Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55191 |
| ensemblid | ENSG00000172890.13 |
| hgncid | 29832 |
| symbol | NADSYN1 |
| name | NAD synthetase 1 |
| refseq_nuc | NM_018161.5 |
| refseq_prot | NP_060631.2 |
| ensembl_nuc | ENST00000319023.7 |
| ensembl_prot | ENSP00000326424.2 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 71453203 |
| end | 71501816 |
| strand | + |
| ver | v1.2 |
| region | chr11:71453203-71501816 |
| region5000 | chr11:71448203-71506816 |
| regionname0 | NADSYN1_chr11_71453203_71501816 |
| regionname5000 | NADSYN1_chr11_71448203_71506816 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/0 | 706 | 183 | 34 | 33 | 86 | 6 | 23 | 64 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0002 | 0/0 | 706 | 114 | 22 | 29 | 51 | 5 | 7 | 37 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0003 | 0/0 | 706 | 37 | 12 | 2 | 16 | 1 | 6 | 14 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0004 | 0/0 | 706 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0005 | 0/0 | 706 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0006 | 0/0 | 706 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0007 | 0/0 | 706 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0008 | 0/0 | 706 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0009 | 0/0 | 706 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0010 | 0/0 | 706 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0011 | 0/0 | 706 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0012 | 0/0 | 706 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| a0013 | 0/1 | 706 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | MGRKV others(701): Show |
chr11 | 71448203 | 71506816 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2118 | 104 | 13 | 13 | 63 | 5 | 10 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0001c0003 | 1/0 | 2118 | 67 | 11 | 19 | 23 | 1 | 12 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0001c0006 | 0/0 | 2118 | 8 | 7 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0001c0012 | 0/0 | 2118 | 2 | 1 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0001c0023 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0001c0024 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0002c0002 | 0/0 | 2118 | 99 | 9 | 28 | 50 | 5 | 7 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0002c0005 | 0/0 | 2118 | 10 | 10 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0002c0015 | 0/0 | 2118 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0002c0016 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0002c0018 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0002c0019 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0002c0020 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0003c0004 | 0/0 | 2118 | 34 | 9 | 2 | 16 | 1 | 6 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0003c0009 | 0/0 | 2118 | 3 | 3 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0004c0007 | 0/0 | 2118 | 5 | 5 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0005c0008 | 0/0 | 2118 | 3 | 3 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0006c0010 | 0/0 | 2118 | 3 | 3 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0007c0011 | 0/0 | 2118 | 2 | 2 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0008c0013 | 0/0 | 2118 | 2 | 0 | 0 | 0 | 0 | 2 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0009c0022 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0010c0017 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0011c0014 | 0/0 | 2118 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0012c0025 | 0/0 | 2118 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 | ||
| a0013c0021 | 0/1 | 2118 | 1 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | ATGGG others(2113): Show |
chr11 | 71448203 | 71506816 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 2679 | 104 | 13 | 13 | 63 | 5 | 10 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0001c0003t0001 | 1/0 | 2679 | 67 | 11 | 19 | 23 | 1 | 12 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0001c0006t0001 | 0/0 | 2679 | 8 | 7 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0001c0012t0001 | 0/0 | 2679 | 2 | 1 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0001c0023t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0001c0024t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0002c0002t0001 | 0/0 | 2679 | 98 | 9 | 27 | 50 | 5 | 7 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0002c0002t0005 | 0/0 | 2679 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0002c0005t0001 | 0/0 | 2679 | 8 | 8 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0002c0005t0004 | 0/0 | 2562 | 2 | 2 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2557): Show |
chr11 | 71448203 | 71506816 |
| a0002c0015t0001 | 0/0 | 2679 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0002c0016t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0002c0018t0001 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0002c0019t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0002c0020t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0003c0004t0001 | 0/0 | 2679 | 23 | 9 | 2 | 6 | 1 | 5 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0003c0004t0002 | 0/0 | 2679 | 11 | 0 | 0 | 10 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0003c0009t0001 | 0/0 | 2679 | 3 | 3 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0004c0007t0001 | 0/0 | 2679 | 5 | 5 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0005c0008t0001 | 0/0 | 2679 | 3 | 3 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0006c0010t0003 | 0/0 | 2679 | 3 | 3 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0007c0011t0001 | 0/0 | 2679 | 2 | 2 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0008c0013t0001 | 0/0 | 2679 | 2 | 0 | 0 | 0 | 0 | 2 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0009c0022t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0010c0017t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0011c0014t0001 | 0/0 | 2679 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0012c0025t0001 | 0/0 | 2679 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| a0013c0021t0001 | 0/1 | 2679 | 1 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | AACCC others(2674): Show |
chr11 | 71448203 | 71506816 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0003 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 2 | 3 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0012 | 0/0 | 3 | 0 | 2 | 0 | 1 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0041 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0043 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0001 | 0/0 | 17 | 3 | 4 | 3 | 1 | 6 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0029 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0031 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0003t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0006t0001g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0006t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0006t0001g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0006t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0006t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0012t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0012t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0023t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0001c0024t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0002 | 0/0 | 8 | 0 | 5 | 2 | 1 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0005 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0006 | 0/0 | 5 | 2 | 0 | 1 | 2 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0009 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0025 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0002t0005g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0005t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0005t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0005t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0005t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0005t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0005t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0005t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0005t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0005t0004g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0005t0004g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0015t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0016t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0018t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0019t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0002c0020t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0016 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0018 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0002g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0004t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0009t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0009t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0003c0009t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0004c0007t0001g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0004c0007t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0005c0008t0001g0044 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0005c0008t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0006c0010t0003g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0006c0010t0003g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0006c0010t0003g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0007c0011t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0007c0011t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0008c0013t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0008c0013t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0009c0022t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0010c0017t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0011c0014t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0012c0025t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| a0013c0021t0001g0088 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0002 | t0001 | g0006 | EUR | GBR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00099 | hp2 | a0001 | c0003 | t0001 | g0001 | EUR | GBR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00140 | hp2 | a0002 | c0002 | t0001 | g0083 | EUR | GBR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00280 | hp1 | a0003 | c0004 | t0001 | g0216 | EUR | FIN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0226 | EUR | FIN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00323 | hp1 | a0002 | c0002 | t0001 | g0002 | EUR | FIN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | FIN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00423 | hp2 | a0002 | c0002 | t0001 | g0060 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00438 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00544 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00558 | hp1 | a0002 | c0018 | t0001 | g0081 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00558 | hp2 | a0001 | c0003 | t0001 | g0140 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00609 | hp1 | a0003 | c0004 | t0001 | g0018 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00609 | hp2 | a0002 | c0002 | t0001 | g0006 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00621 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00621 | hp2 | a0002 | c0002 | t0001 | g0045 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00639 | hp1 | a0002 | c0002 | t0001 | g0047 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0200 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00642 | hp1 | a0003 | c0004 | t0001 | g0016 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00642 | hp2 | a0002 | c0002 | t0001 | g0066 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00673 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00733 | hp1 | a0003 | c0004 | t0001 | g0214 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00733 | hp2 | a0001 | c0003 | t0001 | g0134 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00735 | hp1 | a0002 | c0002 | t0001 | g0059 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00735 | hp2 | a0002 | c0002 | t0001 | g0011 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00738 | hp1 | a0001 | c0003 | t0001 | g0115 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00738 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00741 | hp1 | a0002 | c0002 | t0001 | g0064 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG00741 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01069 | hp1 | a0002 | c0002 | t0001 | g0099 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01069 | hp2 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01070 | hp2 | a0002 | c0002 | t0001 | g0067 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0029 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01074 | hp1 | a0002 | c0015 | t0001 | g0009 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01074 | hp2 | a0001 | c0006 | t0001 | g0026 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01081 | hp1 | a0002 | c0002 | t0001 | g0025 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01081 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01106 | hp1 | a0002 | c0002 | t0001 | g0050 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01167 | hp1 | a0001 | c0003 | t0001 | g0143 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01167 | hp2 | a0002 | c0002 | t0001 | g0075 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01192 | hp2 | a0001 | c0003 | t0001 | g0136 | AMR | PUR | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01255 | hp1 | a0002 | c0002 | t0001 | g0095 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01256 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01256 | hp2 | a0001 | c0003 | t0001 | g0126 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01257 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01257 | hp2 | a0002 | c0002 | t0001 | g0093 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01258 | hp1 | a0002 | c0002 | t0001 | g0002 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01258 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01261 | hp1 | a0002 | c0002 | t0001 | g0092 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0124 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01346 | hp2 | a0002 | c0002 | t0001 | g0070 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01361 | hp2 | a0002 | c0002 | t0001 | g0051 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01433 | hp2 | a0001 | c0003 | t0001 | g0001 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01496 | hp1 | a0002 | c0002 | t0001 | g0011 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01496 | hp2 | a0001 | c0003 | t0001 | g0128 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01515 | hp1 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0154 | EUR | IBS | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01884 | hp1 | a0004 | c0007 | t0001 | g0010 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01884 | hp2 | a0003 | c0004 | t0001 | g0017 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01891 | hp1 | a0002 | c0002 | t0001 | g0073 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01891 | hp2 | a0001 | c0006 | t0001 | g0109 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01952 | hp1 | a0001 | c0003 | t0001 | g0139 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01978 | hp1 | a0001 | c0003 | t0001 | g0141 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01978 | hp2 | a0001 | c0003 | t0001 | g0031 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01981 | hp1 | a0002 | c0002 | t0001 | g0098 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01981 | hp2 | a0001 | c0003 | t0001 | g0145 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01993 | hp1 | a0001 | c0003 | t0001 | g0135 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02015 | hp2 | a0002 | c0002 | t0001 | g0076 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02027 | hp1 | a0002 | c0002 | t0001 | g0254 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02027 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02040 | hp1 | a0001 | c0003 | t0001 | g0007 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02040 | hp2 | a0002 | c0002 | t0001 | g0084 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02055 | hp1 | a0003 | c0004 | t0001 | g0218 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0096 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02080 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02083 | hp1 | a0001 | c0003 | t0001 | g0033 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02083 | hp2 | a0002 | c0002 | t0001 | g0069 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02132 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02132 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | KHV | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02145 | hp1 | a0003 | c0009 | t0001 | g0156 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02145 | hp2 | a0001 | c0006 | t0001 | g0026 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02148 | hp1 | a0001 | c0003 | t0001 | g0001 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02148 | hp2 | a0002 | c0002 | t0001 | g0009 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | CDX | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02155 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | CDX | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02258 | hp1 | a0001 | c0006 | t0001 | g0027 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02258 | hp2 | a0002 | c0005 | t0001 | g0238 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02273 | hp1 | a0002 | c0002 | t0001 | g0048 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02273 | hp2 | a0002 | c0002 | t0001 | g0002 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02293 | hp1 | a0002 | c0002 | t0005 | g0002 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02293 | hp2 | a0001 | c0003 | t0001 | g0138 | AMR | PEL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02451 | hp1 | a0005 | c0008 | t0001 | g0044 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02572 | hp1 | a0003 | c0009 | t0001 | g0157 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02572 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02615 | hp2 | a0002 | c0005 | t0004 | g0244 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02622 | hp2 | a0001 | c0024 | t0001 | g0253 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02630 | hp1 | a0006 | c0010 | t0003 | g0105 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02630 | hp2 | a0009 | c0022 | t0001 | g0205 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02683 | hp2 | a0003 | c0004 | t0001 | g0215 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02698 | hp2 | a0001 | c0012 | t0001 | g0121 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02717 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02717 | hp2 | a0001 | c0006 | t0001 | g0028 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02723 | hp1 | a0001 | c0003 | t0001 | g0030 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02723 | hp2 | a0004 | c0007 | t0001 | g0010 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02735 | hp1 | a0003 | c0004 | t0001 | g0016 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02735 | hp2 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02809 | hp1 | a0002 | c0002 | t0001 | g0091 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02809 | hp2 | a0004 | c0007 | t0001 | g0010 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02818 | hp2 | a0003 | c0004 | t0001 | g0107 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02886 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02886 | hp2 | a0003 | c0004 | t0001 | g0206 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0120 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02895 | hp2 | a0007 | c0011 | t0001 | g0249 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02896 | hp2 | a0001 | c0012 | t0001 | g0113 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02897 | hp1 | a0007 | c0011 | t0001 | g0250 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02965 | hp1 | a0006 | c0010 | t0003 | g0106 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02965 | hp2 | a0001 | c0006 | t0001 | g0108 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02970 | hp2 | a0004 | c0007 | t0001 | g0246 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02976 | hp1 | a0002 | c0016 | t0001 | g0077 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02976 | hp2 | a0002 | c0002 | t0001 | g0243 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03017 | hp1 | a0001 | c0003 | t0001 | g0032 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0172 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03041 | hp1 | a0002 | c0020 | t0001 | g0094 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03041 | hp2 | a0002 | c0005 | t0001 | g0247 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03098 | hp1 | a0004 | c0007 | t0001 | g0010 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03130 | hp1 | a0002 | c0005 | t0001 | g0248 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03130 | hp2 | a0001 | c0006 | t0001 | g0027 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03139 | hp1 | a0003 | c0004 | t0001 | g0212 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03139 | hp2 | a0002 | c0002 | t0001 | g0065 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03195 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0189 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0030 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03225 | hp1 | a0005 | c0008 | t0001 | g0044 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03225 | hp2 | a0001 | c0006 | t0001 | g0028 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03239 | hp1 | a0001 | c0003 | t0001 | g0127 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03239 | hp2 | a0002 | c0002 | t0001 | g0101 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03453 | hp1 | a0010 | c0017 | t0001 | g0055 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03453 | hp2 | a0001 | c0003 | t0001 | g0116 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0019 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03490 | hp2 | a0003 | c0004 | t0001 | g0217 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03491 | hp1 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03491 | hp2 | a0001 | c0003 | t0001 | g0131 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03492 | hp2 | a0002 | c0002 | t0001 | g0023 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03516 | hp1 | a0003 | c0009 | t0001 | g0155 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03516 | hp2 | a0002 | c0005 | t0001 | g0240 | AFR | ESN | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03540 | hp1 | a0002 | c0005 | t0004 | g0245 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03540 | hp2 | a0002 | c0002 | t0001 | g0072 | AFR | GWD | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03579 | hp1 | a0003 | c0004 | t0001 | g0162 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03579 | hp2 | a0003 | c0004 | t0001 | g0204 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03654 | hp1 | a0001 | c0003 | t0001 | g0125 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03688 | hp1 | a0003 | c0004 | t0002 | g0207 | SAS | STU | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03688 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | STU | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03704 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03704 | hp2 | a0003 | c0004 | t0001 | g0016 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03710 | hp1 | a0008 | c0013 | t0001 | g0132 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03710 | hp2 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | BEB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0222 | SAS | BEB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03927 | hp1 | a0002 | c0002 | t0001 | g0054 | SAS | BEB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03927 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | BEB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03942 | hp1 | a0008 | c0013 | t0001 | g0118 | SAS | BEB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03942 | hp2 | a0001 | c0003 | t0001 | g0146 | SAS | BEB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG04199 | hp1 | a0001 | c0003 | t0001 | g0001 | SAS | STU | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG04199 | hp2 | a0003 | c0004 | t0001 | g0233 | SAS | STU | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0178 | SAS | STU | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG04204 | hp2 | a0001 | c0003 | t0001 | g0032 | SAS | STU | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG04228 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | STU | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18612 | hp1 | a0003 | c0004 | t0001 | g0234 | EAS | CHB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18612 | hp2 | a0002 | c0002 | t0001 | g0079 | EAS | CHB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0043 | EAS | CHB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18747 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | CHB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18906 | hp1 | a0002 | c0005 | t0001 | g0239 | AFR | YRI | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18906 | hp2 | a0001 | c0023 | t0001 | g0117 | AFR | YRI | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18941 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18941 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18942 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18944 | hp2 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18945 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18946 | hp2 | a0002 | c0002 | t0001 | g0087 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18947 | hp2 | a0002 | c0002 | t0001 | g0002 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18949 | hp2 | a0002 | c0002 | t0001 | g0009 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18950 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18950 | hp2 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18954 | hp2 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18956 | hp1 | a0001 | c0003 | t0001 | g0031 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18956 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18957 | hp2 | a0002 | c0002 | t0001 | g0063 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18959 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18959 | hp2 | a0003 | c0004 | t0002 | g0202 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18960 | hp1 | a0002 | c0002 | t0001 | g0052 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18962 | hp1 | a0011 | c0014 | t0001 | g0089 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18963 | hp1 | a0001 | c0003 | t0001 | g0142 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18965 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18967 | hp1 | a0003 | c0004 | t0001 | g0211 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18970 | hp1 | a0001 | c0003 | t0001 | g0013 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18970 | hp2 | a0003 | c0004 | t0001 | g0018 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18971 | hp1 | a0002 | c0002 | t0001 | g0046 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18972 | hp2 | a0003 | c0004 | t0001 | g0235 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18973 | hp1 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18973 | hp2 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18974 | hp1 | a0001 | c0003 | t0001 | g0122 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18977 | hp1 | a0001 | c0003 | t0001 | g0130 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18977 | hp2 | a0002 | c0002 | t0001 | g0068 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18978 | hp2 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18980 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18980 | hp2 | a0001 | c0003 | t0001 | g0129 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18985 | hp1 | a0002 | c0002 | t0001 | g0097 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18987 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18987 | hp2 | a0003 | c0004 | t0002 | g0209 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18988 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18989 | hp1 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18991 | hp1 | a0003 | c0004 | t0002 | g0177 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18991 | hp2 | a0002 | c0002 | t0001 | g0102 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18992 | hp2 | a0001 | c0003 | t0001 | g0123 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18995 | hp1 | a0002 | c0002 | t0001 | g0058 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18995 | hp2 | a0001 | c0003 | t0001 | g0007 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19001 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19002 | hp1 | a0003 | c0004 | t0002 | g0176 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19004 | hp1 | a0002 | c0002 | t0001 | g0005 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19004 | hp2 | a0003 | c0004 | t0002 | g0015 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19005 | hp1 | a0003 | c0004 | t0001 | g0018 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19007 | hp1 | a0002 | c0002 | t0001 | g0086 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19011 | hp1 | a0003 | c0004 | t0002 | g0213 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19011 | hp2 | a0002 | c0002 | t0001 | g0057 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19043 | hp1 | a0002 | c0005 | t0001 | g0252 | AFR | LWK | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19043 | hp2 | a0003 | c0004 | t0001 | g0017 | AFR | LWK | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19054 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19056 | hp1 | a0003 | c0004 | t0002 | g0210 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19057 | hp1 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19060 | hp1 | a0002 | c0002 | t0001 | g0004 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19060 | hp2 | a0001 | c0003 | t0001 | g0001 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19063 | hp1 | a0002 | c0002 | t0001 | g0049 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19066 | hp1 | a0001 | c0003 | t0001 | g0137 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19066 | hp2 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19070 | hp2 | a0002 | c0002 | t0001 | g0056 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19072 | hp2 | a0001 | c0003 | t0001 | g0119 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19077 | hp1 | a0002 | c0002 | t0001 | g0078 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19079 | hp1 | a0003 | c0004 | t0002 | g0208 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19086 | hp1 | a0002 | c0002 | t0001 | g0100 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19087 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | TSI | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA20752 | hp2 | a0002 | c0002 | t0001 | g0071 | EUR | TSI | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA20905 | hp1 | a0002 | c0002 | t0001 | g0025 | SAS | GIH | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA20905 | hp2 | a0001 | c0003 | t0001 | g0001 | SAS | GIH | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01123 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG01123 | hp2 | a0002 | c0002 | t0001 | g0024 | AMR | CLM | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02109 | hp1 | a0001 | c0003 | t0001 | g0133 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02109 | hp2 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02559 | hp1 | a0006 | c0010 | t0003 | g0104 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03471 | hp1 | a0001 | c0003 | t0001 | g0014 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG03471 | hp2 | a0003 | c0004 | t0001 | g0017 | AFR | MSL | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG06807 | hp1 | a0002 | c0005 | t0001 | g0241 | AFR | USA | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | USA | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18955 | hp1 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA20300 | hp1 | a0005 | c0008 | t0001 | g0242 | AFR | USA | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA20300 | hp2 | a0002 | c0019 | t0001 | g0061 | AFR | USA | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA21309 | hp1 | a0012 | c0025 | t0001 | g0251 | AFR | LWK | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| NA21309 | hp2 | a0002 | c0005 | t0001 | g0237 | AFR | LWK | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| homoSapiens | chm13v2 | a0013 | c0021 | t0001 | g0088 | REF | REF | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| homoSapiens | grch38p0 | a0001 | c0003 | t0001 | g0144 | REF | REF | NADSYN1_chr11_71448203_71506816 | NADSYN1 | chr11 | 71448203 | 71506816 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:71458501 | G | C | 7 | a0002 a0004 a0005 others(4): Show |
129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
missense_variant | MODERATE | c.220G>C | p.Val74Leu | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/21 | 314/2679 | 220/2121 | 74/706 | chr11 | 71458501 | |||
| chr11:71458537 | G | A | 1 | a0007 | 2 | HG02895.hp2 HG02897.hp1 |
missense_variant | MODERATE | c.256G>A | p.Val86Met | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/21 | 350/2679 | 256/2121 | 86/706 | chr11 | 71458537 | |||
| chr11:71473584 | G | A | 1 | a0011 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.564G>A | p.Met188Ile | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 8/21 | 658/2679 | 564/2121 | 188/706 | chr11 | 71473584 | |||
| chr11:71480771 | C | T | 2 | a0003 a0009 |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
missense_variant | MODERATE | c.890C>T | p.Pro297Leu | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 11/21 | 984/2679 | 890/2121 | 297/706 | chr11 | 71480771 | |||
| chr11:71480845 | G | A | 1 | a0009 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.964G>A | p.Glu322Lys | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 11/21 | 1058/2679 | 964/2121 | 322/706 | chr11 | 71480845 | |||
| chr11:71482016 | A | T | 1 | a0006 | 3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
missense_variant | MODERATE | c.1141A>T | p.Arg381Trp | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/21 | 1235/2679 | 1141/2121 | 381/706 | chr11 | 71482016 | |||
| chr11:71482939 | C | G | 1 | a0012 | 1 | NA21309.hp1 | missense_variant | MODERATE | c.1241C>G | p.Thr414Ser | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/21 | 1335/2679 | 1241/2121 | 414/706 | chr11 | 71482939 | |||
| chr11:71484352 | G | A | 1 | a0008 | 2 | HG03710.hp1 HG03942.hp1 |
missense_variant | MODERATE | c.1360G>A | p.Val454Ile | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/21 | 1454/2679 | 1360/2121 | 454/706 | chr11 | 71484352 | |||
| chr11:71497491 | G | A | 1 | a0004 | 5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.1773G>A | p.Met591Ile | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/21 | 1867/2679 | 1773/2121 | 591/706 | chr11 | 71497491 | |||
| chr11:71498352 | G | A | 1 | a0010 | 1 | HG03453.hp1 | missense_variant&splice_region_variant | MODERATE | c.1894G>A | p.Val632Ile | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/21 | 1988/2679 | 1894/2121 | 632/706 | chr11 | 71498352 | |||
| chr11:71501341 | G | A | 1 | a0005 | 3 | HG02451.hp1 HG03225.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.2110G>A | p.Gly704Ser | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 21/21 | 2204/2679 | 2110/2121 | 704/706 | chr11 | 71501341 | |||
| chr11:71501699 | GGAGGGGT others(2970): Show |
G | 1 | a0002 | 2 | HG02615.hp2 HG03540.hp1 |
splice_region_variant | LOW | c.*349_*3325del | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr11 | 71501699 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:71458434 | C | T | 1 | a0006c0010 | 3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
synonymous_variant | LOW | c.153C>T | p.Tyr51Tyr | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/21 | 247/2679 | 153/2121 | 51/706 | chr11 | 71458434 | |||
| chr11:71474397 | C | T | 2 | a0001c0024 a0012c0025 |
2 | HG02622.hp2 NA21309.hp1 |
splice_region_variant&synonymous_variant | LOW | c.669C>T | p.Asn223Asn | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/21 | 763/2679 | 669/2121 | 223/706 | chr11 | 71474397 | |||
| chr11:71474433 | T | C | 21 | a0001c0001 a0001c0006 a0001c0012 others(18): Show |
283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
synonymous_variant | LOW | c.705T>C | p.Cys235Cys | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/21 | 799/2679 | 705/2121 | 235/706 | chr11 | 71474433 | |||
| chr11:71474472 | T | C | 14 | a0001c0001 a0001c0006 a0002c0002 others(11): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
synonymous_variant | LOW | c.744T>C | p.Ile248Ile | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/21 | 838/2679 | 744/2121 | 248/706 | chr11 | 71474472 | |||
| chr11:71478454 | A | G | 1 | a0002c0020 | 1 | HG03041.hp1 | synonymous_variant | LOW | c.858A>G | p.Ser286Ser | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/21 | 952/2679 | 858/2121 | 286/706 | chr11 | 71478454 | |||
| chr11:71480805 | G | C | 1 | a0003c0009 | 3 | HG02145.hp1 HG02572.hp1 HG03516.hp1 |
synonymous_variant | LOW | c.924G>C | p.Ser308Ser | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 11/21 | 1018/2679 | 924/2121 | 308/706 | chr11 | 71480805 | |||
| chr11:71481393 | C | A | 3 | a0003c0004 a0003c0009 a0009c0022 |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
synonymous_variant | LOW | c.1036C>A | p.Arg346Arg | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 12/21 | 1130/2679 | 1036/2121 | 346/706 | chr11 | 71481393 | |||
| chr11:71484333 | C | T | 1 | a0001c0006 | 8 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(5): Show |
synonymous_variant | LOW | c.1341C>T | p.Ile447Ile | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/21 | 1435/2679 | 1341/2121 | 447/706 | chr11 | 71484333 | |||
| chr11:71491846 | G | A | 1 | a0002c0015 | 1 | HG01074.hp1 | synonymous_variant | LOW | c.1707G>A | p.Ala569Ala | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/21 | 1801/2679 | 1707/2121 | 569/706 | chr11 | 71491846 | |||
| chr11:71497578 | C | T | 1 | a0002c0019 | 1 | NA20300.hp2 | synonymous_variant | LOW | c.1860C>T | p.Leu620Leu | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/21 | 1954/2679 | 1860/2121 | 620/706 | chr11 | 71497578 | |||
| chr11:71497605 | G | A | 2 | a0001c0023 a0002c0016 |
2 | HG02976.hp1 NA18906.hp2 |
synonymous_variant | LOW | c.1887G>A | p.Pro629Pro | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/21 | 1981/2679 | 1887/2121 | 629/706 | chr11 | 71497605 | |||
| chr11:71497608 | A | G | 1 | a0002c0018 | 1 | HG00558.hp1 | synonymous_variant | LOW | c.1890A>G | p.Arg630Arg | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/21 | 1984/2679 | 1890/2121 | 630/706 | chr11 | 71497608 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:71453235 | C | T | 1 | a0006c0010t0003 | 3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
5_prime_UTR_variant | MODIFIER | c.-62C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/21 | 62 | chr11 | 71453235 | ||||||
| chr11:71501473 | G | A | 1 | a0003c0004t0002 | 11 | HG03688.hp1 NA18944.hp2 NA18950.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*121G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 21/21 | 121 | chr11 | 71501473 | ||||||
| chr11:71501553 | A | G | 1 | a0002c0002t0005 | 1 | HG02293.hp1 | 3_prime_UTR_variant | MODIFIER | c.*201A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 21/21 | 201 | chr11 | 71501553 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:71453423 | C | T | 1 | a0002c0002t0001g0254 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.85+42C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71453423 | |||||||
| chr11:71453425 | G | A | 73 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(70): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.85+44G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71453425 | |||||||
| chr11:71453434 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.85+53G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71453434 | |||||||
| chr11:71453471 | T | G | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.85+90T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71453471 | |||||||
| chr11:71453498 | A | C | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.85+117A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71453498 | |||||||
| chr11:71453527 | C | A | 6 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(3): Show |
9 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.85+146C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71453527 | |||||||
| chr11:71453724 | C | A | 2 | a0001c0001t0001g0012 a0001c0001t0001g0110 |
4 | HG00140.hp1 HG01109.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.85+343C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71453724 | |||||||
| chr11:71453919 | T | A | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.85+538T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71453919 | |||||||
| chr11:71453985 | G | T | 19 | a0001c0024t0001g0253 a0002c0002t0001g0243 a0002c0005t0001g0237 others(16): Show |
23 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.85+604G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71453985 | |||||||
| chr11:71454042 | G | A | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.85+661G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71454042 | |||||||
| chr11:71454098 | C | A | 1 | a0001c0001t0001g0111 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.85+717C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71454098 | |||||||
| chr11:71454357 | G | A | 1 | a0001c0001t0001g0112 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.86-753G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71454357 | |||||||
| chr11:71454501 | C | T | 103 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(100): Show |
127 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(124): Show |
intron_variant | MODIFIER | c.86-609C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71454501 | |||||||
| chr11:71454579 | A | G | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.86-531A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71454579 | |||||||
| chr11:71454592 | T | TTGG | 95 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(92): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.86-517_86-515dupTG others(1): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr11 | 71454592 | ||||||
| chr11:71454743 | G | A | 1 | a0002c0002t0001g0045 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.86-367G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71454743 | |||||||
| chr11:71454793 | C | T | 1 | a0001c0001t0001g0236 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.86-317C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71454793 | |||||||
| chr11:71454865 | G | C | 1 | a0006c0010t0003g0104 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.86-245G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71454865 | |||||||
| chr11:71454898 | C | CAT | 95 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(92): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.86-212_86-211insAT | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71454898 | |||||||
| chr11:71455014 | T | TG | 101 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(98): Show |
140 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.86-96_86-95insG | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 1/20 | chr11 | 71455014 | |||||||
| chr11:71455282 | G | T | 2 | a0003c0004t0001g0018 a0003c0004t0001g0235 |
4 | HG00609.hp1 NA18970.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.146+112G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71455282 | |||||||
| chr11:71455291 | A | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(210): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.146+121A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71455291 | |||||||
| chr11:71455359 | A | G | 1 | a0001c0024t0001g0253 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.146+189A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71455359 | |||||||
| chr11:71455552 | C | A | 1 | a0001c0001t0001g0154 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.146+382C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71455552 | |||||||
| chr11:71455748 | G | C | 3 | a0003c0009t0001g0155 a0003c0009t0001g0156 a0003c0009t0001g0157 |
3 | HG02145.hp1 HG02572.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.146+578G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71455748 | |||||||
| chr11:71455936 | A | G | 19 | a0001c0024t0001g0253 a0002c0002t0001g0243 a0002c0005t0001g0237 others(16): Show |
23 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.146+766A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71455936 | |||||||
| chr11:71455946 | T | C | 95 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(92): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.146+776T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71455946 | |||||||
| chr11:71455969 | A | G | 2 | a0003c0004t0001g0233 a0003c0004t0001g0234 |
2 | HG04199.hp2 NA18612.hp1 |
intron_variant | MODIFIER | c.146+799A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71455969 | |||||||
| chr11:71456014 | G | A | 1 | a0002c0002t0001g0046 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.146+844G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456014 | |||||||
| chr11:71456187 | A | G | 1 | a0001c0001t0001g0232 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.146+1017A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456187 | |||||||
| chr11:71456403 | G | T | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.146+1233G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456403 | |||||||
| chr11:71456419 | C | T | 1 | a0002c0005t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.146+1249C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456419 | |||||||
| chr11:71456631 | C | T | 95 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(92): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.146+1461C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456631 | |||||||
| chr11:71456663 | T | C | 1 | a0001c0001t0001g0158 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.146+1493T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456663 | |||||||
| chr11:71456719 | C | T | 95 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(92): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.146+1549C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456719 | |||||||
| chr11:71456735 | C | A | 1 | a0001c0001t0001g0147 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.146+1565C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456735 | |||||||
| chr11:71456748 | CA | C | 3 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0109 |
5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.146+1579delA | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456748 | |||||||
| chr11:71456774 | A | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(210): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.146+1604A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456774 | |||||||
| chr11:71456876 | C | G | 1 | a0003c0009t0001g0157 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.147-1552C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456876 | |||||||
| chr11:71456918 | C | G | 19 | a0001c0024t0001g0253 a0002c0002t0001g0243 a0002c0005t0001g0237 others(16): Show |
23 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.147-1510C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456918 | |||||||
| chr11:71456926 | G | A | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.147-1502G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456926 | |||||||
| chr11:71456989 | A | G | 102 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(99): Show |
141 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(138): Show |
intron_variant | MODIFIER | c.147-1439A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71456989 | |||||||
| chr11:71457027 | A | G | 73 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(70): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.147-1401A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71457027 | |||||||
| chr11:71457100 | G | A | 2 | a0002c0005t0001g0237 a0002c0005t0001g0238 |
2 | HG02258.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.147-1328G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71457100 | |||||||
| chr11:71457188 | T | C | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.147-1240T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71457188 | |||||||
| chr11:71457194 | G | A | 20 | a0001c0001t0001g0159 a0001c0024t0001g0253 a0002c0002t0001g0243 others(17): Show |
24 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(21): Show |
intron_variant | MODIFIER | c.147-1234G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71457194 | |||||||
| chr11:71457218 | T | C | 19 | a0001c0024t0001g0253 a0002c0002t0001g0243 a0002c0005t0001g0237 others(16): Show |
23 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.147-1210T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71457218 | |||||||
| chr11:71457371 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.147-1057C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71457371 | |||||||
| chr11:71457648 | G | A | 6 | a0002c0002t0001g0243 a0002c0005t0001g0239 a0002c0005t0001g0240 others(3): Show |
7 | HG02451.hp1 HG02976.hp2 HG03225.hp1 others(4): Show |
intron_variant | MODIFIER | c.147-780G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71457648 | |||||||
| chr11:71457664 | G | A | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.147-764G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71457664 | |||||||
| chr11:71457669 | C | T | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.147-759C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71457669 | |||||||
| chr11:71457766 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.147-662A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71457766 | |||||||
| chr11:71458037 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.147-391G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71458037 | |||||||
| chr11:71458087 | T | G | 1 | a0001c0001t0001g0160 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.147-341T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71458087 | |||||||
| chr11:71458207 | C | G | 1 | a0001c0003t0001g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.147-221C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71458207 | |||||||
| chr11:71458262 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.147-166G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71458262 | |||||||
| chr11:71458327 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.147-101C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 2/20 | chr11 | 71458327 | |||||||
| chr11:71458602 | A | G | 94 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(91): Show |
130 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(127): Show |
intron_variant | MODIFIER | c.263+58A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71458602 | |||||||
| chr11:71458648 | G | T | 1 | a0001c0001t0001g0012 | 3 | HG00140.hp1 HG01109.hp1 HG01346.hp1 |
intron_variant | MODIFIER | c.263+104G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71458648 | |||||||
| chr11:71458707 | G | A | 19 | a0001c0024t0001g0253 a0002c0002t0001g0243 a0002c0005t0001g0237 others(16): Show |
23 | HG01884.hp1 HG02258.hp2 HG02451.hp1 others(20): Show |
intron_variant | MODIFIER | c.263+163G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71458707 | |||||||
| chr11:71458722 | TC | T | 6 | a0001c0024t0001g0253 a0002c0005t0001g0248 a0002c0005t0001g0252 others(3): Show |
6 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.263+182delC | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 71458722 | ||||||
| chr11:71458756 | G | A | 3 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0114 |
9 | HG00544.hp1 HG00621.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.263+212G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71458756 | |||||||
| chr11:71458974 | G | T | 1 | a0001c0012t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.263+430G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71458974 | |||||||
| chr11:71458988 | C | CGCCGGTC others(53): Show |
1 | a0002c0002t0001g0048 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.263+452_263+453ins others(60): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 71458988 | ||||||
| chr11:71458997 | T | C | 92 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(89): Show |
127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.263+453T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71458997 | |||||||
| chr11:71459016 | C | T | 3 | a0002c0005t0001g0247 a0004c0007t0001g0010 a0004c0007t0001g0246 |
6 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.263+472C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459016 | |||||||
| chr11:71459052 | G | A | 1 | a0002c0002t0001g0047 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.263+508G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459052 | |||||||
| chr11:71459054 | T | TCCCTATG others(397): Show |
3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.263+532_263+935dup others(404): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 71459054 | ||||||
| chr11:71459479 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.263+935G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459479 | |||||||
| chr11:71459607 | T | C | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.263+1063T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459607 | |||||||
| chr11:71459664 | G | A | 1 | a0002c0002t0001g0049 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.263+1120G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459664 | |||||||
| chr11:71459679 | G | A | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.263+1135G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459679 | |||||||
| chr11:71459724 | G | A | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.263+1180G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459724 | |||||||
| chr11:71459747 | C | T | 1 | a0002c0002t0001g0101 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.263+1203C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459747 | |||||||
| chr11:71459761 | C | T | 1 | a0001c0012t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.263+1217C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459761 | |||||||
| chr11:71459771 | C | T | 77 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(74): Show |
109 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(106): Show |
intron_variant | MODIFIER | c.263+1227C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459771 | |||||||
| chr11:71459842 | A | G | 2 | a0002c0002t0001g0100 a0002c0002t0001g0102 |
2 | NA18991.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.263+1298A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459842 | |||||||
| chr11:71459859 | T | C | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.263+1315T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459859 | |||||||
| chr11:71459919 | A | G | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.263+1375A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459919 | |||||||
| chr11:71459920 | A | G | 2 | a0001c0001t0001g0161 a0001c0001t0001g0230 |
2 | HG00408.hp1 NA18945.hp2 |
intron_variant | MODIFIER | c.263+1376A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459920 | |||||||
| chr11:71459957 | G | A | 92 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(89): Show |
127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.263+1413G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71459957 | |||||||
| chr11:71460000 | C | T | 17 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(14): Show |
21 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(18): Show |
intron_variant | MODIFIER | c.263+1456C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460000 | |||||||
| chr11:71460069 | G | A | 5 | a0002c0005t0001g0239 a0002c0005t0001g0240 a0002c0005t0001g0241 others(2): Show |
5 | HG02615.hp2 HG03516.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.263+1525G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460069 | |||||||
| chr11:71460124 | T | C | 92 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(89): Show |
127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.263+1580T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460124 | |||||||
| chr11:71460169 | TC | T | 1 | a0001c0003t0001g0013 | 3 | HG00544.hp1 NA18941.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.263+1628delC | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 71460169 | ||||||
| chr11:71460207 | G | A | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.263+1663G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460207 | |||||||
| chr11:71460268 | G | T | 2 | a0001c0001t0001g0219 a0001c0001t0001g0220 |
2 | HG02451.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.263+1724G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460268 | |||||||
| chr11:71460361 | G | T | 1 | a0002c0002t0001g0099 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.263+1817G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460361 | |||||||
| chr11:71460394 | A | G | 101 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(98): Show |
140 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(137): Show |
intron_variant | MODIFIER | c.263+1850A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460394 | |||||||
| chr11:71460438 | C | A | 1 | a0002c0002t0001g0046 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.263+1894C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460438 | |||||||
| chr11:71460483 | C | T | 1 | a0002c0002t0001g0098 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.263+1939C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460483 | |||||||
| chr11:71460596 | G | A | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.263+2052G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460596 | |||||||
| chr11:71460649 | T | C | 3 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0109 |
5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.263+2105T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460649 | |||||||
| chr11:71460679 | T | A | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.263+2135T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460679 | |||||||
| chr11:71460697 | AG | A | 76 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(73): Show |
108 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(105): Show |
intron_variant | MODIFIER | c.263+2155delG | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr11 | 71460697 | ||||||
| chr11:71460854 | G | C | 1 | a0002c0002t0001g0050 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.263+2310G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460854 | |||||||
| chr11:71460865 | T | C | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.263+2321T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71460865 | |||||||
| chr11:71461146 | C | A | 1 | a0001c0003t0001g0114 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.264-2286C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71461146 | |||||||
| chr11:71461258 | A | G | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.264-2174A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71461258 | |||||||
| chr11:71461287 | T | G | 1 | a0003c0004t0001g0162 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.264-2145T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71461287 | |||||||
| chr11:71461417 | T | C | 1 | a0001c0001t0001g0163 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.264-2015T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71461417 | |||||||
| chr11:71461452 | A | G | 1 | a0002c0002t0001g0025 | 2 | HG01081.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.264-1980A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71461452 | |||||||
| chr11:71461465 | G | A | 1 | a0001c0001t0001g0221 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.264-1967G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71461465 | |||||||
| chr11:71461563 | G | A | 3 | a0001c0003t0001g0007 a0001c0003t0001g0013 a0001c0003t0001g0114 |
9 | HG00544.hp1 HG00621.hp1 HG02027.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-1869G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71461563 | |||||||
| chr11:71461676 | C | T | 3 | a0003c0004t0001g0017 a0003c0004t0001g0162 a0003c0004t0001g0218 |
5 | HG01884.hp2 HG02055.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.264-1756C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71461676 | |||||||
| chr11:71461737 | A | C | 98 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(95): Show |
136 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.264-1695A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71461737 | |||||||
| chr11:71461744 | C | T | 6 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(3): Show |
9 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.264-1688C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71461744 | |||||||
| chr11:71462089 | G | C | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.264-1343G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71462089 | |||||||
| chr11:71462095 | C | T | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.264-1337C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71462095 | |||||||
| chr11:71462129 | G | C | 210 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(207): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.264-1303G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71462129 | |||||||
| chr11:71462169 | C | T | 17 | a0001c0001t0001g0112 a0001c0024t0001g0253 a0002c0005t0001g0237 others(14): Show |
20 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(17): Show |
intron_variant | MODIFIER | c.264-1263C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71462169 | |||||||
| chr11:71462208 | C | T | 92 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(89): Show |
127 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.264-1224C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71462208 | |||||||
| chr11:71462495 | G | A | 1 | a0002c0002t0001g0051 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.264-937G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71462495 | |||||||
| chr11:71462552 | G | T | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.264-880G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71462552 | |||||||
| chr11:71462701 | C | G | 72 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(69): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.264-731C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71462701 | |||||||
| chr11:71462962 | G | A | 1 | a0002c0002t0001g0052 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.264-470G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71462962 | |||||||
| chr11:71463226 | G | A | 2 | a0001c0006t0001g0026 a0001c0006t0001g0108 |
3 | HG01074.hp2 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.264-206G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71463226 | |||||||
| chr11:71463399 | C | T | 1 | a0003c0004t0001g0217 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.264-33C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71463399 | |||||||
| chr11:71463406 | A | G | 91 | a0001c0024t0001g0253 a0002c0002t0001g0002 a0002c0002t0001g0004 others(88): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.264-26A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 3/20 | chr11 | 71463406 | |||||||
| chr11:71463507 | C | T | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.317+22C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 4/20 | chr11 | 71463507 | |||||||
| chr11:71463508 | G | A | 1 | a0001c0003t0001g0115 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.317+23G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 4/20 | chr11 | 71463508 | |||||||
| chr11:71463543 | T | C | 248 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(245): Show |
345 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(342): Show |
intron_variant | MODIFIER | c.317+58T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 4/20 | chr11 | 71463543 | |||||||
| chr11:71463711 | G | A | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.317+226G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 4/20 | chr11 | 71463711 | |||||||
| chr11:71463719 | C | T | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.317+234C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 4/20 | chr11 | 71463719 | |||||||
| chr11:71463900 | C | T | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.318-153C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 4/20 | chr11 | 71463900 | |||||||
| chr11:71463903 | A | C | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.318-150A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 4/20 | chr11 | 71463903 | |||||||
| chr11:71464174 | T | C | 3 | a0002c0005t0001g0239 a0002c0005t0001g0240 a0002c0005t0001g0241 |
3 | HG03516.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.407+32T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464174 | |||||||
| chr11:71464242 | C | T | 9 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(6): Show |
13 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.407+100C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464242 | |||||||
| chr11:71464305 | G | A | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.407+163G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464305 | |||||||
| chr11:71464475 | T | G | 1 | a0001c0001t0001g0164 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.407+333T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464475 | |||||||
| chr11:71464589 | T | C | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.407+447T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464589 | |||||||
| chr11:71464760 | G | A | 2 | a0002c0005t0001g0248 a0002c0005t0001g0252 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.407+618G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464760 | |||||||
| chr11:71464784 | A | G | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.407+642A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464784 | |||||||
| chr11:71464798 | CA | C | 7 | a0001c0024t0001g0253 a0002c0005t0001g0247 a0002c0005t0001g0248 others(4): Show |
7 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+658delA | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71464798 | ||||||
| chr11:71464800 | A | G | 7 | a0001c0024t0001g0253 a0002c0005t0001g0247 a0002c0005t0001g0248 others(4): Show |
7 | HG02622.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.407+658A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464800 | |||||||
| chr11:71464844 | A | G | 3 | a0002c0002t0001g0243 a0005c0008t0001g0044 a0005c0008t0001g0242 |
4 | HG02451.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.407+702A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464844 | |||||||
| chr11:71464847 | A | G | 3 | a0002c0002t0001g0243 a0005c0008t0001g0044 a0005c0008t0001g0242 |
4 | HG02451.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.407+705A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464847 | |||||||
| chr11:71464867 | C | CA | 22 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(19): Show |
28 | HG00423.hp2 HG00735.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.407+751dupA | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71464867 | ||||||
| chr11:71464867 | CA | C | 78 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(75): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.407+751delA | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71464867 | ||||||
| chr11:71464867 | CAA | C | 26 | a0001c0001t0001g0203 a0001c0001t0001g0228 a0002c0005t0004g0245 others(23): Show |
34 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(31): Show |
intron_variant | MODIFIER | c.407+750_407+751del others(2): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71464867 | ||||||
| chr11:71464867 | CAAAAAAA others(3): Show |
C | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.407+742_407+751del others(10): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71464867 | ||||||
| chr11:71464867 | CAAAAAAA others(4): Show |
C | 1 | a0002c0005t0001g0241 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.407+741_407+751del others(11): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71464867 | ||||||
| chr11:71464867 | CAAAAAAA others(7): Show |
C | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.407+738_407+751del others(14): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71464867 | ||||||
| chr11:71464931 | G | A | 10 | a0001c0001t0001g0012 a0001c0001t0001g0110 a0001c0001t0001g0161 others(7): Show |
12 | HG00140.hp1 HG00408.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.407+789G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464931 | |||||||
| chr11:71464971 | G | A | 1 | a0001c0001t0001g0220 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.407+829G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71464971 | |||||||
| chr11:71465008 | G | A | 1 | a0002c0019t0001g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.407+866G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465008 | |||||||
| chr11:71465016 | A | G | 2 | a0001c0003t0001g0014 a0001c0003t0001g0133 |
4 | HG02109.hp1 HG02717.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.407+874A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465016 | |||||||
| chr11:71465095 | C | T | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.407+953C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465095 | |||||||
| chr11:71465183 | G | A | 1 | a0004c0007t0001g0246 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.407+1041G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465183 | |||||||
| chr11:71465201 | G | A | 1 | a0001c0003t0001g0134 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.407+1059G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465201 | |||||||
| chr11:71465212 | C | T | 1 | a0001c0003t0001g0032 | 2 | HG03017.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.407+1070C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465212 | |||||||
| chr11:71465238 | G | C | 2 | a0002c0002t0001g0062 a0002c0002t0001g0063 |
2 | NA18957.hp2 NA18978.hp2 |
intron_variant | MODIFIER | c.407+1096G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465238 | |||||||
| chr11:71465348 | G | A | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.407+1206G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465348 | |||||||
| chr11:71465421 | T | C | 213 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(210): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.407+1279T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465421 | |||||||
| chr11:71465528 | C | T | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.407+1386C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465528 | |||||||
| chr11:71465575 | A | T | 1 | a0001c0001t0001g0201 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.407+1433A>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465575 | |||||||
| chr11:71465682 | C | T | 1 | a0002c0005t0004g0245 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.407+1540C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465682 | |||||||
| chr11:71465851 | A | G | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.407+1709A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71465851 | |||||||
| chr11:71466021 | C | A | 1 | a0002c0002t0001g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.407+1879C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466021 | |||||||
| chr11:71466161 | T | C | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.407+2019T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466161 | |||||||
| chr11:71466311 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.407+2169C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466311 | |||||||
| chr11:71466366 | A | G | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.407+2224A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466366 | |||||||
| chr11:71466481 | C | G | 1 | a0001c0001t0001g0200 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.407+2339C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466481 | |||||||
| chr11:71466500 | C | G | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.407+2358C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466500 | |||||||
| chr11:71466532 | T | C | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.407+2390T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466532 | |||||||
| chr11:71466638 | G | A | 1 | a0002c0002t0001g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.407+2496G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466638 | |||||||
| chr11:71466664 | A | C | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.407+2522A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466664 | |||||||
| chr11:71466815 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.407+2673C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466815 | |||||||
| chr11:71466975 | G | C | 1 | a0002c0005t0001g0248 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.407+2833G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466975 | |||||||
| chr11:71466984 | G | A | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.407+2842G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71466984 | |||||||
| chr11:71467292 | G | A | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.407+3150G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71467292 | |||||||
| chr11:71467352 | G | A | 16 | a0001c0024t0001g0253 a0002c0005t0001g0237 a0002c0005t0001g0238 others(13): Show |
19 | HG01884.hp1 HG02258.hp2 HG02615.hp2 others(16): Show |
intron_variant | MODIFIER | c.407+3210G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71467352 | |||||||
| chr11:71467429 | A | G | 2 | a0001c0001t0001g0012 a0001c0001t0001g0110 |
4 | HG00140.hp1 HG01109.hp1 HG01346.hp1 others(1): Show |
intron_variant | MODIFIER | c.407+3287A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71467429 | |||||||
| chr11:71467480 | A | G | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.407+3338A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71467480 | |||||||
| chr11:71467627 | G | A | 1 | a0001c0001t0001g0229 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.407+3485G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71467627 | |||||||
| chr11:71467647 | ACCTCTCC others(3): Show |
A | 1 | a0001c0003t0001g0141 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.407+3507_407+3516d others(12): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71467647 | ||||||
| chr11:71467826 | A | G | 2 | a0008c0013t0001g0118 a0008c0013t0001g0132 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.407+3684A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71467826 | |||||||
| chr11:71467992 | G | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.407+3850G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71467992 | |||||||
| chr11:71468099 | T | C | 1 | a0001c0003t0001g0135 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.407+3957T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71468099 | |||||||
| chr11:71468215 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.407+4073C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71468215 | |||||||
| chr11:71468241 | G | C | 3 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02155.hp1 NA19001.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.407+4099G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71468241 | |||||||
| chr11:71468302 | G | A | 1 | a0002c0002t0001g0066 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.408-4147G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71468302 | |||||||
| chr11:71468349 | A | G | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.408-4100A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71468349 | |||||||
| chr11:71468447 | T | C | 6 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(3): Show |
9 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.408-4002T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71468447 | |||||||
| chr11:71468534 | AAAG | A | 21 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(18): Show |
29 | HG00408.hp2 HG00423.hp1 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.408-3910_408-3908d others(5): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71468534 | ||||||
| chr11:71468551 | A | G | 2 | a0002c0002t0001g0096 a0002c0002t0001g0097 |
2 | HG02074.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.408-3898A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71468551 | |||||||
| chr11:71469123 | T | C | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.408-3326T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469123 | |||||||
| chr11:71469133 | A | ATT | 7 | a0003c0004t0001g0016 a0003c0004t0001g0214 a0003c0004t0001g0215 others(4): Show |
9 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(6): Show |
intron_variant | MODIFIER | c.408-3316_408-3315i others(4): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469133 | |||||||
| chr11:71469171 | C | T | 1 | a0002c0002t0001g0024 | 2 | HG01123.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.408-3278C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469171 | |||||||
| chr11:71469228 | T | C | 1 | a0001c0003t0001g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.408-3221T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469228 | |||||||
| chr11:71469248 | G | A | 2 | a0002c0005t0004g0244 a0002c0005t0004g0245 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.408-3201G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469248 | |||||||
| chr11:71469267 | G | A | 2 | a0002c0002t0001g0096 a0002c0002t0001g0097 |
2 | HG02074.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.408-3182G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469267 | |||||||
| chr11:71469656 | C | T | 2 | a0002c0005t0004g0244 a0002c0005t0004g0245 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.408-2793C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469656 | |||||||
| chr11:71469665 | T | C | 205 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(202): Show |
268 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(265): Show |
intron_variant | MODIFIER | c.408-2784T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469665 | |||||||
| chr11:71469685 | G | C | 1 | a0001c0003t0001g0119 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.408-2764G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469685 | |||||||
| chr11:71469737 | G | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.408-2712G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469737 | |||||||
| chr11:71469927 | G | GA | 84 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(81): Show |
125 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.408-2505dupA | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71469927 | ||||||
| chr11:71469927 | G | GAAAAAAA others(4): Show |
8 | a0001c0001t0001g0154 a0001c0001t0001g0175 a0001c0001t0001g0188 others(5): Show |
8 | HG01515.hp2 HG02155.hp1 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.408-2515_408-2505d others(13): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71469927 | ||||||
| chr11:71469927 | G | GAAAAAAA others(5): Show |
62 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0035 others(59): Show |
80 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(77): Show |
intron_variant | MODIFIER | c.408-2516_408-2505d others(14): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71469927 | ||||||
| chr11:71469927 | G | GAAAAAAA others(6): Show |
28 | a0001c0001t0001g0034 a0001c0001t0001g0036 a0001c0001t0001g0040 others(25): Show |
34 | HG00408.hp1 HG00642.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.408-2517_408-2505d others(15): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71469927 | ||||||
| chr11:71469927 | G | GAAAAAAA others(7): Show |
4 | a0003c0004t0001g0214 a0003c0004t0002g0176 a0003c0004t0002g0202 others(1): Show |
4 | HG00733.hp1 HG03516.hp1 NA18959.hp2 others(1): Show |
intron_variant | MODIFIER | c.408-2518_408-2505d others(16): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71469927 | ||||||
| chr11:71469946 | A | G | 105 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(102): Show |
129 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.408-2503A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71469946 | |||||||
| chr11:71470039 | A | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(85): Show |
129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.408-2410A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470039 | |||||||
| chr11:71470097 | G | A | 1 | a0001c0003t0001g0029 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.408-2352G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470097 | |||||||
| chr11:71470097 | G | T | 1 | a0002c0002t0001g0092 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.408-2352G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470097 | |||||||
| chr11:71470125 | A | C | 1 | a0002c0002t0001g0091 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.408-2324A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470125 | |||||||
| chr11:71470176 | T | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.408-2273T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470176 | |||||||
| chr11:71470280 | G | C | 9 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0112 others(6): Show |
14 | HG00423.hp1 HG01952.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.408-2169G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470280 | |||||||
| chr11:71470399 | A | C | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.408-2050A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470399 | |||||||
| chr11:71470427 | C | T | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.408-2022C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470427 | |||||||
| chr11:71470439 | C | T | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.408-2010C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470439 | |||||||
| chr11:71470583 | T | C | 2 | a0002c0002t0001g0011 a0002c0002t0001g0093 |
4 | HG00735.hp2 HG01257.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-1866T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470583 | |||||||
| chr11:71470756 | C | G | 20 | a0001c0012t0001g0113 a0001c0024t0001g0253 a0002c0005t0001g0237 others(17): Show |
23 | HG01884.hp1 HG02258.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.408-1693C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470756 | |||||||
| chr11:71470815 | C | T | 13 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(10): Show |
22 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.408-1634C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470815 | |||||||
| chr11:71470861 | A | T | 1 | a0002c0002t0001g0091 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.408-1588A>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470861 | |||||||
| chr11:71470863 | CT | C | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.408-1584delT | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71470863 | ||||||
| chr11:71470958 | G | A | 5 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
8 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.408-1491G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470958 | |||||||
| chr11:71470972 | T | C | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.408-1477T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71470972 | |||||||
| chr11:71471109 | T | TG | 3 | a0002c0002t0001g0243 a0005c0008t0001g0044 a0005c0008t0001g0242 |
4 | HG02451.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-1336dupG | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71471109 | ||||||
| chr11:71471133 | G | A | 105 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(102): Show |
130 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(127): Show |
intron_variant | MODIFIER | c.408-1316G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471133 | |||||||
| chr11:71471139 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(85): Show |
129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.408-1310C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471139 | |||||||
| chr11:71471202 | C | A | 1 | a0001c0003t0001g0120 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.408-1247C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471202 | |||||||
| chr11:71471202 | C | T | 3 | a0002c0002t0001g0243 a0005c0008t0001g0044 a0005c0008t0001g0242 |
4 | HG02451.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.408-1247C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471202 | |||||||
| chr11:71471221 | A | G | 1 | a0001c0003t0001g0131 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.408-1228A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471221 | |||||||
| chr11:71471288 | A | G | 1 | a0002c0002t0001g0090 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.408-1161A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471288 | |||||||
| chr11:71471461 | G | A | 1 | a0002c0002t0001g0090 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.408-988G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471461 | |||||||
| chr11:71471543 | T | A | 9 | a0003c0004t0002g0015 a0003c0004t0002g0176 a0003c0004t0002g0177 others(6): Show |
11 | HG03688.hp1 NA18944.hp2 NA18950.hp2 others(8): Show |
intron_variant | MODIFIER | c.408-906T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471543 | |||||||
| chr11:71471543 | T | C | 95 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(92): Show |
117 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(114): Show |
intron_variant | MODIFIER | c.408-906T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471543 | |||||||
| chr11:71471635 | G | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.408-814G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471635 | |||||||
| chr11:71471638 | G | A | 2 | a0003c0004t0002g0176 a0003c0004t0002g0202 |
2 | NA18959.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.408-811G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471638 | |||||||
| chr11:71471715 | C | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.408-734C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471715 | |||||||
| chr11:71471855 | G | A | 36 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(33): Show |
44 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.408-594G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71471855 | |||||||
| chr11:71471940 | CTCTTGGT others(6): Show |
C | 6 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0175 others(3): Show |
6 | HG01192.hp1 HG02155.hp1 NA18942.hp1 others(3): Show |
intron_variant | MODIFIER | c.408-502_408-490del others(13): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr11 | 71471940 | ||||||
| chr11:71472223 | G | A | 2 | a0001c0006t0001g0026 a0001c0006t0001g0108 |
3 | HG01074.hp2 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.408-226G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71472223 | |||||||
| chr11:71472354 | C | T | 2 | a0003c0004t0001g0206 a0009c0022t0001g0205 |
2 | HG02630.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.408-95C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71472354 | |||||||
| chr11:71472428 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(85): Show |
129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.408-21C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71472428 | |||||||
| chr11:71472431 | C | T | 88 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(85): Show |
129 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(126): Show |
intron_variant | MODIFIER | c.408-18C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 5/20 | chr11 | 71472431 | |||||||
| chr11:71472541 | C | T | 1 | a0002c0005t0001g0248 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.459+41C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472541 | |||||||
| chr11:71472599 | T | C | 209 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(206): Show |
277 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(274): Show |
intron_variant | MODIFIER | c.459+99T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472599 | |||||||
| chr11:71472599 | T | G | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.459+99T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472599 | |||||||
| chr11:71472644 | C | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.459+144C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472644 | |||||||
| chr11:71472691 | T | C | 193 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(190): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.459+191T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472691 | |||||||
| chr11:71472729 | C | G | 2 | a0001c0001t0001g0112 a0001c0001t0001g0195 |
2 | NA18949.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.459+229C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472729 | |||||||
| chr11:71472730 | C | T | 1 | a0002c0002t0001g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.459+230C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472730 | |||||||
| chr11:71472733 | A | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(210): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.459+233A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472733 | |||||||
| chr11:71472800 | G | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.459+300G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472800 | |||||||
| chr11:71472969 | C | G | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.460-309C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472969 | |||||||
| chr11:71472977 | G | C | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.460-301G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71472977 | |||||||
| chr11:71473003 | A | C | 2 | a0001c0024t0001g0253 a0012c0025t0001g0251 |
2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.460-275A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71473003 | |||||||
| chr11:71473143 | A | G | 1 | a0002c0005t0001g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.460-135A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71473143 | |||||||
| chr11:71473144 | C | A | 72 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(69): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.460-134C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71473144 | |||||||
| chr11:71473237 | A | G | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.460-41A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 6/20 | chr11 | 71473237 | |||||||
| chr11:71473452 | G | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.548+86G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 7/20 | chr11 | 71473452 | |||||||
| chr11:71473475 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.549-94C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 7/20 | chr11 | 71473475 | |||||||
| chr11:71473527 | G | A | 2 | a0003c0004t0001g0018 a0003c0004t0001g0235 |
4 | HG00609.hp1 NA18970.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.549-42G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 7/20 | chr11 | 71473527 | |||||||
| chr11:71474014 | G | A | 20 | a0001c0012t0001g0113 a0001c0024t0001g0253 a0002c0005t0001g0237 others(17): Show |
23 | HG01884.hp1 HG02258.hp2 HG02559.hp1 others(20): Show |
intron_variant | MODIFIER | c.666+328G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 8/20 | chr11 | 71474014 | |||||||
| chr11:71474180 | A | G | 1 | a0001c0023t0001g0117 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.667-215A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 8/20 | chr11 | 71474180 | |||||||
| chr11:71474263 | G | A | 2 | a0008c0013t0001g0118 a0008c0013t0001g0132 |
2 | HG03710.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.667-132G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 8/20 | chr11 | 71474263 | |||||||
| chr11:71474311 | G | A | 101 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(98): Show |
123 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(120): Show |
intron_variant | MODIFIER | c.667-84G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 8/20 | chr11 | 71474311 | |||||||
| chr11:71474313 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.667-82G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 8/20 | chr11 | 71474313 | |||||||
| chr11:71474378 | G | A | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.667-17G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 8/20 | chr11 | 71474378 | |||||||
| chr11:71474536 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.798+10G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71474536 | |||||||
| chr11:71474711 | GGGGGTCC others(65): Show |
G | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.798+202_798+273del others(72): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 71474711 | ||||||
| chr11:71474848 | G | A | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.798+322G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71474848 | |||||||
| chr11:71474918 | G | A | 3 | a0002c0002t0001g0024 a0002c0002t0001g0053 a0002c0002t0001g0066 |
4 | HG00642.hp2 HG00741.hp2 HG01123.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+392G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71474918 | |||||||
| chr11:71474999 | C | T | 1 | a0001c0012t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.798+473C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71474999 | |||||||
| chr11:71475091 | C | T | 1 | a0001c0001t0001g0169 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.798+565C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475091 | |||||||
| chr11:71475183 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.798+657C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475183 | |||||||
| chr11:71475251 | G | A | 1 | a0002c0005t0001g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.798+725G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475251 | |||||||
| chr11:71475277 | A | C | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.798+751A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475277 | |||||||
| chr11:71475283 | G | A | 2 | a0001c0024t0001g0253 a0012c0025t0001g0251 |
2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.798+757G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475283 | |||||||
| chr11:71475338 | C | T | 1 | a0001c0003t0001g0130 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.798+812C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475338 | |||||||
| chr11:71475410 | G | A | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+884G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475410 | |||||||
| chr11:71475414 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.798+888C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475414 | |||||||
| chr11:71475430 | G | A | 70 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(67): Show |
101 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.798+904G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475430 | |||||||
| chr11:71475498 | C | T | 5 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
8 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.798+972C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475498 | |||||||
| chr11:71475676 | T | A | 1 | a0002c0005t0001g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.798+1150T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475676 | |||||||
| chr11:71475698 | G | A | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.798+1172G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475698 | |||||||
| chr11:71475800 | C | T | 1 | a0005c0008t0001g0242 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.798+1274C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475800 | |||||||
| chr11:71475828 | G | A | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+1302G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475828 | |||||||
| chr11:71475850 | C | T | 1 | a0001c0003t0001g0129 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.798+1324C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475850 | |||||||
| chr11:71475959 | G | A | 3 | a0002c0002t0001g0243 a0005c0008t0001g0044 a0005c0008t0001g0242 |
4 | HG02451.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.798+1433G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71475959 | |||||||
| chr11:71476015 | C | G | 104 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(101): Show |
128 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.798+1489C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476015 | |||||||
| chr11:71476171 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.798+1645C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476171 | |||||||
| chr11:71476248 | G | T | 92 | a0001c0012t0001g0113 a0001c0024t0001g0253 a0002c0002t0001g0002 others(89): Show |
126 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.798+1722G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476248 | |||||||
| chr11:71476283 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.798+1757G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476283 | |||||||
| chr11:71476299 | G | A | 2 | a0002c0002t0001g0091 a0002c0019t0001g0061 |
2 | HG02809.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.798+1773G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476299 | |||||||
| chr11:71476366 | C | T | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.798+1840C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476366 | |||||||
| chr11:71476397 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.798+1871C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476397 | |||||||
| chr11:71476405 | G | A | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.798+1879G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476405 | |||||||
| chr11:71476532 | C | T | 2 | a0003c0004t0002g0210 a0003c0004t0002g0213 |
2 | NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.799-1863C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476532 | |||||||
| chr11:71476578 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
26 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.799-1817C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476578 | |||||||
| chr11:71476633 | C | T | 72 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(69): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.799-1762C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476633 | |||||||
| chr11:71476721 | T | TCCC | 213 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(210): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.799-1673_799-1672i others(5): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 71476721 | ||||||
| chr11:71476812 | G | A | 2 | a0002c0002t0001g0011 a0002c0002t0001g0093 |
4 | HG00735.hp2 HG01257.hp2 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.799-1583G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476812 | |||||||
| chr11:71476842 | C | T | 1 | a0002c0002t0001g0091 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.799-1553C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476842 | |||||||
| chr11:71476862 | G | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
26 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.799-1533G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476862 | |||||||
| chr11:71476999 | T | C | 3 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0109 |
5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-1396T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71476999 | |||||||
| chr11:71477026 | C | G | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.799-1369C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477026 | |||||||
| chr11:71477067 | T | C | 2 | a0002c0005t0001g0248 a0002c0005t0001g0252 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.799-1328T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477067 | |||||||
| chr11:71477159 | A | T | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.799-1236A>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477159 | |||||||
| chr11:71477213 | C | G | 1 | a0002c0002t0001g0060 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.799-1182C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477213 | |||||||
| chr11:71477216 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.799-1179C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477216 | |||||||
| chr11:71477243 | G | A | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.799-1152G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477243 | |||||||
| chr11:71477277 | C | T | 5 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
8 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.799-1118C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477277 | |||||||
| chr11:71477315 | TCACA | T | 89 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(86): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.799-1078_799-1075d others(6): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 71477315 | ||||||
| chr11:71477406 | G | A | 2 | a0001c0001t0001g0103 a0001c0001t0001g0186 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.799-989G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477406 | |||||||
| chr11:71477456 | G | A | 209 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(206): Show |
278 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(275): Show |
intron_variant | MODIFIER | c.799-939G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477456 | |||||||
| chr11:71477474 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0153 |
2 | NA18999.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.799-921C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477474 | |||||||
| chr11:71477477 | G | A | 3 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0109 |
5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.799-918G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477477 | |||||||
| chr11:71477524 | C | T | 1 | a0002c0019t0001g0061 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.799-871C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477524 | |||||||
| chr11:71477564 | C | G | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.799-831C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477564 | |||||||
| chr11:71477586 | GAT | G | 3 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0189 |
5 | HG02055.hp2 HG02615.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.799-806_799-805del others(2): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 71477586 | ||||||
| chr11:71477708 | A | G | 35 | a0001c0001t0001g0008 a0001c0001t0001g0036 a0001c0001t0001g0037 others(32): Show |
43 | HG00423.hp1 HG00438.hp1 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.799-687A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477708 | |||||||
| chr11:71477732 | C | G | 2 | a0003c0004t0002g0210 a0003c0004t0002g0213 |
2 | NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.799-663C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477732 | |||||||
| chr11:71477754 | G | A | 91 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(88): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.799-641G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477754 | |||||||
| chr11:71477798 | G | C | 5 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
8 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.799-597G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71477798 | |||||||
| chr11:71478020 | C | A | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.799-375C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71478020 | |||||||
| chr11:71478028 | CAG | C | 5 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
8 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.799-366_799-365del others(2): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71478028 | |||||||
| chr11:71478102 | CAG | C | 4 | a0001c0003t0001g0140 a0002c0002t0001g0059 a0002c0005t0001g0239 others(1): Show |
4 | HG00558.hp2 HG00735.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.799-292_799-291del others(2): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71478102 | |||||||
| chr11:71478103 | AGGGGTGT others(11): Show |
A | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.799-278_799-261del others(18): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 71478103 | ||||||
| chr11:71478140 | AG | A | 16 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
26 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.799-252delG | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | INFO_REALIGN_3_PRIME | chr11 | 71478140 | ||||||
| chr11:71478269 | T | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(44): Show |
66 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(63): Show |
intron_variant | MODIFIER | c.799-126T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71478269 | |||||||
| chr11:71478390 | T | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
splice_region_variant&intron_variant | LOW | c.799-5T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 9/20 | chr11 | 71478390 | |||||||
| chr11:71478513 | C | T | 1 | a0001c0003t0001g0133 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.873+44C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71478513 | |||||||
| chr11:71478553 | G | A | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.873+84G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71478553 | |||||||
| chr11:71478728 | G | A | 3 | a0002c0002t0001g0243 a0005c0008t0001g0044 a0005c0008t0001g0242 |
4 | HG02451.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.873+259G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71478728 | |||||||
| chr11:71478811 | G | A | 2 | a0001c0024t0001g0253 a0012c0025t0001g0251 |
2 | HG02622.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.873+342G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71478811 | |||||||
| chr11:71478939 | C | T | 1 | a0002c0005t0001g0247 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.873+470C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71478939 | |||||||
| chr11:71479027 | C | T | 2 | a0002c0002t0001g0005 a0011c0014t0001g0089 |
7 | NA18942.hp2 NA18962.hp1 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.873+558C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479027 | |||||||
| chr11:71479079 | C | G | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.873+610C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479079 | |||||||
| chr11:71479111 | A | G | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.873+642A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479111 | |||||||
| chr11:71479116 | A | G | 213 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(210): Show |
282 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(279): Show |
intron_variant | MODIFIER | c.873+647A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479116 | |||||||
| chr11:71479252 | G | A | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.873+783G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479252 | |||||||
| chr11:71479252 | G | T | 1 | a0001c0001t0001g0168 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.873+783G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479252 | |||||||
| chr11:71479263 | A | T | 8 | a0001c0003t0001g0031 a0001c0003t0001g0134 a0001c0003t0001g0136 others(5): Show |
9 | HG00558.hp2 HG00733.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.873+794A>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479263 | |||||||
| chr11:71479263 | AT | A | 36 | a0001c0003t0001g0143 a0001c0012t0001g0121 a0002c0002t0001g0067 others(33): Show |
44 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.873+809delT | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr11 | 71479263 | ||||||
| chr11:71479386 | G | A | 2 | a0002c0005t0004g0244 a0002c0005t0004g0245 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.873+917G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479386 | |||||||
| chr11:71479566 | C | G | 13 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(10): Show |
22 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(19): Show |
intron_variant | MODIFIER | c.873+1097C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479566 | |||||||
| chr11:71479586 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.873+1117A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479586 | |||||||
| chr11:71479616 | T | C | 1 | a0002c0002t0001g0069 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.874-1139T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479616 | |||||||
| chr11:71479623 | G | A | 1 | a0001c0003t0001g0141 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.874-1132G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479623 | |||||||
| chr11:71479660 | T | TC | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.874-1093dupC | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr11 | 71479660 | ||||||
| chr11:71479818 | G | A | 3 | a0002c0002t0001g0243 a0005c0008t0001g0044 a0005c0008t0001g0242 |
4 | HG02451.hp1 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.874-937G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479818 | |||||||
| chr11:71479847 | T | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.874-908T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479847 | |||||||
| chr11:71479887 | C | T | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.874-868C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479887 | |||||||
| chr11:71479888 | G | T | 2 | a0001c0001t0001g0041 a0001c0001t0001g0226 |
3 | HG00280.hp2 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.874-867G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71479888 | |||||||
| chr11:71480056 | G | T | 2 | a0002c0005t0004g0244 a0002c0005t0004g0245 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.874-699G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71480056 | |||||||
| chr11:71480168 | T | TTTTG | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.874-579_874-576dup others(4): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr11 | 71480168 | ||||||
| chr11:71480235 | G | A | 5 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
8 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.874-520G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71480235 | |||||||
| chr11:71480285 | G | A | 1 | a0002c0002t0001g0254 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.874-470G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71480285 | |||||||
| chr11:71480492 | G | C | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.874-263G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71480492 | |||||||
| chr11:71480557 | C | T | 16 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(13): Show |
26 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(23): Show |
intron_variant | MODIFIER | c.874-198C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71480557 | |||||||
| chr11:71480558 | G | A | 26 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0040 others(23): Show |
32 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(29): Show |
intron_variant | MODIFIER | c.874-197G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71480558 | |||||||
| chr11:71480688 | C | T | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.874-67C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71480688 | |||||||
| chr11:71480714 | G | A | 1 | a0001c0003t0001g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.874-41G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 10/20 | chr11 | 71480714 | |||||||
| chr11:71480957 | C | T | 4 | a0001c0024t0001g0253 a0002c0005t0001g0248 a0002c0005t0001g0252 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.998+78C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 11/20 | chr11 | 71480957 | |||||||
| chr11:71481011 | A | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.998+132A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 11/20 | chr11 | 71481011 | |||||||
| chr11:71481179 | T | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.999-177T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 11/20 | chr11 | 71481179 | |||||||
| chr11:71481267 | G | A | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.999-89G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 11/20 | chr11 | 71481267 | |||||||
| chr11:71481320 | A | G | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.999-36A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 11/20 | chr11 | 71481320 | |||||||
| chr11:71481329 | G | A | 2 | a0003c0004t0002g0210 a0003c0004t0002g0213 |
2 | NA19011.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.999-27G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 11/20 | chr11 | 71481329 | |||||||
| chr11:71481483 | A | AT | 7 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0192 others(4): Show |
7 | HG01981.hp1 HG01981.hp2 HG01993.hp1 others(4): Show |
intron_variant | MODIFIER | c.1047+96dupT | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr11 | 71481483 | ||||||
| chr11:71481483 | AT | A | 11 | a0001c0001t0001g0199 a0001c0001t0001g0222 a0001c0001t0001g0223 others(8): Show |
12 | HG00323.hp2 HG00558.hp2 HG01261.hp1 others(9): Show |
intron_variant | MODIFIER | c.1047+96delT | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 12/20 | INFO_REALIGN_3_PRIME | chr11 | 71481483 | ||||||
| chr11:71481556 | T | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1047+152T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 12/20 | chr11 | 71481556 | |||||||
| chr11:71481677 | T | C | 5 | a0003c0004t0001g0016 a0003c0004t0001g0214 a0003c0004t0001g0215 others(2): Show |
7 | HG00280.hp1 HG00642.hp1 HG00733.hp1 others(4): Show |
intron_variant | MODIFIER | c.1048-246T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 12/20 | chr11 | 71481677 | |||||||
| chr11:71481742 | C | T | 2 | a0002c0002t0001g0100 a0002c0002t0001g0102 |
2 | NA18991.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1048-181C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 12/20 | chr11 | 71481742 | |||||||
| chr11:71481754 | C | T | 15 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(12): Show |
25 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1048-169C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 12/20 | chr11 | 71481754 | |||||||
| chr11:71481770 | G | A | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1048-153G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 12/20 | chr11 | 71481770 | |||||||
| chr11:71481773 | C | T | 2 | a0002c0005t0004g0244 a0002c0005t0004g0245 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1048-150C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 12/20 | chr11 | 71481773 | |||||||
| chr11:71481805 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1048-118A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 12/20 | chr11 | 71481805 | |||||||
| chr11:71482089 | G | C | 77 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(74): Show |
93 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1150+64G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482089 | |||||||
| chr11:71482102 | G | A | 1 | a0002c0005t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1150+77G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482102 | |||||||
| chr11:71482117 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1150+92C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482117 | |||||||
| chr11:71482173 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1150+148A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482173 | |||||||
| chr11:71482230 | C | T | 31 | a0002c0002t0001g0068 a0003c0004t0001g0016 a0003c0004t0001g0017 others(28): Show |
39 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.1150+205C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482230 | |||||||
| chr11:71482340 | A | G | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1150+315A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482340 | |||||||
| chr11:71482403 | T | C | 2 | a0003c0004t0002g0176 a0003c0004t0002g0202 |
2 | NA18959.hp2 NA19002.hp1 |
intron_variant | MODIFIER | c.1150+378T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482403 | |||||||
| chr11:71482447 | G | A | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1151-402G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482447 | |||||||
| chr11:71482457 | G | T | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1151-392G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482457 | |||||||
| chr11:71482465 | G | A | 18 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(15): Show |
28 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(25): Show |
intron_variant | MODIFIER | c.1151-384G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482465 | |||||||
| chr11:71482512 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-337C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482512 | |||||||
| chr11:71482519 | T | C | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-330T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482519 | |||||||
| chr11:71482609 | TCACACGG others(29): Show |
T | 34 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(31): Show |
45 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1151-238_1151-203d others(38): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr11 | 71482609 | ||||||
| chr11:71482611 | A | G | 178 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(175): Show |
236 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(233): Show |
intron_variant | MODIFIER | c.1151-238A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482611 | |||||||
| chr11:71482635 | C | T | 1 | a0003c0004t0001g0206 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1151-214C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482635 | |||||||
| chr11:71482636 | G | A | 2 | a0005c0008t0001g0044 a0005c0008t0001g0242 |
3 | HG02451.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1151-213G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482636 | |||||||
| chr11:71482651 | A | G | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1151-198A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482651 | |||||||
| chr11:71482671 | T | C | 72 | a0001c0001t0001g0171 a0002c0002t0001g0002 a0002c0002t0001g0004 others(69): Show |
103 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1151-178T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482671 | |||||||
| chr11:71482671 | TGGGGTGG others(29): Show |
T | 1 | a0003c0004t0001g0206 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1151-127_1151-92de others(37): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr11 | 71482671 | ||||||
| chr11:71482686 | C | T | 4 | a0001c0024t0001g0253 a0002c0005t0001g0248 a0002c0005t0001g0252 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-163C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482686 | |||||||
| chr11:71482707 | C | T | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1151-142C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482707 | |||||||
| chr11:71482719 | G | A | 4 | a0001c0024t0001g0253 a0002c0005t0001g0248 a0002c0005t0001g0252 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1151-130G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482719 | |||||||
| chr11:71482723 | A | AGGCACCT others(29): Show |
1 | a0001c0001t0001g0159 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1151-97_1151-62dup others(36): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr11 | 71482723 | ||||||
| chr11:71482745 | G | A | 1 | a0012c0025t0001g0251 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1151-104G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482745 | |||||||
| chr11:71482780 | G | A | 2 | a0001c0001t0001g0231 a0002c0002t0001g0019 |
3 | HG02015.hp1 HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1151-69G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 13/20 | chr11 | 71482780 | |||||||
| chr11:71483083 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1319+66C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483083 | |||||||
| chr11:71483121 | G | A | 1 | a0002c0002t0001g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1319+104G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483121 | |||||||
| chr11:71483153 | T | G | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1319+136T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483153 | |||||||
| chr11:71483163 | A | G | 211 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(208): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1319+146A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483163 | |||||||
| chr11:71483309 | G | A | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1319+292G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483309 | |||||||
| chr11:71483370 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.1319+353G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483370 | |||||||
| chr11:71483398 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1319+381A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483398 | |||||||
| chr11:71483447 | T | A | 1 | a0002c0002t0001g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1319+430T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483447 | |||||||
| chr11:71483490 | T | C | 253 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(250): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.1319+473T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483490 | |||||||
| chr11:71483513 | G | A | 77 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(74): Show |
93 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.1319+496G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483513 | |||||||
| chr11:71483555 | G | A | 92 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(89): Show |
108 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.1319+538G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483555 | |||||||
| chr11:71483556 | G | A | 1 | a0002c0002t0001g0020 | 2 | HG00438.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.1319+539G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483556 | |||||||
| chr11:71483562 | A | G | 10 | a0002c0002t0001g0020 a0002c0002t0001g0021 a0002c0002t0001g0022 others(7): Show |
13 | HG00423.hp2 HG00438.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.1319+545A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483562 | |||||||
| chr11:71483692 | T | C | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1320-620T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483692 | |||||||
| chr11:71483743 | A | C | 1 | a0001c0003t0001g0143 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1320-569A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483743 | |||||||
| chr11:71483809 | C | T | 1 | a0002c0002t0001g0084 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1320-503C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483809 | |||||||
| chr11:71483875 | T | C | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1320-437T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483875 | |||||||
| chr11:71483917 | C | T | 3 | a0001c0001t0001g0163 a0001c0001t0001g0174 a0001c0001t0001g0175 |
3 | HG02155.hp1 NA19001.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1320-395C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483917 | |||||||
| chr11:71483986 | C | T | 19 | a0002c0002t0001g0009 a0002c0002t0001g0024 a0002c0002t0001g0025 others(16): Show |
23 | HG00140.hp2 HG00639.hp1 HG00642.hp2 others(20): Show |
intron_variant | MODIFIER | c.1320-326C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71483986 | |||||||
| chr11:71484197 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1320-115C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71484197 | |||||||
| chr11:71484198 | G | C | 1 | a0001c0001t0001g0230 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1320-114G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71484198 | |||||||
| chr11:71484231 | C | T | 1 | a0001c0001t0001g0225 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1320-81C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71484231 | |||||||
| chr11:71484254 | G | A | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18954.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.1320-58G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 14/20 | chr11 | 71484254 | |||||||
| chr11:71484456 | G | A | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1455+9G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71484456 | |||||||
| chr11:71484886 | A | AGT | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1455+443_1455+444d others(4): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr11 | 71484886 | ||||||
| chr11:71484913 | G | A | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1455+466G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71484913 | |||||||
| chr11:71484941 | G | A | 1 | a0002c0002t0001g0072 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1455+494G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71484941 | |||||||
| chr11:71484957 | G | A | 1 | a0003c0004t0002g0176 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.1455+510G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71484957 | |||||||
| chr11:71485071 | C | T | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1456-471C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71485071 | |||||||
| chr11:71485128 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1456-414C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71485128 | |||||||
| chr11:71485147 | G | A | 1 | a0002c0002t0001g0062 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.1456-395G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71485147 | |||||||
| chr11:71485247 | C | T | 1 | a0001c0012t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1456-295C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71485247 | |||||||
| chr11:71485260 | C | T | 1 | a0001c0023t0001g0117 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1456-282C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71485260 | |||||||
| chr11:71485468 | A | G | 1 | a0003c0004t0002g0209 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1456-74A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71485468 | |||||||
| chr11:71485516 | G | A | 15 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(12): Show |
25 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(22): Show |
intron_variant | MODIFIER | c.1456-26G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 15/20 | chr11 | 71485516 | |||||||
| chr11:71485711 | T | C | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1562+63T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71485711 | |||||||
| chr11:71485748 | C | T | 2 | a0005c0008t0001g0044 a0005c0008t0001g0242 |
3 | HG02451.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1562+100C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71485748 | |||||||
| chr11:71485882 | T | C | 5 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(2): Show |
8 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.1562+234T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71485882 | |||||||
| chr11:71485910 | G | A | 2 | a0002c0002t0001g0049 a0002c0002t0001g0052 |
2 | NA18960.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.1562+262G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71485910 | |||||||
| chr11:71486037 | C | T | 90 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(87): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(103): Show |
intron_variant | MODIFIER | c.1562+389C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71486037 | |||||||
| chr11:71486488 | C | T | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1562+840C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71486488 | |||||||
| chr11:71486494 | T | G | 163 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(160): Show |
213 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(210): Show |
intron_variant | MODIFIER | c.1562+846T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71486494 | |||||||
| chr11:71486609 | A | G | 1 | a0001c0001t0001g0185 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1562+961A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71486609 | |||||||
| chr11:71486751 | C | T | 1 | a0001c0024t0001g0253 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1562+1103C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71486751 | |||||||
| chr11:71486796 | C | CT | 36 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0013 others(33): Show |
54 | HG00099.hp2 HG00544.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.1562+1175dupT | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71486796 | ||||||
| chr11:71486796 | C | CTT | 10 | a0001c0003t0001g0001 a0001c0003t0001g0007 a0001c0003t0001g0014 others(7): Show |
15 | HG00621.hp1 HG01071.hp1 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.1562+1174_1562+117 others(6): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71486796 | ||||||
| chr11:71486796 | CT | C | 47 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(44): Show |
53 | HG00280.hp1 HG00438.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.1562+1175delT | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71486796 | ||||||
| chr11:71486796 | CTT | C | 94 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(91): Show |
132 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.1562+1174_1562+117 others(6): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71486796 | ||||||
| chr11:71486796 | CTTT | C | 77 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(74): Show |
86 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.1562+1173_1562+117 others(7): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71486796 | ||||||
| chr11:71486906 | C | T | 3 | a0002c0005t0001g0239 a0002c0005t0001g0240 a0002c0005t0001g0241 |
3 | HG03516.hp2 HG06807.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1562+1258C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71486906 | |||||||
| chr11:71486951 | G | A | 1 | a0002c0005t0001g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1562+1303G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71486951 | |||||||
| chr11:71486979 | T | C | 1 | a0001c0003t0001g0145 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1562+1331T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71486979 | |||||||
| chr11:71486993 | A | G | 2 | a0001c0001t0001g0039 a0001c0001t0001g0191 |
3 | NA18939.hp2 NA18946.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.1562+1345A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71486993 | |||||||
| chr11:71487008 | G | A | 1 | a0002c0005t0001g0240 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1562+1360G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487008 | |||||||
| chr11:71487028 | C | A | 2 | a0005c0008t0001g0044 a0005c0008t0001g0242 |
3 | HG02451.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1562+1380C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487028 | |||||||
| chr11:71487142 | T | C | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1562+1494T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487142 | |||||||
| chr11:71487342 | T | A | 1 | a0002c0002t0001g0096 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1562+1694T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487342 | |||||||
| chr11:71487347 | G | A | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1562+1699G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487347 | |||||||
| chr11:71487348 | C | T | 1 | a0001c0001t0001g0229 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1562+1700C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487348 | |||||||
| chr11:71487465 | A | G | 1 | a0002c0002t0001g0071 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1562+1817A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487465 | |||||||
| chr11:71487549 | G | A | 1 | a0002c0005t0001g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1562+1901G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487549 | |||||||
| chr11:71487786 | G | A | 2 | a0001c0006t0001g0026 a0001c0006t0001g0108 |
3 | HG01074.hp2 HG02145.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1562+2138G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487786 | |||||||
| chr11:71487796 | A | G | 6 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(3): Show |
10 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1562+2148A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487796 | |||||||
| chr11:71487825 | C | T | 1 | a0002c0005t0001g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1562+2177C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487825 | |||||||
| chr11:71487830 | C | CA | 20 | a0001c0001t0001g0037 a0001c0001t0001g0172 a0001c0001t0001g0190 others(17): Show |
23 | HG00423.hp1 HG00558.hp2 HG00733.hp2 others(20): Show |
intron_variant | MODIFIER | c.1562+2202dupA | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71487830 | ||||||
| chr11:71487830 | C | CAA | 8 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(5): Show |
14 | NA18906.hp1 NA18955.hp2 NA18956.hp2 others(11): Show |
intron_variant | MODIFIER | c.1562+2201_1562+220 others(6): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71487830 | ||||||
| chr11:71487830 | C | CAAAA | 56 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(53): Show |
86 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(83): Show |
intron_variant | MODIFIER | c.1562+2199_1562+220 others(8): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71487830 | ||||||
| chr11:71487830 | C | CAAAAA | 9 | a0002c0002t0001g0021 a0002c0002t0001g0053 a0002c0002t0001g0054 others(6): Show |
10 | HG00741.hp2 HG01891.hp1 HG02132.hp1 others(7): Show |
intron_variant | MODIFIER | c.1562+2198_1562+220 others(9): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71487830 | ||||||
| chr11:71487830 | CAAAAAAA others(2): Show |
C | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1562+2194_1562+220 others(13): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71487830 | ||||||
| chr11:71487911 | G | A | 100 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(97): Show |
119 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(116): Show |
intron_variant | MODIFIER | c.1562+2263G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71487911 | |||||||
| chr11:71488001 | C | T | 2 | a0002c0005t0004g0244 a0002c0005t0004g0245 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1562+2353C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488001 | |||||||
| chr11:71488072 | T | C | 1 | a0002c0002t0001g0075 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1562+2424T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488072 | |||||||
| chr11:71488084 | T | A | 1 | a0001c0024t0001g0253 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1562+2436T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488084 | |||||||
| chr11:71488213 | A | G | 1 | a0002c0002t0001g0064 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1562+2565A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488213 | |||||||
| chr11:71488315 | A | AGG | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1563-2528_1563-252 others(6): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr11 | 71488315 | ||||||
| chr11:71488531 | G | A | 1 | a0002c0002t0001g0076 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1563-2314G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488531 | |||||||
| chr11:71488608 | C | T | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1563-2237C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488608 | |||||||
| chr11:71488620 | G | A | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1563-2225G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488620 | |||||||
| chr11:71488633 | C | T | 1 | a0002c0005t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1563-2212C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488633 | |||||||
| chr11:71488690 | C | A | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1563-2155C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488690 | |||||||
| chr11:71488712 | C | T | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
38 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1563-2133C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488712 | |||||||
| chr11:71488870 | A | G | 2 | a0005c0008t0001g0044 a0005c0008t0001g0242 |
3 | HG02451.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1563-1975A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488870 | |||||||
| chr11:71488903 | G | A | 167 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(164): Show |
217 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(214): Show |
intron_variant | MODIFIER | c.1563-1942G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71488903 | |||||||
| chr11:71489093 | A | G | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1563-1752A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489093 | |||||||
| chr11:71489110 | A | C | 2 | a0002c0005t0004g0244 a0002c0005t0004g0245 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1563-1735A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489110 | |||||||
| chr11:71489165 | A | G | 4 | a0001c0024t0001g0253 a0002c0005t0001g0248 a0002c0005t0001g0252 others(1): Show |
4 | HG02622.hp2 HG03130.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.1563-1680A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489165 | |||||||
| chr11:71489215 | C | T | 1 | a0002c0002t0001g0069 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1563-1630C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489215 | |||||||
| chr11:71489272 | A | T | 1 | a0001c0001t0001g0221 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1563-1573A>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489272 | |||||||
| chr11:71489274 | T | C | 212 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(209): Show |
281 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(278): Show |
intron_variant | MODIFIER | c.1563-1571T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489274 | |||||||
| chr11:71489443 | C | CT | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1563-1402_1563-140 others(5): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489443 | |||||||
| chr11:71489572 | T | C | 2 | a0001c0001t0001g0042 a0001c0001t0001g0228 |
3 | NA18939.hp1 NA18957.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.1563-1273T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489572 | |||||||
| chr11:71489597 | G | A | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1563-1248G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489597 | |||||||
| chr11:71489622 | T | C | 29 | a0001c0003t0001g0137 a0003c0004t0001g0016 a0003c0004t0001g0017 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1563-1223T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489622 | |||||||
| chr11:71489715 | G | C | 7 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
13 | NA18955.hp2 NA18956.hp2 NA18962.hp2 others(10): Show |
intron_variant | MODIFIER | c.1563-1130G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489715 | |||||||
| chr11:71489914 | T | A | 29 | a0002c0005t0001g0238 a0003c0004t0001g0016 a0003c0004t0001g0017 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1563-931T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489914 | |||||||
| chr11:71489927 | A | G | 32 | a0002c0005t0001g0238 a0003c0004t0001g0016 a0003c0004t0001g0017 others(29): Show |
40 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1563-918A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489927 | |||||||
| chr11:71489963 | G | A | 1 | a0002c0005t0001g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1563-882G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489963 | |||||||
| chr11:71489972 | G | A | 1 | a0003c0004t0001g0218 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1563-873G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71489972 | |||||||
| chr11:71490149 | G | A | 3 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0203 |
3 | HG02683.hp1 HG02698.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1563-696G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71490149 | |||||||
| chr11:71490152 | A | T | 27 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(24): Show |
35 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.1563-693A>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71490152 | |||||||
| chr11:71490215 | C | T | 1 | a0001c0006t0001g0108 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1563-630C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71490215 | |||||||
| chr11:71490481 | C | A | 83 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(80): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.1563-364C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71490481 | |||||||
| chr11:71490720 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1563-125G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 16/20 | chr11 | 71490720 | |||||||
| chr11:71491042 | C | T | 1 | a0001c0003t0001g0128 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1694+66C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491042 | |||||||
| chr11:71491056 | C | T | 1 | a0001c0003t0001g0126 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1694+80C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491056 | |||||||
| chr11:71491067 | G | A | 1 | a0001c0001t0001g0181 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.1694+91G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491067 | |||||||
| chr11:71491243 | C | T | 13 | a0002c0002t0001g0004 a0002c0002t0001g0005 a0002c0002t0001g0046 others(10): Show |
23 | HG00423.hp2 HG00558.hp1 HG02015.hp2 others(20): Show |
intron_variant | MODIFIER | c.1694+267C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491243 | |||||||
| chr11:71491258 | C | T | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694+282C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491258 | |||||||
| chr11:71491259 | G | A | 1 | a0002c0002t0001g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1694+283G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491259 | |||||||
| chr11:71491284 | G | C | 7 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(4): Show |
11 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1694+308G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491284 | |||||||
| chr11:71491349 | T | A | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694+373T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491349 | |||||||
| chr11:71491443 | T | TAGTC | 210 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(207): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1695-389_1695-388i others(6): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | INFO_REALIGN_3_PRIME | chr11 | 71491443 | ||||||
| chr11:71491450 | G | A | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695-384G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491450 | |||||||
| chr11:71491493 | T | G | 1 | a0002c0002t0001g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1695-341T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491493 | |||||||
| chr11:71491513 | T | C | 1 | a0002c0005t0001g0248 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1695-321T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491513 | |||||||
| chr11:71491625 | G | A | 1 | a0001c0001t0001g0197 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1695-209G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491625 | |||||||
| chr11:71491650 | C | A | 1 | a0002c0016t0001g0077 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1695-184C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491650 | |||||||
| chr11:71491671 | C | T | 28 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(25): Show |
36 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1695-163C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491671 | |||||||
| chr11:71491691 | C | T | 1 | a0001c0001t0001g0183 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1695-143C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491691 | |||||||
| chr11:71491707 | G | A | 5 | a0001c0001t0001g0161 a0001c0001t0001g0165 a0001c0001t0001g0173 others(2): Show |
5 | HG00408.hp1 HG00408.hp2 HG02074.hp2 others(2): Show |
intron_variant | MODIFIER | c.1695-127G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491707 | |||||||
| chr11:71491780 | G | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(17): Show |
31 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.1695-54G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491780 | |||||||
| chr11:71491795 | G | A | 2 | a0002c0005t0001g0248 a0002c0005t0001g0252 |
2 | HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1695-39G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 17/20 | chr11 | 71491795 | |||||||
| chr11:71491981 | T | C | 1 | a0002c0002t0001g0068 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1764+78T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71491981 | |||||||
| chr11:71491998 | A | AACT | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
41 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1764+95_1764+96ins others(3): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71491998 | |||||||
| chr11:71491999 | C | G | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
41 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1764+96C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71491999 | |||||||
| chr11:71492000 | A | T | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
41 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1764+97A>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492000 | |||||||
| chr11:71492149 | G | A | 11 | a0001c0001t0001g0012 a0001c0001t0001g0110 a0001c0001t0001g0161 others(8): Show |
13 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(10): Show |
intron_variant | MODIFIER | c.1764+246G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492149 | |||||||
| chr11:71492390 | C | T | 73 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(70): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(86): Show |
intron_variant | MODIFIER | c.1764+487C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492390 | |||||||
| chr11:71492485 | A | G | 1 | a0002c0002t0001g0049 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1764+582A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492485 | |||||||
| chr11:71492641 | G | C | 1 | a0002c0005t0001g0241 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1764+738G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492641 | |||||||
| chr11:71492693 | C | T | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1764+790C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492693 | |||||||
| chr11:71492720 | C | T | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+817C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492720 | |||||||
| chr11:71492744 | A | C | 74 | a0001c0001t0001g0167 a0001c0001t0001g0168 a0001c0001t0001g0231 others(71): Show |
105 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1764+841A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492744 | |||||||
| chr11:71492756 | G | A | 1 | a0003c0004t0001g0215 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1764+853G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492756 | |||||||
| chr11:71492805 | G | A | 14 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(11): Show |
24 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(21): Show |
intron_variant | MODIFIER | c.1764+902G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492805 | |||||||
| chr11:71492841 | A | G | 1 | a0001c0012t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1764+938A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492841 | |||||||
| chr11:71492887 | AT | A | 131 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(128): Show |
166 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.1764+1002delT | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr11 | 71492887 | ||||||
| chr11:71492887 | ATT | A | 6 | a0001c0001t0001g0112 a0001c0012t0001g0113 a0002c0002t0001g0243 others(3): Show |
6 | HG02895.hp2 HG02896.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1764+1001_1764+100 others(6): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr11 | 71492887 | ||||||
| chr11:71492912 | T | C | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+1009T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71492912 | |||||||
| chr11:71493037 | A | G | 1 | a0003c0004t0001g0234 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1764+1134A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493037 | |||||||
| chr11:71493046 | T | C | 210 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(207): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.1764+1143T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493046 | |||||||
| chr11:71493114 | G | A | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1764+1211G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493114 | |||||||
| chr11:71493190 | G | A | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1764+1287G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493190 | |||||||
| chr11:71493201 | T | G | 1 | a0001c0001t0001g0172 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1764+1298T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493201 | |||||||
| chr11:71493260 | G | A | 1 | a0001c0001t0001g0224 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1764+1357G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493260 | |||||||
| chr11:71493329 | AT | A | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+1428delT | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr11 | 71493329 | ||||||
| chr11:71493452 | T | G | 1 | a0002c0002t0001g0065 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1764+1549T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493452 | |||||||
| chr11:71493456 | C | T | 2 | a0001c0001t0001g0103 a0001c0001t0001g0186 |
2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1764+1553C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493456 | |||||||
| chr11:71493569 | A | T | 1 | a0002c0002t0001g0078 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1764+1666A>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493569 | |||||||
| chr11:71493580 | TA | T | 32 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(29): Show |
40 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1764+1687delA | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr11 | 71493580 | ||||||
| chr11:71493593 | AT | A | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1764+1697delT | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr11 | 71493593 | ||||||
| chr11:71493651 | G | A | 1 | a0001c0003t0001g0123 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.1764+1748G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493651 | |||||||
| chr11:71493732 | T | A | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1764+1829T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493732 | |||||||
| chr11:71493753 | T | G | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1764+1850T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493753 | |||||||
| chr11:71493950 | G | A | 1 | a0003c0004t0002g0208 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1764+2047G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493950 | |||||||
| chr11:71493952 | T | A | 1 | a0003c0004t0002g0208 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1764+2049T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493952 | |||||||
| chr11:71493955 | A | G | 1 | a0003c0004t0002g0208 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1764+2052A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493955 | |||||||
| chr11:71493957 | C | T | 1 | a0003c0004t0002g0208 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1764+2054C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493957 | |||||||
| chr11:71493958 | C | A | 1 | a0003c0004t0002g0208 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1764+2055C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493958 | |||||||
| chr11:71493959 | C | G | 1 | a0003c0004t0002g0208 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1764+2056C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493959 | |||||||
| chr11:71493960 | T | C | 30 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(27): Show |
41 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.1764+2057T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493960 | |||||||
| chr11:71493961 | G | A | 1 | a0003c0004t0002g0208 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1764+2058G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493961 | |||||||
| chr11:71493963 | C | T | 1 | a0003c0004t0002g0208 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1764+2060C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71493963 | |||||||
| chr11:71494036 | G | A | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1764+2133G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71494036 | |||||||
| chr11:71494048 | T | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
13 | NA18955.hp2 NA18956.hp2 NA18962.hp2 others(10): Show |
intron_variant | MODIFIER | c.1764+2145T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71494048 | |||||||
| chr11:71494201 | C | T | 1 | a0006c0010t0003g0106 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1764+2298C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71494201 | |||||||
| chr11:71494324 | A | G | 1 | a0001c0003t0001g0143 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1764+2421A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71494324 | |||||||
| chr11:71494354 | C | A | 1 | a0001c0003t0001g0127 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1764+2451C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71494354 | |||||||
| chr11:71494468 | A | G | 80 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(77): Show |
96 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(93): Show |
intron_variant | MODIFIER | c.1764+2565A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71494468 | |||||||
| chr11:71494524 | T | C | 12 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(9): Show |
17 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1764+2621T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71494524 | |||||||
| chr11:71494538 | C | CTTTTG | 160 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(157): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1764+2654_1764+265 others(9): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr11 | 71494538 | ||||||
| chr11:71494538 | CTTTTG | C | 28 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(25): Show |
36 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.1764+2654_1764+265 others(9): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr11 | 71494538 | ||||||
| chr11:71494558 | G | T | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1764+2655G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71494558 | |||||||
| chr11:71494728 | T | C | 1 | a0002c0002t0001g0086 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1765-2755T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71494728 | |||||||
| chr11:71494774 | C | T | 54 | a0002c0002t0001g0002 a0002c0002t0001g0004 a0002c0002t0001g0005 others(51): Show |
80 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(77): Show |
intron_variant | MODIFIER | c.1765-2709C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71494774 | |||||||
| chr11:71495096 | T | C | 1 | a0001c0003t0001g0115 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1765-2387T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495096 | |||||||
| chr11:71495097 | A | G | 1 | a0002c0005t0001g0239 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1765-2386A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495097 | |||||||
| chr11:71495108 | G | C | 1 | a0002c0005t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1765-2375G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495108 | |||||||
| chr11:71495120 | G | A | 31 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(28): Show |
42 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1765-2363G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495120 | |||||||
| chr11:71495314 | A | G | 1 | a0001c0001t0001g0197 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1765-2169A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495314 | |||||||
| chr11:71495320 | G | C | 31 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(28): Show |
42 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.1765-2163G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495320 | |||||||
| chr11:71495322 | A | G | 160 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(157): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1765-2161A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495322 | |||||||
| chr11:71495425 | T | C | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765-2058T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495425 | |||||||
| chr11:71495426 | C | A | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1765-2057C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495426 | |||||||
| chr11:71495462 | C | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
13 | NA18955.hp2 NA18956.hp2 NA18962.hp2 others(10): Show |
intron_variant | MODIFIER | c.1765-2021C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495462 | |||||||
| chr11:71495496 | C | T | 2 | a0005c0008t0001g0044 a0005c0008t0001g0242 |
3 | HG02451.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1765-1987C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495496 | |||||||
| chr11:71495517 | G | C | 2 | a0005c0008t0001g0044 a0005c0008t0001g0242 |
3 | HG02451.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1765-1966G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495517 | |||||||
| chr11:71495556 | A | G | 2 | a0002c0005t0004g0244 a0002c0005t0004g0245 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1765-1927A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495556 | |||||||
| chr11:71495820 | C | G | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765-1663C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495820 | |||||||
| chr11:71495909 | C | T | 1 | a0001c0001t0001g0161 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1765-1574C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495909 | |||||||
| chr11:71495938 | C | T | 1 | a0002c0005t0001g0252 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1765-1545C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495938 | |||||||
| chr11:71495998 | G | A | 1 | a0002c0005t0001g0241 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1765-1485G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71495998 | |||||||
| chr11:71496128 | A | G | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765-1355A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496128 | |||||||
| chr11:71496159 | C | G | 160 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(157): Show |
207 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(204): Show |
intron_variant | MODIFIER | c.1765-1324C>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496159 | |||||||
| chr11:71496176 | C | T | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765-1307C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496176 | |||||||
| chr11:71496301 | A | G | 50 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(47): Show |
72 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.1765-1182A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496301 | |||||||
| chr11:71496310 | C | T | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765-1173C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496310 | |||||||
| chr11:71496311 | G | A | 1 | a0002c0002t0001g0045 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.1765-1172G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496311 | |||||||
| chr11:71496434 | C | T | 1 | a0002c0020t0001g0094 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1765-1049C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496434 | |||||||
| chr11:71496448 | G | A | 1 | a0001c0024t0001g0253 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1765-1035G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496448 | |||||||
| chr11:71496464 | G | A | 19 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(16): Show |
30 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.1765-1019G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496464 | |||||||
| chr11:71496520 | C | T | 1 | a0001c0001t0001g0194 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1765-963C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496520 | |||||||
| chr11:71496560 | A | G | 7 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
13 | NA18955.hp2 NA18956.hp2 NA18962.hp2 others(10): Show |
intron_variant | MODIFIER | c.1765-923A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496560 | |||||||
| chr11:71496638 | G | A | 7 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(4): Show |
11 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1765-845G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496638 | |||||||
| chr11:71496655 | G | C | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765-828G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496655 | |||||||
| chr11:71496686 | A | C | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.1765-797A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496686 | |||||||
| chr11:71496706 | C | T | 1 | a0001c0012t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1765-777C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496706 | |||||||
| chr11:71496720 | T | A | 1 | a0003c0004t0001g0211 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1765-763T>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496720 | |||||||
| chr11:71496851 | A | C | 19 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(16): Show |
30 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(27): Show |
intron_variant | MODIFIER | c.1765-632A>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496851 | |||||||
| chr11:71496872 | TTTC | T | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765-599_1765-597d others(5): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr11 | 71496872 | ||||||
| chr11:71496936 | T | C | 228 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(225): Show |
302 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(299): Show |
intron_variant | MODIFIER | c.1765-547T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496936 | |||||||
| chr11:71496954 | C | T | 5 | a0005c0008t0001g0044 a0005c0008t0001g0242 a0006c0010t0003g0104 others(2): Show |
6 | HG02451.hp1 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.1765-529C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71496954 | |||||||
| chr11:71497215 | C | A | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1765-268C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71497215 | |||||||
| chr11:71497252 | C | T | 1 | a0002c0002t0001g0085 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1765-231C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71497252 | |||||||
| chr11:71497322 | T | G | 7 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(4): Show |
11 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1765-161T>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71497322 | |||||||
| chr11:71497432 | C | T | 1 | a0002c0002t0001g0019 | 2 | HG02572.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1765-51C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 18/20 | chr11 | 71497432 | |||||||
| chr11:71497829 | C | T | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1893+218C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/20 | chr11 | 71497829 | |||||||
| chr11:71497842 | G | GC | 38 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(35): Show |
53 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.1893+233dupC | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr11 | 71497842 | ||||||
| chr11:71497920 | G | A | 12 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(9): Show |
19 | HG02451.hp1 HG02559.hp1 HG02630.hp1 others(16): Show |
intron_variant | MODIFIER | c.1893+309G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/20 | chr11 | 71497920 | |||||||
| chr11:71497950 | A | G | 1 | a0002c0005t0001g0237 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1893+339A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/20 | chr11 | 71497950 | |||||||
| chr11:71498127 | T | C | 207 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(204): Show |
276 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(273): Show |
intron_variant | MODIFIER | c.1894-225T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/20 | chr11 | 71498127 | |||||||
| chr11:71498137 | C | T | 11 | a0003c0004t0002g0015 a0003c0004t0002g0176 a0003c0004t0002g0177 others(8): Show |
16 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(13): Show |
intron_variant | MODIFIER | c.1894-215C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/20 | chr11 | 71498137 | |||||||
| chr11:71498138 | G | A | 7 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(4): Show |
11 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.1894-214G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/20 | chr11 | 71498138 | |||||||
| chr11:71498295 | G | C | 1 | a0001c0003t0001g0138 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1894-57G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/20 | chr11 | 71498295 | |||||||
| chr11:71498342 | C | T | 3 | a0001c0006t0001g0027 a0001c0006t0001g0028 a0001c0006t0001g0109 |
5 | HG01891.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1894-10C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 19/20 | chr11 | 71498342 | |||||||
| chr11:71498550 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2070+22C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71498550 | |||||||
| chr11:71498642 | G | C | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2070+114G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71498642 | |||||||
| chr11:71498700 | C | T | 1 | a0002c0002t0001g0082 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.2070+172C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71498700 | |||||||
| chr11:71498817 | G | A | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.2070+289G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71498817 | |||||||
| chr11:71498907 | G | T | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.2070+379G>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71498907 | |||||||
| chr11:71498977 | G | A | 181 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(178): Show |
242 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(239): Show |
intron_variant | MODIFIER | c.2070+449G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71498977 | |||||||
| chr11:71498980 | G | A | 2 | a0005c0008t0001g0044 a0005c0008t0001g0242 |
3 | HG02451.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.2070+452G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71498980 | |||||||
| chr11:71499024 | C | T | 76 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(73): Show |
92 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.2070+496C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499024 | |||||||
| chr11:71499039 | G | A | 7 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(4): Show |
11 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.2070+511G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499039 | |||||||
| chr11:71499097 | C | T | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2070+569C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499097 | |||||||
| chr11:71499141 | A | G | 2 | a0002c0005t0004g0244 a0002c0005t0004g0245 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2070+613A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499141 | |||||||
| chr11:71499186 | C | T | 3 | a0002c0005t0001g0247 a0007c0011t0001g0249 a0007c0011t0001g0250 |
3 | HG02895.hp2 HG02897.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.2070+658C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499186 | |||||||
| chr11:71499190 | C | T | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2070+662C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499190 | |||||||
| chr11:71499276 | T | C | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2070+748T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499276 | |||||||
| chr11:71499387 | A | G | 1 | a0001c0001t0001g0182 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2070+859A>G | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499387 | |||||||
| chr11:71499543 | T | C | 1 | a0001c0001t0001g0110 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2070+1015T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499543 | |||||||
| chr11:71499557 | C | T | 1 | a0001c0012t0001g0113 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2070+1029C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499557 | |||||||
| chr11:71499565 | T | C | 1 | a0001c0003t0001g0146 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2070+1037T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499565 | |||||||
| chr11:71499631 | T | C | 89 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(86): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.2070+1103T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499631 | |||||||
| chr11:71499699 | C | T | 4 | a0001c0006t0001g0026 a0001c0006t0001g0108 a0002c0002t0001g0019 others(1): Show |
6 | HG01074.hp2 HG02145.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.2070+1171C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499699 | |||||||
| chr11:71499772 | C | T | 1 | a0002c0002t0001g0087 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.2070+1244C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499772 | |||||||
| chr11:71499851 | C | T | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2070+1323C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499851 | |||||||
| chr11:71499881 | C | T | 1 | a0002c0005t0004g0244 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.2070+1353C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71499881 | |||||||
| chr11:71500034 | G | A | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2071-1268G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71500034 | |||||||
| chr11:71500109 | C | A | 2 | a0001c0001t0001g0148 a0001c0001t0001g0151 |
2 | NA18956.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.2071-1193C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71500109 | |||||||
| chr11:71500255 | C | T | 20 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(17): Show |
31 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(28): Show |
intron_variant | MODIFIER | c.2071-1047C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71500255 | |||||||
| chr11:71500342 | G | C | 2 | a0004c0007t0001g0010 a0004c0007t0001g0246 |
5 | HG01884.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2071-960G>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71500342 | |||||||
| chr11:71500366 | A | T | 3 | a0006c0010t0003g0104 a0006c0010t0003g0105 a0006c0010t0003g0106 |
3 | HG02559.hp1 HG02630.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2071-936A>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71500366 | |||||||
| chr11:71500382 | A | AC | 192 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(189): Show |
257 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(254): Show |
intron_variant | MODIFIER | c.2071-914dupC | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr11 | 71500382 | ||||||
| chr11:71500382 | A | ACC | 18 | a0001c0001t0001g0040 a0001c0001t0001g0041 a0001c0001t0001g0042 others(15): Show |
22 | HG00280.hp2 HG00323.hp2 HG00544.hp2 others(19): Show |
intron_variant | MODIFIER | c.2071-915_2071-914d others(4): Show |
NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr11 | 71500382 | ||||||
| chr11:71500440 | T | C | 2 | a0002c0005t0004g0244 a0002c0005t0004g0245 |
2 | HG02615.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2071-862T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71500440 | |||||||
| chr11:71500530 | C | T | 1 | a0001c0003t0001g0139 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2071-772C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71500530 | |||||||
| chr11:71500587 | GA | G | 210 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(207): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.2071-713delA | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr11 | 71500587 | ||||||
| chr11:71500608 | G | A | 167 | a0001c0001t0001g0008 a0001c0001t0001g0012 a0001c0001t0001g0034 others(164): Show |
218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.2071-694G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71500608 | |||||||
| chr11:71500659 | G | A | 1 | a0002c0002t0001g0083 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.2071-643G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71500659 | |||||||
| chr11:71500763 | TC | T | 7 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
13 | NA18955.hp2 NA18956.hp2 NA18962.hp2 others(10): Show |
intron_variant | MODIFIER | c.2071-535delC | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr11 | 71500763 | ||||||
| chr11:71500913 | C | A | 29 | a0003c0004t0001g0016 a0003c0004t0001g0017 a0003c0004t0001g0018 others(26): Show |
37 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.2071-389C>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71500913 | |||||||
| chr11:71501094 | G | A | 5 | a0005c0008t0001g0044 a0005c0008t0001g0242 a0006c0010t0003g0104 others(2): Show |
6 | HG02451.hp1 HG02559.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2071-208G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71501094 | |||||||
| chr11:71501123 | G | A | 1 | a0002c0002t0001g0078 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.2071-179G>A | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71501123 | |||||||
| chr11:71501126 | A | T | 210 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0012 others(207): Show |
279 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(276): Show |
intron_variant | MODIFIER | c.2071-176A>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71501126 | |||||||
| chr11:71501173 | T | C | 50 | a0001c0001t0001g0003 a0001c0001t0001g0147 a0001c0001t0001g0148 others(47): Show |
72 | HG00280.hp1 HG00609.hp1 HG00642.hp1 others(69): Show |
intron_variant | MODIFIER | c.2071-129T>C | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71501173 | |||||||
| chr11:71501219 | C | T | 12 | a0001c0006t0001g0026 a0001c0006t0001g0027 a0001c0006t0001g0028 others(9): Show |
17 | HG01074.hp2 HG01891.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.2071-83C>T | NADSYN1 | ENSG00000172890.13 | transcript | ENST00000319023.7 | protein_coding | 20/20 | chr11 | 71501219 |