 | A | T | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-38-30191A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152063999 | |||||||
| chr7:152064067 | T | C | 1 | a0001c0001t0001g0222 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-38-30123T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152064067 | |||||||
| chr7:152064076 | A | G | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-30114A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152064076 | |||||||
| chr7:152064198 | C | G | 1 | a0001c0001t0002g0060 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-38-29992C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152064198 | |||||||
| chr7:152064385 | C | T | 2 | a0001c0001t0001g0134 a0001c0001t0001g0255 |
2 | HG02015.hp1 HG02080.hp2 |
intron_variant | MODIFIER | c.-38-29805C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152064385 | |||||||
| chr7:152064437 | A | G | 6 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0018 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-29753A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152064437 | |||||||
| chr7:152064614 | G | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-29576G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152064614 | |||||||
| chr7:152064682 | G | A | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-29508G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152064682 | |||||||
| chr7:152064752 | T | A | 10 | a0001c0001t0001g0184 a0001c0001t0001g0185 a0001c0001t0001g0186 others(7): Show |
10 | HG00140.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-29438T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152064752 | |||||||
| chr7:152064821 | C | A | 2 | a0001c0001t0001g0131 a0001c0001t0015g0144 |
2 | NA18964.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-38-29369C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152064821 | |||||||
| chr7:152064895 | T | G | 1 | a0001c0001t0001g0234 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-38-29295T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152064895 | |||||||
| chr7:152065108 | G | A | 4 | a0001c0001t0001g0208 a0001c0001t0001g0209 a0001c0001t0001g0266 others(1): Show |
4 | NA18942.hp2 NA19058.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-29082G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152065108 | |||||||
| chr7:152065498 | C | T | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01433.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-38-28692C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152065498 | |||||||
| chr7:152065660 | G | A | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-28530G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152065660 | |||||||
| chr7:152065954 | A | G | 1 | a0001c0001t0003g0005 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-38-28236A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152065954 | |||||||
| chr7:152066035 | A | G | 1 | a0001c0001t0003g0044 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-38-28155A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066035 | |||||||
| chr7:152066074 | G | A | 54 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(51): Show |
56 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-38-28116G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066074 | |||||||
| chr7:152066159 | C | T | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38-28031C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066159 | |||||||
| chr7:152066169 | T | A | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-28021T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066169 | |||||||
| chr7:152066215 | G | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG00597.hp1 HG02056.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-27975G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066215 | |||||||
| chr7:152066267 | AT | A | 46 | a0001c0001t0001g0016 a0001c0001t0001g0101 a0001c0001t0001g0104 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.-38-27920delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152066267 | ||||||
| chr7:152066311 | A | G | 1 | a0001c0001t0001g0120 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-38-27879A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066311 | |||||||
| chr7:152066431 | C | T | 1 | a0001c0001t0001g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-38-27759C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066431 | |||||||
| chr7:152066485 | GT | G | 92 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(89): Show |
94 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-38-27703delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152066485 | ||||||
| chr7:152066533 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-38-27657C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066533 | |||||||
| chr7:152066921 | C | A | 23 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0017 others(20): Show |
23 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-38-27269C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066921 | |||||||
| chr7:152066922 | G | A | 1 | a0001c0001t0011g0162 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-38-27268G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066922 | |||||||
| chr7:152066975 | T | C | 23 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0017 others(20): Show |
23 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-38-27215T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152066975 | |||||||
| chr7:152067039 | C | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-38-27151C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067039 | |||||||
| chr7:152067238 | A | G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-26952A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067238 | |||||||
| chr7:152067359 | A | G | 1 | a0001c0001t0003g0026 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-38-26831A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067359 | |||||||
| chr7:152067367 | A | G | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-26823A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067367 | |||||||
| chr7:152067454 | C | T | 2 | a0001c0001t0001g0147 a0001c0001t0013g0145 |
2 | HG01169.hp2 HG02145.hp1 |
intron_variant | MODIFIER | c.-38-26736C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067454 | |||||||
| chr7:152067478 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-38-26712A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067478 | |||||||
| chr7:152067508 | A | G | 2 | a0004c0005t0005g0256 a0004c0005t0005g0257 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-38-26682A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067508 | |||||||
| chr7:152067534 | G | A | 8 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-26656G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067534 | |||||||
| chr7:152067703 | A | T | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-26487A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067703 | |||||||
| chr7:152067775 | C | T | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-38-26415C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067775 | |||||||
| chr7:152067816 | T | C | 1 | a0001c0001t0003g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-38-26374T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067816 | |||||||
| chr7:152067830 | G | A | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02257.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-38-26360G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067830 | |||||||
| chr7:152067841 | A | G | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-26349A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067841 | |||||||
| chr7:152067921 | A | G | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-26269A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152067921 | |||||||
| chr7:152068002 | C | T | 1 | a0002c0003t0003g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-38-26188C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152068002 | |||||||
| chr7:152068103 | T | G | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-26087T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152068103 | |||||||
| chr7:152068185 | C | A | 1 | a0001c0001t0002g0002 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.-38-26005C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152068185 | |||||||
| chr7:152068345 | G | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-25845G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152068345 | |||||||
| chr7:152068449 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-25741C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152068449 | |||||||
| chr7:152068652 | C | CT | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-25532dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152068652 | ||||||
| chr7:152069002 | G | T | 4 | a0001c0001t0001g0197 a0001c0001t0001g0216 a0001c0001t0001g0218 others(1): Show |
4 | HG01192.hp2 HG01346.hp2 HG01975.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-25188G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152069002 | |||||||
| chr7:152069188 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38-25002G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152069188 | |||||||
| chr7:152069251 | G | A | 3 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 |
3 | HG02897.hp1 HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-38-24939G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152069251 | |||||||
| chr7:152069326 | G | C | 23 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0017 others(20): Show |
23 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.-38-24864G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152069326 | |||||||
| chr7:152069595 | T | C | 1 | a0001c0001t0003g0005 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-38-24595T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152069595 | |||||||
| chr7:152069791 | G | T | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38-24399G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152069791 | |||||||
| chr7:152069837 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-38-24353C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152069837 | |||||||
| chr7:152069868 | C | G | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-24322C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152069868 | |||||||
| chr7:152069888 | A | G | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-38-24302A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152069888 | |||||||
| chr7:152069997 | C | CT | 27 | a0001c0001t0003g0001 a0001c0001t0003g0017 a0001c0001t0003g0021 others(24): Show |
28 | HG00639.hp2 HG00735.hp2 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-38-24188dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152069997 | ||||||
| chr7:152069997 | C | CTT | 45 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(42): Show |
46 | HG00438.hp2 HG00558.hp2 HG00673.hp2 others(43): Show |
intron_variant | MODIFIER | c.-38-24189_-38-2418 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152069997 | ||||||
| chr7:152070000 | T | TC | 12 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0038 others(9): Show |
12 | HG02055.hp1 HG02257.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38-24190_-38-2418 others(5): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070000 | |||||||
| chr7:152070003 | C | T | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-24187C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070003 | |||||||
| chr7:152070057 | T | C | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-24133T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070057 | |||||||
| chr7:152070154 | G | A | 1 | a0001c0001t0001g0177 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-38-24036G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070154 | |||||||
| chr7:152070218 | G | A | 20 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0017 others(17): Show |
20 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-38-23972G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070218 | |||||||
| chr7:152070273 | G | C | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38-23917G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070273 | |||||||
| chr7:152070285 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-23905C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070285 | |||||||
| chr7:152070390 | C | T | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-23800C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070390 | |||||||
| chr7:152070486 | ATC | A | 36 | a0001c0001t0001g0016 a0001c0001t0001g0101 a0001c0001t0001g0104 others(33): Show |
36 | HG00099.hp2 HG00544.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.-38-23702_-38-2370 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152070486 | ||||||
| chr7:152070798 | G | A | 20 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0017 others(17): Show |
20 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-38-23392G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070798 | |||||||
| chr7:152070907 | C | T | 8 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-23283C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070907 | |||||||
| chr7:152070978 | G | A | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-23212G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070978 | |||||||
| chr7:152070981 | A | G | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-23209A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152070981 | |||||||
| chr7:152071109 | G | A | 41 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0107 others(38): Show |
41 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.-38-23081G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152071109 | |||||||
| chr7:152071199 | T | G | 1 | a0001c0001t0001g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-38-22991T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152071199 | |||||||
| chr7:152071285 | T | TG | 54 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(51): Show |
56 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.-38-22900dupG | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152071285 | ||||||
| chr7:152071291 | T | G | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-22899T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152071291 | |||||||
| chr7:152071432 | G | T | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG00621.hp2 HG00673.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-38-22758G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152071432 | |||||||
| chr7:152071576 | A | G | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-22614A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152071576 | |||||||
| chr7:152071651 | T | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-22539T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152071651 | |||||||
| chr7:152071673 | C | T | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-22517C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152071673 | |||||||
| chr7:152071744 | G | A | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.-38-22446G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152071744 | |||||||
| chr7:152071863 | G | A | 1 | a0001c0001t0001g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-38-22327G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152071863 | |||||||
| chr7:152072009 | C | CA | 12 | a0001c0001t0001g0098 a0001c0001t0001g0126 a0001c0001t0001g0147 others(9): Show |
12 | HG01361.hp1 HG01433.hp2 HG02027.hp2 others(9): Show |
intron_variant | MODIFIER | c.-38-22160dupA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152072009 | ||||||
| chr7:152072009 | CA | C | 96 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(93): Show |
98 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-22160delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152072009 | ||||||
| chr7:152072044 | G | C | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-22146G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152072044 | |||||||
| chr7:152072191 | C | T | 4 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0023 others(1): Show |
4 | HG01891.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-21999C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152072191 | |||||||
| chr7:152072232 | T | C | 6 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0018 others(3): Show |
6 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-21958T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152072232 | |||||||
| chr7:152072314 | C | CA | 7 | a0001c0001t0001g0207 a0001c0001t0001g0268 a0001c0001t0001g0269 others(4): Show |
7 | HG03098.hp1 HG03831.hp1 HG04199.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-21858dupA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152072314 | ||||||
| chr7:152072314 | CA | C | 7 | a0001c0001t0001g0135 a0001c0001t0001g0229 a0001c0001t0006g0093 others(4): Show |
7 | HG00639.hp2 HG02572.hp2 HG03490.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-21858delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152072314 | ||||||
| chr7:152072326 | A | G | 25 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(22): Show |
25 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38-21864A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152072326 | |||||||
| chr7:152072590 | A | C | 2 | a0001c0001t0003g0014 a0001c0001t0003g0281 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-38-21600A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152072590 | |||||||
| chr7:152072647 | C | CT | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-21540dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152072647 | ||||||
| chr7:152072651 | G | C | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-21539G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152072651 | |||||||
| chr7:152072735 | A | G | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-21455A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152072735 | |||||||
| chr7:152072779 | A | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-38-21411A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152072779 | |||||||
| chr7:152072870 | C | T | 2 | a0001c0001t0001g0142 a0001c0001t0001g0143 |
2 | HG03669.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.-38-21320C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152072870 | |||||||
| chr7:152072953 | C | T | 6 | a0001c0001t0003g0001 a0001c0001t0003g0018 a0001c0001t0003g0019 others(3): Show |
7 | HG01243.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-21237C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152072953 | |||||||
| chr7:152073000 | C | T | 2 | a0001c0001t0001g0242 a0001c0001t0001g0244 |
2 | NA18971.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-38-21190C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073000 | |||||||
| chr7:152073059 | A | G | 11 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(8): Show |
11 | HG00558.hp2 HG00673.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.-38-21131A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073059 | |||||||
| chr7:152073150 | T | G | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-38-21040T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073150 | |||||||
| chr7:152073258 | C | T | 1 | a0003c0002t0001g0214 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-38-20932C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073258 | |||||||
| chr7:152073310 | C | T | 1 | a0001c0001t0012g0062 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.-38-20880C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073310 | |||||||
| chr7:152073333 | T | G | 1 | a0001c0001t0007g0132 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-38-20857T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073333 | |||||||
| chr7:152073422 | C | T | 1 | a0001c0001t0001g0266 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-38-20768C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073422 | |||||||
| chr7:152073445 | G | T | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38-20745G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073445 | |||||||
| chr7:152073526 | T | C | 6 | a0001c0001t0003g0001 a0001c0001t0003g0018 a0001c0001t0003g0019 others(3): Show |
7 | HG01243.hp1 HG02451.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-20664T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073526 | |||||||
| chr7:152073690 | T | C | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-20500T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073690 | |||||||
| chr7:152073884 | T | C | 27 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(24): Show |
27 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.-38-20306T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073884 | |||||||
| chr7:152073986 | A | G | 8 | a0001c0001t0001g0134 a0001c0001t0001g0163 a0001c0001t0001g0255 others(5): Show |
8 | HG02015.hp1 HG02040.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.-38-20204A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152073986 | |||||||
| chr7:152074032 | C | G | 7 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0034 others(4): Show |
7 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-20158C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152074032 | |||||||
| chr7:152074036 | G | A | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-20154G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152074036 | |||||||
| chr7:152074115 | T | C | 3 | a0001c0001t0001g0106 a0001c0001t0001g0107 a0001c0001t0001g0108 |
3 | NA18951.hp2 NA18987.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.-38-20075T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152074115 | |||||||
| chr7:152074226 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0141 others(2): Show |
5 | HG01109.hp2 HG02886.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-19964G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152074226 | |||||||
| chr7:152074310 | T | A | 1 | a0001c0001t0001g0123 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-38-19880T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152074310 | |||||||
| chr7:152074497 | A | AT | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-38-19692dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152074497 | ||||||
| chr7:152075039 | T | C | 92 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(89): Show |
94 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(91): Show |
intron_variant | MODIFIER | c.-38-19151T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075039 | |||||||
| chr7:152075065 | G | A | 1 | a0001c0001t0001g0224 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-38-19125G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075065 | |||||||
| chr7:152075137 | G | A | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-38-19053G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075137 | |||||||
| chr7:152075137 | G | C | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-19053G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075137 | |||||||
| chr7:152075250 | C | G | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-18940C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075250 | |||||||
| chr7:152075262 | G | A | 2 | a0001c0001t0001g0109 a0001c0001t0001g0110 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-38-18928G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075262 | |||||||
| chr7:152075279 | T | C | 31 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0001 others(28): Show |
32 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38-18911T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075279 | |||||||
| chr7:152075558 | T | C | 2 | a0001c0001t0001g0252 a0001c0001t0001g0253 |
2 | HG00280.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.-38-18632T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075558 | |||||||
| chr7:152075611 | A | G | 8 | a0001c0001t0003g0017 a0001c0001t0003g0027 a0001c0001t0003g0030 others(5): Show |
8 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-18579A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075611 | |||||||
| chr7:152075648 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-38-18542A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075648 | |||||||
| chr7:152075796 | C | CA | 24 | a0001c0001t0001g0104 a0001c0001t0001g0119 a0001c0001t0001g0142 others(21): Show |
24 | HG00621.hp1 HG00639.hp2 HG00735.hp2 others(21): Show |
intron_variant | MODIFIER | c.-38-18379dupA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152075796 | ||||||
| chr7:152075796 | C | CAA | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0001 others(23): Show |
27 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.-38-18380_-38-1837 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152075796 | ||||||
| chr7:152075889 | G | C | 1 | a0001c0001t0003g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.-38-18301G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152075889 | |||||||
| chr7:152076016 | C | T | 1 | a0001c0001t0007g0132 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-38-18174C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152076016 | |||||||
| chr7:152076056 | C | T | 1 | a0001c0001t0002g0056 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-38-18134C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152076056 | |||||||
| chr7:152076061 | CA | C | 67 | a0001c0001t0001g0016 a0001c0001t0001g0101 a0001c0001t0001g0104 others(64): Show |
68 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(65): Show |
intron_variant | MODIFIER | c.-38-18100delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152076061 | ||||||
| chr7:152076061 | CAA | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(149): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-38-18101_-38-1810 others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152076061 | ||||||
| chr7:152076061 | CAAA | C | 10 | a0001c0001t0001g0137 a0001c0001t0001g0153 a0001c0001t0001g0193 others(7): Show |
10 | HG01070.hp1 HG01361.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38-18102_-38-1810 others(7): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152076061 | ||||||
| chr7:152076061 | CAAAAA | C | 6 | a0001c0001t0002g0049 a0001c0001t0003g0043 a0001c0001t0003g0044 others(3): Show |
6 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38-18104_-38-1810 others(9): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152076061 | ||||||
| chr7:152076061 | CAAAAAA | C | 10 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(7): Show |
10 | HG00558.hp2 HG00673.hp2 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38-18105_-38-1810 others(10): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152076061 | ||||||
| chr7:152076065 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-38-18125A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152076065 | |||||||
| chr7:152076090 | A | C | 3 | a0001c0001t0001g0186 a0001c0001t0001g0190 a0001c0001t0001g0192 |
3 | HG00140.hp1 HG00738.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.-38-18100A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152076090 | |||||||
| chr7:152076098 | AG | A | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-18091delG | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152076098 | |||||||
| chr7:152076150 | T | C | 1 | a0001c0001t0001g0197 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-38-18040T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152076150 | |||||||
| chr7:152076399 | A | G | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-17791A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152076399 | |||||||
| chr7:152076442 | TA | T | 8 | a0001c0001t0003g0001 a0001c0001t0003g0018 a0001c0001t0003g0019 others(5): Show |
9 | HG01243.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38-17745delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152076442 | ||||||
| chr7:152076731 | C | T | 14 | a0001c0001t0001g0100 a0001c0001t0001g0122 a0001c0001t0001g0135 others(11): Show |
14 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-38-17459C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152076731 | |||||||
| chr7:152076995 | G | A | 1 | a0001c0001t0001g0268 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-38-17195G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152076995 | |||||||
| chr7:152077023 | G | C | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-38-17167G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152077023 | |||||||
| chr7:152077270 | G | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-16920G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152077270 | |||||||
| chr7:152077354 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0157 |
2 | HG00673.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.-38-16836G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152077354 | |||||||
| chr7:152077690 | A | C | 4 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0023 others(1): Show |
4 | HG01891.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-16500A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152077690 | |||||||
| chr7:152077696 | C | T | 1 | a0001c0001t0006g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-38-16494C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152077696 | |||||||
| chr7:152077802 | G | A | 1 | a0001c0001t0001g0265 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-38-16388G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152077802 | |||||||
| chr7:152077858 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-38-16332C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152077858 | |||||||
| chr7:152077859 | G | A | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-38-16331G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152077859 | |||||||
| chr7:152077888 | A | G | 1 | a0001c0001t0001g0233 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-38-16302A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152077888 | |||||||
| chr7:152077989 | C | T | 7 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0034 others(4): Show |
7 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-16201C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152077989 | |||||||
| chr7:152078077 | C | T | 3 | a0001c0001t0001g0133 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG01928.hp1 HG01975.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.-38-16113C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078077 | |||||||
| chr7:152078095 | G | A | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38-16095G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078095 | |||||||
| chr7:152078106 | G | A | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-16084G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078106 | |||||||
| chr7:152078192 | A | G | 1 | a0001c0001t0003g0027 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-38-15998A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078192 | |||||||
| chr7:152078238 | A | G | 31 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0001 others(28): Show |
32 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38-15952A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078238 | |||||||
| chr7:152078257 | G | C | 192 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0037 others(189): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-38-15933G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078257 | |||||||
| chr7:152078272 | A | G | 2 | a0001c0001t0002g0086 a0001c0001t0002g0087 |
2 | NA18962.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.-38-15918A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078272 | |||||||
| chr7:152078392 | G | T | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-38-15798G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078392 | |||||||
| chr7:152078501 | G | A | 97 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(94): Show |
99 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.-38-15689G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078501 | |||||||
| chr7:152078663 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-38-15527C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078663 | |||||||
| chr7:152078733 | T | G | 1 | a0001c0001t0002g0058 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-38-15457T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078733 | |||||||
| chr7:152078751 | T | A | 2 | a0001c0001t0001g0260 a0001c0001t0001g0261 |
2 | HG01261.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.-38-15439T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078751 | |||||||
| chr7:152078885 | A | G | 1 | a0001c0001t0006g0091 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-38-15305A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078885 | |||||||
| chr7:152078928 | C | T | 3 | a0001c0001t0001g0187 a0001c0001t0001g0188 a0001c0001t0001g0189 |
3 | HG02257.hp1 HG02717.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-38-15262C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078928 | |||||||
| chr7:152078996 | T | TG | 31 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0001 others(28): Show |
32 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38-15193dupG | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152078996 | ||||||
| chr7:152078997 | G | T | 1 | a0001c0007t0001g0148 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-38-15193G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152078997 | |||||||
| chr7:152079127 | A | G | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-15063A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152079127 | |||||||
| chr7:152079221 | A | T | 1 | a0001c0001t0001g0203 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.-38-14969A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152079221 | |||||||
| chr7:152079258 | G | A | 3 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0060 |
3 | NA18960.hp1 NA18985.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.-38-14932G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152079258 | |||||||
| chr7:152079530 | T | C | 8 | a0001c0001t0003g0001 a0001c0001t0003g0018 a0001c0001t0003g0019 others(5): Show |
9 | HG01243.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38-14660T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152079530 | |||||||
| chr7:152079533 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-38-14657A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152079533 | |||||||
| chr7:152079853 | G | A | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-14337G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152079853 | |||||||
| chr7:152080122 | A | G | 31 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0001 others(28): Show |
32 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38-14068A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152080122 | |||||||
| chr7:152080156 | G | C | 1 | a0005c0009t0001g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-38-14034G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152080156 | |||||||
| chr7:152080360 | A | G | 1 | a0002c0003t0003g0008 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-38-13830A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152080360 | |||||||
| chr7:152080496 | G | C | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38-13694G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152080496 | |||||||
| chr7:152080539 | A | T | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-13651A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152080539 | |||||||
| chr7:152080670 | A | AT | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-38-13518dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152080670 | ||||||
| chr7:152080680 | G | A | 7 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(4): Show |
7 | HG01433.hp2 HG02559.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.-38-13510G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152080680 | |||||||
| chr7:152080704 | G | A | 2 | a0001c0001t0003g0014 a0001c0001t0003g0281 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-38-13486G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152080704 | |||||||
| chr7:152080799 | T | TA | 9 | a0001c0001t0002g0181 a0001c0001t0003g0001 a0001c0001t0003g0018 others(6): Show |
10 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-13379dupA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152080799 | ||||||
| chr7:152081116 | G | T | 1 | a0001c0001t0001g0255 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-38-13074G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152081116 | |||||||
| chr7:152081388 | C | T | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-12802C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152081388 | |||||||
| chr7:152081531 | A | G | 1 | a0001c0001t0001g0271 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-38-12659A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152081531 | |||||||
| chr7:152081633 | T | G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0281 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-38-12557T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152081633 | |||||||
| chr7:152081736 | G | A | 5 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-12454G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152081736 | |||||||
| chr7:152081762 | C | G | 2 | a0001c0001t0001g0225 a0006c0006t0001g0227 |
2 | NA19000.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.-38-12428C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152081762 | |||||||
| chr7:152081923 | T | C | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-12267T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152081923 | |||||||
| chr7:152081963 | A | C | 1 | a0001c0001t0003g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-38-12227A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152081963 | |||||||
| chr7:152081969 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0186 |
2 | HG00738.hp1 HG01074.hp2 |
intron_variant | MODIFIER | c.-38-12221T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152081969 | |||||||
| chr7:152082491 | A | C | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-11699A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152082491 | |||||||
| chr7:152082532 | C | T | 1 | a0001c0001t0006g0092 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-38-11658C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152082532 | |||||||
| chr7:152082585 | T | C | 20 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0017 others(17): Show |
20 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-38-11605T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152082585 | |||||||
| chr7:152082600 | G | A | 2 | a0001c0001t0001g0196 a0001c0001t0001g0226 |
2 | HG02895.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-38-11590G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152082600 | |||||||
| chr7:152083081 | C | T | 1 | a0001c0001t0001g0192 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-38-11109C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152083081 | |||||||
| chr7:152083092 | G | A | 7 | a0001c0001t0001g0134 a0001c0001t0001g0255 a0001c0001t0001g0269 others(4): Show |
7 | HG02015.hp1 HG02040.hp1 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-38-11098G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152083092 | |||||||
| chr7:152083328 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-38-10862C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152083328 | |||||||
| chr7:152083752 | T | C | 1 | a0003c0002t0001g0211 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-38-10438T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152083752 | |||||||
| chr7:152083793 | A | G | 46 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(43): Show |
47 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-38-10397A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152083793 | |||||||
| chr7:152083876 | G | A | 1 | a0001c0001t0003g0005 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-38-10314G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152083876 | |||||||
| chr7:152084340 | TTGAGTC | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-38-9848_-38-9843d others(8): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152084340 | ||||||
| chr7:152084380 | T | TA | 60 | a0001c0001t0001g0108 a0001c0001t0001g0112 a0001c0001t0001g0142 others(57): Show |
61 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.-38-9786dupA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152084380 | ||||||
| chr7:152084380 | T | TAA | 14 | a0001c0001t0001g0207 a0001c0001t0002g0048 a0001c0001t0002g0049 others(11): Show |
15 | HG01243.hp1 HG01891.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.-38-9787_-38-9786d others(4): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152084380 | ||||||
| chr7:152084380 | TA | T | 19 | a0001c0001t0001g0015 a0001c0001t0001g0105 a0001c0001t0001g0110 others(16): Show |
19 | HG01243.hp2 HG02109.hp2 HG02523.hp2 others(16): Show |
intron_variant | MODIFIER | c.-38-9786delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152084380 | ||||||
| chr7:152084380 | TAA | T | 25 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(22): Show |
25 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.-38-9787_-38-9786d others(4): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152084380 | ||||||
| chr7:152084402 | A | C | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-9788A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152084402 | |||||||
| chr7:152084467 | T | C | 1 | a0001c0001t0003g0018 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-38-9723T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152084467 | |||||||
| chr7:152084537 | G | A | 1 | a0001c0001t0001g0237 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-38-9653G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152084537 | |||||||
| chr7:152084555 | C | G | 1 | a0001c0001t0001g0268 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-38-9635C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152084555 | |||||||
| chr7:152084672 | T | G | 5 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0139 others(2): Show |
5 | HG01928.hp1 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38-9518T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152084672 | |||||||
| chr7:152084673 | C | T | 5 | a0001c0001t0001g0131 a0001c0001t0001g0133 a0001c0001t0001g0139 others(2): Show |
5 | HG01928.hp1 HG01975.hp1 HG01978.hp1 others(2): Show |
intron_variant | MODIFIER | c.-38-9517C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152084673 | |||||||
| chr7:152084693 | G | A | 20 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0017 others(17): Show |
20 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-38-9497G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152084693 | |||||||
| chr7:152084782 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-38-9408G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152084782 | |||||||
| chr7:152084855 | A | G | 1 | a0001c0001t0001g0122 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-38-9335A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152084855 | |||||||
| chr7:152084934 | C | CATTA | 38 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(35): Show |
38 | HG00639.hp2 HG00735.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.-38-9255_-38-9254i others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152084934 | ||||||
| chr7:152084936 | A | T | 38 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(35): Show |
38 | HG00639.hp2 HG00735.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.-38-9254A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152084936 | |||||||
| chr7:152085435 | T | G | 1 | a0001c0001t0001g0274 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-38-8755T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152085435 | |||||||
| chr7:152085579 | A | ATTAT | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-8610_-38-8609i others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152085579 | ||||||
| chr7:152085604 | A | T | 20 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0017 others(17): Show |
20 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.-38-8586A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152085604 | |||||||
| chr7:152085791 | G | GC | 13 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(10): Show |
13 | HG00558.hp2 HG00673.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.-38-8398dupC | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152085791 | ||||||
| chr7:152085895 | G | GT | 58 | a0001c0001t0001g0118 a0001c0001t0001g0173 a0001c0001t0002g0002 others(55): Show |
60 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.-38-8284dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152085895 | ||||||
| chr7:152085923 | C | G | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-8267C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152085923 | |||||||
| chr7:152085964 | T | G | 8 | a0001c0001t0003g0001 a0001c0001t0003g0018 a0001c0001t0003g0019 others(5): Show |
9 | HG01243.hp1 HG02451.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.-38-8226T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152085964 | |||||||
| chr7:152086179 | C | A | 1 | a0001c0001t0002g0082 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-38-8011C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152086179 | |||||||
| chr7:152086315 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-38-7875G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152086315 | |||||||
| chr7:152086369 | T | C | 1 | a0001c0001t0001g0254 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-38-7821T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152086369 | |||||||
| chr7:152086698 | G | A | 28 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(25): Show |
28 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-38-7492G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152086698 | |||||||
| chr7:152086763 | A | C | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.-38-7427A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152086763 | |||||||
| chr7:152086899 | T | G | 2 | a0003c0002t0001g0211 a0003c0002t0001g0214 |
2 | NA18951.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.-38-7291T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152086899 | |||||||
| chr7:152087013 | C | A | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-7177C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152087013 | |||||||
| chr7:152087039 | AT | A | 47 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(44): Show |
48 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(45): Show |
intron_variant | MODIFIER | c.-38-7149delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152087039 | ||||||
| chr7:152087306 | G | A | 6 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(3): Show |
6 | HG00639.hp2 HG01884.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.-38-6884G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152087306 | |||||||
| chr7:152087521 | C | T | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-6669C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152087521 | |||||||
| chr7:152087661 | G | T | 1 | a0001c0001t0001g0265 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-38-6529G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152087661 | |||||||
| chr7:152087772 | G | A | 1 | a0001c0001t0002g0075 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.-38-6418G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152087772 | |||||||
| chr7:152087854 | A | G | 31 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0001 others(28): Show |
32 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.-38-6336A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152087854 | |||||||
| chr7:152087896 | T | A | 1 | a0001c0001t0001g0106 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.-38-6294T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152087896 | |||||||
| chr7:152088083 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-6107C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152088083 | |||||||
| chr7:152088103 | G | A | 3 | a0001c0001t0001g0216 a0001c0001t0001g0218 a0001c0001t0001g0220 |
3 | HG01192.hp2 HG01346.hp2 HG01975.hp2 |
intron_variant | MODIFIER | c.-38-6087G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152088103 | |||||||
| chr7:152088386 | G | GT | 5 | a0001c0001t0001g0217 a0001c0001t0005g0258 a0001c0001t0005g0259 others(2): Show |
5 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.-38-5796dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152088386 | ||||||
| chr7:152088412 | T | G | 1 | a0001c0001t0001g0217 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-38-5778T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152088412 | |||||||
| chr7:152088413 | G | C | 1 | a0001c0001t0001g0217 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-38-5777G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152088413 | |||||||
| chr7:152088516 | G | GT | 66 | a0001c0001t0001g0004 a0001c0001t0001g0131 a0001c0001t0001g0217 others(63): Show |
67 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.-38-5660dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152088516 | ||||||
| chr7:152088516 | GT | G | 6 | a0001c0001t0001g0104 a0001c0001t0001g0206 a0001c0001t0001g0221 others(3): Show |
6 | HG02056.hp1 HG02056.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.-38-5660delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152088516 | ||||||
| chr7:152088536 | T | A | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-38-5654T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152088536 | |||||||
| chr7:152088592 | T | G | 1 | a0001c0001t0001g0102 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-38-5598T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152088592 | |||||||
| chr7:152088598 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-38-5592C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152088598 | |||||||
| chr7:152088906 | C | T | 1 | a0001c0001t0001g0253 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-38-5284C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152088906 | |||||||
| chr7:152089368 | C | T | 27 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(24): Show |
27 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.-38-4822C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152089368 | |||||||
| chr7:152089378 | C | A | 8 | a0001c0001t0001g0102 a0001c0001t0001g0228 a0001c0001t0001g0229 others(5): Show |
8 | HG00408.hp2 HG00639.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.-38-4812C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152089378 | |||||||
| chr7:152089718 | A | G | 1 | a0001c0001t0004g0032 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-38-4472A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152089718 | |||||||
| chr7:152089839 | T | G | 1 | a0001c0001t0001g0103 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.-38-4351T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152089839 | |||||||
| chr7:152090050 | T | C | 1 | a0001c0001t0003g0039 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-38-4140T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152090050 | |||||||
| chr7:152090300 | CTGT | C | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-3885_-38-3883d others(5): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152090300 | ||||||
| chr7:152090646 | A | AC | 13 | a0001c0001t0001g0112 a0001c0001t0001g0117 a0001c0001t0001g0142 others(10): Show |
13 | HG00597.hp1 HG00597.hp2 HG01261.hp2 others(10): Show |
intron_variant | MODIFIER | c.-38-3537dupC | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152090646 | ||||||
| chr7:152090647 | C | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-38-3543C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152090647 | |||||||
| chr7:152090656 | C | A | 1 | a0001c0001t0003g0040 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-38-3534C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152090656 | |||||||
| chr7:152090657 | CCA | C | 10 | a0001c0001t0001g0037 a0001c0001t0003g0038 a0001c0001t0003g0039 others(7): Show |
10 | HG02257.hp2 HG02486.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.-38-3531_-38-3530d others(4): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152090657 | ||||||
| chr7:152090659 | A | C | 1 | a0001c0001t0003g0040 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-38-3531A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152090659 | |||||||
| chr7:152090776 | C | T | 8 | a0001c0001t0003g0017 a0001c0001t0003g0027 a0001c0001t0003g0030 others(5): Show |
8 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-3414C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152090776 | |||||||
| chr7:152090792 | C | T | 8 | a0001c0001t0003g0017 a0001c0001t0003g0027 a0001c0001t0003g0030 others(5): Show |
8 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.-38-3398C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152090792 | |||||||
| chr7:152091040 | T | G | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-3150T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091040 | |||||||
| chr7:152091061 | T | G | 67 | a0001c0001t0001g0004 a0001c0001t0002g0002 a0001c0001t0002g0045 others(64): Show |
69 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(66): Show |
intron_variant | MODIFIER | c.-38-3129T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091061 | |||||||
| chr7:152091196 | C | T | 1 | a0002c0003t0003g0010 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-38-2994C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091196 | |||||||
| chr7:152091272 | G | A | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-2918G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091272 | |||||||
| chr7:152091329 | C | A | 1 | a0001c0001t0001g0159 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-38-2861C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091329 | |||||||
| chr7:152091333 | C | T | 2 | a0001c0001t0001g0217 a0002c0003t0003g0010 |
2 | HG03041.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.-38-2857C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091333 | |||||||
| chr7:152091365 | C | T | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38-2825C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091365 | |||||||
| chr7:152091392 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-38-2798C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091392 | |||||||
| chr7:152091457 | G | C | 1 | a0001c0001t0001g0250 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.-38-2733G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091457 | |||||||
| chr7:152091538 | C | T | 1 | a0001c0001t0001g0264 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-38-2652C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091538 | |||||||
| chr7:152091568 | G | T | 1 | a0001c0001t0001g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-38-2622G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091568 | |||||||
| chr7:152091869 | C | A | 1 | a0001c0001t0001g0219 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.-38-2321C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152091869 | |||||||
| chr7:152092149 | A | T | 1 | a0001c0001t0001g0217 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-38-2041A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152092149 | |||||||
| chr7:152092486 | C | G | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-1704C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152092486 | |||||||
| chr7:152092634 | C | G | 28 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(25): Show |
28 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.-38-1556C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152092634 | |||||||
| chr7:152092842 | C | G | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-1348C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152092842 | |||||||
| chr7:152092941 | G | A | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.-38-1249G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152092941 | |||||||
| chr7:152092971 | G | A | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-38-1219G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152092971 | |||||||
| chr7:152093000 | G | A | 1 | a0001c0001t0003g0025 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-38-1190G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152093000 | |||||||
| chr7:152093058 | A | G | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-38-1132A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152093058 | |||||||
| chr7:152093235 | G | GA | 21 | a0001c0001t0001g0097 a0001c0001t0001g0176 a0001c0001t0001g0239 others(18): Show |
21 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(18): Show |
intron_variant | MODIFIER | c.-38-940dupA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152093235 | ||||||
| chr7:152093236 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-38-954A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152093236 | |||||||
| chr7:152093236 | A | T | 2 | a0001c0001t0001g0105 a0001c0001t0001g0249 |
2 | NA20905.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.-38-954A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152093236 | |||||||
| chr7:152093402 | A | AT | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.-38-780dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr7 | 152093402 | ||||||
| chr7:152093610 | A | G | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.-38-580A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152093610 | |||||||
| chr7:152093758 | A | G | 2 | a0001c0001t0001g0166 a0001c0001t0001g0167 |
2 | HG01433.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.-38-432A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152093758 | |||||||
| chr7:152093975 | C | G | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-38-215C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152093975 | |||||||
| chr7:152094005 | C | A | 46 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(43): Show |
47 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-38-185C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152094005 | |||||||
| chr7:152094073 | A | C | 38 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(35): Show |
38 | HG00639.hp2 HG00735.hp2 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.-38-117A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152094073 | |||||||
| chr7:152094085 | T | G | 46 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(43): Show |
47 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.-38-105T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 1/11 | chr7 | 152094085 | |||||||
| chr7:152094951 | G | A | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.295+429G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152094951 | |||||||
| chr7:152095124 | A | G | 1 | a0001c0001t0003g0031 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.295+602A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152095124 | |||||||
| chr7:152095172 | T | C | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.295+650T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152095172 | |||||||
| chr7:152095183 | T | TAGAA | 31 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0001 others(28): Show |
32 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.295+663_295+664ins others(4): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152095183 | ||||||
| chr7:152095279 | T | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+757T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152095279 | |||||||
| chr7:152095285 | CATTTT | C | 20 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0017 others(17): Show |
20 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.295+770_295+774del others(5): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152095285 | ||||||
| chr7:152095486 | A | G | 23 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(20): Show |
23 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.295+964A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152095486 | |||||||
| chr7:152095528 | G | C | 3 | a0001c0001t0001g0184 a0001c0001t0001g0191 a0001c0001t0001g0277 |
3 | HG02055.hp2 HG03225.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.295+1006G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152095528 | |||||||
| chr7:152096646 | C | T | 2 | a0001c0001t0006g0091 a0001c0001t0006g0092 |
2 | HG02083.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.295+2124C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152096646 | |||||||
| chr7:152096693 | C | A | 26 | a0001c0001t0001g0037 a0001c0001t0002g0082 a0001c0001t0003g0005 others(23): Show |
26 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.295+2171C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152096693 | |||||||
| chr7:152096714 | C | CA | 8 | a0001c0001t0001g0142 a0001c0001t0001g0168 a0001c0001t0001g0240 others(5): Show |
8 | HG02055.hp2 HG02622.hp2 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.295+2210dupA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152096714 | ||||||
| chr7:152096714 | CA | C | 12 | a0001c0001t0001g0015 a0001c0001t0001g0196 a0001c0001t0001g0201 others(9): Show |
12 | HG00558.hp1 HG00639.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.295+2210delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152096714 | ||||||
| chr7:152097225 | A | G | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.295+2703A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152097225 | |||||||
| chr7:152097251 | C | T | 3 | a0001c0001t0001g0135 a0001c0001t0001g0149 a0001c0001t0001g0150 |
3 | HG00099.hp1 HG00738.hp2 HG03490.hp1 |
intron_variant | MODIFIER | c.295+2729C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152097251 | |||||||
| chr7:152097447 | C | G | 8 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.295+2925C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152097447 | |||||||
| chr7:152097531 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.295+3009C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152097531 | |||||||
| chr7:152097807 | G | A | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.296-2991G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152097807 | |||||||
| chr7:152098429 | A | T | 3 | a0001c0001t0003g0001 a0001c0001t0003g0025 a0001c0001t0003g0026 |
4 | HG01243.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-2369A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152098429 | |||||||
| chr7:152098433 | T | A | 21 | a0001c0001t0001g0112 a0001c0001t0001g0147 a0001c0001t0001g0166 others(18): Show |
21 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.296-2365T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152098433 | |||||||
| chr7:152098437 | T | A | 2 | a0004c0005t0005g0256 a0004c0005t0005g0257 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.296-2361T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152098437 | |||||||
| chr7:152098545 | G | A | 1 | a0002c0003t0003g0013 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.296-2253G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152098545 | |||||||
| chr7:152098680 | A | G | 1 | a0001c0001t0003g0281 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.296-2118A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152098680 | |||||||
| chr7:152098985 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.296-1813C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152098985 | |||||||
| chr7:152099003 | GGCATGAT others(13): Show |
G | 1 | a0001c0001t0001g0195 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.296-1794_296-1775d others(22): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099003 | |||||||
| chr7:152099127 | A | G | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.296-1671A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099127 | |||||||
| chr7:152099130 | C | T | 35 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0107 others(32): Show |
35 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.296-1668C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099130 | |||||||
| chr7:152099259 | T | C | 1 | a0001c0001t0001g0111 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.296-1539T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099259 | |||||||
| chr7:152099338 | G | T | 1 | a0001c0001t0001g0216 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.296-1460G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099338 | |||||||
| chr7:152099342 | T | A | 2 | a0001c0001t0002g0076 a0001c0001t0002g0088 |
2 | NA19001.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.296-1456T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099342 | |||||||
| chr7:152099342 | T | TTTTA | 57 | a0001c0001t0001g0015 a0001c0001t0001g0016 a0001c0001t0001g0098 others(54): Show |
57 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(54): Show |
intron_variant | MODIFIER | c.296-1416_296-1413d others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099342 | ||||||
| chr7:152099342 | T | TTTTATTT others(1): Show |
35 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0112 others(32): Show |
35 | HG00408.hp1 HG00438.hp1 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.296-1420_296-1413d others(10): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099342 | ||||||
| chr7:152099342 | TTTTA | T | 14 | a0001c0001t0001g0037 a0001c0001t0001g0109 a0001c0001t0001g0110 others(11): Show |
14 | HG00597.hp2 HG00735.hp2 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.296-1416_296-1413d others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099342 | ||||||
| chr7:152099342 | TTTTATTT others(1): Show |
T | 17 | a0001c0001t0003g0017 a0001c0001t0003g0027 a0001c0001t0003g0030 others(14): Show |
17 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.296-1420_296-1413d others(10): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099342 | ||||||
| chr7:152099342 | TTTTATTT others(5): Show |
T | 17 | a0001c0001t0002g0002 a0001c0001t0002g0087 a0001c0001t0003g0001 others(14): Show |
19 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.296-1424_296-1413d others(14): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099342 | ||||||
| chr7:152099454 | T | C | 96 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.296-1344T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099454 | |||||||
| chr7:152099456 | C | T | 1 | a0001c0001t0004g0095 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.296-1342C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099456 | |||||||
| chr7:152099530 | G | GT | 109 | a0001c0001t0001g0098 a0001c0001t0001g0100 a0001c0001t0001g0104 others(106): Show |
109 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.296-1239dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099530 | ||||||
| chr7:152099530 | G | GTT | 26 | a0001c0001t0001g0134 a0001c0001t0001g0154 a0001c0001t0001g0213 others(23): Show |
27 | HG00408.hp2 HG00621.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.296-1240_296-1239d others(4): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099530 | ||||||
| chr7:152099530 | GT | G | 16 | a0001c0001t0001g0186 a0001c0001t0001g0254 a0001c0001t0003g0027 others(13): Show |
16 | HG00639.hp2 HG00738.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.296-1239delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099530 | ||||||
| chr7:152099530 | GTT | G | 13 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0038 others(10): Show |
13 | HG02109.hp2 HG02257.hp2 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.296-1240_296-1239d others(4): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099530 | ||||||
| chr7:152099530 | GTTTTTTT others(5): Show |
G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.296-1250_296-1239d others(14): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099530 | ||||||
| chr7:152099530 | GTTTTTTT others(6): Show |
G | 1 | a0001c0001t0001g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.296-1251_296-1239d others(15): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099530 | ||||||
| chr7:152099588 | G | A | 27 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(24): Show |
27 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.296-1210G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099588 | |||||||
| chr7:152099635 | G | A | 1 | a0001c0001t0001g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.296-1163G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099635 | |||||||
| chr7:152099677 | C | T | 27 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(24): Show |
27 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.296-1121C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099677 | |||||||
| chr7:152099756 | C | CT | 57 | a0001c0001t0001g0102 a0001c0001t0001g0106 a0001c0001t0001g0107 others(54): Show |
57 | HG00140.hp1 HG00597.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.296-1019dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099756 | ||||||
| chr7:152099756 | C | CTT | 7 | a0001c0001t0001g0037 a0001c0001t0001g0207 a0001c0001t0001g0277 others(4): Show |
7 | HG01361.hp2 HG02055.hp2 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.296-1020_296-1019d others(4): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099756 | ||||||
| chr7:152099756 | CT | C | 10 | a0001c0001t0001g0110 a0001c0001t0001g0153 a0001c0001t0001g0232 others(7): Show |
11 | HG00639.hp1 HG01070.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.296-1019delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099756 | ||||||
| chr7:152099780 | G | T | 27 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(24): Show |
27 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(24): Show |
intron_variant | MODIFIER | c.296-1018G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152099780 | |||||||
| chr7:152099947 | A | AT | 85 | a0001c0001t0001g0097 a0001c0001t0001g0100 a0001c0001t0001g0101 others(82): Show |
87 | HG00408.hp1 HG00438.hp2 HG00558.hp2 others(84): Show |
intron_variant | MODIFIER | c.296-828dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099947 | ||||||
| chr7:152099947 | A | ATT | 14 | a0001c0001t0001g0004 a0001c0001t0001g0127 a0001c0001t0001g0240 others(11): Show |
14 | HG00673.hp2 HG01433.hp1 HG02027.hp1 others(11): Show |
intron_variant | MODIFIER | c.296-829_296-828dup others(2): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr7 | 152099947 | ||||||
| chr7:152100057 | G | T | 1 | a0001c0001t0001g0135 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.296-741G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152100057 | |||||||
| chr7:152100080 | G | A | 1 | a0001c0001t0001g0280 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.296-718G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152100080 | |||||||
| chr7:152100218 | T | A | 1 | a0001c0001t0001g0163 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.296-580T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152100218 | |||||||
| chr7:152100248 | T | C | 278 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0015 others(275): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.296-550T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152100248 | |||||||
| chr7:152100289 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.296-509C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152100289 | |||||||
| chr7:152100326 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.296-472G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152100326 | |||||||
| chr7:152100459 | G | A | 35 | a0001c0001t0001g0100 a0001c0001t0001g0106 a0001c0001t0001g0107 others(32): Show |
35 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(32): Show |
intron_variant | MODIFIER | c.296-339G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152100459 | |||||||
| chr7:152100738 | G | C | 8 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0018 others(5): Show |
8 | HG02572.hp1 HG02615.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.296-60G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 2/11 | chr7 | 152100738 | |||||||
| chr7:152101173 | A | G | 8 | a0001c0001t0003g0017 a0001c0001t0003g0027 a0001c0001t0003g0030 others(5): Show |
8 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.419+252A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101173 | |||||||
| chr7:152101252 | G | T | 1 | a0001c0001t0014g0272 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.419+331G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101252 | |||||||
| chr7:152101261 | T | TC | 71 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(68): Show |
73 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.419+341dupC | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 152101261 | ||||||
| chr7:152101346 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.419+425G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101346 | |||||||
| chr7:152101374 | G | A | 71 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(68): Show |
73 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.419+453G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101374 | |||||||
| chr7:152101578 | C | G | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+657C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101578 | |||||||
| chr7:152101634 | C | CT | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.419+721dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 152101634 | ||||||
| chr7:152101642 | T | TG | 25 | a0001c0001t0001g0037 a0001c0001t0001g0100 a0001c0001t0001g0102 others(22): Show |
25 | HG00140.hp1 HG00544.hp1 HG00544.hp2 others(22): Show |
intron_variant | MODIFIER | c.419+733dupG | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 152101642 | ||||||
| chr7:152101642 | T | TTG | 4 | a0001c0001t0003g0019 a0001c0001t0003g0020 a0001c0001t0003g0275 others(1): Show |
4 | HG02615.hp2 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.419+721_419+722ins others(2): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101642 | |||||||
| chr7:152101642 | TG | T | 55 | a0001c0001t0001g0176 a0001c0001t0001g0240 a0001c0001t0002g0002 others(52): Show |
57 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.419+733delG | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 152101642 | ||||||
| chr7:152101643 | G | T | 2 | a0001c0001t0001g0108 a0005c0009t0001g0178 |
2 | HG02572.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.419+722G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101643 | |||||||
| chr7:152101644 | G | T | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.419+723G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101644 | |||||||
| chr7:152101645 | G | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.419+724G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101645 | |||||||
| chr7:152101646 | G | T | 1 | a0001c0001t0001g0101 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.419+725G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101646 | |||||||
| chr7:152101647 | G | C | 3 | a0001c0001t0006g0091 a0001c0001t0006g0092 a0001c0001t0006g0093 |
3 | HG02083.hp1 HG02135.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.419+726G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101647 | |||||||
| chr7:152101647 | G | T | 2 | a0004c0005t0005g0256 a0004c0005t0005g0257 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.419+726G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101647 | |||||||
| chr7:152101648 | G | C | 1 | a0001c0001t0003g0022 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.419+727G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101648 | |||||||
| chr7:152101650 | G | T | 11 | a0001c0001t0001g0177 a0001c0001t0003g0043 a0001c0001t0003g0044 others(8): Show |
11 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.419+729G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101650 | |||||||
| chr7:152101652 | G | A | 5 | a0001c0001t0001g0170 a0001c0001t0001g0173 a0001c0001t0001g0174 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.419+731G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101652 | |||||||
| chr7:152101823 | A | G | 1 | a0001c0001t0002g0081 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.419+902A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152101823 | |||||||
| chr7:152102185 | T | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.420-927T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102185 | |||||||
| chr7:152102195 | T | G | 1 | a0001c0001t0001g0205 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.420-917T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102195 | |||||||
| chr7:152102235 | A | C | 1 | a0001c0001t0001g0141 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.420-877A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102235 | |||||||
| chr7:152102271 | T | C | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.420-841T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102271 | |||||||
| chr7:152102309 | C | T | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.420-803C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102309 | |||||||
| chr7:152102464 | C | A | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.420-648C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102464 | |||||||
| chr7:152102496 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.420-616C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102496 | |||||||
| chr7:152102535 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(66): Show |
71 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(68): Show |
intron_variant | MODIFIER | c.420-577C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102535 | |||||||
| chr7:152102555 | T | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.420-557T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102555 | |||||||
| chr7:152102632 | C | T | 1 | a0001c0001t0001g0182 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.420-480C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102632 | |||||||
| chr7:152102874 | G | T | 1 | a0001c0001t0002g0063 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.420-238G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102874 | |||||||
| chr7:152102929 | C | T | 1 | a0002c0003t0003g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.420-183C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102929 | |||||||
| chr7:152102935 | A | C | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.420-177A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102935 | |||||||
| chr7:152102968 | C | T | 60 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(57): Show |
61 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.420-144C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152102968 | |||||||
| chr7:152102981 | CA | C | 69 | a0001c0001t0001g0159 a0001c0001t0001g0193 a0001c0001t0002g0002 others(66): Show |
70 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(67): Show |
intron_variant | MODIFIER | c.420-116delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 152102981 | ||||||
| chr7:152102981 | CAA | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.420-117_420-116del others(2): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr7 | 152102981 | ||||||
| chr7:152103000 | A | G | 74 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(71): Show |
76 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.420-112A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152103000 | |||||||
| chr7:152103067 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.420-45C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 3/11 | chr7 | 152103067 | |||||||
| chr7:152103368 | G | A | 11 | a0001c0001t0001g0196 a0001c0001t0003g0043 a0001c0001t0003g0044 others(8): Show |
11 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.586+90G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152103368 | |||||||
| chr7:152103448 | C | T | 2 | a0001c0001t0001g0100 a0001c0001t0001g0183 |
2 | HG00280.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.586+170C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152103448 | |||||||
| chr7:152103518 | C | T | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+240C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152103518 | |||||||
| chr7:152103568 | C | T | 97 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(94): Show |
99 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(96): Show |
intron_variant | MODIFIER | c.586+290C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152103568 | |||||||
| chr7:152103637 | A | G | 1 | a0001c0001t0001g0168 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.586+359A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152103637 | |||||||
| chr7:152103795 | G | A | 5 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.586+517G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152103795 | |||||||
| chr7:152103862 | G | A | 1 | a0001c0001t0002g0072 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.586+584G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152103862 | |||||||
| chr7:152103915 | A | T | 10 | a0001c0001t0003g0043 a0001c0001t0003g0044 a0002c0003t0003g0006 others(7): Show |
10 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.586+637A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152103915 | |||||||
| chr7:152103957 | A | C | 1 | a0001c0001t0001g0236 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.586+679A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152103957 | |||||||
| chr7:152104021 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.586+743C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152104021 | |||||||
| chr7:152104029 | A | G | 1 | a0001c0008t0002g0094 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.586+751A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152104029 | |||||||
| chr7:152104039 | C | T | 2 | a0001c0001t0002g0053 a0001c0001t0002g0054 |
2 | NA18522.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.586+761C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152104039 | |||||||
| chr7:152104323 | C | T | 1 | a0001c0001t0001g0104 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.587-922C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152104323 | |||||||
| chr7:152104360 | G | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.587-885G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152104360 | |||||||
| chr7:152104653 | G | A | 11 | a0001c0001t0002g0082 a0001c0001t0003g0038 a0001c0001t0003g0039 others(8): Show |
11 | HG02055.hp1 HG02486.hp2 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.587-592G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152104653 | |||||||
| chr7:152104975 | C | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.587-270C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152104975 | |||||||
| chr7:152105067 | T | C | 5 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.587-178T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 4/11 | chr7 | 152105067 | |||||||
| chr7:152105534 | G | A | 1 | a0001c0001t0002g0046 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.712+164G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152105534 | |||||||
| chr7:152105622 | C | G | 2 | a0001c0004t0002g0071 a0001c0004t0002g0073 |
2 | NA19004.hp2 NA19068.hp1 |
intron_variant | MODIFIER | c.712+252C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152105622 | |||||||
| chr7:152105887 | C | T | 60 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(57): Show |
62 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.712+517C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152105887 | |||||||
| chr7:152105888 | T | C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG00280.hp2 HG01978.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.712+518T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152105888 | |||||||
| chr7:152105912 | C | T | 70 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(67): Show |
72 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.712+542C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152105912 | |||||||
| chr7:152106005 | GGTTA | G | 46 | a0001c0001t0001g0016 a0001c0001t0001g0101 a0001c0001t0001g0113 others(43): Show |
46 | HG00099.hp2 HG00140.hp1 HG00544.hp1 others(43): Show |
intron_variant | MODIFIER | c.712+638_712+641del others(4): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 152106005 | ||||||
| chr7:152106244 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0201 a0001c0001t0001g0203 others(4): Show |
8 | HG00558.hp1 HG02523.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+874C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152106244 | |||||||
| chr7:152106259 | T | C | 1 | a0001c0001t0010g0202 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.712+889T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152106259 | |||||||
| chr7:152106336 | C | G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.712+966C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152106336 | |||||||
| chr7:152106482 | T | C | 78 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(75): Show |
80 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(77): Show |
intron_variant | MODIFIER | c.712+1112T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152106482 | |||||||
| chr7:152106582 | A | T | 1 | a0001c0001t0014g0272 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.712+1212A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152106582 | |||||||
| chr7:152106667 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.712+1297G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152106667 | |||||||
| chr7:152106699 | A | G | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.712+1329A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152106699 | |||||||
| chr7:152106762 | C | A | 96 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0045 others(93): Show |
98 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(95): Show |
intron_variant | MODIFIER | c.713-1276C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152106762 | |||||||
| chr7:152106878 | C | G | 3 | a0001c0001t0001g0102 a0001c0001t0001g0230 a0001c0001t0001g0232 |
3 | HG00639.hp1 HG01106.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.713-1160C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152106878 | |||||||
| chr7:152107027 | G | A | 49 | a0001c0001t0001g0197 a0001c0001t0002g0002 a0001c0001t0002g0045 others(46): Show |
50 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(47): Show |
intron_variant | MODIFIER | c.713-1011G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107027 | |||||||
| chr7:152107222 | G | A | 1 | a0001c0001t0002g0056 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.713-816G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107222 | |||||||
| chr7:152107224 | G | GGAGCTCT others(33): Show |
1 | a0001c0001t0001g0171 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.713-813_713-774dup others(40): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 152107224 | ||||||
| chr7:152107246 | TA | T | 98 | a0001c0001t0001g0197 a0001c0001t0001g0205 a0001c0001t0002g0002 others(95): Show |
100 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.713-778delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 152107246 | ||||||
| chr7:152107293 | TTAAAATG others(5): Show |
T | 2 | a0001c0001t0001g0194 a0001c0001t0001g0195 |
2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.713-737_713-726del others(12): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr7 | 152107293 | ||||||
| chr7:152107527 | A | G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0170 a0001c0001t0001g0173 others(4): Show |
7 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.713-511A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107527 | |||||||
| chr7:152107740 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.713-298G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107740 | |||||||
| chr7:152107786 | T | G | 1 | a0005c0009t0001g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.713-252T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107786 | |||||||
| chr7:152107797 | C | T | 5 | a0001c0001t0001g0015 a0001c0001t0001g0170 a0001c0001t0001g0174 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.713-241C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107797 | |||||||
| chr7:152107798 | G | A | 5 | a0001c0001t0001g0136 a0001c0001t0001g0137 a0001c0001t0001g0171 others(2): Show |
5 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.713-240G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107798 | |||||||
| chr7:152107853 | A | G | 3 | a0001c0001t0001g0156 a0001c0001t0001g0157 a0001c0001t0001g0158 |
3 | HG00621.hp2 HG00673.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.713-185A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107853 | |||||||
| chr7:152107866 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.713-172C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107866 | |||||||
| chr7:152107883 | G | A | 1 | a0001c0001t0001g0016 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.713-155G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107883 | |||||||
| chr7:152107938 | G | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.713-100G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 5/11 | chr7 | 152107938 | |||||||
| chr7:152108334 | A | G | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.962+47A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152108334 | |||||||
| chr7:152108427 | G | T | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | NA18981.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.962+140G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152108427 | |||||||
| chr7:152108572 | G | A | 70 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(67): Show |
72 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(69): Show |
intron_variant | MODIFIER | c.962+285G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152108572 | |||||||
| chr7:152109007 | G | GTTA | 71 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(68): Show |
73 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(70): Show |
intron_variant | MODIFIER | c.962+722_962+723ins others(3): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr7 | 152109007 | ||||||
| chr7:152109120 | T | G | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.962+833T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152109120 | |||||||
| chr7:152109296 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.962+1009A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152109296 | |||||||
| chr7:152109297 | A | G | 98 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(95): Show |
100 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.962+1010A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152109297 | |||||||
| chr7:152109528 | C | T | 2 | a0001c0001t0001g0198 a0001c0001t0001g0199 |
2 | HG03669.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.963-1000C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152109528 | |||||||
| chr7:152109593 | C | A | 5 | a0001c0001t0001g0221 a0001c0001t0001g0222 a0001c0001t0001g0223 others(2): Show |
5 | HG00597.hp1 HG02056.hp1 NA18947.hp2 others(2): Show |
intron_variant | MODIFIER | c.963-935C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152109593 | |||||||
| chr7:152109626 | C | G | 1 | a0001c0001t0001g0236 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.963-902C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152109626 | |||||||
| chr7:152109809 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.963-719C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152109809 | |||||||
| chr7:152109886 | G | T | 8 | a0001c0001t0003g0017 a0001c0001t0003g0027 a0001c0001t0003g0030 others(5): Show |
8 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.963-642G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152109886 | |||||||
| chr7:152110267 | T | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.963-261T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152110267 | |||||||
| chr7:152110404 | A | G | 4 | a0001c0001t0001g0163 a0001c0001t0001g0246 a0001c0001t0001g0250 others(1): Show |
4 | HG00408.hp1 HG00438.hp1 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.963-124A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 6/11 | chr7 | 152110404 | |||||||
| chr7:152110738 | A | AT | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1080+102dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152110738 | ||||||
| chr7:152110738 | A | T | 2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+93A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152110738 | |||||||
| chr7:152110751 | G | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1080+106G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152110751 | |||||||
| chr7:152110791 | C | T | 4 | a0001c0001t0001g0169 a0001c0001t0003g0005 a0001c0001t0003g0014 others(1): Show |
4 | HG02809.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+146C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152110791 | |||||||
| chr7:152110902 | G | A | 5 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1080+257G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152110902 | |||||||
| chr7:152110913 | C | G | 98 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(95): Show |
100 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.1080+268C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152110913 | |||||||
| chr7:152110922 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1080+277A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152110922 | |||||||
| chr7:152110969 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1080+324G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152110969 | |||||||
| chr7:152110973 | C | G | 2 | a0001c0001t0009g0129 a0001c0001t0009g0130 |
2 | NA18963.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.1080+328C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152110973 | |||||||
| chr7:152110974 | G | A | 50 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(47): Show |
51 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1080+329G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152110974 | |||||||
| chr7:152111151 | T | C | 2 | a0001c0001t0001g0128 a0001c0001t0001g0185 |
2 | HG00099.hp2 HG01175.hp1 |
intron_variant | MODIFIER | c.1080+506T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111151 | |||||||
| chr7:152111354 | T | C | 7 | a0001c0001t0004g0032 a0001c0001t0004g0033 a0001c0001t0004g0034 others(4): Show |
7 | HG02486.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.1080+709T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111354 | |||||||
| chr7:152111407 | A | G | 98 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(95): Show |
100 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.1080+762A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111407 | |||||||
| chr7:152111543 | G | A | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1080+898G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111543 | |||||||
| chr7:152111565 | T | C | 94 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(91): Show |
96 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.1080+920T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111565 | |||||||
| chr7:152111576 | T | C | 94 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(91): Show |
96 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(93): Show |
intron_variant | MODIFIER | c.1080+931T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111576 | |||||||
| chr7:152111628 | G | A | 3 | a0001c0001t0001g0109 a0001c0001t0001g0110 a0001c0001t0003g0005 |
3 | HG02965.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1080+983G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111628 | |||||||
| chr7:152111628 | G | GTATATA | 3 | a0001c0001t0003g0001 a0001c0001t0003g0025 a0001c0001t0003g0026 |
4 | HG01243.hp1 HG02451.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+995_1080+1000 others(9): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152111628 | ||||||
| chr7:152111628 | G | GTGTA | 8 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1080+984_1080+985i others(6): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152111628 | ||||||
| chr7:152111628 | G | GTGTATAT others(3): Show |
2 | a0001c0001t0003g0043 a0001c0001t0003g0044 |
2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1080+984_1080+985i others(12): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152111628 | ||||||
| chr7:152111630 | A | G | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1080+985A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111630 | |||||||
| chr7:152111641 | TA | T | 5 | a0001c0001t0002g0053 a0001c0001t0002g0054 a0001c0001t0002g0082 others(2): Show |
5 | HG02647.hp1 HG02886.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.1080+997delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111641 | |||||||
| chr7:152111643 | TA | T | 46 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(43): Show |
47 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(44): Show |
intron_variant | MODIFIER | c.1080+999delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111643 | |||||||
| chr7:152111644 | A | AT | 20 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(17): Show |
20 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1080+1006dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152111644 | ||||||
| chr7:152111644 | A | ATATATAT others(1): Show |
3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0003g0024 |
3 | HG01891.hp1 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1080+1000_1080+100 others(12): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152111644 | ||||||
| chr7:152111644 | A | T | 33 | a0001c0001t0001g0015 a0001c0001t0001g0108 a0001c0001t0001g0175 others(30): Show |
33 | HG00597.hp1 HG01192.hp2 HG01981.hp2 others(30): Show |
intron_variant | MODIFIER | c.1080+999A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111644 | |||||||
| chr7:152111646 | T | A | 11 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0002c0003t0003g0006 others(8): Show |
11 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(8): Show |
intron_variant | MODIFIER | c.1080+1001T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111646 | |||||||
| chr7:152111652 | A | T | 98 | a0001c0001t0001g0037 a0001c0001t0002g0002 a0001c0001t0002g0045 others(95): Show |
100 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(97): Show |
intron_variant | MODIFIER | c.1080+1007A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111652 | |||||||
| chr7:152111805 | A | C | 3 | a0001c0001t0001g0241 a0001c0001t0001g0247 a0001c0001t0001g0248 |
3 | HG00544.hp2 HG02074.hp2 HG02155.hp1 |
intron_variant | MODIFIER | c.1080+1160A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111805 | |||||||
| chr7:152111831 | C | G | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1080+1186C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152111831 | |||||||
| chr7:152112000 | TA | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0246 a0001c0001t0001g0250 |
3 | HG00408.hp1 HG00438.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.1081-1244delA | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152112000 | ||||||
| chr7:152112086 | CGAG | C | 71 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0102 others(68): Show |
72 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1081-1158_1081-115 others(7): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr7 | 152112086 | ||||||
| chr7:152112455 | C | T | 50 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(47): Show |
51 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(48): Show |
intron_variant | MODIFIER | c.1081-791C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152112455 | |||||||
| chr7:152112571 | T | C | 1 | a0001c0001t0002g0060 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.1081-675T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152112571 | |||||||
| chr7:152112604 | G | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1081-642G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152112604 | |||||||
| chr7:152112694 | C | T | 4 | a0001c0001t0005g0258 a0001c0001t0005g0259 a0004c0005t0005g0256 others(1): Show |
4 | HG02895.hp1 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1081-552C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152112694 | |||||||
| chr7:152112935 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG02027.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1081-311G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152112935 | |||||||
| chr7:152112960 | T | C | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1081-286T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152112960 | |||||||
| chr7:152113191 | T | C | 2 | a0001c0001t0002g0084 a0001c0001t0002g0085 |
2 | NA18981.hp2 NA19064.hp2 |
intron_variant | MODIFIER | c.1081-55T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 7/11 | chr7 | 152113191 | |||||||
| chr7:152113630 | G | A | 28 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0014 others(25): Show |
29 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.1233+232G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152113630 | |||||||
| chr7:152113671 | C | T | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1233+273C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152113671 | |||||||
| chr7:152113681 | CTCTATTG others(31): Show |
C | 2 | a0001c0001t0005g0258 a0001c0001t0005g0259 |
2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1233+285_1233+322d others(40): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113681 | ||||||
| chr7:152113681 | CTCTATTG others(33): Show |
C | 1 | a0004c0005t0005g0257 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1233+285_1233+324d others(42): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113681 | ||||||
| chr7:152113681 | CTCTATTG others(34): Show |
C | 1 | a0004c0005t0005g0256 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1233+285_1233+325d others(43): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113681 | ||||||
| chr7:152113693 | G | A | 1 | a0001c0001t0002g0067 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.1233+295G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152113693 | |||||||
| chr7:152113711 | T | G | 1 | a0003c0002t0001g0243 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1233+313T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152113711 | |||||||
| chr7:152113712 | C | CTTTTTTT others(4): Show |
1 | a0005c0009t0001g0178 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1233+346_1233+356d others(13): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0136 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1233+345_1233+356d others(14): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0001g0208 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1233+343_1233+356d others(16): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | C | CTTTTTTT others(10): Show |
1 | a0001c0001t0001g0177 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1233+340_1233+356d others(19): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | C | CTTTTTTT others(11): Show |
1 | a0001c0001t0001g0225 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1233+339_1233+356d others(20): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | C | CTTTTTTT others(19): Show |
1 | a0001c0001t0001g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1233+331_1233+356d others(28): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTT | C | 9 | a0001c0001t0001g0101 a0001c0001t0001g0104 a0001c0001t0001g0106 others(6): Show |
9 | HG01261.hp1 HG02040.hp1 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.1233+352_1233+356d others(7): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTT | C | 6 | a0001c0001t0001g0138 a0001c0001t0001g0143 a0001c0001t0001g0151 others(3): Show |
6 | HG01358.hp2 HG02135.hp2 HG03669.hp2 others(3): Show |
intron_variant | MODIFIER | c.1233+351_1233+356d others(8): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0135 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1233+347_1233+356d others(12): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0118 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1233+346_1233+356d others(13): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0098 a0001c0001t0001g0170 a0001c0001t0001g0174 |
3 | HG02145.hp2 HG02559.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1233+345_1233+356d others(14): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(6): Show |
C | 8 | a0001c0001t0001g0015 a0001c0001t0001g0097 a0001c0001t0001g0116 others(5): Show |
8 | HG02071.hp1 HG02622.hp2 HG03041.hp2 others(5): Show |
intron_variant | MODIFIER | c.1233+344_1233+356d others(15): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(7): Show |
C | 12 | a0001c0001t0001g0126 a0001c0001t0001g0187 a0001c0001t0003g0043 others(9): Show |
12 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1233+343_1233+356d others(16): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(8): Show |
C | 5 | a0001c0001t0001g0127 a0001c0001t0001g0253 a0001c0001t0002g0180 others(2): Show |
5 | HG00280.hp1 HG01109.hp1 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.1233+342_1233+356d others(17): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(9): Show |
C | 3 | a0001c0001t0001g0100 a0001c0001t0001g0182 a0001c0001t0001g0183 |
3 | HG00280.hp2 HG01978.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1233+341_1233+356d others(18): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(10): Show |
C | 5 | a0001c0001t0001g0131 a0001c0001t0001g0140 a0001c0001t0001g0220 others(2): Show |
5 | HG01192.hp1 HG01928.hp1 HG01975.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+340_1233+356d others(19): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(11): Show |
C | 2 | a0001c0001t0001g0133 a0001c0001t0003g0018 |
2 | HG01978.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.1233+339_1233+356d others(20): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(12): Show |
C | 5 | a0001c0001t0001g0172 a0001c0001t0001g0252 a0001c0001t0003g0019 others(2): Show |
5 | HG01167.hp1 HG01167.hp2 HG02071.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+338_1233+356d others(21): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(13): Show |
C | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1233+337_1233+356d others(22): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(14): Show |
C | 1 | a0001c0001t0002g0078 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1233+336_1233+356d others(23): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(19): Show |
C | 12 | a0001c0001t0001g0037 a0001c0001t0003g0022 a0001c0001t0003g0038 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1233+331_1233+356d others(28): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(20): Show |
C | 17 | a0001c0001t0003g0001 a0001c0001t0003g0005 a0001c0001t0003g0014 others(14): Show |
18 | HG01243.hp1 HG01361.hp2 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.1233+330_1233+356d others(29): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(21): Show |
C | 3 | a0001c0001t0001g0179 a0001c0001t0001g0200 a0001c0001t0001g0216 |
3 | HG01074.hp1 HG01346.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.1233+329_1233+356d others(30): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(22): Show |
C | 78 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0102 others(75): Show |
79 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.1233+328_1233+356d others(31): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113712 | CTTTTTTT others(23): Show |
C | 1 | a0001c0001t0001g0204 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1233+327_1233+356d others(32): Show |
GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113712 | ||||||
| chr7:152113782 | G | A | 1 | a0001c0001t0001g0150 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1233+384G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152113782 | |||||||
| chr7:152113790 | G | A | 1 | a0001c0001t0002g0079 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1233+392G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152113790 | |||||||
| chr7:152113919 | GT | G | 142 | a0001c0001t0001g0016 a0001c0001t0001g0037 a0001c0001t0001g0101 others(139): Show |
144 | HG00099.hp2 HG00140.hp1 HG00438.hp2 others(141): Show |
intron_variant | MODIFIER | c.1233+532delT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152113919 | ||||||
| chr7:152113927 | T | G | 2 | a0001c0001t0003g0014 a0001c0001t0003g0281 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1233+529T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152113927 | |||||||
| chr7:152113978 | G | T | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1233+580G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152113978 | |||||||
| chr7:152114364 | A | T | 12 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0003g0043 others(9): Show |
12 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.1233+966A>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152114364 | |||||||
| chr7:152114392 | A | G | 5 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(2): Show |
5 | HG02572.hp1 HG02615.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.1233+994A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152114392 | |||||||
| chr7:152114405 | T | G | 18 | a0001c0001t0003g0017 a0001c0001t0003g0027 a0001c0001t0003g0030 others(15): Show |
18 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.1233+1007T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152114405 | |||||||
| chr7:152114464 | G | A | 48 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(45): Show |
49 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(46): Show |
intron_variant | MODIFIER | c.1233+1066G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152114464 | |||||||
| chr7:152114562 | C | CT | 8 | a0001c0001t0001g0141 a0001c0001t0003g0001 a0001c0001t0003g0021 others(5): Show |
9 | HG01109.hp2 HG01243.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.1233+1179dupT | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr7 | 152114562 | ||||||
| chr7:152114622 | G | A | 1 | a0001c0001t0001g0135 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1233+1224G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152114622 | |||||||
| chr7:152114807 | G | A | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1233+1409G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152114807 | |||||||
| chr7:152115273 | G | C | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1233+1875G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152115273 | |||||||
| chr7:152115732 | C | T | 2 | a0001c0001t0003g0275 a0001c0001t0003g0276 |
2 | HG03209.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.1234-1425C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152115732 | |||||||
| chr7:152115784 | C | T | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1234-1373C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152115784 | |||||||
| chr7:152115816 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1234-1341C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152115816 | |||||||
| chr7:152115845 | T | A | 1 | a0001c0001t0001g0207 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1234-1312T>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152115845 | |||||||
| chr7:152115913 | G | A | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1234-1244G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152115913 | |||||||
| chr7:152115928 | T | C | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1234-1229T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152115928 | |||||||
| chr7:152116011 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1234-1146G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116011 | |||||||
| chr7:152116023 | T | G | 34 | a0001c0001t0001g0016 a0001c0001t0001g0097 a0001c0001t0001g0098 others(31): Show |
34 | HG00544.hp1 HG01109.hp2 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.1234-1134T>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116023 | |||||||
| chr7:152116111 | A | G | 2 | a0001c0001t0001g0208 a0001c0001t0001g0225 |
2 | NA18942.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.1234-1046A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116111 | |||||||
| chr7:152116180 | C | A | 1 | a0001c0001t0001g0101 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1234-977C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116180 | |||||||
| chr7:152116197 | C | T | 1 | a0001c0001t0001g0261 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1234-960C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116197 | |||||||
| chr7:152116218 | G | A | 1 | a0002c0003t0003g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1234-939G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116218 | |||||||
| chr7:152116238 | T | C | 45 | a0001c0001t0002g0045 a0001c0001t0002g0046 a0001c0001t0002g0047 others(42): Show |
45 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(42): Show |
intron_variant | MODIFIER | c.1234-919T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116238 | |||||||
| chr7:152116286 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1234-871T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116286 | |||||||
| chr7:152116313 | C | T | 3 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0040 |
3 | HG02055.hp1 HG02965.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1234-844C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116313 | |||||||
| chr7:152116317 | C | G | 2 | a0001c0001t0002g0180 a0001c0001t0002g0181 |
2 | HG03471.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1234-840C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116317 | |||||||
| chr7:152116322 | T | C | 1 | a0001c0001t0014g0272 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.1234-835T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116322 | |||||||
| chr7:152116385 | C | T | 2 | a0001c0001t0001g0190 a0001c0001t0001g0192 |
2 | HG00140.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.1234-772C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116385 | |||||||
| chr7:152116391 | C | A | 8 | a0002c0003t0003g0006 a0002c0003t0003g0007 a0002c0003t0003g0008 others(5): Show |
8 | HG00639.hp2 HG00735.hp2 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.1234-766C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116391 | |||||||
| chr7:152116428 | C | G | 21 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0017 others(18): Show |
21 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1234-729C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116428 | |||||||
| chr7:152116768 | A | G | 7 | a0001c0001t0003g0001 a0001c0001t0003g0021 a0001c0001t0003g0022 others(4): Show |
8 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.1234-389A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116768 | |||||||
| chr7:152116959 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1234-198C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116959 | |||||||
| chr7:152116976 | G | A | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1234-181G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116976 | |||||||
| chr7:152116990 | C | T | 1 | a0001c0001t0010g0202 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1234-167C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 8/11 | chr7 | 152116990 | |||||||
| chr7:152117611 | G | A | 1 | a0001c0001t0003g0042 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1452+236G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 9/11 | chr7 | 152117611 | |||||||
| chr7:152117679 | G | T | 10 | a0001c0001t0001g0177 a0001c0001t0001g0184 a0001c0001t0001g0187 others(7): Show |
10 | HG00140.hp1 HG01106.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.1452+304G>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 9/11 | chr7 | 152117679 | |||||||
| chr7:152117803 | G | A | 4 | a0001c0001t0003g0021 a0001c0001t0003g0022 a0001c0001t0003g0023 others(1): Show |
4 | HG01891.hp1 HG03471.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.1452+428G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 9/11 | chr7 | 152117803 | |||||||
| chr7:152117850 | T | C | 1 | a0002c0003t0003g0011 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1452+475T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 9/11 | chr7 | 152117850 | |||||||
| chr7:152118179 | A | C | 10 | a0001c0001t0003g0001 a0001c0001t0003g0018 a0001c0001t0003g0019 others(7): Show |
11 | HG01243.hp1 HG01891.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.1453-499A>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 9/11 | chr7 | 152118179 | |||||||
| chr7:152118809 | C | T | 1 | a0001c0001t0002g0051 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1557+27C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152118809 | |||||||
| chr7:152119068 | AC | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG02572.hp1 HG02615.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1557+287delC | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152119068 | |||||||
| chr7:152119109 | G | A | 4 | a0001c0001t0003g0027 a0001c0001t0003g0031 a0001c0001t0003g0041 others(1): Show |
4 | HG01884.hp1 HG02809.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1557+327G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152119109 | |||||||
| chr7:152119117 | G | C | 19 | a0001c0001t0001g0037 a0001c0001t0003g0017 a0001c0001t0003g0027 others(16): Show |
19 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.1557+335G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152119117 | |||||||
| chr7:152119558 | G | A | 2 | a0001c0001t0003g0014 a0001c0001t0003g0281 |
2 | HG02818.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1557+776G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152119558 | |||||||
| chr7:152119704 | C | A | 1 | a0001c0001t0001g0237 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1557+922C>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152119704 | |||||||
| chr7:152119862 | A | G | 22 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(19): Show |
22 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1558-969A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152119862 | |||||||
| chr7:152119952 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.1558-879C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152119952 | |||||||
| chr7:152120004 | G | C | 1 | a0001c0001t0001g0244 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1558-827G>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152120004 | |||||||
| chr7:152120223 | C | G | 22 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(19): Show |
22 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1558-608C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152120223 | |||||||
| chr7:152120452 | G | A | 3 | a0001c0001t0003g0005 a0001c0001t0003g0014 a0001c0001t0003g0281 |
3 | HG02818.hp1 HG02965.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1558-379G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152120452 | |||||||
| chr7:152120498 | G | A | 1 | a0001c0001t0007g0125 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1558-333G>A | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152120498 | |||||||
| chr7:152120504 | C | T | 1 | a0001c0001t0001g0135 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1558-327C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152120504 | |||||||
| chr7:152120508 | C | T | 2 | a0001c0001t0002g0056 a0001c0001t0002g0072 |
2 | HG02027.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1558-323C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152120508 | |||||||
| chr7:152120587 | A | G | 1 | a0002c0003t0003g0007 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1558-244A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 10/11 | chr7 | 152120587 | |||||||
| chr7:152121028 | A | G | 22 | a0001c0001t0001g0037 a0001c0001t0003g0005 a0001c0001t0003g0014 others(19): Show |
22 | HG01361.hp2 HG01884.hp1 HG01891.hp2 others(19): Show |
intron_variant | MODIFIER | c.1695+60A>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 11/11 | chr7 | 152121028 | |||||||
| chr7:152121092 | C | G | 1 | a0001c0001t0003g0041 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1695+124C>G | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 11/11 | chr7 | 152121092 | |||||||
| chr7:152121141 | C | T | 1 | a0001c0001t0003g0005 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1695+173C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 11/11 | chr7 | 152121141 | |||||||
| chr7:152121150 | C | T | 21 | a0001c0001t0001g0016 a0001c0001t0001g0101 a0001c0001t0001g0121 others(18): Show |
21 | HG00544.hp1 HG01358.hp1 HG01928.hp1 others(18): Show |
intron_variant | MODIFIER | c.1695+182C>T | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 11/11 | chr7 | 152121150 | |||||||
| chr7:152121385 | T | C | 53 | a0001c0001t0002g0002 a0001c0001t0002g0045 a0001c0001t0002g0046 others(50): Show |
54 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(51): Show |
intron_variant | MODIFIER | c.1696-161T>C | GALNT11 | ENSG00000178234.13 | transcript | ENST00000430044.7 | protein_coding | 11/11 | chr7 | 152121385 |