Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 56006 |
| ensemblid | ENSG00000105771.14 |
| hgncid | 25763 |
| symbol | SMG9 |
| name | SMG9 nonsense mediated mRNA decay factor |
| refseq_nuc | NM_019108.4 |
| refseq_prot | NP_061981.2 |
| ensembl_nuc | ENST00000270066.11 |
| ensembl_prot | ENSP00000270066.6 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 43727983 |
| end | 43754962 |
| strand | - |
| ver | v1.2 |
| region | chr19:43727983-43754962 |
| region5000 | chr19:43722983-43759962 |
| regionname0 | SMG9_chr19_43727983_43754962 |
| regionname5000 | SMG9_chr19_43722983_43759962 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 520 | 315 | 93 | 52 | 122 | 12 | 34 | 86 | SMG9_chr19_43722983_43759962 | SMG9 | MSESG others(515): Show |
chr19 | 43722983 | 43759962 |
| a0002 | 0/0 | 520 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | MSESG others(515): Show |
chr19 | 43722983 | 43759962 |
| a0003 | 0/0 | 520 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | MSESG others(515): Show |
chr19 | 43722983 | 43759962 |
| a0004 | 0/0 | 520 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | MSESG others(515): Show |
chr19 | 43722983 | 43759962 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1560 | 304 | 86 | 52 | 120 | 12 | 32 | SMG9_chr19_43722983_43759962 | SMG9 | ATGTC others(1555): Show |
chr19 | 43722983 | 43759962 | ||
| a0001c0002 | 0/0 | 1560 | 7 | 7 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATGTC others(1555): Show |
chr19 | 43722983 | 43759962 | ||
| a0001c0004 | 0/0 | 1560 | 2 | 0 | 0 | 2 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATGTC others(1555): Show |
chr19 | 43722983 | 43759962 | ||
| a0001c0006 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | ATGTC others(1555): Show |
chr19 | 43722983 | 43759962 | ||
| a0001c0007 | 0/0 | 1560 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | ATGTC others(1555): Show |
chr19 | 43722983 | 43759962 | ||
| a0002c0003 | 0/0 | 1560 | 3 | 1 | 2 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATGTC others(1555): Show |
chr19 | 43722983 | 43759962 | ||
| a0003c0005 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATGTC others(1555): Show |
chr19 | 43722983 | 43759962 | ||
| a0004c0008 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATGTC others(1555): Show |
chr19 | 43722983 | 43759962 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5491 | 157 | 10 | 36 | 85 | 7 | 17 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0002 | 0/0 | 5491 | 38 | 12 | 8 | 14 | 1 | 3 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0003 | 0/0 | 5491 | 11 | 11 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0004 | 0/0 | 5491 | 6 | 6 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0005 | 0/0 | 5491 | 6 | 6 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0006 | 0/0 | 5491 | 5 | 0 | 1 | 0 | 1 | 3 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0007 | 0/0 | 5492 | 5 | 0 | 1 | 4 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5487): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0008 | 0/0 | 5491 | 5 | 3 | 0 | 0 | 2 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0009 | 0/0 | 5491 | 4 | 0 | 0 | 4 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0010 | 0/0 | 5491 | 4 | 4 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0011 | 0/0 | 5491 | 4 | 4 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0012 | 0/0 | 5491 | 3 | 3 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0013 | 0/0 | 5492 | 3 | 0 | 0 | 1 | 0 | 2 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5487): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0014 | 0/0 | 5491 | 3 | 3 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0015 | 0/0 | 5491 | 3 | 3 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0016 | 0/0 | 5492 | 2 | 1 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5487): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0017 | 0/0 | 5492 | 2 | 0 | 0 | 2 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5487): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0018 | 0/0 | 5491 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0022 | 0/0 | 5491 | 2 | 0 | 0 | 0 | 0 | 2 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0023 | 0/0 | 5513 | 2 | 1 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5508): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0024 | 0/0 | 5491 | 2 | 0 | 0 | 1 | 1 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0025 | 0/0 | 5491 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0026 | 0/0 | 5491 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0027 | 0/0 | 5491 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0029 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0030 | 0/0 | 5491 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0031 | 0/0 | 5491 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0032 | 0/0 | 5492 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5487): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0033 | 0/0 | 5491 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0034 | 0/0 | 5492 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5487): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0035 | 0/0 | 5491 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0036 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0038 | 0/0 | 5491 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0039 | 0/0 | 5491 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0040 | 0/0 | 5491 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0041 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0042 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0044 | 0/0 | 5491 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0045 | 0/0 | 5493 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5488): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0046 | 0/0 | 5491 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0047 | 0/0 | 5492 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5487): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0048 | 0/0 | 5491 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0049 | 0/0 | 5491 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0050 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0051 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0052 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0053 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0054 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0055 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0057 | 0/0 | 5491 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0058 | 0/0 | 5491 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0059 | 0/0 | 5491 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0001t0060 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0002t0019 | 0/0 | 5491 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0002t0020 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0002t0028 | 0/0 | 5491 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0002t0043 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0002t0056 | 0/0 | 5491 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0004t0001 | 0/0 | 5491 | 2 | 0 | 0 | 2 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0006t0002 | 0/0 | 5491 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0001c0007t0002 | 0/0 | 5491 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0002c0003t0020 | 0/0 | 5491 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0002c0003t0021 | 0/0 | 5491 | 2 | 1 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0003c0005t0037 | 0/0 | 5491 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| a0004c0008t0001 | 0/0 | 5491 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | ATTCA others(5486): Show |
chr19 | 43722983 | 43759962 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/1 | 37 | 6 | 8 | 17 | 2 | 3 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0002 | 0/0 | 18 | 2 | 3 | 10 | 2 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0004 | 0/0 | 6 | 1 | 2 | 1 | 0 | 2 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0005 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0008 | 0/0 | 5 | 0 | 5 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0013 | 1/0 | 3 | 0 | 0 | 0 | 2 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0014 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0016 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0017 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0026 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0030 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0003 | 0/0 | 7 | 1 | 5 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0011 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0022 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0003g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0003g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0003g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0003g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0004g0006 | 0/0 | 5 | 5 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0004g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0005g0012 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0005g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0005g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0005g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0006g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0006g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0006g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0007g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0007g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0007g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0007g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0007g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0008g0019 | 0/0 | 3 | 1 | 0 | 0 | 2 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0008g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0008g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0009g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0009g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0009g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0009g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0010g0010 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0011g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0011g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0011g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0011g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0012g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0012g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0012g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0013g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0013g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0013g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0014g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0015g0033 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0015g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0016g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0016g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0017g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0017g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0018g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0018g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0022g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0023g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0024g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0024g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0025g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0025g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0026g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0026g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0027g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0029g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0030g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0031g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0032g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0033g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0034g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0035g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0036g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0038g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0039g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0040g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0041g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0042g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0044g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0045g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0046g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0047g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0048g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0049g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0050g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0051g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0052g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0053g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0054g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0055g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0057g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0058g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0059g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0001t0060g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0002t0019g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0002t0019g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0002t0020g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0002t0028g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0002t0028g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0002t0043g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0002t0056g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0004t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0004t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0006t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0001c0007t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0002c0003t0020g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0002c0003t0021g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0002c0003t0021g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0003c0005t0037g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| a0004c0008t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0013 | EUR | GBR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00099 | hp2 | a0001 | c0001 | t0002 | g0011 | EUR | GBR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | GBR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | GBR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00323 | hp1 | a0001 | c0001 | t0008 | g0019 | EUR | FIN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00323 | hp2 | a0001 | c0001 | t0024 | g0132 | EUR | FIN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00438 | hp1 | a0001 | c0001 | t0024 | g0116 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00597 | hp1 | a0001 | c0004 | t0001 | g0134 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00621 | hp1 | a0001 | c0001 | t0017 | g0057 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00733 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0035 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01109 | hp1 | a0002 | c0003 | t0021 | g0090 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01175 | hp1 | a0001 | c0001 | t0040 | g0088 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01175 | hp2 | a0001 | c0001 | t0007 | g0186 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01243 | hp1 | a0001 | c0001 | t0023 | g0025 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01243 | hp2 | a0001 | c0001 | t0044 | g0150 | AMR | PUR | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01255 | hp2 | a0001 | c0001 | t0006 | g0073 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01256 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01358 | hp1 | a0001 | c0001 | t0035 | g0049 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0027 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01515 | hp1 | a0001 | c0001 | t0008 | g0019 | EUR | IBS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0013 | EUR | IBS | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01884 | hp2 | a0001 | c0001 | t0018 | g0085 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01891 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PEL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01978 | hp1 | a0001 | c0001 | t0032 | g0074 | AMR | PEL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02004 | hp2 | a0001 | c0001 | t0057 | g0198 | AMR | PEL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02027 | hp2 | a0001 | c0001 | t0007 | g0122 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02040 | hp1 | a0001 | c0001 | t0049 | g0157 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02040 | hp2 | a0001 | c0001 | t0009 | g0064 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02055 | hp1 | a0001 | c0001 | t0004 | g0187 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02055 | hp2 | a0001 | c0001 | t0041 | g0177 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02071 | hp2 | a0001 | c0001 | t0009 | g0056 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02083 | hp2 | a0001 | c0001 | t0009 | g0042 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02129 | hp1 | a0001 | c0001 | t0009 | g0077 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02145 | hp1 | a0001 | c0001 | t0015 | g0033 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02145 | hp2 | a0001 | c0002 | t0028 | g0100 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | CDX | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | CDX | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CDX | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02257 | hp1 | a0001 | c0001 | t0036 | g0058 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02258 | hp1 | a0001 | c0002 | t0056 | g0097 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02258 | hp2 | a0001 | c0001 | t0011 | g0104 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02451 | hp1 | a0001 | c0001 | t0027 | g0024 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02451 | hp2 | a0001 | c0002 | t0043 | g0095 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02615 | hp1 | a0001 | c0001 | t0015 | g0197 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02615 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02622 | hp1 | a0001 | c0002 | t0028 | g0101 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02647 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02647 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0014 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0118 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02698 | hp1 | a0001 | c0001 | t0006 | g0071 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02698 | hp2 | a0001 | c0001 | t0039 | g0089 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02717 | hp1 | a0001 | c0001 | t0012 | g0137 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02717 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02723 | hp1 | a0001 | c0001 | t0003 | g0081 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02723 | hp2 | a0001 | c0001 | t0011 | g0106 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02818 | hp1 | a0001 | c0001 | t0016 | g0048 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02818 | hp2 | a0001 | c0001 | t0003 | g0082 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02886 | hp1 | a0001 | c0001 | t0011 | g0105 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02886 | hp2 | a0001 | c0001 | t0012 | g0179 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02895 | hp1 | a0001 | c0002 | t0019 | g0093 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02897 | hp1 | a0001 | c0001 | t0003 | g0063 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02897 | hp2 | a0001 | c0002 | t0019 | g0094 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0108 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02965 | hp1 | a0001 | c0001 | t0055 | g0195 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02965 | hp2 | a0001 | c0001 | t0026 | g0098 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02970 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02970 | hp2 | a0001 | c0001 | t0003 | g0083 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02976 | hp1 | a0001 | c0001 | t0011 | g0109 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03017 | hp1 | a0001 | c0001 | t0038 | g0087 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03017 | hp2 | a0001 | c0001 | t0006 | g0036 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03041 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03041 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03098 | hp2 | a0001 | c0001 | t0060 | g0201 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03139 | hp1 | a0001 | c0001 | t0008 | g0193 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03139 | hp2 | a0001 | c0001 | t0005 | g0012 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03195 | hp1 | a0001 | c0001 | t0003 | g0059 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03195 | hp2 | a0001 | c0001 | t0002 | g0022 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03209 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03225 | hp1 | a0001 | c0001 | t0051 | g0112 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03225 | hp2 | a0001 | c0001 | t0052 | g0182 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03453 | hp1 | a0001 | c0001 | t0012 | g0136 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03453 | hp2 | a0001 | c0001 | t0005 | g0102 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03486 | hp1 | a0002 | c0003 | t0021 | g0091 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03486 | hp2 | a0001 | c0001 | t0014 | g0018 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03516 | hp1 | a0001 | c0001 | t0008 | g0192 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03516 | hp2 | a0001 | c0001 | t0003 | g0079 | AFR | ESN | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03540 | hp1 | a0001 | c0001 | t0008 | g0019 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03540 | hp2 | a0001 | c0001 | t0042 | g0178 | AFR | GWD | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03579 | hp1 | a0001 | c0001 | t0025 | g0114 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03579 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03654 | hp1 | a0001 | c0001 | t0022 | g0031 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03654 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03669 | hp1 | a0001 | c0007 | t0002 | g0055 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03669 | hp2 | a0001 | c0001 | t0058 | g0199 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03710 | hp2 | a0001 | c0001 | t0046 | g0120 | SAS | PJL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03831 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03831 | hp2 | a0001 | c0001 | t0013 | g0158 | SAS | BEB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03834 | hp2 | a0001 | c0001 | t0059 | g0200 | SAS | BEB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03927 | hp1 | a0001 | c0001 | t0013 | g0127 | SAS | BEB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03927 | hp2 | a0001 | c0001 | t0006 | g0075 | SAS | BEB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0139 | SAS | BEB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03942 | hp2 | a0001 | c0001 | t0002 | g0066 | SAS | BEB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0183 | SAS | STU | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG04199 | hp1 | a0001 | c0006 | t0002 | g0050 | SAS | STU | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | STU | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG04204 | hp2 | a0001 | c0001 | t0022 | g0031 | SAS | STU | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18522 | hp1 | a0001 | c0001 | t0053 | g0115 | AFR | YRI | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18522 | hp2 | a0001 | c0001 | t0023 | g0025 | AFR | YRI | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | CHB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18906 | hp1 | a0001 | c0001 | t0004 | g0006 | AFR | YRI | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18906 | hp2 | a0001 | c0001 | t0027 | g0024 | AFR | YRI | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18941 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18941 | hp2 | a0001 | c0001 | t0030 | g0043 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18948 | hp1 | a0003 | c0005 | t0037 | g0084 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18950 | hp1 | a0001 | c0001 | t0048 | g0154 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18950 | hp2 | a0001 | c0001 | t0033 | g0061 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18965 | hp1 | a0001 | c0001 | t0017 | g0034 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18973 | hp2 | a0001 | c0001 | t0034 | g0060 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18974 | hp1 | a0001 | c0001 | t0016 | g0044 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18975 | hp2 | a0001 | c0001 | t0031 | g0052 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18977 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18983 | hp1 | a0004 | c0008 | t0001 | g0126 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18994 | hp2 | a0001 | c0001 | t0007 | g0175 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19000 | hp2 | a0001 | c0001 | t0045 | g0189 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19007 | hp2 | a0001 | c0001 | t0007 | g0130 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19030 | hp1 | a0001 | c0001 | t0005 | g0107 | AFR | LWK | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19030 | hp2 | a0001 | c0001 | t0004 | g0006 | AFR | LWK | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19043 | hp1 | a0001 | c0001 | t0029 | g0068 | AFR | LWK | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19043 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | LWK | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19056 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19058 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19058 | hp2 | a0001 | c0004 | t0001 | g0194 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19060 | hp1 | a0001 | c0001 | t0047 | g0151 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19086 | hp1 | a0001 | c0001 | t0007 | g0144 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19086 | hp2 | a0001 | c0001 | t0002 | g0011 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19087 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19089 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0039 | AFR | YRI | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA19240 | hp2 | a0001 | c0002 | t0020 | g0096 | AFR | YRI | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA20129 | hp1 | a0001 | c0001 | t0054 | g0110 | AFR | ASW | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA20805 | hp1 | a0001 | c0001 | t0006 | g0072 | EUR | TSI | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0002 | EUR | TSI | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | GIH | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | GIH | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG01123 | hp2 | a0002 | c0003 | t0020 | g0092 | AMR | CLM | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02109 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0010 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02486 | hp1 | a0001 | c0001 | t0018 | g0086 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02486 | hp2 | a0001 | c0001 | t0026 | g0099 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02559 | hp1 | a0001 | c0001 | t0010 | g0010 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03471 | hp1 | a0001 | c0001 | t0003 | g0046 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| HG03471 | hp2 | a0001 | c0001 | t0025 | g0113 | AFR | MSL | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA18955 | hp2 | a0001 | c0001 | t0013 | g0153 | EAS | JPT | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA20300 | hp1 | a0001 | c0001 | t0015 | g0033 | AFR | USA | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA20300 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | USA | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA21309 | hp1 | a0001 | c0001 | t0050 | g0152 | AFR | LWK | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | LWK | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0001 | REF | REF | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0013 | REF | REF | SMG9_chr19_43722983_43759962 | SMG9 | chr19 | 43722983 | 43759962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:43733682 | C | T | 1 | a0002 | 3 | HG01109.hp1 HG01123.hp2 HG03486.hp1 |
missense_variant | MODERATE | c.1154G>A | p.Arg385Gln | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 11/14 | 1469/5491 | 1154/1563 | 385/520 | chr19 | 43733682 | |||
| chr19:43747537 | C | T | 1 | a0003 | 1 | NA18948.hp1 | missense_variant&splice_region_variant | MODERATE | c.493G>A | p.Val165Ile | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/14 | 808/5491 | 493/1563 | 165/520 | chr19 | 43747537 | |||
| chr19:43750618 | T | C | 1 | a0004 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.124A>G | p.Ile42Val | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/14 | 439/5491 | 124/1563 | 42/520 | chr19 | 43750618 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:43733373 | C | T | 1 | a0001c0006 | 1 | HG04199.hp1 | synonymous_variant | LOW | c.1290G>A | p.Leu430Leu | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 12/14 | 1605/5491 | 1290/1563 | 430/520 | chr19 | 43733373 | |||
| chr19:43734444 | G | A | 2 | a0001c0002 a0002c0003 |
10 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(7): Show |
synonymous_variant | LOW | c.1047C>T | p.His349His | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/14 | 1362/5491 | 1047/1563 | 349/520 | chr19 | 43734444 | |||
| chr19:43747769 | G | C | 1 | a0001c0004 | 2 | HG00597.hp1 NA19058.hp2 |
synonymous_variant | LOW | c.354C>G | p.Thr118Thr | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 4/14 | 669/5491 | 354/1563 | 118/520 | chr19 | 43747769 | |||
| chr19:43748035 | T | C | 1 | a0001c0007 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.168A>G | p.Thr56Thr | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 3/14 | 483/5491 | 168/1563 | 56/520 | chr19 | 43748035 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:43728084 | C | T | 1 | a0001c0001t0039 | 1 | HG02698.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3512G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 3512 | chr19 | 43728084 | ||||||
| chr19:43728106 | A | G | 3 | a0001c0001t0027 a0001c0002t0020 a0002c0003t0020 |
4 | HG01123.hp2 HG02451.hp1 NA18906.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3490T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 3490 | chr19 | 43728106 | ||||||
| chr19:43728187 | T | C | 1 | a0001c0001t0026 | 2 | HG02486.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3409A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 3409 | chr19 | 43728187 | ||||||
| chr19:43728213 | C | T | 1 | a0001c0001t0026 | 2 | HG02486.hp2 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3383G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 3383 | chr19 | 43728213 | ||||||
| chr19:43728340 | T | TGGGCATG others(15): Show |
1 | a0001c0001t0023 | 2 | HG01243.hp1 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3234_*3255dupGGAG others(18): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 3255 | chr19 | 43728340 | ||||||
| chr19:43728347 | G | A | 1 | a0001c0001t0022 | 2 | HG03654.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3249C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 3249 | chr19 | 43728347 | ||||||
| chr19:43728388 | A | C | 1 | a0001c0001t0035 | 1 | HG01358.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3208T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 3208 | chr19 | 43728388 | ||||||
| chr19:43728556 | A | C | 1 | a0001c0001t0048 | 1 | NA18950.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3040T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 3040 | chr19 | 43728556 | ||||||
| chr19:43728584 | T | C | 15 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0014 others(12): Show |
34 | HG01109.hp1 HG01123.hp2 HG01243.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3012A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 3012 | chr19 | 43728584 | ||||||
| chr19:43728620 | G | C | 2 | a0001c0001t0025 a0001c0001t0051 |
3 | HG03225.hp1 HG03471.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2976C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2976 | chr19 | 43728620 | ||||||
| chr19:43728708 | G | A | 1 | a0001c0001t0024 | 2 | HG00323.hp2 HG00438.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2888C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2888 | chr19 | 43728708 | ||||||
| chr19:43728735 | C | T | 1 | a0001c0001t0051 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2861G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2861 | chr19 | 43728735 | ||||||
| chr19:43728757 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2839G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2839 | chr19 | 43728757 | ||||||
| chr19:43728758 | C | A | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2838G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2838 | chr19 | 43728758 | ||||||
| chr19:43728759 | A | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2837T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2837 | chr19 | 43728759 | ||||||
| chr19:43728762 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2834G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2834 | chr19 | 43728762 | ||||||
| chr19:43728763 | A | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2833T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2833 | chr19 | 43728763 | ||||||
| chr19:43728765 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2831G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2831 | chr19 | 43728765 | ||||||
| chr19:43728769 | C | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2827G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2827 | chr19 | 43728769 | ||||||
| chr19:43728772 | C | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2824G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2824 | chr19 | 43728772 | ||||||
| chr19:43728773 | A | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2823T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2823 | chr19 | 43728773 | ||||||
| chr19:43728774 | C | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2822G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2822 | chr19 | 43728774 | ||||||
| chr19:43728775 | A | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2821T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2821 | chr19 | 43728775 | ||||||
| chr19:43728776 | A | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2820T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2820 | chr19 | 43728776 | ||||||
| chr19:43728777 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2819G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2819 | chr19 | 43728777 | ||||||
| chr19:43728778 | A | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2818T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2818 | chr19 | 43728778 | ||||||
| chr19:43728779 | T | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2817A>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2817 | chr19 | 43728779 | ||||||
| chr19:43728782 | C | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2814G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2814 | chr19 | 43728782 | ||||||
| chr19:43728783 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2813G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2813 | chr19 | 43728783 | ||||||
| chr19:43728786 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2810G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2810 | chr19 | 43728786 | ||||||
| chr19:43728787 | T | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2809A>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2809 | chr19 | 43728787 | ||||||
| chr19:43728788 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2808G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2808 | chr19 | 43728788 | ||||||
| chr19:43728790 | A | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2806T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2806 | chr19 | 43728790 | ||||||
| chr19:43728793 | G | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2803C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2803 | chr19 | 43728793 | ||||||
| chr19:43728795 | A | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2801T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2801 | chr19 | 43728795 | ||||||
| chr19:43728797 | A | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2799T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2799 | chr19 | 43728797 | ||||||
| chr19:43728798 | A | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2798T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2798 | chr19 | 43728798 | ||||||
| chr19:43728800 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2796G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2796 | chr19 | 43728800 | ||||||
| chr19:43728807 | A | G | 2 | a0001c0001t0001 a0001c0001t0002 |
4 | HG00544.hp1 NA18943.hp1 NA18969.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2789T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2789 | chr19 | 43728807 | ||||||
| chr19:43728809 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2787G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2787 | chr19 | 43728809 | ||||||
| chr19:43728827 | C | A | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2769G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2769 | chr19 | 43728827 | ||||||
| chr19:43728828 | A | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2768T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2768 | chr19 | 43728828 | ||||||
| chr19:43728839 | A | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2757T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2757 | chr19 | 43728839 | ||||||
| chr19:43728841 | A | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2755T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2755 | chr19 | 43728841 | ||||||
| chr19:43728842 | A | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2754T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2754 | chr19 | 43728842 | ||||||
| chr19:43728845 | A | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2751T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2751 | chr19 | 43728845 | ||||||
| chr19:43728847 | A | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2749T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2749 | chr19 | 43728847 | ||||||
| chr19:43728848 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2748G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2748 | chr19 | 43728848 | ||||||
| chr19:43728849 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2747G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2747 | chr19 | 43728849 | ||||||
| chr19:43728886 | C | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2710G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2710 | chr19 | 43728886 | ||||||
| chr19:43728888 | A | C | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2708T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2708 | chr19 | 43728888 | ||||||
| chr19:43728889 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2707G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2707 | chr19 | 43728889 | ||||||
| chr19:43728890 | C | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2706G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2706 | chr19 | 43728890 | ||||||
| chr19:43728893 | C | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2703G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2703 | chr19 | 43728893 | ||||||
| chr19:43728904 | G | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2692C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2692 | chr19 | 43728904 | ||||||
| chr19:43728905 | A | T | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2691T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2691 | chr19 | 43728905 | ||||||
| chr19:43728906 | A | G | 1 | a0001c0001t0047 | 1 | NA19060.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2690T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2690 | chr19 | 43728906 | ||||||
| chr19:43729060 | A | AG | 5 | a0001c0001t0013 a0001c0001t0017 a0001c0001t0034 others(2): Show |
8 | HG00621.hp1 HG03831.hp2 HG03927.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2535dupC | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2535 | chr19 | 43729060 | ||||||
| chr19:43729165 | C | A | 1 | a0001c0001t0004 | 6 | HG02055.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2431G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2431 | chr19 | 43729165 | ||||||
| chr19:43729269 | G | A | 1 | a0001c0001t0036 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2327C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2327 | chr19 | 43729269 | ||||||
| chr19:43729343 | C | T | 1 | a0001c0001t0046 | 1 | HG03710.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2253G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2253 | chr19 | 43729343 | ||||||
| chr19:43729536 | C | T | 7 | a0001c0001t0011 a0001c0001t0027 a0001c0001t0041 others(4): Show |
13 | HG01109.hp1 HG01123.hp2 HG02055.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2060G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 2060 | chr19 | 43729536 | ||||||
| chr19:43729636 | A | G | 1 | a0001c0001t0060 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1960T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1960 | chr19 | 43729636 | ||||||
| chr19:43729638 | C | A | 2 | a0001c0001t0029 a0001c0001t0052 |
2 | HG03225.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1958G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1958 | chr19 | 43729638 | ||||||
| chr19:43729678 | G | C | 1 | a0001c0001t0030 | 1 | NA18941.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1918C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1918 | chr19 | 43729678 | ||||||
| chr19:43730020 | C | G | 1 | a0001c0001t0054 | 1 | NA20129.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1576G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1576 | chr19 | 43730020 | ||||||
| chr19:43730047 | C | T | 1 | a0001c0002t0056 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1549 | chr19 | 43730047 | ||||||
| chr19:43730219 | G | A | 1 | a0001c0001t0049 | 1 | HG02040.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1377C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1377 | chr19 | 43730219 | ||||||
| chr19:43730279 | C | T | 1 | a0001c0001t0034 | 1 | NA18973.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1317G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1317 | chr19 | 43730279 | ||||||
| chr19:43730282 | T | C | 1 | a0001c0001t0031 | 1 | NA18975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1314A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1314 | chr19 | 43730282 | ||||||
| chr19:43730363 | T | C | 4 | a0001c0001t0006 a0001c0001t0032 a0001c0001t0044 others(1): Show |
8 | HG01243.hp2 HG01255.hp2 HG01978.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1233A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1233 | chr19 | 43730363 | ||||||
| chr19:43730424 | T | C | 9 | a0001c0001t0005 a0001c0001t0010 a0001c0001t0011 others(6): Show |
22 | HG01891.hp1 HG02109.hp2 HG02258.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1172A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1172 | chr19 | 43730424 | ||||||
| chr19:43730547 | C | T | 2 | a0001c0001t0015 a0001c0001t0026 |
5 | HG02145.hp1 HG02486.hp2 HG02615.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1049G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1049 | chr19 | 43730547 | ||||||
| chr19:43730552 | G | A | 7 | a0001c0001t0053 a0001c0002t0019 a0001c0002t0020 others(4): Show |
10 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1044C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1044 | chr19 | 43730552 | ||||||
| chr19:43730554 | C | T | 1 | a0001c0001t0033 | 1 | NA18950.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1042G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1042 | chr19 | 43730554 | ||||||
| chr19:43730564 | C | CT | 4 | a0001c0001t0007 a0001c0001t0016 a0001c0001t0032 others(1): Show |
9 | HG01175.hp2 HG01978.hp1 HG02027.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1031dupA | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1031 | chr19 | 43730564 | ||||||
| chr19:43730584 | C | T | 1 | a0001c0002t0019 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1012G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 1012 | chr19 | 43730584 | ||||||
| chr19:43730606 | A | G | 1 | a0001c0001t0044 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*990T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 990 | chr19 | 43730606 | ||||||
| chr19:43730709 | G | A | 8 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0011 others(5): Show |
24 | HG00323.hp1 HG01515.hp1 HG01891.hp1 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*887C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 887 | chr19 | 43730709 | ||||||
| chr19:43730756 | C | T | 1 | a0001c0001t0058 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*840G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 840 | chr19 | 43730756 | ||||||
| chr19:43730788 | G | A | 2 | a0001c0002t0028 a0001c0002t0056 |
3 | HG02145.hp2 HG02258.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*808C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 808 | chr19 | 43730788 | ||||||
| chr19:43731365 | A | G | 26 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(23): Show |
85 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(82): Show |
3_prime_UTR_variant | MODIFIER | c.*231T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 231 | chr19 | 43731365 | ||||||
| chr19:43731383 | G | A | 15 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(12): Show |
69 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*213C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 213 | chr19 | 43731383 | ||||||
| chr19:43731428 | T | G | 2 | a0001c0002t0028 a0001c0002t0056 |
3 | HG02145.hp2 HG02258.hp1 HG02622.hp1 |
3_prime_UTR_variant | MODIFIER | c.*168A>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 14/14 | 168 | chr19 | 43731428 | ||||||
| chr19:43754658 | C | A | 1 | a0001c0001t0015 | 3 | HG02145.hp1 HG02615.hp1 NA20300.hp1 |
5_prime_UTR_variant | MODIFIER | c.-11G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/14 | 3917 | chr19 | 43754658 | ||||||
| chr19:43754718 | G | A | 1 | a0003c0005t0037 | 1 | NA18948.hp1 | 5_prime_UTR_variant | MODIFIER | c.-71C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/14 | 3977 | chr19 | 43754718 | ||||||
| chr19:43754736 | C | G | 2 | a0001c0001t0039 a0001c0001t0040 |
2 | HG01175.hp1 HG02698.hp2 |
5_prime_UTR_variant | MODIFIER | c.-89G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/14 | 3995 | chr19 | 43754736 | ||||||
| chr19:43754744 | C | T | 1 | a0001c0001t0038 | 1 | HG03017.hp1 | 5_prime_UTR_variant | MODIFIER | c.-97G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/14 | 4003 | chr19 | 43754744 | ||||||
| chr19:43754822 | G | C | 1 | a0001c0001t0018 | 2 | HG01884.hp2 HG02486.hp1 |
5_prime_UTR_variant | MODIFIER | c.-175C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/14 | 4081 | chr19 | 43754822 | ||||||
| chr19:43754890 | C | A | 1 | a0001c0001t0057 | 1 | HG02004.hp2 | 5_prime_UTR_variant | MODIFIER | c.-243G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/14 | 4149 | chr19 | 43754890 | ||||||
| chr19:43754893 | G | A | 1 | a0001c0001t0058 | 1 | HG03669.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-246C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/14 | chr19 | 43754893 | |||||||
| chr19:43754898 | G | A | 1 | a0001c0001t0059 | 1 | HG03834.hp2 | 5_prime_UTR_variant | MODIFIER | c.-251C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/14 | 4157 | chr19 | 43754898 | ||||||
| chr19:43754925 | C | T | 19 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0006 others(16): Show |
76 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(73): Show |
5_prime_UTR_variant | MODIFIER | c.-278G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/14 | 4184 | chr19 | 43754925 | ||||||
| chr19:43754941 | G | A | 1 | a0001c0001t0060 | 1 | HG03098.hp2 | 5_prime_UTR_variant | MODIFIER | c.-294C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/14 | 4200 | chr19 | 43754941 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:43731709 | G | A | 1 | a0001c0001t0005g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1485-35C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43731709 | |||||||
| chr19:43731801 | C | T | 2 | a0001c0001t0006g0072 a0001c0001t0032g0074 |
2 | HG01978.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.1485-127G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43731801 | |||||||
| chr19:43731833 | C | T | 2 | a0001c0001t0015g0033 a0001c0001t0015g0197 |
3 | HG02145.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1485-159G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43731833 | |||||||
| chr19:43731970 | G | A | 1 | a0001c0002t0056g0097 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1485-296C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43731970 | |||||||
| chr19:43731984 | T | C | 2 | a0001c0001t0004g0006 a0001c0001t0004g0187 |
6 | HG02055.hp1 HG02717.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1485-310A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43731984 | |||||||
| chr19:43732196 | G | A | 1 | a0001c0001t0005g0107 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1485-522C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43732196 | |||||||
| chr19:43732259 | T | C | 9 | a0001c0001t0001g0111 a0001c0001t0010g0010 a0001c0001t0015g0033 others(6): Show |
14 | HG00738.hp1 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1485-585A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43732259 | |||||||
| chr19:43732307 | A | G | 10 | a0001c0002t0019g0093 a0001c0002t0019g0094 a0001c0002t0020g0096 others(7): Show |
10 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1484+551T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43732307 | |||||||
| chr19:43732562 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1484+296C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43732562 | |||||||
| chr19:43732625 | C | A | 3 | a0001c0001t0001g0125 a0001c0001t0001g0172 a0001c0001t0058g0199 |
3 | HG01358.hp2 HG01361.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.1484+233G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43732625 | |||||||
| chr19:43732763 | G | A | 2 | a0001c0001t0001g0117 a0001c0001t0001g0138 |
2 | NA18955.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.1484+95C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43732763 | |||||||
| chr19:43732809 | C | T | 1 | a0001c0001t0007g0186 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1484+49G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 13/13 | chr19 | 43732809 | |||||||
| chr19:43733017 | C | A | 1 | a0001c0001t0018g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1340-15G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 12/13 | chr19 | 43733017 | |||||||
| chr19:43733066 | G | A | 1 | a0001c0001t0001g0117 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1340-64C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 12/13 | chr19 | 43733066 | |||||||
| chr19:43733101 | C | A | 1 | a0001c0001t0001g0156 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1340-99G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 12/13 | chr19 | 43733101 | |||||||
| chr19:43733239 | T | C | 15 | a0001c0001t0001g0005 a0001c0001t0001g0027 a0001c0001t0001g0124 others(12): Show |
22 | HG00673.hp2 HG01071.hp1 HG01168.hp2 others(19): Show |
intron_variant | MODIFIER | c.1339+85A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 12/13 | chr19 | 43733239 | |||||||
| chr19:43733496 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1211-44A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 11/13 | chr19 | 43733496 | |||||||
| chr19:43733556 | G | T | 9 | a0001c0001t0001g0111 a0001c0001t0010g0010 a0001c0001t0015g0033 others(6): Show |
14 | HG00738.hp1 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1210+70C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 11/13 | chr19 | 43733556 | |||||||
| chr19:43733566 | C | T | 1 | a0001c0001t0001g0149 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1210+60G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 11/13 | chr19 | 43733566 | |||||||
| chr19:43733957 | G | A | 2 | a0001c0001t0002g0040 a0001c0001t0003g0046 |
2 | HG02572.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1103-224C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43733957 | |||||||
| chr19:43733986 | A | C | 10 | a0001c0002t0019g0093 a0001c0002t0019g0094 a0001c0002t0020g0096 others(7): Show |
10 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.1103-253T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43733986 | |||||||
| chr19:43734000 | G | A | 59 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(56): Show |
74 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1103-267C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734000 | |||||||
| chr19:43734131 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+258T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734131 | |||||||
| chr19:43734136 | G | C | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+253C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734136 | |||||||
| chr19:43734138 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+251T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734138 | |||||||
| chr19:43734139 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+250C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734139 | |||||||
| chr19:43734140 | A | G | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+249T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734140 | |||||||
| chr19:43734142 | C | CTTCCCAA others(12): Show |
1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+246_1102+247i others(21): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734142 | |||||||
| chr19:43734145 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+244C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734145 | |||||||
| chr19:43734177 | G | T | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+212C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734177 | |||||||
| chr19:43734178 | T | A | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+211A>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734178 | |||||||
| chr19:43734184 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+205G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734184 | |||||||
| chr19:43734187 | C | G | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+202G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734187 | |||||||
| chr19:43734195 | A | G | 59 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(56): Show |
74 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.1102+194T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734195 | |||||||
| chr19:43734197 | G | A | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1102+192C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 10/13 | chr19 | 43734197 | |||||||
| chr19:43735000 | T | G | 1 | a0001c0001t0009g0064 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.996-505A>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735000 | |||||||
| chr19:43735111 | T | C | 2 | a0001c0001t0002g0054 a0001c0001t0002g0065 |
2 | HG01081.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.996-616A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735111 | |||||||
| chr19:43735136 | T | A | 10 | a0001c0002t0019g0093 a0001c0002t0019g0094 a0001c0002t0020g0096 others(7): Show |
10 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.996-641A>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735136 | |||||||
| chr19:43735176 | T | A | 10 | a0001c0002t0019g0093 a0001c0002t0019g0094 a0001c0002t0020g0096 others(7): Show |
10 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.996-681A>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735176 | |||||||
| chr19:43735176 | T | C | 1 | a0001c0001t0001g0142 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.996-681A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735176 | |||||||
| chr19:43735308 | T | C | 2 | a0001c0001t0012g0136 a0001c0001t0012g0137 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.996-813A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735308 | |||||||
| chr19:43735440 | A | C | 1 | a0001c0001t0001g0169 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.996-945T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735440 | |||||||
| chr19:43735498 | G | A | 1 | a0001c0001t0029g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.996-1003C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735498 | |||||||
| chr19:43735546 | C | T | 2 | a0001c0002t0019g0093 a0001c0002t0019g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.996-1051G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735546 | |||||||
| chr19:43735552 | T | C | 9 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0029 others(6): Show |
29 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(26): Show |
intron_variant | MODIFIER | c.996-1057A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735552 | |||||||
| chr19:43735583 | C | T | 1 | a0001c0001t0002g0047 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.996-1088G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735583 | |||||||
| chr19:43735614 | C | CA | 13 | a0001c0001t0001g0016 a0001c0001t0001g0029 a0001c0001t0001g0129 others(10): Show |
16 | HG00544.hp1 HG02055.hp2 HG02071.hp2 others(13): Show |
intron_variant | MODIFIER | c.996-1120dupT | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735614 | |||||||
| chr19:43735614 | C | CAA | 21 | a0001c0001t0001g0170 a0001c0001t0002g0020 a0001c0001t0002g0022 others(18): Show |
23 | HG01123.hp2 HG01255.hp2 HG01884.hp2 others(20): Show |
intron_variant | MODIFIER | c.996-1121_996-1120d others(4): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735614 | |||||||
| chr19:43735614 | C | CAAA | 28 | a0001c0001t0002g0003 a0001c0001t0002g0037 a0001c0001t0002g0040 others(25): Show |
35 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(32): Show |
intron_variant | MODIFIER | c.996-1122_996-1120d others(5): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735614 | |||||||
| chr19:43735614 | C | CAAAA | 11 | a0001c0001t0002g0011 a0001c0001t0002g0051 a0001c0001t0002g0053 others(8): Show |
13 | HG00099.hp2 HG00621.hp1 HG01192.hp1 others(10): Show |
intron_variant | MODIFIER | c.996-1123_996-1120d others(6): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735614 | |||||||
| chr19:43735614 | C | CAAAAAAA others(3): Show |
2 | a0001c0001t0005g0108 a0001c0001t0054g0110 |
2 | HG02922.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.996-1129_996-1120d others(12): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735614 | |||||||
| chr19:43735614 | C | CAAAAAAA others(4): Show |
2 | a0001c0001t0011g0104 a0001c0001t0011g0105 |
2 | HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.996-1130_996-1120d others(13): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735614 | |||||||
| chr19:43735614 | C | CAAAAAAA others(5): Show |
2 | a0001c0001t0011g0106 a0001c0001t0011g0109 |
2 | HG02723.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.996-1131_996-1120d others(14): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735614 | |||||||
| chr19:43735614 | CA | C | 6 | a0001c0001t0001g0141 a0001c0001t0001g0148 a0001c0001t0014g0018 others(3): Show |
8 | HG02486.hp2 HG02615.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.996-1120delT | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735614 | |||||||
| chr19:43735631 | AAAAAAAA others(2): Show |
A | 4 | a0001c0001t0002g0009 a0001c0001t0002g0021 a0001c0001t0002g0069 others(1): Show |
8 | HG00408.hp1 HG00558.hp1 HG02015.hp2 others(5): Show |
intron_variant | MODIFIER | c.996-1145_996-1137d others(11): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735631 | |||||||
| chr19:43735640 | T | A | 50 | a0001c0001t0002g0003 a0001c0001t0002g0011 a0001c0001t0002g0020 others(47): Show |
61 | HG00099.hp2 HG00621.hp1 HG00733.hp2 others(58): Show |
intron_variant | MODIFIER | c.996-1145A>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735640 | |||||||
| chr19:43735702 | G | A | 9 | a0001c0001t0001g0111 a0001c0001t0010g0010 a0001c0001t0015g0033 others(6): Show |
14 | HG00738.hp1 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.996-1207C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735702 | |||||||
| chr19:43735775 | T | C | 94 | a0001c0001t0001g0111 a0001c0001t0002g0003 a0001c0001t0002g0009 others(91): Show |
119 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(116): Show |
intron_variant | MODIFIER | c.996-1280A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735775 | |||||||
| chr19:43735876 | G | A | 1 | a0001c0001t0006g0036 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.996-1381C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43735876 | |||||||
| chr19:43736025 | A | G | 199 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(196): Show |
315 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.996-1530T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43736025 | |||||||
| chr19:43736219 | T | C | 1 | a0001c0001t0046g0120 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.995+1378A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43736219 | |||||||
| chr19:43736429 | G | GT | 10 | a0001c0001t0005g0012 a0001c0001t0005g0102 a0001c0001t0005g0107 others(7): Show |
13 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.995+1167dupA | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43736429 | |||||||
| chr19:43736864 | T | C | 1 | a0001c0001t0012g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.995+733A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43736864 | |||||||
| chr19:43736924 | G | A | 1 | a0001c0001t0059g0200 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.995+673C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43736924 | |||||||
| chr19:43737033 | G | A | 1 | a0001c0001t0049g0157 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.995+564C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737033 | |||||||
| chr19:43737046 | G | A | 1 | a0001c0001t0001g0121 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.995+551C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737046 | |||||||
| chr19:43737081 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.995+516G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737081 | |||||||
| chr19:43737221 | C | T | 2 | a0001c0002t0019g0093 a0001c0002t0019g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.995+376G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737221 | |||||||
| chr19:43737251 | C | T | 2 | a0001c0002t0019g0093 a0001c0002t0019g0094 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.995+346G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737251 | |||||||
| chr19:43737252 | G | A | 6 | a0001c0001t0001g0139 a0001c0001t0001g0159 a0001c0001t0001g0183 others(3): Show |
6 | HG01175.hp1 HG02698.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.995+345C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737252 | |||||||
| chr19:43737272 | C | CAATA | 91 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(88): Show |
174 | HG00140.hp2 HG00323.hp2 HG00408.hp2 others(171): Show |
intron_variant | MODIFIER | c.995+321_995+324dup others(4): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737272 | |||||||
| chr19:43737272 | C | CAATAAAT others(1): Show |
2 | a0001c0001t0001g0160 a0001c0001t0022g0031 |
3 | HG03654.hp1 HG04204.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.995+317_995+324dup others(8): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737272 | |||||||
| chr19:43737399 | G | T | 10 | a0001c0002t0019g0093 a0001c0002t0019g0094 a0001c0002t0020g0096 others(7): Show |
10 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.995+198C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737399 | |||||||
| chr19:43737424 | CT | C | 3 | a0001c0001t0001g0014 a0001c0001t0001g0191 a0001c0001t0007g0130 |
5 | HG02683.hp1 NA18747.hp1 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.995+172delA | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737424 | |||||||
| chr19:43737435 | C | T | 9 | a0001c0001t0001g0111 a0001c0001t0010g0010 a0001c0001t0015g0033 others(6): Show |
14 | HG00738.hp1 HG01243.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.995+162G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 9/13 | chr19 | 43737435 | |||||||
| chr19:43737723 | T | C | 1 | a0001c0001t0002g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.910-41A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 8/13 | chr19 | 43737723 | |||||||
| chr19:43737757 | C | G | 6 | a0001c0001t0001g0111 a0001c0001t0010g0010 a0001c0001t0023g0025 others(3): Show |
10 | HG00738.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.910-75G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 8/13 | chr19 | 43737757 | |||||||
| chr19:43737831 | T | C | 1 | a0001c0001t0001g0161 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.910-149A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 8/13 | chr19 | 43737831 | |||||||
| chr19:43737868 | T | C | 1 | a0001c0001t0001g0140 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.910-186A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 8/13 | chr19 | 43737868 | |||||||
| chr19:43738017 | T | C | 10 | a0001c0001t0005g0012 a0001c0001t0005g0102 a0001c0001t0005g0107 others(7): Show |
13 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.909+105A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 8/13 | chr19 | 43738017 | |||||||
| chr19:43738255 | C | T | 1 | a0001c0001t0012g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.814-38G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43738255 | |||||||
| chr19:43738297 | G | T | 1 | a0001c0001t0034g0060 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.814-80C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43738297 | |||||||
| chr19:43738471 | C | T | 1 | a0001c0001t0053g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.814-254G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43738471 | |||||||
| chr19:43738545 | CTAAGA | C | 55 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(52): Show |
70 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(67): Show |
intron_variant | MODIFIER | c.814-333_814-329del others(5): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43738545 | |||||||
| chr19:43738647 | C | T | 1 | a0001c0001t0001g0146 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.814-430G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43738647 | |||||||
| chr19:43738773 | G | A | 7 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0179 others(4): Show |
8 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.814-556C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43738773 | |||||||
| chr19:43738795 | G | T | 7 | a0001c0001t0012g0136 a0001c0001t0012g0137 a0001c0001t0012g0179 others(4): Show |
8 | HG02055.hp2 HG02145.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.814-578C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43738795 | |||||||
| chr19:43738861 | C | T | 1 | a0001c0001t0002g0041 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.814-644G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43738861 | |||||||
| chr19:43738865 | C | T | 1 | a0001c0001t0001g0148 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.814-648G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43738865 | |||||||
| chr19:43738987 | A | C | 10 | a0001c0001t0005g0012 a0001c0001t0005g0102 a0001c0001t0005g0107 others(7): Show |
13 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.814-770T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43738987 | |||||||
| chr19:43739320 | C | G | 1 | a0001c0004t0001g0134 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.813+787G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43739320 | |||||||
| chr19:43739605 | C | T | 1 | a0001c0001t0013g0127 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.813+502G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43739605 | |||||||
| chr19:43739640 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0165 |
2 | HG02165.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.813+467C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 7/13 | chr19 | 43739640 | |||||||
| chr19:43740271 | A | G | 28 | a0001c0001t0001g0111 a0001c0001t0005g0012 a0001c0001t0005g0102 others(25): Show |
38 | HG00323.hp1 HG00738.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.702-53T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43740271 | |||||||
| chr19:43740279 | G | A | 1 | a0001c0001t0036g0058 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.702-61C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43740279 | |||||||
| chr19:43740344 | C | A | 1 | a0001c0001t0001g0162 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.702-126G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43740344 | |||||||
| chr19:43740991 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(164): Show |
269 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(266): Show |
intron_variant | MODIFIER | c.702-773A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43740991 | |||||||
| chr19:43741321 | G | A | 1 | a0001c0001t0001g0163 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.702-1103C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43741321 | |||||||
| chr19:43741414 | A | G | 1 | a0001c0001t0014g0018 | 3 | HG02615.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.702-1196T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43741414 | |||||||
| chr19:43741515 | C | G | 15 | a0001c0001t0002g0022 a0001c0001t0002g0038 a0001c0001t0002g0040 others(12): Show |
17 | HG01884.hp2 HG01891.hp2 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.702-1297G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43741515 | |||||||
| chr19:43741560 | C | A | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.702-1342G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43741560 | |||||||
| chr19:43741604 | A | G | 3 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0007g0144 |
3 | NA18962.hp1 NA18977.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.702-1386T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43741604 | |||||||
| chr19:43741679 | A | G | 1 | a0001c0001t0012g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.702-1461T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43741679 | |||||||
| chr19:43741796 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.702-1578G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43741796 | |||||||
| chr19:43741862 | A | T | 1 | a0001c0001t0057g0198 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.702-1644T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43741862 | |||||||
| chr19:43741941 | A | G | 1 | a0001c0002t0028g0101 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.702-1723T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43741941 | |||||||
| chr19:43741981 | C | G | 2 | a0001c0001t0012g0136 a0001c0001t0012g0137 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.702-1763G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43741981 | |||||||
| chr19:43742009 | G | A | 1 | a0001c0001t0002g0065 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.702-1791C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43742009 | |||||||
| chr19:43742448 | T | A | 72 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(69): Show |
87 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.702-2230A>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43742448 | |||||||
| chr19:43742554 | A | G | 74 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(71): Show |
89 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.701+2218T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43742554 | |||||||
| chr19:43742673 | T | C | 1 | a0001c0001t0012g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.701+2099A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43742673 | |||||||
| chr19:43742818 | C | T | 73 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(70): Show |
88 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.701+1954G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43742818 | |||||||
| chr19:43742856 | C | T | 1 | a0001c0001t0055g0195 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+1916G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43742856 | |||||||
| chr19:43743002 | G | A | 2 | a0001c0001t0015g0033 a0001c0001t0015g0197 |
3 | HG02145.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.701+1770C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743002 | |||||||
| chr19:43743062 | G | A | 10 | a0001c0002t0019g0093 a0001c0002t0019g0094 a0001c0002t0020g0096 others(7): Show |
10 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.701+1710C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743062 | |||||||
| chr19:43743072 | C | CA | 10 | a0001c0001t0001g0164 a0001c0001t0005g0012 a0001c0001t0005g0107 others(7): Show |
13 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.701+1699dupT | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743072 | |||||||
| chr19:43743126 | A | G | 3 | a0001c0001t0001g0007 a0001c0001t0001g0169 a0001c0001t0001g0170 |
7 | NA18948.hp2 NA18966.hp2 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.701+1646T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743126 | |||||||
| chr19:43743162 | C | T | 7 | a0001c0001t0005g0107 a0001c0001t0005g0108 a0001c0001t0011g0104 others(4): Show |
7 | HG02258.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.701+1610G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743162 | |||||||
| chr19:43743163 | G | A | 1 | a0001c0001t0002g0054 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.701+1609C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743163 | |||||||
| chr19:43743218 | C | G | 1 | a0001c0001t0036g0058 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.701+1554G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743218 | |||||||
| chr19:43743338 | G | C | 3 | a0001c0001t0001g0123 a0001c0001t0001g0165 a0001c0001t0007g0122 |
3 | HG02027.hp2 HG02165.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.701+1434C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743338 | |||||||
| chr19:43743417 | T | C | 11 | a0001c0001t0001g0111 a0001c0001t0008g0019 a0001c0001t0008g0192 others(8): Show |
17 | HG00323.hp1 HG00738.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.701+1355A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743417 | |||||||
| chr19:43743433 | C | T | 1 | a0001c0001t0012g0179 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.701+1339G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743433 | |||||||
| chr19:43743571 | G | A | 1 | a0001c0001t0002g0076 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.701+1201C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743571 | |||||||
| chr19:43743574 | T | C | 1 | a0001c0001t0001g0143 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.701+1198A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743574 | |||||||
| chr19:43743906 | T | C | 1 | a0001c0001t0055g0195 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.701+866A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43743906 | |||||||
| chr19:43744473 | G | A | 72 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(69): Show |
87 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.701+299C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43744473 | |||||||
| chr19:43744726 | A | G | 94 | a0001c0001t0001g0111 a0001c0001t0002g0003 a0001c0001t0002g0009 others(91): Show |
118 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.701+46T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 6/13 | chr19 | 43744726 | |||||||
| chr19:43744900 | T | G | 1 | a0001c0001t0002g0066 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.589-16A>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43744900 | |||||||
| chr19:43744911 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.589-27C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43744911 | |||||||
| chr19:43744916 | G | A | 3 | a0002c0003t0020g0092 a0002c0003t0021g0090 a0002c0003t0021g0091 |
3 | HG01109.hp1 HG01123.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.589-32C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43744916 | |||||||
| chr19:43744949 | G | C | 4 | a0001c0001t0011g0104 a0001c0001t0011g0105 a0001c0001t0011g0106 others(1): Show |
4 | HG02258.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.589-65C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43744949 | |||||||
| chr19:43745365 | G | GT | 12 | a0001c0001t0002g0067 a0001c0001t0005g0102 a0001c0002t0019g0093 others(9): Show |
12 | HG01109.hp1 HG01123.hp2 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.589-482dupA | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43745365 | |||||||
| chr19:43745526 | G | T | 1 | a0001c0001t0015g0197 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.589-642C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43745526 | |||||||
| chr19:43745719 | C | T | 1 | a0001c0001t0001g0145 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.589-835G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43745719 | |||||||
| chr19:43745766 | C | T | 1 | a0001c0001t0006g0036 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.589-882G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43745766 | |||||||
| chr19:43745768 | G | A | 2 | a0001c0004t0001g0134 a0001c0004t0001g0194 |
2 | HG00597.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.589-884C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43745768 | |||||||
| chr19:43745902 | G | C | 2 | a0001c0001t0015g0033 a0001c0001t0015g0197 |
3 | HG02145.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.589-1018C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43745902 | |||||||
| chr19:43745914 | T | C | 1 | a0001c0002t0020g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.589-1030A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43745914 | |||||||
| chr19:43745923 | C | T | 3 | a0001c0001t0008g0019 a0001c0001t0008g0192 a0001c0001t0008g0193 |
5 | HG00323.hp1 HG01515.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.589-1039G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43745923 | |||||||
| chr19:43745985 | G | A | 1 | a0001c0001t0002g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.589-1101C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43745985 | |||||||
| chr19:43746091 | T | C | 3 | a0001c0001t0005g0102 a0001c0002t0019g0093 a0001c0002t0019g0094 |
3 | HG02895.hp1 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.589-1207A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746091 | |||||||
| chr19:43746098 | G | A | 10 | a0001c0001t0001g0111 a0001c0001t0008g0019 a0001c0001t0008g0192 others(7): Show |
16 | HG00323.hp1 HG00738.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.589-1214C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746098 | |||||||
| chr19:43746135 | T | C | 2 | a0001c0001t0026g0098 a0001c0001t0026g0099 |
2 | HG02486.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.589-1251A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746135 | |||||||
| chr19:43746158 | G | A | 1 | a0001c0001t0001g0138 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.589-1274C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746158 | |||||||
| chr19:43746180 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.588+1262A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746180 | |||||||
| chr19:43746589 | G | A | 9 | a0001c0001t0005g0012 a0001c0001t0005g0107 a0001c0001t0005g0108 others(6): Show |
12 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.588+853C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746589 | |||||||
| chr19:43746623 | ATCTGAGC others(5): Show |
A | 11 | a0001c0001t0001g0111 a0001c0001t0008g0019 a0001c0001t0008g0192 others(8): Show |
17 | HG00323.hp1 HG00738.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.588+807_588+818del others(12): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746623 | |||||||
| chr19:43746679 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(80): Show |
101 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.588+763T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746679 | |||||||
| chr19:43746771 | G | C | 1 | a0001c0001t0001g0190 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.588+671C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746771 | |||||||
| chr19:43746793 | C | G | 1 | a0001c0001t0001g0030 | 2 | NA18966.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.588+649G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746793 | |||||||
| chr19:43746819 | C | CT | 6 | a0001c0001t0001g0118 a0001c0001t0001g0119 a0001c0001t0005g0102 others(3): Show |
6 | HG01261.hp1 HG02683.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.588+622dupA | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746819 | |||||||
| chr19:43746819 | CT | C | 81 | a0001c0001t0001g0111 a0001c0001t0001g0124 a0001c0001t0001g0168 others(78): Show |
103 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.588+622delA | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43746819 | |||||||
| chr19:43747002 | G | A | 6 | a0001c0001t0001g0111 a0001c0001t0010g0010 a0001c0001t0023g0025 others(3): Show |
10 | HG00738.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.588+440C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43747002 | |||||||
| chr19:43747273 | C | T | 101 | a0001c0001t0001g0111 a0001c0001t0002g0003 a0001c0001t0002g0009 others(98): Show |
126 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.588+169G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43747273 | |||||||
| chr19:43747318 | A | T | 101 | a0001c0001t0001g0111 a0001c0001t0002g0003 a0001c0001t0002g0009 others(98): Show |
126 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.588+124T>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43747318 | |||||||
| chr19:43747337 | G | T | 1 | a0001c0001t0012g0136 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.588+105C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43747337 | |||||||
| chr19:43747382 | G | A | 1 | a0001c0001t0002g0020 | 2 | HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.588+60C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43747382 | |||||||
| chr19:43747404 | A | G | 9 | a0001c0001t0005g0012 a0001c0001t0005g0107 a0001c0001t0005g0108 others(6): Show |
12 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.588+38T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43747404 | |||||||
| chr19:43747437 | G | A | 7 | a0001c0001t0005g0012 a0001c0001t0005g0107 a0001c0001t0011g0104 others(4): Show |
10 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
splice_region_variant&intron_variant | LOW | c.588+5C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 5/13 | chr19 | 43747437 | |||||||
| chr19:43747595 | G | A | 9 | a0001c0001t0005g0012 a0001c0001t0005g0107 a0001c0001t0005g0108 others(6): Show |
12 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.490+38C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 4/13 | chr19 | 43747595 | |||||||
| chr19:43747607 | C | T | 8 | a0001c0001t0001g0002 a0001c0001t0001g0015 a0001c0001t0001g0029 others(5): Show |
28 | HG00544.hp2 HG00558.hp2 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.490+26G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 4/13 | chr19 | 43747607 | |||||||
| chr19:43747908 | A | G | 3 | a0001c0001t0002g0045 a0001c0001t0016g0044 a0001c0001t0017g0057 |
3 | HG00621.hp1 NA18974.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.226-11T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 3/13 | chr19 | 43747908 | |||||||
| chr19:43747946 | C | T | 9 | a0001c0001t0005g0012 a0001c0001t0005g0107 a0001c0001t0005g0108 others(6): Show |
12 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.225+32G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 3/13 | chr19 | 43747946 | |||||||
| chr19:43747952 | C | T | 2 | a0001c0002t0028g0100 a0001c0002t0028g0101 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.225+26G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 3/13 | chr19 | 43747952 | |||||||
| chr19:43748167 | A | G | 2 | a0001c0001t0041g0177 a0001c0001t0042g0178 |
2 | HG02055.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.151-115T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43748167 | |||||||
| chr19:43748366 | T | C | 1 | a0001c0002t0028g0101 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.151-314A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43748366 | |||||||
| chr19:43748380 | C | T | 1 | a0001c0001t0055g0195 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-328G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43748380 | |||||||
| chr19:43748385 | C | T | 2 | a0001c0001t0012g0136 a0001c0001t0012g0137 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.151-333G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43748385 | |||||||
| chr19:43748594 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.151-542T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43748594 | |||||||
| chr19:43748614 | C | A | 7 | a0001c0001t0005g0012 a0001c0001t0005g0107 a0001c0001t0011g0104 others(4): Show |
10 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.151-562G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43748614 | |||||||
| chr19:43748721 | C | T | 1 | a0001c0001t0001g0118 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.151-669G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43748721 | |||||||
| chr19:43748753 | G | C | 3 | a0001c0001t0012g0179 a0001c0001t0041g0177 a0001c0001t0042g0178 |
3 | HG02055.hp2 HG02886.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.151-701C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43748753 | |||||||
| chr19:43748926 | A | C | 3 | a0001c0001t0005g0102 a0001c0002t0019g0093 a0001c0002t0019g0094 |
3 | HG02895.hp1 HG02897.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.151-874T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43748926 | |||||||
| chr19:43748964 | C | T | 1 | a0001c0001t0055g0195 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.151-912G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43748964 | |||||||
| chr19:43749060 | C | G | 9 | a0001c0001t0005g0012 a0001c0001t0005g0107 a0001c0001t0005g0108 others(6): Show |
12 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.151-1008G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749060 | |||||||
| chr19:43749074 | C | T | 1 | a0001c0001t0006g0071 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.151-1022G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749074 | |||||||
| chr19:43749165 | C | T | 2 | a0001c0001t0012g0136 a0001c0001t0012g0137 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.151-1113G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749165 | |||||||
| chr19:43749257 | G | A | 6 | a0001c0001t0001g0111 a0001c0001t0010g0010 a0001c0001t0023g0025 others(3): Show |
10 | HG00738.hp1 HG01243.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.151-1205C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749257 | |||||||
| chr19:43749259 | C | T | 2 | a0001c0001t0012g0136 a0001c0001t0012g0137 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.151-1207G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749259 | |||||||
| chr19:43749436 | G | A | 101 | a0001c0001t0001g0111 a0001c0001t0002g0003 a0001c0001t0002g0009 others(98): Show |
126 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.150+1156C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749436 | |||||||
| chr19:43749473 | T | G | 1 | a0001c0001t0002g0067 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.150+1119A>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749473 | |||||||
| chr19:43749518 | A | C | 1 | a0001c0001t0001g0015 | 3 | NA18962.hp2 NA18964.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.150+1074T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749518 | |||||||
| chr19:43749526 | C | T | 11 | a0001c0001t0005g0102 a0001c0002t0019g0093 a0001c0002t0019g0094 others(8): Show |
11 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.150+1066G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749526 | |||||||
| chr19:43749638 | G | A | 30 | a0001c0001t0001g0111 a0001c0001t0005g0012 a0001c0001t0005g0102 others(27): Show |
39 | HG00323.hp1 HG00738.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.150+954C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749638 | |||||||
| chr19:43749698 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.150+894T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749698 | |||||||
| chr19:43749748 | C | T | 5 | a0001c0001t0005g0107 a0001c0001t0011g0104 a0001c0001t0011g0105 others(2): Show |
5 | HG02258.hp2 HG02723.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+844G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749748 | |||||||
| chr19:43749819 | C | T | 3 | a0001c0001t0008g0019 a0001c0001t0008g0192 a0001c0001t0008g0193 |
5 | HG00323.hp1 HG01515.hp1 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.150+773G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749819 | |||||||
| chr19:43749820 | G | A | 1 | a0001c0001t0018g0086 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.150+772C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749820 | |||||||
| chr19:43749842 | T | C | 4 | a0001c0002t0020g0096 a0001c0002t0028g0100 a0001c0002t0028g0101 others(1): Show |
4 | HG02145.hp2 HG02258.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.150+750A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749842 | |||||||
| chr19:43749959 | C | T | 13 | a0001c0001t0005g0102 a0001c0001t0026g0098 a0001c0001t0026g0099 others(10): Show |
13 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.150+633G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43749959 | |||||||
| chr19:43750189 | C | T | 1 | a0001c0001t0008g0193 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.150+403G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43750189 | |||||||
| chr19:43750511 | A | G | 1 | a0001c0001t0001g0174 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.150+81T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 2/13 | chr19 | 43750511 | |||||||
| chr19:43750820 | C | T | 182 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(179): Show |
291 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.-6-73G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43750820 | |||||||
| chr19:43750826 | C | T | 2 | a0001c0001t0012g0136 a0001c0001t0012g0137 |
2 | HG02717.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-6-79G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43750826 | |||||||
| chr19:43750907 | C | T | 1 | a0001c0002t0043g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-6-160G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43750907 | |||||||
| chr19:43750998 | T | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(80): Show |
101 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-6-251A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43750998 | |||||||
| chr19:43751009 | G | A | 2 | a0001c0001t0015g0033 a0001c0001t0015g0197 |
3 | HG02145.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-6-262C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751009 | |||||||
| chr19:43751104 | T | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(80): Show |
101 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-6-357A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751104 | |||||||
| chr19:43751123 | C | T | 2 | a0001c0001t0002g0022 a0001c0001t0002g0067 |
3 | HG02109.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.-6-376G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751123 | |||||||
| chr19:43751176 | G | A | 3 | a0001c0001t0001g0007 a0001c0001t0001g0169 a0001c0001t0001g0170 |
7 | NA18948.hp2 NA18966.hp2 NA18975.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6-429C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751176 | |||||||
| chr19:43751195 | G | A | 1 | a0001c0001t0053g0115 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-6-448C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751195 | |||||||
| chr19:43751294 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-6-547G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751294 | |||||||
| chr19:43751301 | T | C | 1 | a0001c0001t0001g0135 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-6-554A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751301 | |||||||
| chr19:43751416 | C | T | 4 | a0001c0001t0011g0104 a0001c0001t0011g0105 a0001c0001t0011g0106 others(1): Show |
4 | HG02258.hp2 HG02723.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.-6-669G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751416 | |||||||
| chr19:43751536 | G | C | 10 | a0001c0001t0005g0012 a0001c0001t0005g0102 a0001c0001t0005g0107 others(7): Show |
13 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.-6-789C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751536 | |||||||
| chr19:43751606 | G | A | 2 | a0001c0001t0015g0033 a0001c0001t0015g0197 |
3 | HG02145.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-6-859C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751606 | |||||||
| chr19:43751826 | C | A | 1 | a0001c0001t0001g0171 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.-6-1079G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43751826 | |||||||
| chr19:43752035 | T | C | 1 | a0001c0001t0009g0056 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.-6-1288A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752035 | |||||||
| chr19:43752053 | T | C | 88 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(85): Show |
106 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.-6-1306A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752053 | |||||||
| chr19:43752229 | T | G | 11 | a0001c0001t0005g0102 a0001c0002t0019g0093 a0001c0002t0019g0094 others(8): Show |
11 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-6-1482A>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752229 | |||||||
| chr19:43752234 | T | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(80): Show |
101 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-6-1487A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752234 | |||||||
| chr19:43752713 | C | A | 4 | a0001c0001t0001g0008 a0001c0001t0001g0125 a0001c0001t0001g0172 others(1): Show |
8 | HG00733.hp1 HG01074.hp1 HG01099.hp2 others(5): Show |
intron_variant | MODIFIER | c.-7+1941G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752713 | |||||||
| chr19:43752735 | A | G | 4 | a0001c0001t0001g0028 a0001c0001t0001g0117 a0001c0001t0001g0138 others(1): Show |
5 | NA18747.hp2 NA18941.hp1 NA18952.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+1919T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752735 | |||||||
| chr19:43752758 | T | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(80): Show |
101 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-7+1896A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752758 | |||||||
| chr19:43752881 | G | A | 80 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(77): Show |
162 | HG00140.hp2 HG00408.hp2 HG00438.hp2 others(159): Show |
intron_variant | MODIFIER | c.-7+1773C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752881 | |||||||
| chr19:43752900 | T | G | 9 | a0001c0001t0005g0012 a0001c0001t0005g0107 a0001c0001t0005g0108 others(6): Show |
12 | HG01891.hp1 HG02258.hp2 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.-7+1754A>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752900 | |||||||
| chr19:43752902 | T | TA | 12 | a0001c0001t0001g0017 a0001c0001t0001g0111 a0001c0001t0001g0173 others(9): Show |
18 | HG00738.hp1 HG01070.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.-7+1751dupT | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAA | 6 | a0001c0001t0005g0102 a0001c0001t0008g0019 a0001c0001t0008g0192 others(3): Show |
8 | HG00323.hp1 HG01515.hp1 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.-7+1750_-7+1751dup others(2): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(2): Show |
7 | a0001c0001t0005g0107 a0001c0001t0005g0108 a0001c0001t0011g0104 others(4): Show |
7 | HG02258.hp2 HG02723.hp2 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+1743_-7+1751dup others(9): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(3): Show |
2 | a0001c0001t0005g0012 a0001c0001t0027g0024 |
5 | HG01891.hp1 HG02451.hp1 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+1742_-7+1751dup others(10): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(4): Show |
5 | a0001c0001t0006g0036 a0001c0001t0006g0071 a0001c0001t0006g0072 others(2): Show |
5 | HG01255.hp2 HG01978.hp1 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+1741_-7+1751dup others(11): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(5): Show |
1 | a0001c0001t0006g0075 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-7+1740_-7+1751dup others(12): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(12): Show |
1 | a0001c0002t0043g0095 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-7+1751_-7+1752ins others(19): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(13): Show |
1 | a0002c0003t0021g0090 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-7+1751_-7+1752ins others(20): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(14): Show |
2 | a0001c0001t0002g0076 a0002c0003t0021g0091 |
2 | HG02809.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-7+1751_-7+1752ins others(21): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(15): Show |
2 | a0001c0001t0002g0020 a0002c0003t0020g0092 |
3 | HG01123.hp2 HG02572.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.-7+1751_-7+1752ins others(22): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(16): Show |
1 | a0001c0002t0020g0096 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.-7+1751_-7+1752ins others(23): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(17): Show |
13 | a0001c0001t0002g0009 a0001c0001t0002g0038 a0001c0001t0002g0040 others(10): Show |
16 | HG00408.hp1 HG00558.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.-7+1751_-7+1752ins others(24): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(18): Show |
21 | a0001c0001t0002g0003 a0001c0001t0002g0021 a0001c0001t0002g0045 others(18): Show |
28 | HG00733.hp2 HG00738.hp2 HG01074.hp2 others(25): Show |
intron_variant | MODIFIER | c.-7+1751_-7+1752ins others(25): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(19): Show |
18 | a0001c0001t0002g0011 a0001c0001t0002g0022 a0001c0001t0002g0035 others(15): Show |
22 | HG00099.hp2 HG00621.hp1 HG01081.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7+1751_-7+1752ins others(26): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(20): Show |
2 | a0001c0001t0002g0067 a0001c0001t0026g0099 |
2 | HG02109.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.-7+1751_-7+1752ins others(27): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752902 | T | TAAAAAAA others(21): Show |
1 | a0001c0001t0029g0068 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-7+1751_-7+1752ins others(28): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752902 | |||||||
| chr19:43752916 | A | AAAAAAAA others(52): Show |
1 | a0001c0002t0056g0097 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-7+1737_-7+1738ins others(59): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752916 | |||||||
| chr19:43752916 | A | AAAAAAAA others(7): Show |
1 | a0001c0002t0028g0100 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-7+1737_-7+1738ins others(14): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752916 | |||||||
| chr19:43752916 | A | AAAAAAAA others(6): Show |
1 | a0001c0002t0028g0101 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-7+1737_-7+1738ins others(13): Show |
SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43752916 | |||||||
| chr19:43753295 | T | C | 1 | a0001c0001t0014g0018 | 3 | HG02615.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.-7+1359A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753295 | |||||||
| chr19:43753336 | A | C | 1 | a0004c0008t0001g0126 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-7+1318T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753336 | |||||||
| chr19:43753432 | G | A | 11 | a0001c0001t0001g0111 a0001c0001t0008g0019 a0001c0001t0008g0192 others(8): Show |
17 | HG00323.hp1 HG00738.hp1 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7+1222C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753432 | |||||||
| chr19:43753458 | C | CT | 20 | a0001c0001t0001g0026 a0001c0001t0001g0027 a0001c0001t0001g0117 others(17): Show |
22 | HG00438.hp1 HG01109.hp1 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.-7+1195dupA | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753458 | |||||||
| chr19:43753458 | CT | C | 12 | a0001c0001t0001g0176 a0001c0001t0001g0180 a0001c0001t0001g0181 others(9): Show |
12 | HG01167.hp1 HG01168.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7+1195delA | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753458 | |||||||
| chr19:43753462 | T | C | 57 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(54): Show |
72 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.-7+1192A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753462 | |||||||
| chr19:43753463 | T | C | 3 | a0001c0001t0001g0032 a0001c0001t0002g0069 a0001c0001t0002g0070 |
4 | HG01070.hp1 HG01071.hp2 HG03831.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+1191A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753463 | |||||||
| chr19:43753465 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-7+1189A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753465 | |||||||
| chr19:43753466 | T | C | 7 | a0001c0001t0002g0076 a0001c0001t0006g0036 a0001c0001t0006g0071 others(4): Show |
7 | HG01255.hp2 HG01978.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+1188A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753466 | |||||||
| chr19:43753506 | G | C | 1 | a0001c0001t0009g0077 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-7+1148C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753506 | |||||||
| chr19:43753645 | G | T | 1 | a0001c0001t0006g0036 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-7+1009C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753645 | |||||||
| chr19:43753650 | G | A | 3 | a0001c0002t0028g0100 a0001c0002t0028g0101 a0001c0002t0056g0097 |
3 | HG02145.hp2 HG02258.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-7+1004C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753650 | |||||||
| chr19:43753678 | A | C | 94 | a0001c0001t0001g0111 a0001c0001t0002g0003 a0001c0001t0002g0009 others(91): Show |
118 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.-7+976T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753678 | |||||||
| chr19:43753872 | G | A | 1 | a0001c0001t0001g0184 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.-7+782C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753872 | |||||||
| chr19:43753919 | G | GA | 7 | a0001c0001t0001g0185 a0001c0001t0001g0188 a0001c0001t0001g0190 others(4): Show |
7 | HG00621.hp2 HG01175.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-7+734dupT | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753919 | |||||||
| chr19:43753932 | AAC | A | 75 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(72): Show |
92 | HG00099.hp2 HG00323.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.-7+720_-7+721delGT | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753932 | |||||||
| chr19:43753933 | AC | A | 25 | a0001c0001t0001g0111 a0001c0001t0002g0035 a0001c0001t0005g0012 others(22): Show |
33 | HG00738.hp1 HG01106.hp2 HG01243.hp1 others(30): Show |
intron_variant | MODIFIER | c.-7+720delG | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753933 | |||||||
| chr19:43753934 | C | A | 1 | a0001c0001t0011g0104 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-7+720G>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753934 | |||||||
| chr19:43753951 | C | G | 1 | a0001c0001t0027g0024 | 2 | HG02451.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-7+703G>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43753951 | |||||||
| chr19:43754306 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(80): Show |
101 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(98): Show |
intron_variant | MODIFIER | c.-7+348T>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754306 | |||||||
| chr19:43754322 | A | C | 1 | a0001c0001t0001g0103 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-7+332T>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754322 | |||||||
| chr19:43754343 | C | T | 11 | a0001c0001t0005g0102 a0001c0002t0019g0093 a0001c0002t0019g0094 others(8): Show |
11 | HG01109.hp1 HG01123.hp2 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.-7+311G>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754343 | |||||||
| chr19:43754382 | T | C | 2 | a0001c0002t0028g0100 a0001c0002t0028g0101 |
2 | HG02145.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.-7+272A>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754382 | |||||||
| chr19:43754479 | G | C | 1 | a0001c0004t0001g0194 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-7+175C>G | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754479 | |||||||
| chr19:43754487 | T | G | 1 | a0001c0001t0002g0078 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-7+167A>C | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754487 | |||||||
| chr19:43754513 | G | A | 2 | a0001c0001t0015g0033 a0001c0001t0015g0197 |
3 | HG02145.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-7+141C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754513 | |||||||
| chr19:43754550 | G | T | 73 | a0001c0001t0002g0003 a0001c0001t0002g0009 a0001c0001t0002g0011 others(70): Show |
88 | HG00099.hp2 HG00408.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.-7+104C>A | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754550 | |||||||
| chr19:43754567 | T | A | 1 | a0001c0001t0055g0195 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-7+87A>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754567 | |||||||
| chr19:43754571 | T | A | 8 | a0001c0001t0003g0023 a0001c0001t0003g0079 a0001c0001t0003g0080 others(5): Show |
9 | HG01884.hp2 HG02486.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+83A>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754571 | |||||||
| chr19:43754582 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-7+72C>T | SMG9 | ENSG00000105771.14 | transcript | ENST00000270066.11 | protein_coding | 1/13 | chr19 | 43754582 |