Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 55226 |
| ensemblid | ENSG00000135372.10 |
| hgncid | 29830 |
| symbol | NAT10 |
| name | N-acetyltransferase 10 |
| refseq_nuc | NM_024662.3 |
| refseq_prot | NP_078938.3 |
| ensembl_nuc | ENST00000257829.8 |
| ensembl_prot | ENSP00000257829.3 |
| mane_status | MANE Select |
| chr | chr11 |
| start | 34105629 |
| end | 34146908 |
| strand | + |
| ver | v1.2 |
| region | chr11:34105629-34146908 |
| region5000 | chr11:34100629-34151908 |
| regionname0 | NAT10_chr11_34105629_34146908 |
| regionname5000 | NAT10_chr11_34100629_34151908 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 1025 | 240 | 81 | 45 | 75 | 8 | 30 | 46 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0002 | 0/0 | 1025 | 4 | 0 | 0 | 4 | 0 | 0 | 2 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0003 | 0/0 | 1025 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0004 | 1/0 | 1025 | 2 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0005 | 0/0 | 1025 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0006 | 0/0 | 1025 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0007 | 0/0 | 1025 | 2 | 0 | 0 | 0 | 0 | 2 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0008 | 0/0 | 1025 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0009 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0010 | 0/0 | 1025 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0011 | 0/0 | 1025 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0012 | 0/0 | 1025 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(1020): Show |
chr11 | 34100629 | 34151908 |
| a0013 | 0/0 | 58 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | MHRKK others(53): Show |
chr11 | 34100629 | 34151908 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3075 | 187 | 36 | 41 | 73 | 7 | 29 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0001c0002 | 0/0 | 3075 | 22 | 21 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0001c0003 | 0/0 | 3075 | 11 | 9 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0001c0004 | 0/0 | 3075 | 7 | 7 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0001c0005 | 0/0 | 3075 | 6 | 6 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0001c0009 | 0/0 | 3075 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0001c0015 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0001c0016 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0001c0019 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0001c0020 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0001c0022 | 0/0 | 3075 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0002c0006 | 0/0 | 3075 | 4 | 0 | 0 | 4 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0003c0007 | 0/0 | 3075 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0004c0011 | 1/0 | 3075 | 2 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0005c0008 | 0/0 | 3075 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0006c0010 | 0/0 | 3075 | 2 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0007c0012 | 0/0 | 3075 | 2 | 0 | 0 | 0 | 0 | 2 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0008c0023 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0009c0017 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0010c0021 | 0/0 | 3075 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0011c0014 | 0/0 | 3075 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0012c0018 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 | ||
| a0013c0013 | 0/0 | 3075 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | ATGCA others(3070): Show |
chr11 | 34100629 | 34151908 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3973 | 118 | 28 | 21 | 42 | 7 | 19 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0001t0002 | 0/0 | 3973 | 64 | 7 | 20 | 27 | 0 | 10 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0001t0006 | 0/0 | 3973 | 3 | 0 | 0 | 3 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0001t0010 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0001t0011 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0002t0001 | 0/0 | 3973 | 20 | 20 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0002t0002 | 0/0 | 3973 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0002t0009 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0003t0001 | 0/0 | 3973 | 9 | 7 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0003t0003 | 0/0 | 3973 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0004t0003 | 0/0 | 3973 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0004t0005 | 0/0 | 3973 | 4 | 4 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0004t0008 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0005t0004 | 0/0 | 3973 | 6 | 6 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0009t0007 | 0/0 | 3973 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0015t0001 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0016t0001 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0019t0001 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0020t0005 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0001c0022t0001 | 0/0 | 3973 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0002c0006t0001 | 0/0 | 3973 | 4 | 0 | 0 | 4 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0003c0007t0001 | 0/0 | 3973 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0004c0011t0001 | 1/0 | 3973 | 2 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0005c0008t0003 | 0/0 | 3973 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0006c0010t0001 | 0/0 | 3973 | 2 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0007c0012t0001 | 0/0 | 3973 | 2 | 0 | 0 | 0 | 0 | 2 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0008c0023t0001 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0009c0017t0001 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0010c0021t0002 | 0/0 | 3973 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0011c0014t0001 | 0/0 | 3973 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0012c0018t0001 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| a0013c0013t0002 | 0/0 | 3973 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | AGTTC others(3968): Show |
chr11 | 34100629 | 34151908 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0005 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0007 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0023 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0137 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0001 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0003 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0006 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0002g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0006g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0006g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0006g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0010g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0001t0011g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0002t0009g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0003t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0003g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0005g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0005g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0005g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0005g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0004t0008g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0005t0004g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0005t0004g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0005t0004g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0005t0004g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0005t0004g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0009t0007g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0015t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0016t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0019t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0020t0005g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0001c0022t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0002c0006t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0002c0006t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0002c0006t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0002c0006t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0003c0007t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0003c0007t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0003c0007t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0004c0011t0001g0223 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0004c0011t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0005c0008t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0005c0008t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0005c0008t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0006c0010t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0006c0010t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0007c0012t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0007c0012t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0008c0023t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0009c0017t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0010c0021t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0011c0014t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0012c0018t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| a0013c0013t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0155 | EUR | GBR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0204 | EUR | GBR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0158 | EUR | FIN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | FIN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00597 | hp2 | a0002 | c0006 | t0001 | g0164 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0119 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00621 | hp2 | a0002 | c0006 | t0001 | g0163 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00639 | hp1 | a0006 | c0010 | t0001 | g0054 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | CHS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00735 | hp1 | a0001 | c0001 | t0002 | g0145 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00738 | hp1 | a0001 | c0022 | t0001 | g0038 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG00741 | hp2 | a0001 | c0001 | t0002 | g0069 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01109 | hp1 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01168 | hp1 | a0001 | c0009 | t0007 | g0010 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01169 | hp2 | a0001 | c0009 | t0007 | g0010 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01175 | hp1 | a0001 | c0001 | t0002 | g0125 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0070 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01243 | hp2 | a0001 | c0003 | t0001 | g0037 | AMR | PUR | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0075 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01361 | hp1 | a0001 | c0001 | t0002 | g0154 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0144 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01433 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01433 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01515 | hp1 | a0001 | c0002 | t0002 | g0057 | EUR | IBS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0019 | EUR | IBS | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01928 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01928 | hp2 | a0001 | c0001 | t0002 | g0083 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0080 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02015 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0213 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0063 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0065 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0132 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0133 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02145 | hp1 | a0001 | c0004 | t0005 | g0034 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CDX | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0134 | EAS | CDX | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02165 | hp2 | a0009 | c0017 | t0001 | g0061 | EAS | CDX | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02258 | hp1 | a0001 | c0004 | t0003 | g0033 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02258 | hp2 | a0010 | c0021 | t0002 | g0066 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0129 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0097 | AMR | PEL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02451 | hp1 | a0001 | c0002 | t0009 | g0215 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0118 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02572 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02572 | hp2 | a0001 | c0002 | t0001 | g0146 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0052 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02615 | hp1 | a0001 | c0020 | t0005 | g0028 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02622 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0009 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02647 | hp1 | a0001 | c0002 | t0001 | g0201 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02647 | hp2 | a0001 | c0002 | t0001 | g0126 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02683 | hp1 | a0001 | c0001 | t0002 | g0116 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02683 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02717 | hp1 | a0001 | c0019 | t0001 | g0147 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02717 | hp2 | a0003 | c0007 | t0001 | g0095 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02735 | hp2 | a0011 | c0014 | t0001 | g0082 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0079 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02809 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02818 | hp1 | a0001 | c0005 | t0004 | g0046 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0202 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02896 | hp1 | a0001 | c0003 | t0001 | g0041 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02896 | hp2 | a0001 | c0005 | t0004 | g0008 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02897 | hp1 | a0001 | c0005 | t0004 | g0008 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02922 | hp2 | a0001 | c0004 | t0008 | g0031 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02965 | hp1 | a0001 | c0002 | t0001 | g0199 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03041 | hp1 | a0001 | c0005 | t0004 | g0047 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03041 | hp2 | a0001 | c0003 | t0003 | g0044 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03098 | hp1 | a0004 | c0011 | t0001 | g0224 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03098 | hp2 | a0001 | c0001 | t0002 | g0120 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0130 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03195 | hp2 | a0001 | c0005 | t0004 | g0045 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03209 | hp1 | a0005 | c0008 | t0003 | g0025 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03209 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03225 | hp1 | a0001 | c0004 | t0005 | g0029 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03225 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0139 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0197 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03486 | hp2 | a0001 | c0003 | t0001 | g0002 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0219 | AFR | ESN | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03540 | hp2 | a0001 | c0005 | t0004 | g0048 | AFR | GWD | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03579 | hp1 | a0001 | c0002 | t0001 | g0200 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0211 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03654 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03654 | hp2 | a0007 | c0012 | t0001 | g0040 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03669 | hp1 | a0001 | c0003 | t0001 | g0042 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0006 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | PJL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0098 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03927 | hp1 | a0001 | c0001 | t0002 | g0122 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0023 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04115 | hp1 | a0001 | c0001 | t0002 | g0081 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0073 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04184 | hp2 | a0007 | c0012 | t0001 | g0043 | SAS | BEB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0053 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04204 | hp1 | a0006 | c0010 | t0001 | g0055 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG04204 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18522 | hp1 | a0001 | c0003 | t0001 | g0036 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18522 | hp2 | a0001 | c0004 | t0003 | g0032 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | CHB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18906 | hp1 | a0001 | c0001 | t0010 | g0207 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18950 | hp2 | a0012 | c0018 | t0001 | g0121 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18954 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18960 | hp1 | a0002 | c0006 | t0001 | g0191 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18968 | hp1 | a0001 | c0001 | t0006 | g0058 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18968 | hp2 | a0001 | c0016 | t0001 | g0050 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18970 | hp2 | a0002 | c0006 | t0001 | g0005 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18977 | hp1 | a0001 | c0001 | t0002 | g0112 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18983 | hp2 | a0013 | c0013 | t0002 | g0222 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0135 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18995 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18998 | hp1 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19011 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19011 | hp2 | a0001 | c0015 | t0001 | g0004 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19030 | hp1 | a0005 | c0008 | t0003 | g0024 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19043 | hp1 | a0001 | c0002 | t0001 | g0049 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19043 | hp2 | a0001 | c0004 | t0005 | g0027 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19056 | hp2 | a0001 | c0001 | t0002 | g0114 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0128 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19070 | hp2 | a0001 | c0001 | t0002 | g0113 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19074 | hp2 | a0001 | c0001 | t0002 | g0115 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19078 | hp1 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19085 | hp1 | a0001 | c0001 | t0006 | g0117 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19085 | hp2 | a0001 | c0001 | t0011 | g0087 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA19240 | hp2 | a0005 | c0008 | t0003 | g0026 | AFR | YRI | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ASW | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA20129 | hp2 | a0001 | c0002 | t0001 | g0198 | AFR | ASW | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01123 | hp1 | a0001 | c0001 | t0002 | g0131 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02109 | hp1 | a0008 | c0023 | t0001 | g0002 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02109 | hp2 | a0003 | c0007 | t0001 | g0096 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02486 | hp1 | a0001 | c0002 | t0001 | g0208 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02559 | hp1 | a0001 | c0002 | t0001 | g0148 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | ACB | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03471 | hp1 | a0001 | c0003 | t0003 | g0035 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0017 | AFR | USA | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | USA | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0039 | AFR | USA | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0160 | AFR | USA | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA21309 | hp1 | a0001 | c0004 | t0005 | g0030 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| NA21309 | hp2 | a0003 | c0007 | t0001 | g0001 | AFR | LWK | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0137 | REF | REF | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| homoSapiens | grch38p0 | a0004 | c0011 | t0001 | g0223 | REF | REF | NAT10_chr11_34100629_34151908 | NAT10 | chr11 | 34100629 | 34151908 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34108810 | T | G | 1 | a0013 | 1 | NA18983.hp2 | stop_gained | HIGH | c.177T>G | p.Tyr59* | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/29 | 356/3973 | 177/3078 | 59/1025 | chr11 | 34108810 | |||
| chr11:34113726 | C | G | 1 | a0010 | 1 | HG02258.hp2 | missense_variant | MODERATE | c.383C>G | p.Ala128Gly | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/29 | 562/3973 | 383/3078 | 128/1025 | chr11 | 34113726 | |||
| chr11:34118230 | A | G | 1 | a0008 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.608A>G | p.Gln203Arg | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/29 | 787/3973 | 608/3078 | 203/1025 | chr11 | 34118230 | |||
| chr11:34118259 | G | A | 1 | a0011 | 1 | HG02735.hp2 | missense_variant | MODERATE | c.637G>A | p.Val213Ile | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/29 | 816/3973 | 637/3078 | 213/1025 | chr11 | 34118259 | |||
| chr11:34118293 | C | T | 1 | a0003 | 3 | HG02109.hp2 HG02717.hp2 NA21309.hp2 |
missense_variant&splice_region_variant | MODERATE | c.671C>T | p.Pro224Leu | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/29 | 850/3973 | 671/3078 | 224/1025 | chr11 | 34118293 | |||
| chr11:34130863 | G | A | 1 | a0009 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.1295G>A | p.Arg432His | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/29 | 1474/3973 | 1295/3078 | 432/1025 | chr11 | 34130863 | |||
| chr11:34131392 | T | C | 12 | a0001 a0002 a0003 others(9): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
missense_variant | MODERATE | c.1381T>C | p.Tyr461His | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/29 | 1560/3973 | 1381/3078 | 461/1025 | chr11 | 34131392 | |||
| chr11:34133032 | C | T | 1 | a0006 | 2 | HG00639.hp1 HG04204.hp1 |
missense_variant | MODERATE | c.1624C>T | p.Pro542Ser | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/29 | 1803/3973 | 1624/3078 | 542/1025 | chr11 | 34133032 | |||
| chr11:34133098 | C | T | 1 | a0002 | 4 | HG00597.hp2 HG00621.hp2 NA18960.hp1 others(1): Show |
missense_variant | MODERATE | c.1690C>T | p.Pro564Ser | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/29 | 1869/3973 | 1690/3078 | 564/1025 | chr11 | 34133098 | |||
| chr11:34135175 | A | G | 1 | a0007 | 2 | HG03654.hp2 HG04184.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1912A>G | p.Met638Val | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/29 | 2091/3973 | 1912/3078 | 638/1025 | chr11 | 34135175 | |||
| chr11:34142340 | C | A | 1 | a0012 | 1 | NA18950.hp2 | missense_variant | MODERATE | c.2877C>A | p.Asp959Glu | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/29 | 3056/3973 | 2877/3078 | 959/1025 | chr11 | 34142340 | |||
| chr11:34143506 | G | A | 1 | a0005 | 3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
missense_variant | MODERATE | c.2947G>A | p.Ala983Thr | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/29 | 3126/3973 | 2947/3078 | 983/1025 | chr11 | 34143506 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34108795 | A | G | 5 | a0001c0003 a0001c0022 a0005c0008 others(2): Show |
18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
synonymous_variant | LOW | c.162A>G | p.Ser54Ser | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/29 | 341/3973 | 162/3078 | 54/1025 | chr11 | 34108795 | |||
| chr11:34108810 | T | C | 1 | a0001c0005 | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
synonymous_variant | LOW | c.177T>C | p.Tyr59Tyr | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/29 | 356/3973 | 177/3078 | 59/1025 | chr11 | 34108810 | |||
| chr11:34112220 | G | A | 1 | a0001c0005 | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
synonymous_variant | LOW | c.369G>A | p.Leu123Leu | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/29 | 548/3973 | 369/3078 | 123/1025 | chr11 | 34112220 | |||
| chr11:34113802 | C | T | 2 | a0001c0004 a0001c0020 |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
synonymous_variant | LOW | c.459C>T | p.Thr153Thr | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/29 | 638/3973 | 459/3078 | 153/1025 | chr11 | 34113802 | |||
| chr11:34122485 | G | A | 1 | a0001c0015 | 1 | NA19011.hp2 | synonymous_variant | LOW | c.807G>A | p.Glu269Glu | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/29 | 986/3973 | 807/3078 | 269/1025 | chr11 | 34122485 | |||
| chr11:34124397 | T | C | 1 | a0001c0016 | 1 | NA18968.hp2 | synonymous_variant | LOW | c.1104T>C | p.Ile368Ile | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/29 | 1283/3973 | 1104/3078 | 368/1025 | chr11 | 34124397 | |||
| chr11:34127528 | C | T | 1 | a0001c0019 | 1 | HG02717.hp1 | synonymous_variant | LOW | c.1173C>T | p.Ala391Ala | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/29 | 1352/3973 | 1173/3078 | 391/1025 | chr11 | 34127528 | |||
| chr11:34133094 | C | T | 13 | a0001c0001 a0001c0015 a0001c0016 others(10): Show |
204 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(201): Show |
synonymous_variant | LOW | c.1686C>T | p.Pro562Pro | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/29 | 1865/3973 | 1686/3078 | 562/1025 | chr11 | 34133094 | |||
| chr11:34140401 | C | A | 2 | a0001c0009 a0005c0008 |
5 | HG01168.hp1 HG01169.hp2 HG03209.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.2421C>A | p.Ala807Ala | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/29 | 2600/3973 | 2421/3078 | 807/1025 | chr11 | 34140401 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34105714 | C | T | 1 | a0001c0001t0011 | 1 | NA19085.hp2 | 5_prime_UTR_variant | MODIFIER | c.-94C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/29 | 2512 | chr11 | 34105714 | ||||||
| chr11:34105756 | T | G | 1 | a0001c0004t0008 | 1 | HG02922.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-52T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/29 | chr11 | 34105756 | |||||||
| chr11:34146447 | C | A | 1 | a0001c0005t0004 | 6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*255C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 255 | chr11 | 34146447 | ||||||
| chr11:34146548 | T | G | 1 | a0001c0009t0007 | 2 | HG01168.hp1 HG01169.hp2 |
3_prime_UTR_variant | MODIFIER | c.*356T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 356 | chr11 | 34146548 | ||||||
| chr11:34146566 | C | T | 1 | a0001c0001t0006 | 3 | HG00621.hp1 NA18968.hp1 NA19085.hp1 |
3_prime_UTR_variant | MODIFIER | c.*374C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 374 | chr11 | 34146566 | ||||||
| chr11:34146606 | G | A | 5 | a0001c0001t0002 a0001c0001t0011 a0001c0002t0002 others(2): Show |
68 | HG00673.hp2 HG00733.hp1 HG00735.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*414G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 414 | chr11 | 34146606 | ||||||
| chr11:34146610 | C | T | 3 | a0001c0004t0005 a0001c0004t0008 a0001c0020t0005 |
6 | HG02145.hp1 HG02615.hp1 HG02922.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*418C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 418 | chr11 | 34146610 | ||||||
| chr11:34146623 | C | A | 1 | a0001c0002t0009 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*431C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 431 | chr11 | 34146623 | ||||||
| chr11:34146793 | C | T | 4 | a0001c0003t0003 a0001c0004t0003 a0001c0009t0007 others(1): Show |
9 | HG01168.hp1 HG01169.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*601C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 601 | chr11 | 34146793 | ||||||
| chr11:34146897 | A | T | 1 | a0001c0001t0010 | 1 | NA18906.hp1 | 3_prime_UTR_variant | MODIFIER | c.*705A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 29/29 | 705 | chr11 | 34146897 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr11:34105853 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.-16+61T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34105853 | |||||||
| chr11:34105916 | T | C | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16+124T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34105916 | |||||||
| chr11:34105925 | A | T | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-16+133A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34105925 | |||||||
| chr11:34106292 | A | G | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16+500A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106292 | |||||||
| chr11:34106362 | A | G | 1 | a0013c0013t0002g0222 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-16+570A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106362 | |||||||
| chr11:34106379 | A | C | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.-16+587A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106379 | |||||||
| chr11:34106421 | A | AT | 16 | a0001c0001t0001g0218 a0001c0001t0002g0219 a0001c0003t0001g0002 others(13): Show |
19 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-16+643dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr11 | 34106421 | ||||||
| chr11:34106421 | A | ATT | 9 | a0001c0003t0003g0044 a0001c0004t0003g0032 a0001c0004t0003g0033 others(6): Show |
9 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-16+642_-16+643dup others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr11 | 34106421 | ||||||
| chr11:34106484 | A | G | 15 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(12): Show |
18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-16+692A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106484 | |||||||
| chr11:34106710 | G | C | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-16+918G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106710 | |||||||
| chr11:34106712 | C | G | 2 | a0001c0002t0001g0216 a0001c0002t0001g0217 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-16+920C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106712 | |||||||
| chr11:34106786 | C | T | 2 | a0001c0001t0002g0219 a0001c0002t0009g0215 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-16+994C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106786 | |||||||
| chr11:34106863 | G | A | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.-16+1071G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106863 | |||||||
| chr11:34106906 | G | C | 2 | a0001c0002t0001g0216 a0001c0002t0001g0217 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.-16+1114G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106906 | |||||||
| chr11:34106990 | T | C | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-16+1198T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34106990 | |||||||
| chr11:34107031 | C | CT | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(188): Show |
220 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.-15-1162dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr11 | 34107031 | ||||||
| chr11:34107031 | C | CTT | 20 | a0001c0001t0001g0205 a0001c0001t0001g0209 a0001c0001t0001g0210 others(17): Show |
20 | HG01081.hp2 HG02055.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-15-1163_-15-1162d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr11 | 34107031 | ||||||
| chr11:34107031 | C | CTTT | 13 | a0001c0001t0001g0214 a0001c0003t0001g0002 a0001c0003t0001g0036 others(10): Show |
16 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.-15-1164_-15-1162d others(5): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr11 | 34107031 | ||||||
| chr11:34107235 | T | G | 3 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0053 |
3 | HG00733.hp2 HG02602.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.-15-976T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107235 | |||||||
| chr11:34107325 | T | C | 1 | a0001c0004t0005g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-15-886T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107325 | |||||||
| chr11:34107395 | A | G | 1 | a0001c0001t0001g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-15-816A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107395 | |||||||
| chr11:34107493 | C | T | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.-15-718C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107493 | |||||||
| chr11:34107654 | A | G | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.-15-557A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107654 | |||||||
| chr11:34107656 | G | A | 2 | a0006c0010t0001g0054 a0006c0010t0001g0055 |
2 | HG00639.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.-15-555G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107656 | |||||||
| chr11:34107847 | C | T | 52 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0020 others(49): Show |
60 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(57): Show |
intron_variant | MODIFIER | c.-15-364C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107847 | |||||||
| chr11:34107852 | C | A | 15 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(12): Show |
18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-15-359C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107852 | |||||||
| chr11:34107901 | G | T | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-15-310G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 1/28 | chr11 | 34107901 | |||||||
| chr11:34108421 | T | G | 3 | a0005c0008t0003g0024 a0005c0008t0003g0025 a0005c0008t0003g0026 |
3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.108+88T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108421 | |||||||
| chr11:34108468 | C | G | 15 | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0152 others(12): Show |
17 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(14): Show |
intron_variant | MODIFIER | c.108+135C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108468 | |||||||
| chr11:34108476 | C | T | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18971.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.108+143C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108476 | |||||||
| chr11:34108512 | C | T | 1 | a0001c0001t0002g0149 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.108+179C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108512 | |||||||
| chr11:34108608 | T | C | 2 | a0002c0006t0001g0163 a0002c0006t0001g0164 |
2 | HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.109-134T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108608 | |||||||
| chr11:34108617 | A | G | 24 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(21): Show |
28 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.109-125A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108617 | |||||||
| chr11:34108648 | G | A | 29 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(26): Show |
34 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.109-94G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 2/28 | chr11 | 34108648 | |||||||
| chr11:34108847 | T | G | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.200+14T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34108847 | |||||||
| chr11:34108855 | T | C | 1 | a0001c0001t0001g0220 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.200+22T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34108855 | |||||||
| chr11:34108859 | A | G | 15 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(12): Show |
18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.200+26A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34108859 | |||||||
| chr11:34109010 | A | C | 1 | a0001c0001t0001g0203 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.200+177A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109010 | |||||||
| chr11:34109164 | C | T | 1 | a0001c0002t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.200+331C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109164 | |||||||
| chr11:34109259 | G | T | 1 | a0001c0019t0001g0147 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.200+426G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109259 | |||||||
| chr11:34109286 | A | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.200+453A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109286 | |||||||
| chr11:34109411 | T | A | 1 | a0001c0003t0003g0035 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.200+578T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109411 | |||||||
| chr11:34109460 | G | T | 1 | a0001c0002t0001g0146 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.200+627G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109460 | |||||||
| chr11:34109474 | A | T | 7 | a0001c0002t0001g0197 a0001c0002t0001g0198 a0001c0002t0001g0199 others(4): Show |
7 | HG02055.hp1 HG02647.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.200+641A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109474 | |||||||
| chr11:34109896 | T | C | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.200+1063T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34109896 | |||||||
| chr11:34110108 | T | C | 1 | a0001c0019t0001g0147 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.200+1275T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110108 | |||||||
| chr11:34110169 | C | T | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.200+1336C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110169 | |||||||
| chr11:34110170 | G | A | 1 | a0001c0002t0009g0215 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.200+1337G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110170 | |||||||
| chr11:34110248 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.200+1415G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110248 | |||||||
| chr11:34110354 | A | G | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.200+1521A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110354 | |||||||
| chr11:34110361 | C | T | 1 | a0001c0004t0005g0034 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.200+1528C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110361 | |||||||
| chr11:34110410 | A | G | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.200+1577A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110410 | |||||||
| chr11:34110427 | C | T | 1 | a0001c0001t0002g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.200+1594C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110427 | |||||||
| chr11:34110491 | A | G | 1 | a0001c0001t0002g0144 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.201-1561A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110491 | |||||||
| chr11:34110559 | C | CT | 14 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(11): Show |
14 | HG00597.hp2 HG02040.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.201-1468dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | ||||||
| chr11:34110559 | C | CTT | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | HG02572.hp1 HG02818.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-1469_201-1468d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | ||||||
| chr11:34110559 | CT | C | 15 | a0001c0001t0001g0020 a0001c0001t0001g0056 a0001c0001t0001g0059 others(12): Show |
16 | HG00323.hp2 HG01515.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.201-1468delT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | ||||||
| chr11:34110559 | CTT | C | 7 | a0001c0001t0001g0018 a0001c0001t0001g0152 a0001c0003t0001g0042 others(4): Show |
8 | HG02976.hp2 HG03209.hp1 HG03669.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-1469_201-1468d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | ||||||
| chr11:34110559 | CTTT | C | 10 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(7): Show |
13 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.201-1470_201-1468d others(5): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | ||||||
| chr11:34110559 | CTTTTTTT others(3): Show |
C | 1 | a0001c0005t0004g0045 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.201-1477_201-1468d others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34110559 | ||||||
| chr11:34110915 | C | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
257 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.201-1137C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34110915 | |||||||
| chr11:34111010 | G | A | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.201-1042G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111010 | |||||||
| chr11:34111019 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.201-1033T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111019 | |||||||
| chr11:34111062 | A | G | 4 | a0001c0001t0001g0018 a0001c0001t0001g0152 a0001c0001t0001g0161 others(1): Show |
5 | HG02451.hp2 HG02976.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.201-990A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111062 | |||||||
| chr11:34111196 | GC | G | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-852delC | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34111196 | ||||||
| chr11:34111417 | C | G | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.201-635C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111417 | |||||||
| chr11:34111842 | C | T | 1 | a0001c0019t0001g0147 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.201-210C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111842 | |||||||
| chr11:34111881 | A | G | 1 | a0001c0001t0002g0060 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.201-171A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34111881 | |||||||
| chr11:34111931 | T | TTC | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.201-120_201-119dup others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr11 | 34111931 | ||||||
| chr11:34112005 | T | C | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.201-47T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34112005 | |||||||
| chr11:34112007 | C | T | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.201-45C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34112007 | |||||||
| chr11:34112039 | T | C | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.201-13T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34112039 | |||||||
| chr11:34112040 | G | A | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.201-12G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 3/28 | chr11 | 34112040 | |||||||
| chr11:34112331 | T | C | 3 | a0005c0008t0003g0024 a0005c0008t0003g0025 a0005c0008t0003g0026 |
3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.372+108T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34112331 | |||||||
| chr11:34112470 | A | G | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.372+247A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34112470 | |||||||
| chr11:34112471 | C | T | 1 | a0001c0001t0002g0139 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.372+248C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34112471 | |||||||
| chr11:34112600 | C | T | 1 | a0001c0001t0002g0138 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.372+377C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34112600 | |||||||
| chr11:34112930 | T | C | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.372+707T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34112930 | |||||||
| chr11:34113054 | C | T | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.373-662C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113054 | |||||||
| chr11:34113151 | G | A | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.373-565G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113151 | |||||||
| chr11:34113264 | T | C | 1 | a0009c0017t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.373-452T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113264 | |||||||
| chr11:34113327 | G | A | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-389G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113327 | |||||||
| chr11:34113344 | CGTTTTTG others(4): Show |
C | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-371_373-361del others(11): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113344 | |||||||
| chr11:34113345 | G | A | 24 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(21): Show |
28 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(25): Show |
intron_variant | MODIFIER | c.373-371G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113345 | |||||||
| chr11:34113366 | G | A | 7 | a0001c0004t0003g0032 a0001c0004t0005g0027 a0001c0004t0005g0029 others(4): Show |
7 | HG02145.hp1 HG02615.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.373-350G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113366 | |||||||
| chr11:34113379 | C | T | 88 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0018 others(85): Show |
101 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.373-337C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113379 | |||||||
| chr11:34113525 | A | G | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.373-191A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113525 | |||||||
| chr11:34113541 | G | T | 1 | a0001c0019t0001g0147 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.373-175G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113541 | |||||||
| chr11:34113636 | C | CA | 14 | a0001c0001t0001g0167 a0001c0001t0001g0205 a0001c0003t0001g0036 others(11): Show |
14 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.373-56dupA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr11 | 34113636 | ||||||
| chr11:34113636 | C | CAA | 7 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(4): Show |
9 | HG01168.hp1 HG01169.hp2 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.373-57_373-56dupAA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr11 | 34113636 | ||||||
| chr11:34113636 | CA | C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
199 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(196): Show |
intron_variant | MODIFIER | c.373-56delA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr11 | 34113636 | ||||||
| chr11:34113636 | CAA | C | 5 | a0001c0002t0001g0009 a0001c0002t0001g0049 a0001c0002t0001g0208 others(2): Show |
6 | HG02451.hp1 HG02486.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.373-57_373-56delAA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr11 | 34113636 | ||||||
| chr11:34113636 | CAAAAAAA others(3): Show |
C | 1 | a0002c0006t0001g0191 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.373-65_373-56delAA others(8): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr11 | 34113636 | ||||||
| chr11:34113703 | C | T | 1 | a0001c0002t0001g0202 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.373-13C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113703 | |||||||
| chr11:34113709 | C | T | 6 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(3): Show |
6 | HG02145.hp1 HG02258.hp1 HG02922.hp2 others(3): Show |
splice_region_variant&intron_variant | LOW | c.373-7C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 4/28 | chr11 | 34113709 | |||||||
| chr11:34114024 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
257 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.495+186A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114024 | |||||||
| chr11:34114068 | C | G | 1 | a0001c0001t0001g0190 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.495+230C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114068 | |||||||
| chr11:34114227 | C | T | 1 | a0006c0010t0001g0055 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.495+389C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114227 | |||||||
| chr11:34114383 | G | A | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+545G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114383 | |||||||
| chr11:34114384 | T | A | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+546T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114384 | |||||||
| chr11:34114385 | T | C | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+547T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114385 | |||||||
| chr11:34114387 | C | CTGAT | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+549_495+550ins others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114387 | |||||||
| chr11:34114388 | C | A | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.495+550C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114388 | |||||||
| chr11:34114401 | A | G | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.495+563A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114401 | |||||||
| chr11:34114451 | C | T | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.495+613C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114451 | |||||||
| chr11:34114481 | T | C | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.495+643T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114481 | |||||||
| chr11:34114549 | A | G | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.495+711A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114549 | |||||||
| chr11:34114673 | C | T | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.495+835C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114673 | |||||||
| chr11:34114760 | G | A | 3 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG00323.hp2 HG01109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.495+922G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114760 | |||||||
| chr11:34114874 | C | T | 1 | a0001c0001t0001g0136 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.496-949C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34114874 | |||||||
| chr11:34115097 | G | A | 2 | a0001c0001t0001g0140 a0001c0002t0001g0217 |
2 | HG02040.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.496-726G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34115097 | |||||||
| chr11:34115251 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.496-572G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34115251 | |||||||
| chr11:34115540 | G | A | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.496-283G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34115540 | |||||||
| chr11:34115665 | A | G | 4 | a0001c0001t0002g0132 a0001c0001t0002g0133 a0001c0001t0002g0134 others(1): Show |
4 | HG02080.hp1 HG02132.hp1 HG02165.hp1 others(1): Show |
intron_variant | MODIFIER | c.496-158A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34115665 | |||||||
| chr11:34115805 | G | A | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.496-18G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 5/28 | chr11 | 34115805 | |||||||
| chr11:34115905 | A | G | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | HG02818.hp2 HG02922.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.557+21A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34115905 | |||||||
| chr11:34115906 | A | G | 1 | a0001c0001t0001g0189 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.557+22A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34115906 | |||||||
| chr11:34115929 | G | A | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.557+45G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34115929 | |||||||
| chr11:34115977 | G | A | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.557+93G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34115977 | |||||||
| chr11:34116139 | T | C | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.557+255T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116139 | |||||||
| chr11:34116166 | T | C | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.557+282T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116166 | |||||||
| chr11:34116267 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.557+383T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116267 | |||||||
| chr11:34116314 | A | C | 7 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0005t0004g0008 others(4): Show |
8 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.557+430A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116314 | |||||||
| chr11:34116328 | G | A | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.557+444G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116328 | |||||||
| chr11:34116385 | T | C | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.557+501T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116385 | |||||||
| chr11:34116481 | C | T | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.557+597C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116481 | |||||||
| chr11:34116904 | A | G | 16 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(13): Show |
19 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.557+1020A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34116904 | |||||||
| chr11:34117172 | CT | C | 15 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(12): Show |
18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.558-1007delT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117172 | |||||||
| chr11:34117208 | A | C | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-972A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117208 | |||||||
| chr11:34117210 | A | G | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-970A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117210 | |||||||
| chr11:34117211 | AAATTT | A | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-967_558-963del others(5): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | INFO_REALIGN_3_PRIME | chr11 | 34117211 | ||||||
| chr11:34117217 | A | G | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-963A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117217 | |||||||
| chr11:34117224 | T | G | 2 | a0001c0001t0001g0051 a0001c0001t0001g0052 |
2 | HG00733.hp2 HG02602.hp2 |
intron_variant | MODIFIER | c.558-956T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117224 | |||||||
| chr11:34117226 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
257 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.558-954A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117226 | |||||||
| chr11:34117396 | G | A | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.558-784G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117396 | |||||||
| chr11:34117446 | G | A | 15 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(12): Show |
18 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.558-734G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117446 | |||||||
| chr11:34117670 | G | A | 26 | a0001c0001t0002g0069 a0001c0001t0002g0070 a0001c0002t0002g0057 others(23): Show |
29 | HG00738.hp1 HG00741.hp2 HG01175.hp2 others(26): Show |
intron_variant | MODIFIER | c.558-510G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117670 | |||||||
| chr11:34117691 | A | G | 1 | a0001c0001t0002g0131 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.558-489A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117691 | |||||||
| chr11:34117731 | A | C | 23 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(20): Show |
26 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.558-449A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117731 | |||||||
| chr11:34117803 | G | T | 2 | a0001c0001t0001g0187 a0001c0001t0001g0188 |
2 | HG01168.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.558-377G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117803 | |||||||
| chr11:34117811 | A | T | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.558-369A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117811 | |||||||
| chr11:34117901 | C | T | 2 | a0001c0001t0001g0017 a0001c0001t0001g0059 |
3 | HG02615.hp2 HG02976.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.558-279C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 6/28 | chr11 | 34117901 | |||||||
| chr11:34118334 | C | T | 1 | a0001c0005t0004g0048 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.672+40C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/28 | chr11 | 34118334 | |||||||
| chr11:34118347 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.673-49G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/28 | chr11 | 34118347 | |||||||
| chr11:34118392 | G | A | 1 | a0001c0004t0005g0027 | 1 | NA19043.hp2 | splice_region_variant&intron_variant | LOW | c.673-4G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 7/28 | chr11 | 34118392 | |||||||
| chr11:34118637 | C | T | 1 | a0001c0002t0001g0130 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.780+134C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34118637 | |||||||
| chr11:34118689 | G | C | 2 | a0001c0001t0002g0219 a0001c0002t0009g0215 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.780+186G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34118689 | |||||||
| chr11:34118818 | C | G | 1 | a0001c0001t0002g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.780+315C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34118818 | |||||||
| chr11:34118954 | A | G | 5 | a0001c0003t0001g0039 a0001c0003t0001g0042 a0001c0022t0001g0038 others(2): Show |
5 | HG00738.hp1 HG03654.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.780+451A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34118954 | |||||||
| chr11:34119014 | C | T | 1 | a0007c0012t0001g0043 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.780+511C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119014 | |||||||
| chr11:34119071 | T | G | 3 | a0005c0008t0003g0024 a0005c0008t0003g0025 a0005c0008t0003g0026 |
3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.780+568T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119071 | |||||||
| chr11:34119079 | G | A | 1 | a0001c0002t0009g0215 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.780+576G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119079 | |||||||
| chr11:34119142 | G | A | 2 | a0001c0002t0001g0071 a0001c0002t0001g0072 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.780+639G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119142 | |||||||
| chr11:34119159 | A | G | 1 | a0001c0001t0002g0128 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.780+656A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119159 | |||||||
| chr11:34119404 | T | C | 2 | a0001c0001t0002g0003 a0001c0001t0002g0073 |
5 | HG00733.hp1 HG01928.hp1 HG01934.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+901T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119404 | |||||||
| chr11:34119415 | T | C | 1 | a0001c0002t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.780+912T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119415 | |||||||
| chr11:34119594 | A | C | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.780+1091A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119594 | |||||||
| chr11:34119694 | A | G | 3 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0148 |
3 | HG02559.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.780+1191A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119694 | |||||||
| chr11:34119917 | A | G | 5 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0130 others(2): Show |
5 | HG02486.hp1 HG02572.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.780+1414A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119917 | |||||||
| chr11:34119927 | G | A | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.780+1424G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119927 | |||||||
| chr11:34119946 | T | C | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.780+1443T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119946 | |||||||
| chr11:34119981 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(183): Show |
214 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.780+1478C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34119981 | |||||||
| chr11:34120085 | A | G | 20 | a0001c0002t0001g0009 a0001c0002t0001g0049 a0001c0003t0001g0002 others(17): Show |
26 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(23): Show |
intron_variant | MODIFIER | c.780+1582A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120085 | |||||||
| chr11:34120118 | TTTG | T | 29 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(26): Show |
34 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.780+1631_780+1633d others(5): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34120118 | ||||||
| chr11:34120143 | G | GT | 174 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(171): Show |
203 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(200): Show |
intron_variant | MODIFIER | c.780+1660dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34120143 | ||||||
| chr11:34120143 | G | GTT | 18 | a0001c0001t0001g0023 a0001c0001t0001g0185 a0001c0001t0001g0186 others(15): Show |
19 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(16): Show |
intron_variant | MODIFIER | c.780+1659_780+1660d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34120143 | ||||||
| chr11:34120143 | GT | G | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.780+1660delT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34120143 | ||||||
| chr11:34120172 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.780+1669G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120172 | |||||||
| chr11:34120200 | T | A | 29 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(26): Show |
34 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.780+1697T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120200 | |||||||
| chr11:34120222 | G | A | 2 | a0001c0002t0001g0216 a0001c0002t0001g0217 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.780+1719G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120222 | |||||||
| chr11:34120319 | A | G | 2 | a0001c0004t0005g0029 a0001c0020t0005g0028 |
2 | HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.780+1816A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120319 | |||||||
| chr11:34120328 | A | G | 29 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(26): Show |
34 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(31): Show |
intron_variant | MODIFIER | c.780+1825A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120328 | |||||||
| chr11:34120417 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.780+1914G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120417 | |||||||
| chr11:34120623 | T | A | 1 | a0001c0001t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.781-1836T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120623 | |||||||
| chr11:34120769 | A | G | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.781-1690A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120769 | |||||||
| chr11:34120793 | G | A | 2 | a0001c0001t0002g0074 a0001c0001t0002g0075 |
2 | HG01261.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.781-1666G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120793 | |||||||
| chr11:34120825 | G | T | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.781-1634G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34120825 | |||||||
| chr11:34121102 | C | T | 3 | a0001c0001t0002g0125 a0001c0001t0002g0131 a0001c0001t0002g0144 |
3 | HG01123.hp1 HG01175.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.781-1357C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121102 | |||||||
| chr11:34121103 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.781-1356A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121103 | |||||||
| chr11:34121131 | T | C | 3 | a0001c0002t0001g0127 a0001c0002t0001g0130 a0001c0002t0001g0146 |
3 | HG02572.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.781-1328T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121131 | |||||||
| chr11:34121179 | A | G | 4 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0130 others(1): Show |
4 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.781-1280A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121179 | |||||||
| chr11:34121206 | G | A | 1 | a0001c0001t0002g0118 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.781-1253G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121206 | |||||||
| chr11:34121637 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.781-822G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121637 | |||||||
| chr11:34121689 | G | A | 1 | a0001c0002t0001g0126 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.781-770G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121689 | |||||||
| chr11:34121814 | C | G | 1 | a0001c0001t0006g0117 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.781-645C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121814 | |||||||
| chr11:34121840 | CAG | C | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.781-616_781-615del others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34121840 | ||||||
| chr11:34121858 | C | CA | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(117): Show |
142 | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.781-577dupA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34121858 | ||||||
| chr11:34121858 | C | CAA | 18 | a0001c0001t0001g0076 a0001c0001t0001g0077 a0001c0001t0001g0078 others(15): Show |
18 | HG00738.hp1 HG00741.hp1 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.781-578_781-577dup others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34121858 | ||||||
| chr11:34121858 | CAA | C | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.781-578_781-577del others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34121858 | ||||||
| chr11:34121858 | CAAAAAAA others(5): Show |
C | 1 | a0001c0001t0002g0116 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.781-588_781-577del others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | INFO_REALIGN_3_PRIME | chr11 | 34121858 | ||||||
| chr11:34121882 | A | T | 1 | a0001c0001t0001g0210 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.781-577A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121882 | |||||||
| chr11:34121885 | T | C | 1 | a0001c0001t0001g0168 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.781-574T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121885 | |||||||
| chr11:34121950 | C | T | 2 | a0001c0001t0002g0016 a0010c0021t0002g0066 |
3 | HG01070.hp1 HG01071.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.781-509C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34121950 | |||||||
| chr11:34122048 | C | T | 1 | a0001c0004t0005g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.781-411C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34122048 | |||||||
| chr11:34122049 | G | T | 1 | a0001c0001t0002g0124 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.781-410G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34122049 | |||||||
| chr11:34122180 | A | C | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.781-279A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34122180 | |||||||
| chr11:34122453 | C | G | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | HG02818.hp2 HG02922.hp1 HG03540.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.781-6C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 8/28 | chr11 | 34122453 | |||||||
| chr11:34122931 | G | C | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.914+339G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34122931 | |||||||
| chr11:34122945 | C | A | 1 | a0001c0002t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.914+353C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34122945 | |||||||
| chr11:34122966 | T | G | 3 | a0005c0008t0003g0024 a0005c0008t0003g0025 a0005c0008t0003g0026 |
3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.914+374T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34122966 | |||||||
| chr11:34123000 | A | G | 1 | a0001c0002t0001g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.914+408A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123000 | |||||||
| chr11:34123032 | T | C | 31 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0003t0001g0002 others(28): Show |
36 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(33): Show |
intron_variant | MODIFIER | c.914+440T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123032 | |||||||
| chr11:34123126 | T | C | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.914+534T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123126 | |||||||
| chr11:34123201 | G | C | 1 | a0001c0002t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.915-561G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123201 | |||||||
| chr11:34123291 | G | C | 1 | a0001c0001t0001g0196 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.915-471G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123291 | |||||||
| chr11:34123399 | C | T | 1 | a0001c0019t0001g0147 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.915-363C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123399 | |||||||
| chr11:34123424 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.915-338C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123424 | |||||||
| chr11:34123456 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.915-306G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 9/28 | chr11 | 34123456 | |||||||
| chr11:34123912 | G | A | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1008+57G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 10/28 | chr11 | 34123912 | |||||||
| chr11:34123965 | T | G | 1 | a0011c0014t0001g0082 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1008+110T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 10/28 | chr11 | 34123965 | |||||||
| chr11:34124135 | C | T | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG02818.hp2 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1009-167C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 10/28 | chr11 | 34124135 | |||||||
| chr11:34124558 | A | G | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1107+158A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124558 | |||||||
| chr11:34124600 | T | C | 2 | a0001c0001t0001g0177 a0001c0001t0001g0193 |
2 | HG02738.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1107+200T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124600 | |||||||
| chr11:34124686 | T | C | 1 | a0001c0001t0002g0083 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1107+286T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124686 | |||||||
| chr11:34124709 | T | C | 2 | a0001c0001t0002g0219 a0001c0002t0009g0215 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1107+309T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124709 | |||||||
| chr11:34124755 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1107+355A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124755 | |||||||
| chr11:34124843 | A | C | 2 | a0001c0001t0002g0015 a0001c0001t0002g0065 |
3 | HG02015.hp1 HG02071.hp1 NA18970.hp1 |
intron_variant | MODIFIER | c.1107+443A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124843 | |||||||
| chr11:34124856 | C | T | 1 | a0005c0008t0003g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1107+456C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124856 | |||||||
| chr11:34124955 | A | G | 184 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(181): Show |
211 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.1107+555A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34124955 | |||||||
| chr11:34125099 | C | A | 3 | a0001c0001t0006g0058 a0001c0001t0006g0117 a0001c0001t0006g0119 |
3 | HG00621.hp1 NA18968.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1107+699C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125099 | |||||||
| chr11:34125215 | A | G | 2 | a0002c0006t0001g0163 a0002c0006t0001g0164 |
2 | HG00597.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1107+815A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125215 | |||||||
| chr11:34125330 | T | C | 1 | a0001c0001t0001g0076 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.1107+930T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125330 | |||||||
| chr11:34125798 | A | G | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1107+1398A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125798 | |||||||
| chr11:34125930 | G | A | 2 | a0001c0002t0001g0216 a0001c0002t0001g0217 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1107+1530G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125930 | |||||||
| chr11:34125941 | A | G | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1108-1522A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125941 | |||||||
| chr11:34125959 | C | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG00323.hp2 HG01109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1108-1504C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125959 | |||||||
| chr11:34125998 | A | G | 1 | a0013c0013t0002g0222 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1108-1465A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34125998 | |||||||
| chr11:34126319 | A | G | 1 | a0001c0001t0001g0106 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1108-1144A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126319 | |||||||
| chr11:34126691 | C | T | 2 | a0001c0002t0001g0216 a0001c0002t0001g0217 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.1108-772C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126691 | |||||||
| chr11:34126856 | A | G | 2 | a0001c0001t0002g0062 a0001c0001t0002g0105 |
2 | HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1108-607A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126856 | |||||||
| chr11:34126903 | G | A | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1108-560G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126903 | |||||||
| chr11:34126955 | CAG | C | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108-507_1108-506d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126955 | |||||||
| chr11:34126998 | C | T | 1 | a0001c0002t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1108-465C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34126998 | |||||||
| chr11:34127023 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0152 a0001c0001t0001g0162 |
4 | HG02976.hp2 HG03516.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.1108-440C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34127023 | |||||||
| chr11:34127100 | ATC | A | 7 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(4): Show |
7 | HG02818.hp2 HG02886.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108-358_1108-357d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr11 | 34127100 | ||||||
| chr11:34127179 | A | G | 1 | a0001c0004t0005g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1108-284A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34127179 | |||||||
| chr11:34127183 | G | C | 3 | a0005c0008t0003g0024 a0005c0008t0003g0025 a0005c0008t0003g0026 |
3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1108-280G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34127183 | |||||||
| chr11:34127340 | A | G | 1 | a0001c0001t0001g0104 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1108-123A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34127340 | |||||||
| chr11:34127445 | A | T | 3 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0148 |
3 | HG02559.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1108-18A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 11/28 | chr11 | 34127445 | |||||||
| chr11:34127619 | A | T | 13 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(10): Show |
14 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244+20A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34127619 | |||||||
| chr11:34127652 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1244+53T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34127652 | |||||||
| chr11:34127706 | AGTCTCTG others(3): Show |
A | 1 | a0001c0001t0001g0184 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1244+110_1244+119d others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34127706 | ||||||
| chr11:34127708 | T | G | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1244+109T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34127708 | |||||||
| chr11:34127786 | G | A | 1 | a0001c0022t0001g0038 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1244+187G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34127786 | |||||||
| chr11:34128122 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1244+523G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128122 | |||||||
| chr11:34128130 | C | T | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244+531C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128130 | |||||||
| chr11:34128213 | G | C | 3 | a0005c0008t0003g0024 a0005c0008t0003g0025 a0005c0008t0003g0026 |
3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1244+614G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128213 | |||||||
| chr11:34128236 | C | T | 1 | a0001c0001t0001g0171 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1244+637C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128236 | |||||||
| chr11:34128293 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1244+694G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128293 | |||||||
| chr11:34128362 | C | CA | 6 | a0001c0001t0001g0012 a0001c0001t0001g0067 a0001c0001t0001g0168 others(3): Show |
8 | HG01109.hp1 HG01109.hp2 HG01168.hp1 others(5): Show |
intron_variant | MODIFIER | c.1244+779dupA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34128362 | ||||||
| chr11:34128362 | CA | C | 13 | a0001c0002t0001g0217 a0001c0004t0003g0032 a0001c0004t0003g0033 others(10): Show |
14 | HG02145.hp1 HG02258.hp1 HG02572.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244+779delA | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34128362 | ||||||
| chr11:34128367 | A | C | 29 | a0001c0001t0002g0003 a0001c0001t0002g0014 a0001c0001t0002g0015 others(26): Show |
35 | HG00673.hp2 HG00733.hp1 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.1244+768A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128367 | |||||||
| chr11:34128372 | A | C | 1 | a0001c0001t0002g0065 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1244+773A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128372 | |||||||
| chr11:34128437 | A | G | 13 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(10): Show |
14 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1244+838A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128437 | |||||||
| chr11:34128502 | A | G | 1 | a0001c0001t0002g0016 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1244+903A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128502 | |||||||
| chr11:34128562 | G | A | 1 | a0001c0001t0001g0204 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1244+963G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128562 | |||||||
| chr11:34128680 | A | G | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1244+1081A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128680 | |||||||
| chr11:34128694 | C | A | 1 | a0001c0001t0001g0187 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1244+1095C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128694 | |||||||
| chr11:34128711 | A | G | 1 | a0001c0001t0001g0052 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1244+1112A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128711 | |||||||
| chr11:34128836 | G | C | 1 | a0001c0002t0001g0216 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1244+1237G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128836 | |||||||
| chr11:34128876 | C | T | 4 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0029 others(1): Show |
4 | HG02258.hp1 HG02615.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1244+1277C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128876 | |||||||
| chr11:34128888 | A | G | 224 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
257 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.1244+1289A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128888 | |||||||
| chr11:34128905 | G | A | 1 | a0001c0001t0002g0145 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1244+1306G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128905 | |||||||
| chr11:34128955 | C | T | 170 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(167): Show |
197 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(194): Show |
intron_variant | MODIFIER | c.1244+1356C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34128955 | |||||||
| chr11:34129011 | A | G | 1 | a0001c0003t0001g0037 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1244+1412A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129011 | |||||||
| chr11:34129039 | T | G | 1 | a0001c0002t0001g0148 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1244+1440T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129039 | |||||||
| chr11:34129165 | G | A | 1 | a0001c0001t0001g0086 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1244+1566G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129165 | |||||||
| chr11:34129174 | T | C | 1 | a0001c0002t0001g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1244+1575T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129174 | |||||||
| chr11:34129186 | T | C | 1 | a0001c0001t0001g0155 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1244+1587T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129186 | |||||||
| chr11:34129242 | G | C | 2 | a0001c0004t0005g0027 a0001c0004t0005g0034 |
2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1245-1571G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129242 | |||||||
| chr11:34129278 | T | C | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1245-1535T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129278 | |||||||
| chr11:34129292 | C | G | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(189): Show |
219 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(216): Show |
intron_variant | MODIFIER | c.1245-1521C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129292 | |||||||
| chr11:34129347 | G | A | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245-1466G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129347 | |||||||
| chr11:34129407 | A | G | 5 | a0001c0003t0001g0039 a0001c0003t0001g0042 a0001c0022t0001g0038 others(2): Show |
5 | HG00738.hp1 HG03654.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1245-1406A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129407 | |||||||
| chr11:34129584 | TTTC | T | 6 | a0001c0004t0005g0027 a0001c0004t0005g0029 a0001c0004t0005g0034 others(3): Show |
6 | HG02145.hp1 HG02922.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1245-1214_1245-121 others(7): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34129584 | ||||||
| chr11:34129599 | C | CT | 16 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0078 others(13): Show |
17 | HG00438.hp1 HG01071.hp1 HG01106.hp2 others(14): Show |
intron_variant | MODIFIER | c.1245-1188dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34129599 | ||||||
| chr11:34129599 | CT | C | 127 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(124): Show |
145 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1245-1188delT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34129599 | ||||||
| chr11:34129599 | CTT | C | 8 | a0001c0001t0001g0188 a0001c0002t0001g0126 a0001c0002t0001g0127 others(5): Show |
8 | HG01168.hp2 HG02647.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1245-1189_1245-118 others(6): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34129599 | ||||||
| chr11:34129599 | CTTTTTTT others(8): Show |
C | 7 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0005t0004g0008 others(4): Show |
8 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.1245-1202_1245-118 others(19): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34129599 | ||||||
| chr11:34129603 | T | C | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1245-1210T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129603 | |||||||
| chr11:34129625 | T | G | 3 | a0005c0008t0003g0024 a0005c0008t0003g0025 a0005c0008t0003g0026 |
3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1245-1188T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129625 | |||||||
| chr11:34129709 | C | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1245-1104C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34129709 | |||||||
| chr11:34130044 | A | ACACT | 15 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0004t0003g0032 others(12): Show |
16 | HG02145.hp1 HG02258.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1245-767_1245-766i others(6): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | INFO_REALIGN_3_PRIME | chr11 | 34130044 | ||||||
| chr11:34130161 | T | C | 1 | a0001c0002t0001g0127 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1245-652T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130161 | |||||||
| chr11:34130224 | A | G | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.1245-589A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130224 | |||||||
| chr11:34130247 | A | G | 1 | a0001c0001t0002g0139 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1245-566A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130247 | |||||||
| chr11:34130342 | A | G | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1245-471A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130342 | |||||||
| chr11:34130383 | C | G | 1 | a0001c0001t0001g0182 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1245-430C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130383 | |||||||
| chr11:34130422 | A | G | 2 | a0001c0004t0005g0029 a0001c0020t0005g0028 |
2 | HG02615.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1245-391A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130422 | |||||||
| chr11:34130489 | A | G | 1 | a0001c0001t0002g0129 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1245-324A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130489 | |||||||
| chr11:34130527 | C | G | 1 | a0001c0001t0001g0020 | 2 | HG02015.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1245-286C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 12/28 | chr11 | 34130527 | |||||||
| chr11:34130941 | C | T | 1 | a0001c0002t0009g0215 | 1 | HG02451.hp1 | splice_region_variant&intron_variant | LOW | c.1369+4C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/28 | chr11 | 34130941 | |||||||
| chr11:34130977 | A | G | 1 | a0001c0001t0001g0143 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1369+40A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/28 | chr11 | 34130977 | |||||||
| chr11:34131313 | C | G | 2 | a0001c0003t0003g0035 a0001c0003t0003g0044 |
2 | HG03041.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.1370-68C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/28 | chr11 | 34131313 | |||||||
| chr11:34131333 | A | C | 1 | a0001c0001t0002g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1370-48A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/28 | chr11 | 34131333 | |||||||
| chr11:34131360 | G | A | 1 | a0001c0001t0011g0087 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1370-21G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 13/28 | chr11 | 34131360 | |||||||
| chr11:34131560 | G | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0001t0001g0068 |
3 | HG00323.hp2 HG01109.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1520+29G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131560 | |||||||
| chr11:34131657 | TTTCCTTT others(5): Show |
T | 1 | a0001c0016t0001g0050 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1520+136_1520+147d others(14): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | INFO_REALIGN_3_PRIME | chr11 | 34131657 | ||||||
| chr11:34131685 | TC | T | 6 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0041 others(3): Show |
9 | HG02109.hp1 HG02895.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1520+155delC | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131685 | |||||||
| chr11:34131686 | C | T | 5 | a0001c0003t0001g0039 a0001c0003t0001g0042 a0001c0022t0001g0038 others(2): Show |
5 | HG00738.hp1 HG03654.hp2 HG03669.hp1 others(2): Show |
intron_variant | MODIFIER | c.1520+155C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131686 | |||||||
| chr11:34131723 | G | C | 1 | a0001c0003t0003g0044 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1520+192G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131723 | |||||||
| chr11:34131735 | G | A | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1520+204G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131735 | |||||||
| chr11:34131805 | C | T | 2 | a0001c0001t0002g0103 a0001c0001t0002g0114 |
2 | NA19056.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1520+274C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131805 | |||||||
| chr11:34131842 | C | T | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | HG02818.hp2 HG02922.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1521-283C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131842 | |||||||
| chr11:34131858 | G | T | 1 | a0001c0001t0002g0138 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1521-267G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 14/28 | chr11 | 34131858 | |||||||
| chr11:34132500 | CGGT | C | 19 | a0001c0001t0001g0011 a0001c0001t0001g0052 a0001c0001t0001g0053 others(16): Show |
20 | HG00621.hp1 HG00741.hp1 HG01081.hp1 others(17): Show |
intron_variant | MODIFIER | c.1617+284_1617+286d others(5): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 15/28 | INFO_REALIGN_3_PRIME | chr11 | 34132500 | ||||||
| chr11:34132689 | A | G | 1 | a0001c0001t0002g0120 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1618-337A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 15/28 | chr11 | 34132689 | |||||||
| chr11:34132885 | A | G | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(190): Show |
221 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(218): Show |
intron_variant | MODIFIER | c.1618-141A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 15/28 | chr11 | 34132885 | |||||||
| chr11:34132914 | C | T | 1 | a0001c0002t0001g0197 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1618-112C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 15/28 | chr11 | 34132914 | |||||||
| chr11:34133366 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1734+224C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133366 | |||||||
| chr11:34133374 | C | G | 3 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0130 |
3 | HG02647.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1734+232C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133374 | |||||||
| chr11:34133426 | C | T | 1 | a0001c0002t0001g0049 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1734+284C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133426 | |||||||
| chr11:34133463 | A | G | 2 | a0001c0001t0001g0220 a0001c0001t0001g0221 |
2 | HG02886.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1734+321A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133463 | |||||||
| chr11:34133559 | C | T | 2 | a0001c0001t0002g0062 a0001c0001t0002g0105 |
2 | HG02132.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1734+417C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133559 | |||||||
| chr11:34133734 | T | C | 1 | a0001c0004t0005g0030 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1735-585T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133734 | |||||||
| chr11:34133838 | G | T | 5 | a0001c0001t0001g0209 a0001c0001t0001g0210 a0001c0001t0001g0211 others(2): Show |
5 | HG02818.hp2 HG02922.hp1 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1735-481G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133838 | |||||||
| chr11:34133882 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.1735-437A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133882 | |||||||
| chr11:34133919 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1735-400G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133919 | |||||||
| chr11:34133927 | C | T | 3 | a0001c0001t0006g0058 a0001c0001t0006g0117 a0001c0001t0006g0119 |
3 | HG00621.hp1 NA18968.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.1735-392C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133927 | |||||||
| chr11:34133928 | G | A | 1 | a0001c0002t0009g0215 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1735-391G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133928 | |||||||
| chr11:34133959 | T | C | 9 | a0001c0003t0001g0037 a0001c0004t0003g0032 a0001c0004t0003g0033 others(6): Show |
9 | HG01243.hp2 HG02145.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1735-360T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133959 | |||||||
| chr11:34133968 | C | T | 1 | a0001c0001t0001g0175 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1735-351C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34133968 | |||||||
| chr11:34134006 | T | A | 1 | a0001c0001t0002g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1735-313T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34134006 | |||||||
| chr11:34134022 | G | T | 1 | a0001c0001t0001g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1735-297G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34134022 | |||||||
| chr11:34134032 | T | C | 1 | a0001c0001t0002g0100 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1735-287T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34134032 | |||||||
| chr11:34134105 | A | T | 1 | a0001c0001t0001g0108 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1735-214A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34134105 | |||||||
| chr11:34134143 | G | A | 1 | a0001c0001t0001g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1735-176G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 16/28 | chr11 | 34134143 | |||||||
| chr11:34134425 | C | T | 3 | a0001c0001t0001g0168 a0001c0001t0001g0170 a0001c0001t0001g0203 |
3 | HG00673.hp1 HG02040.hp1 HG02135.hp2 |
splice_region_variant&intron_variant | LOW | c.1836+5C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 17/28 | chr11 | 34134425 | |||||||
| chr11:34134596 | C | T | 1 | a0001c0001t0001g0142 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1911+10C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34134596 | |||||||
| chr11:34134897 | A | C | 2 | a0001c0004t0003g0032 a0001c0004t0003g0033 |
2 | HG02258.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1912-278A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34134897 | |||||||
| chr11:34134995 | A | G | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.1912-180A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34134995 | |||||||
| chr11:34135084 | G | C | 1 | a0001c0002t0009g0215 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1912-91G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34135084 | |||||||
| chr11:34135084 | G | T | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1912-91G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34135084 | |||||||
| chr11:34135107 | A | T | 1 | a0001c0002t0009g0215 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1912-68A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 18/28 | chr11 | 34135107 | |||||||
| chr11:34135325 | G | A | 1 | a0001c0001t0001g0088 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.2028+34G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34135325 | |||||||
| chr11:34135594 | G | C | 1 | a0001c0002t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2028+303G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34135594 | |||||||
| chr11:34135729 | T | C | 17 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(14): Show |
21 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2028+438T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34135729 | |||||||
| chr11:34135836 | G | A | 1 | a0001c0001t0002g0100 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2028+545G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34135836 | |||||||
| chr11:34136084 | A | AT | 5 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0009t0007g0010 others(2): Show |
6 | HG01168.hp1 HG01169.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.2029-543dupT | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | INFO_REALIGN_3_PRIME | chr11 | 34136084 | ||||||
| chr11:34136162 | A | C | 12 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(9): Show |
15 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.2029-480A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34136162 | |||||||
| chr11:34136345 | G | A | 3 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0130 |
3 | HG02647.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2029-297G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34136345 | |||||||
| chr11:34136441 | T | C | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2029-201T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 19/28 | chr11 | 34136441 | |||||||
| chr11:34136864 | A | G | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2162+89A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 20/28 | chr11 | 34136864 | |||||||
| chr11:34136884 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2163-94T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 20/28 | chr11 | 34136884 | |||||||
| chr11:34137034 | A | G | 3 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0130 |
3 | HG02647.hp2 HG02809.hp1 HG03195.hp1 |
splice_region_variant&intron_variant | LOW | c.2211+8A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137034 | |||||||
| chr11:34137038 | A | G | 7 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0005t0004g0008 others(4): Show |
8 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2211+12A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137038 | |||||||
| chr11:34137161 | T | C | 3 | a0005c0008t0003g0024 a0005c0008t0003g0025 a0005c0008t0003g0026 |
3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2211+135T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137161 | |||||||
| chr11:34137262 | G | A | 4 | a0001c0002t0001g0208 a0005c0008t0003g0024 a0005c0008t0003g0025 others(1): Show |
4 | HG02486.hp1 HG03209.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.2211+236G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137262 | |||||||
| chr11:34137337 | A | C | 1 | a0001c0004t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2211+311A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137337 | |||||||
| chr11:34137375 | G | A | 6 | a0001c0004t0005g0027 a0001c0004t0005g0029 a0001c0004t0005g0030 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2211+349G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137375 | |||||||
| chr11:34137772 | A | C | 1 | a0001c0001t0001g0068 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2211+746A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137772 | |||||||
| chr11:34137858 | G | C | 2 | a0005c0008t0003g0024 a0005c0008t0003g0025 |
2 | HG03209.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2211+832G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137858 | |||||||
| chr11:34137985 | G | T | 1 | a0001c0001t0002g0132 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2211+959G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34137985 | |||||||
| chr11:34138025 | A | G | 2 | a0001c0001t0002g0219 a0001c0002t0009g0215 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2211+999A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138025 | |||||||
| chr11:34138083 | G | T | 1 | a0001c0002t0001g0217 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2211+1057G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138083 | |||||||
| chr11:34138226 | A | G | 2 | a0001c0001t0002g0069 a0001c0002t0002g0057 |
2 | HG00741.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.2212-965A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138226 | |||||||
| chr11:34138285 | G | A | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2212-906G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138285 | |||||||
| chr11:34138359 | C | T | 1 | a0004c0011t0001g0224 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.2212-832C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138359 | |||||||
| chr11:34138567 | C | A | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2212-624C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138567 | |||||||
| chr11:34138646 | C | G | 13 | a0001c0001t0001g0205 a0001c0003t0001g0002 a0001c0003t0001g0036 others(10): Show |
16 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(13): Show |
intron_variant | MODIFIER | c.2212-545C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138646 | |||||||
| chr11:34138665 | T | G | 3 | a0001c0002t0001g0009 a0001c0002t0001g0049 a0001c0019t0001g0147 |
4 | HG02622.hp2 HG02630.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2212-526T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138665 | |||||||
| chr11:34138667 | T | C | 2 | a0001c0001t0002g0219 a0001c0002t0009g0215 |
2 | HG02451.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.2212-524T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138667 | |||||||
| chr11:34138675 | G | A | 3 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0130 |
3 | HG02647.hp2 HG02809.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2212-516G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138675 | |||||||
| chr11:34138779 | T | A | 45 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0020 others(42): Show |
53 | HG00438.hp2 HG00597.hp2 HG00621.hp2 others(50): Show |
intron_variant | MODIFIER | c.2212-412T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34138779 | |||||||
| chr11:34139024 | G | A | 1 | a0001c0001t0001g0021 | 2 | NA18944.hp2 NA18953.hp1 |
intron_variant | MODIFIER | c.2212-167G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34139024 | |||||||
| chr11:34139132 | T | C | 1 | a0001c0001t0001g0156 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2212-59T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 21/28 | chr11 | 34139132 | |||||||
| chr11:34139309 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2308+22G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 22/28 | chr11 | 34139309 | |||||||
| chr11:34139365 | T | C | 1 | a0001c0002t0001g0202 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2309-20T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 22/28 | chr11 | 34139365 | |||||||
| chr11:34139917 | ATG | A | 3 | a0001c0001t0006g0058 a0001c0001t0006g0117 a0001c0001t0006g0119 |
3 | HG00621.hp1 NA18968.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.2419+426_2419+427d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | INFO_REALIGN_3_PRIME | chr11 | 34139917 | ||||||
| chr11:34140039 | A | G | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2420-361A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140039 | |||||||
| chr11:34140086 | A | G | 1 | a0001c0001t0001g0011 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.2420-314A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140086 | |||||||
| chr11:34140109 | G | A | 1 | a0005c0008t0003g0024 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2420-291G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140109 | |||||||
| chr11:34140194 | G | A | 1 | a0001c0001t0001g0189 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.2420-206G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140194 | |||||||
| chr11:34140327 | G | A | 3 | a0001c0002t0001g0071 a0001c0002t0001g0072 a0001c0002t0001g0148 |
3 | HG02559.hp1 HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2420-73G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140327 | |||||||
| chr11:34140357 | C | T | 1 | a0001c0001t0001g0099 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2420-43C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140357 | |||||||
| chr11:34140360 | C | T | 7 | a0001c0001t0002g0080 a0001c0001t0002g0097 a0001c0001t0002g0098 others(4): Show |
7 | HG01123.hp1 HG01175.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.2420-40C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 23/28 | chr11 | 34140360 | |||||||
| chr11:34140641 | G | A | 2 | a0001c0001t0001g0150 a0001c0001t0001g0151 |
2 | NA18971.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.2592+69G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/28 | chr11 | 34140641 | |||||||
| chr11:34140676 | C | A | 1 | a0009c0017t0001g0061 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.2592+104C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/28 | chr11 | 34140676 | |||||||
| chr11:34140683 | C | T | 1 | a0001c0004t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2592+111C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/28 | chr11 | 34140683 | |||||||
| chr11:34140684 | A | C | 1 | a0012c0018t0001g0121 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2592+112A>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/28 | chr11 | 34140684 | |||||||
| chr11:34140953 | A | G | 7 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0005t0004g0008 others(4): Show |
8 | HG02486.hp2 HG02723.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.2593-136A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 24/28 | chr11 | 34140953 | |||||||
| chr11:34141229 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2712+21G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141229 | |||||||
| chr11:34141287 | CAT | C | 8 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02615.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.2712+80_2712+81del others(2): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141287 | |||||||
| chr11:34141321 | T | TCA | 13 | a0001c0001t0001g0013 a0001c0001t0001g0017 a0001c0001t0001g0059 others(10): Show |
15 | HG01071.hp1 HG01106.hp2 HG01358.hp2 others(12): Show |
intron_variant | MODIFIER | c.2712+138_2712+139d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141321 | ||||||
| chr11:34141321 | TCA | T | 30 | a0001c0001t0001g0142 a0001c0001t0001g0143 a0001c0001t0001g0205 others(27): Show |
32 | HG01168.hp1 HG01169.hp2 HG02145.hp2 others(29): Show |
intron_variant | MODIFIER | c.2712+138_2712+139d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141321 | ||||||
| chr11:34141340 | C | G | 38 | a0001c0001t0001g0161 a0001c0001t0002g0003 a0001c0001t0002g0014 others(35): Show |
44 | HG00673.hp2 HG00733.hp1 HG00741.hp2 others(41): Show |
intron_variant | MODIFIER | c.2712+132C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141340 | |||||||
| chr11:34141407 | A | ATC | 24 | a0001c0001t0001g0007 a0001c0001t0001g0053 a0001c0001t0001g0094 others(21): Show |
27 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(24): Show |
intron_variant | MODIFIER | c.2712+200_2712+201d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141407 | ||||||
| chr11:34141408 | T | TCACACAC others(3): Show |
1 | a0001c0004t0005g0034 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2712+234_2712+243d others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | T | TCACACAC others(5): Show |
1 | a0001c0004t0005g0027 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.2712+232_2712+243d others(14): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | T | TCACACAC others(7): Show |
1 | a0001c0004t0005g0029 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2712+230_2712+243d others(16): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | T | TCACACAC others(11): Show |
1 | a0001c0004t0005g0030 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2712+226_2712+243d others(20): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | T | TCACACAC others(17): Show |
1 | a0001c0020t0005g0028 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2712+220_2712+243d others(26): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | T | TCTCA | 12 | a0001c0001t0001g0064 a0001c0001t0001g0078 a0001c0001t0001g0093 others(9): Show |
12 | HG02071.hp2 HG02129.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2712+201_2712+202i others(6): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | T | TCTCACA | 4 | a0001c0001t0001g0004 a0001c0001t0001g0013 a0001c0001t0001g0140 others(1): Show |
7 | HG00597.hp1 HG01071.hp1 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.2712+201_2712+202i others(8): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | T | TCTCACAC others(3): Show |
1 | a0001c0001t0001g0086 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.2712+201_2712+202i others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | TCA | T | 37 | a0001c0001t0001g0018 a0001c0001t0001g0153 a0001c0001t0001g0159 others(34): Show |
46 | HG00673.hp2 HG00733.hp1 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.2712+242_2712+243d others(4): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | TCACA | T | 14 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0001t0001g0068 others(11): Show |
15 | HG00323.hp2 HG01109.hp2 HG01261.hp2 others(12): Show |
intron_variant | MODIFIER | c.2712+240_2712+243d others(6): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | TCACACA | T | 18 | a0001c0001t0001g0011 a0001c0001t0001g0052 a0001c0001t0001g0077 others(15): Show |
19 | HG00621.hp1 HG00741.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.2712+238_2712+243d others(8): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | TCACACAC others(1): Show |
T | 11 | a0001c0001t0001g0051 a0001c0001t0001g0076 a0001c0001t0001g0107 others(8): Show |
12 | HG00733.hp2 HG02486.hp2 HG02622.hp2 others(9): Show |
intron_variant | MODIFIER | c.2712+236_2712+243d others(10): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | TCACACAC others(3): Show |
T | 3 | a0001c0001t0001g0205 a0001c0004t0003g0032 a0001c0004t0003g0033 |
3 | HG02258.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2712+234_2712+243d others(12): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | TCACACAC others(5): Show |
T | 2 | a0001c0002t0001g0130 a0001c0002t0001g0208 |
2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2712+232_2712+243d others(14): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141408 | TCACACAC others(7): Show |
T | 1 | a0001c0003t0001g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2712+230_2712+243d others(16): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | INFO_REALIGN_3_PRIME | chr11 | 34141408 | ||||||
| chr11:34141410 | A | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0012 others(89): Show |
107 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.2712+202A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141410 | |||||||
| chr11:34141412 | A | T | 37 | a0001c0001t0001g0153 a0001c0001t0001g0159 a0001c0001t0001g0189 others(34): Show |
45 | HG00673.hp2 HG00733.hp1 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.2712+204A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141412 | |||||||
| chr11:34141414 | A | T | 19 | a0001c0001t0001g0056 a0001c0001t0001g0067 a0001c0001t0001g0068 others(16): Show |
20 | HG00323.hp2 HG01109.hp2 HG01261.hp2 others(17): Show |
intron_variant | MODIFIER | c.2712+206A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141414 | |||||||
| chr11:34141416 | A | T | 17 | a0001c0001t0001g0011 a0001c0001t0001g0052 a0001c0001t0001g0077 others(14): Show |
18 | HG00621.hp1 HG00741.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.2712+208A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141416 | |||||||
| chr11:34141418 | A | T | 9 | a0001c0001t0001g0076 a0001c0001t0001g0107 a0001c0002t0001g0009 others(6): Show |
10 | HG02622.hp2 HG02630.hp2 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.2712+210A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141418 | |||||||
| chr11:34141420 | A | T | 3 | a0001c0001t0001g0205 a0001c0004t0003g0032 a0001c0004t0003g0033 |
3 | HG02258.hp1 HG03471.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2712+212A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141420 | |||||||
| chr11:34141422 | A | T | 2 | a0001c0002t0001g0130 a0001c0002t0001g0208 |
2 | HG02486.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2712+214A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141422 | |||||||
| chr11:34141424 | A | G | 1 | a0001c0001t0001g0180 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.2712+216A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141424 | |||||||
| chr11:34141424 | A | T | 1 | a0001c0003t0001g0036 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2712+216A>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141424 | |||||||
| chr11:34141452 | G | A | 2 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
2 | HG00323.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2712+244G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141452 | |||||||
| chr11:34141659 | G | A | 1 | a0001c0001t0002g0006 | 3 | HG03654.hp1 HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.2713-60G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 25/28 | chr11 | 34141659 | |||||||
| chr11:34142019 | T | G | 6 | a0001c0004t0005g0027 a0001c0004t0005g0029 a0001c0004t0005g0030 others(3): Show |
6 | HG02145.hp1 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.2811+202T>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142019 | |||||||
| chr11:34142069 | T | C | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2812-206T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142069 | |||||||
| chr11:34142080 | G | A | 2 | a0001c0002t0001g0216 a0001c0002t0001g0217 |
2 | HG02145.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.2812-195G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142080 | |||||||
| chr11:34142141 | A | G | 4 | a0001c0001t0001g0166 a0001c0001t0001g0173 a0001c0001t0001g0174 others(1): Show |
4 | HG00639.hp2 HG01243.hp1 HG02300.hp1 others(1): Show |
intron_variant | MODIFIER | c.2812-134A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142141 | |||||||
| chr11:34142158 | T | C | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(223): Show |
259 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(256): Show |
intron_variant | MODIFIER | c.2812-117T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142158 | |||||||
| chr11:34142229 | C | G | 1 | a0001c0001t0001g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.2812-46C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 26/28 | chr11 | 34142229 | |||||||
| chr11:34142354 | G | C | 3 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0130 |
3 | HG02647.hp2 HG02809.hp1 HG03195.hp1 |
splice_region_variant&intron_variant | LOW | c.2885+6G>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142354 | |||||||
| chr11:34142433 | C | T | 1 | a0001c0001t0001g0076 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2885+85C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142433 | |||||||
| chr11:34142501 | T | C | 1 | a0001c0001t0002g0091 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.2885+153T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142501 | |||||||
| chr11:34142536 | C | T | 17 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(14): Show |
21 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.2885+188C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142536 | |||||||
| chr11:34142549 | C | T | 2 | a0001c0002t0001g0071 a0001c0002t0001g0072 |
2 | HG02559.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.2885+201C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142549 | |||||||
| chr11:34142550 | G | A | 1 | a0001c0001t0001g0178 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.2885+202G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142550 | |||||||
| chr11:34142622 | G | A | 1 | a0001c0002t0001g0198 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2885+274G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142622 | |||||||
| chr11:34142681 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2885+333G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142681 | |||||||
| chr11:34142877 | G | A | 1 | a0005c0008t0003g0025 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2885+529G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34142877 | |||||||
| chr11:34143027 | A | G | 1 | a0001c0004t0008g0031 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2886-418A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34143027 | |||||||
| chr11:34143313 | A | G | 1 | a0001c0001t0002g0219 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2886-132A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 27/28 | chr11 | 34143313 | |||||||
| chr11:34143532 | A | G | 2 | a0001c0001t0001g0104 a0001c0001t0001g0136 |
2 | HG01081.hp1 HG01261.hp1 |
splice_region_variant&intron_variant | LOW | c.2969+4A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34143532 | |||||||
| chr11:34143696 | C | T | 1 | a0001c0001t0001g0188 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2969+168C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34143696 | |||||||
| chr11:34143962 | C | T | 1 | a0001c0019t0001g0147 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2969+434C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34143962 | |||||||
| chr11:34144163 | A | G | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2969+635A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144163 | |||||||
| chr11:34144172 | C | T | 1 | a0001c0009t0007g0010 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2969+644C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144172 | |||||||
| chr11:34144181 | T | C | 1 | a0001c0001t0002g0084 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.2969+653T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144181 | |||||||
| chr11:34144246 | G | A | 1 | a0001c0001t0002g0133 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.2969+718G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144246 | |||||||
| chr11:34144307 | G | T | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2969+779G>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144307 | |||||||
| chr11:34144313 | T | A | 2 | a0001c0001t0002g0081 a0001c0001t0002g0101 |
2 | HG01433.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.2969+785T>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144313 | |||||||
| chr11:34144332 | C | T | 3 | a0005c0008t0003g0024 a0005c0008t0003g0025 a0005c0008t0003g0026 |
3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2969+804C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144332 | |||||||
| chr11:34144400 | G | A | 5 | a0001c0005t0004g0008 a0001c0005t0004g0045 a0001c0005t0004g0046 others(2): Show |
6 | HG02818.hp1 HG02896.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.2969+872G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144400 | |||||||
| chr11:34144489 | C | A | 1 | a0001c0001t0001g0012 | 2 | HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.2969+961C>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144489 | |||||||
| chr11:34144629 | C | G | 1 | a0001c0001t0001g0205 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2969+1101C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144629 | |||||||
| chr11:34144746 | A | G | 4 | a0001c0002t0001g0126 a0001c0002t0001g0127 a0001c0002t0001g0130 others(1): Show |
4 | HG02572.hp2 HG02647.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2969+1218A>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34144746 | |||||||
| chr11:34145000 | C | G | 15 | a0001c0001t0001g0012 a0001c0001t0001g0142 a0001c0002t0001g0071 others(12): Show |
17 | HG02258.hp1 HG02280.hp2 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.2970-1084C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145000 | |||||||
| chr11:34145237 | C | T | 1 | a0001c0019t0001g0147 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2970-847C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145237 | |||||||
| chr11:34145349 | T | C | 2 | a0001c0001t0001g0092 a0001c0001t0001g0094 |
2 | HG00438.hp1 HG02155.hp1 |
intron_variant | MODIFIER | c.2970-735T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145349 | |||||||
| chr11:34145425 | G | A | 2 | a0001c0002t0001g0126 a0001c0002t0001g0130 |
2 | HG02647.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2970-659G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145425 | |||||||
| chr11:34145438 | G | A | 3 | a0005c0008t0003g0024 a0005c0008t0003g0025 a0005c0008t0003g0026 |
3 | HG03209.hp1 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.2970-646G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145438 | |||||||
| chr11:34145529 | T | C | 1 | a0001c0001t0002g0138 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2970-555T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145529 | |||||||
| chr11:34145633 | T | C | 11 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(8): Show |
14 | HG00738.hp1 HG01243.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.2970-451T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145633 | |||||||
| chr11:34145694 | G | A | 1 | a0001c0002t0001g0208 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2970-390G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145694 | |||||||
| chr11:34145700 | A | ATATGT | 5 | a0001c0003t0001g0002 a0001c0003t0001g0036 a0001c0003t0001g0037 others(2): Show |
8 | HG01243.hp2 HG02109.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.2970-383_2970-379d others(7): Show |
NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr11 | 34145700 | ||||||
| chr11:34145729 | G | A | 2 | a0001c0002t0001g0009 a0001c0002t0001g0049 |
3 | HG02622.hp2 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.2970-355G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145729 | |||||||
| chr11:34145825 | G | A | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2970-259G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145825 | |||||||
| chr11:34145880 | G | A | 224 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(221): Show |
257 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.2970-204G>A | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145880 | |||||||
| chr11:34145953 | T | C | 8 | a0001c0004t0003g0032 a0001c0004t0003g0033 a0001c0004t0005g0027 others(5): Show |
8 | HG02145.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2970-131T>C | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145953 | |||||||
| chr11:34145966 | C | G | 5 | a0001c0003t0003g0035 a0001c0003t0003g0044 a0005c0008t0003g0024 others(2): Show |
5 | HG03041.hp2 HG03209.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.2970-118C>G | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145966 | |||||||
| chr11:34145984 | C | T | 2 | a0001c0001t0001g0156 a0001c0001t0001g0158 |
2 | HG00323.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.2970-100C>T | NAT10 | ENSG00000135372.10 | transcript | ENST00000257829.8 | protein_coding | 28/28 | chr11 | 34145984 |