Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 27130 |
| ensemblid | ENSG00000119509.13 |
| hgncid | 17870 |
| symbol | INVS |
| name | inversin |
| refseq_nuc | NM_014425.5 |
| refseq_prot | NP_055240.2 |
| ensembl_nuc | ENST00000262457.7 |
| ensembl_prot | ENSP00000262457.2 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 100099243 |
| end | 100302175 |
| strand | + |
| ver | v1.2 |
| region | chr9:100099243-100302175 |
| region5000 | chr9:100094243-100307175 |
| regionname0 | INVS_chr9_100099243_100302175 |
| regionname5000 | INVS_chr9_100094243_100307175 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1065 | 169 | 63 | 40 | 41 | 9 | 14 | 22 | INVS_chr9_100094243_100307175 | INVS | MNKSE others(1060): Show |
chr9 | 100094243 | 100307175 |
| a0002 | 0/0 | 1065 | 7 | 2 | 4 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | MNKSE others(1060): Show |
chr9 | 100094243 | 100307175 |
| a0003 | 0/0 | 1065 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | MNKSE others(1060): Show |
chr9 | 100094243 | 100307175 |
| a0004 | 0/0 | 1065 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | MNKSE others(1060): Show |
chr9 | 100094243 | 100307175 |
| a0005 | 0/0 | 283 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | MNKSE others(278): Show |
chr9 | 100094243 | 100307175 |
| a0006 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | MNKSE others(1060): Show |
chr9 | 100094243 | 100307175 |
| a0007 | 0/0 | 1065 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | MNKSE others(1060): Show |
chr9 | 100094243 | 100307175 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 3195 | 94 | 39 | 21 | 21 | 4 | 8 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(3190): Show |
chr9 | 100094243 | 100307175 | ||
| a0001c0002 | 1/0 | 3195 | 72 | 21 | 19 | 20 | 5 | 6 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(3190): Show |
chr9 | 100094243 | 100307175 | ||
| a0001c0004 | 0/0 | 3195 | 2 | 2 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(3190): Show |
chr9 | 100094243 | 100307175 | ||
| a0001c0009 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(3190): Show |
chr9 | 100094243 | 100307175 | ||
| a0002c0003 | 0/0 | 3195 | 7 | 2 | 4 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(3190): Show |
chr9 | 100094243 | 100307175 | ||
| a0003c0005 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(3190): Show |
chr9 | 100094243 | 100307175 | ||
| a0003c0008 | 0/0 | 3195 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(3190): Show |
chr9 | 100094243 | 100307175 | ||
| a0004c0010 | 0/0 | 3195 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(3190): Show |
chr9 | 100094243 | 100307175 | ||
| a0005c0011 | 0/0 | 4192 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(4187): Show |
chr9 | 100094243 | 100307175 | ||
| a0006c0007 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(3190): Show |
chr9 | 100094243 | 100307175 | ||
| a0007c0006 | 0/0 | 3195 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | ATGAA others(3190): Show |
chr9 | 100094243 | 100307175 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 4897 | 16 | 13 | 3 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4892): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0003 | 0/1 | 4897 | 16 | 0 | 10 | 1 | 2 | 2 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4892): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0004 | 0/0 | 4895 | 19 | 1 | 1 | 14 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4890): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0005 | 0/0 | 4903 | 7 | 7 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4898): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0007 | 0/0 | 4893 | 5 | 5 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4888): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0008 | 0/0 | 4895 | 3 | 0 | 0 | 2 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4890): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0009 | 0/0 | 4881 | 3 | 3 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4876): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0010 | 0/0 | 4879 | 4 | 4 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4874): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0011 | 0/0 | 4907 | 4 | 0 | 1 | 0 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4902): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0012 | 0/0 | 4895 | 3 | 0 | 0 | 3 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4890): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0013 | 0/0 | 4913 | 3 | 0 | 2 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4908): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0014 | 0/0 | 4909 | 2 | 1 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4904): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0015 | 0/0 | 4905 | 2 | 0 | 2 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4900): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0017 | 0/0 | 4901 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4896): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0022 | 0/0 | 4895 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4890): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0023 | 0/0 | 4887 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4882): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0024 | 0/0 | 4919 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4914): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0025 | 0/0 | 4917 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4912): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0026 | 0/0 | 4911 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4906): Show |
chr9 | 100094243 | 100307175 |
| a0001c0001t0028 | 0/0 | 4895 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4890): Show |
chr9 | 100094243 | 100307175 |
| a0001c0002t0001 | 0/0 | 4897 | 37 | 21 | 8 | 5 | 1 | 2 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4892): Show |
chr9 | 100094243 | 100307175 |
| a0001c0002t0002 | 0/0 | 4897 | 29 | 0 | 10 | 15 | 1 | 3 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4892): Show |
chr9 | 100094243 | 100307175 |
| a0001c0002t0003 | 1/0 | 4897 | 2 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4892): Show |
chr9 | 100094243 | 100307175 |
| a0001c0002t0008 | 0/0 | 4895 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4890): Show |
chr9 | 100094243 | 100307175 |
| a0001c0002t0016 | 0/0 | 4897 | 2 | 0 | 0 | 0 | 2 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4892): Show |
chr9 | 100094243 | 100307175 |
| a0001c0002t0027 | 0/0 | 4897 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4892): Show |
chr9 | 100094243 | 100307175 |
| a0001c0004t0001 | 0/0 | 4897 | 2 | 2 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4892): Show |
chr9 | 100094243 | 100307175 |
| a0001c0009t0007 | 0/0 | 4893 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4888): Show |
chr9 | 100094243 | 100307175 |
| a0002c0003t0006 | 0/0 | 4901 | 6 | 1 | 4 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4896): Show |
chr9 | 100094243 | 100307175 |
| a0002c0003t0021 | 0/0 | 4905 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4900): Show |
chr9 | 100094243 | 100307175 |
| a0003c0005t0020 | 0/0 | 4905 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4900): Show |
chr9 | 100094243 | 100307175 |
| a0003c0008t0019 | 0/0 | 4907 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4902): Show |
chr9 | 100094243 | 100307175 |
| a0004c0010t0003 | 0/0 | 4897 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4892): Show |
chr9 | 100094243 | 100307175 |
| a0005c0011t0002 | 0/0 | 5894 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(5889): Show |
chr9 | 100094243 | 100307175 |
| a0006c0007t0009 | 0/0 | 4881 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4876): Show |
chr9 | 100094243 | 100307175 |
| a0007c0006t0018 | 0/0 | 4913 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | AGAAG others(4908): Show |
chr9 | 100094243 | 100307175 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0098 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0003g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0007g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0007g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0007g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0008g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0008g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0008g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0009g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0009g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0009g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0010g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0010g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0010g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0010g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0011g0022 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0011g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0011g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0012g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0012g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0012g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0013g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0013g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0013g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0014g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0014g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0015g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0015g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0017g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0022g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0023g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0024g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0025g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0026g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0001t0028g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0002g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0003g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0003g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0008g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0016g0148 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0016g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0002t0027g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0001c0009t0007g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0096 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0006g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0002c0003t0021g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0003c0005t0020g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0003c0008t0019g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0004c0010t0003g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0005c0011t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0006c0007t0009g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| a0007c0006t0018g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0003 | g0045 | EUR | GBR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00140 | hp2 | a0001 | c0002 | t0002 | g0041 | EUR | GBR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00280 | hp1 | a0001 | c0002 | t0001 | g0128 | EUR | FIN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00280 | hp2 | a0001 | c0001 | t0004 | g0052 | EUR | FIN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00323 | hp1 | a0001 | c0001 | t0011 | g0022 | EUR | FIN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00323 | hp2 | a0001 | c0002 | t0008 | g0126 | EUR | FIN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00423 | hp1 | a0001 | c0002 | t0001 | g0171 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00423 | hp2 | a0001 | c0001 | t0028 | g0075 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0169 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00544 | hp2 | a0001 | c0001 | t0004 | g0072 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00609 | hp1 | a0001 | c0001 | t0004 | g0061 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00609 | hp2 | a0001 | c0002 | t0002 | g0118 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00621 | hp1 | a0001 | c0001 | t0012 | g0080 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00621 | hp2 | a0001 | c0002 | t0002 | g0139 | EAS | CHS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00642 | hp1 | a0001 | c0002 | t0001 | g0143 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00642 | hp2 | a0001 | c0001 | t0015 | g0023 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00733 | hp1 | a0001 | c0002 | t0002 | g0156 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00733 | hp2 | a0003 | c0008 | t0019 | g0001 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00735 | hp1 | a0002 | c0003 | t0006 | g0094 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00735 | hp2 | a0001 | c0002 | t0002 | g0152 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00738 | hp1 | a0002 | c0003 | t0006 | g0093 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00738 | hp2 | a0001 | c0001 | t0015 | g0024 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0127 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG00741 | hp2 | a0001 | c0001 | t0013 | g0026 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0132 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01069 | hp2 | a0001 | c0001 | t0003 | g0177 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01071 | hp1 | a0001 | c0002 | t0001 | g0142 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01071 | hp2 | a0001 | c0001 | t0003 | g0178 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01074 | hp1 | a0001 | c0001 | t0003 | g0070 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01074 | hp2 | a0001 | c0002 | t0002 | g0154 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01081 | hp2 | a0001 | c0001 | t0022 | g0182 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01106 | hp1 | a0001 | c0001 | t0011 | g0078 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01106 | hp2 | a0001 | c0001 | t0003 | g0042 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01109 | hp2 | a0001 | c0002 | t0001 | g0172 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01167 | hp1 | a0001 | c0001 | t0003 | g0176 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01167 | hp2 | a0001 | c0002 | t0002 | g0157 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01168 | hp1 | a0001 | c0001 | t0013 | g0025 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01168 | hp2 | a0001 | c0002 | t0002 | g0161 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01169 | hp1 | a0001 | c0002 | t0002 | g0162 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01169 | hp2 | a0001 | c0001 | t0003 | g0179 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01175 | hp1 | a0002 | c0003 | t0006 | g0097 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0165 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01192 | hp1 | a0001 | c0002 | t0002 | g0125 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01192 | hp2 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01243 | hp1 | a0001 | c0001 | t0003 | g0090 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01346 | hp1 | a0001 | c0002 | t0002 | g0175 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01346 | hp2 | a0001 | c0001 | t0003 | g0089 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01433 | hp1 | a0001 | c0002 | t0002 | g0153 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01433 | hp2 | a0001 | c0002 | t0003 | g0130 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0131 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01496 | hp2 | a0004 | c0010 | t0003 | g0044 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01516 | hp1 | a0001 | c0002 | t0016 | g0151 | EUR | IBS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01516 | hp2 | a0001 | c0001 | t0003 | g0083 | EUR | IBS | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0163 | AMR | PEL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01952 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | PEL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01975 | hp1 | a0001 | c0002 | t0002 | g0173 | AMR | PEL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01975 | hp2 | a0002 | c0003 | t0006 | g0095 | AMR | PEL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02055 | hp2 | a0002 | c0003 | t0021 | g0087 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02056 | hp1 | a0001 | c0001 | t0004 | g0066 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02056 | hp2 | a0005 | c0011 | t0002 | g0103 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02080 | hp1 | a0001 | c0002 | t0002 | g0119 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02080 | hp2 | a0001 | c0001 | t0004 | g0059 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02083 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02083 | hp2 | a0001 | c0002 | t0002 | g0158 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0065 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02135 | hp2 | a0001 | c0002 | t0002 | g0141 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0014 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02145 | hp2 | a0001 | c0001 | t0024 | g0031 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02155 | hp1 | a0001 | c0001 | t0004 | g0062 | EAS | CDX | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02155 | hp2 | a0001 | c0002 | t0002 | g0140 | EAS | CDX | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02280 | hp1 | a0001 | c0001 | t0010 | g0136 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02280 | hp2 | a0001 | c0001 | t0014 | g0011 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02451 | hp1 | a0001 | c0001 | t0017 | g0063 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02451 | hp2 | a0001 | c0001 | t0005 | g0005 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02523 | hp1 | a0001 | c0001 | t0008 | g0123 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02523 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | KHV | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02602 | hp1 | a0001 | c0001 | t0013 | g0071 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02602 | hp2 | a0001 | c0002 | t0002 | g0155 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0106 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0040 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02647 | hp1 | a0001 | c0001 | t0007 | g0060 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02717 | hp1 | a0001 | c0001 | t0023 | g0030 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02717 | hp2 | a0001 | c0001 | t0005 | g0009 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02809 | hp1 | a0001 | c0009 | t0007 | g0049 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0108 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02897 | hp1 | a0001 | c0002 | t0001 | g0016 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02897 | hp2 | a0001 | c0001 | t0007 | g0048 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02922 | hp1 | a0001 | c0001 | t0005 | g0007 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0144 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0018 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02970 | hp2 | a0001 | c0001 | t0010 | g0138 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02976 | hp1 | a0001 | c0002 | t0001 | g0135 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02976 | hp2 | a0001 | c0001 | t0005 | g0006 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03041 | hp2 | a0001 | c0001 | t0004 | g0055 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03098 | hp1 | a0003 | c0005 | t0020 | g0002 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03098 | hp2 | a0001 | c0001 | t0009 | g0058 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03130 | hp1 | a0001 | c0002 | t0001 | g0105 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03139 | hp1 | a0001 | c0001 | t0007 | g0054 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0137 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03209 | hp1 | a0001 | c0001 | t0026 | g0008 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03209 | hp2 | a0006 | c0007 | t0009 | g0181 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03225 | hp1 | a0001 | c0001 | t0005 | g0012 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03225 | hp2 | a0001 | c0004 | t0001 | g0109 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03239 | hp1 | a0001 | c0001 | t0004 | g0046 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03239 | hp2 | a0001 | c0002 | t0001 | g0129 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0082 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03453 | hp2 | a0001 | c0001 | t0009 | g0101 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03490 | hp1 | a0001 | c0002 | t0027 | g0113 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03490 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0166 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03516 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | ESN | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03540 | hp1 | a0001 | c0004 | t0001 | g0110 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03669 | hp1 | a0001 | c0001 | t0008 | g0124 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03669 | hp2 | a0001 | c0001 | t0011 | g0076 | SAS | PJL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03831 | hp1 | a0001 | c0001 | t0011 | g0081 | SAS | BEB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03831 | hp2 | a0001 | c0002 | t0002 | g0149 | SAS | BEB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03927 | hp1 | a0001 | c0001 | t0004 | g0047 | SAS | BEB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0160 | SAS | BEB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18522 | hp1 | a0001 | c0001 | t0009 | g0100 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18522 | hp2 | a0001 | c0002 | t0001 | g0104 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18906 | hp1 | a0001 | c0002 | t0001 | g0057 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18962 | hp1 | a0001 | c0002 | t0002 | g0115 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18962 | hp2 | a0001 | c0002 | t0001 | g0145 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18964 | hp1 | a0001 | c0001 | t0004 | g0067 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18964 | hp2 | a0001 | c0002 | t0002 | g0114 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18970 | hp1 | a0001 | c0002 | t0002 | g0150 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18970 | hp2 | a0001 | c0001 | t0004 | g0043 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18983 | hp1 | a0001 | c0001 | t0008 | g0159 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18983 | hp2 | a0001 | c0002 | t0001 | g0168 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18999 | hp1 | a0001 | c0001 | t0004 | g0051 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA18999 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19005 | hp1 | a0001 | c0001 | t0004 | g0116 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19005 | hp2 | a0001 | c0002 | t0002 | g0122 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0117 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19012 | hp2 | a0001 | c0001 | t0004 | g0068 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19030 | hp1 | a0001 | c0002 | t0001 | g0112 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19030 | hp2 | a0007 | c0006 | t0018 | g0099 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19043 | hp1 | a0001 | c0001 | t0005 | g0010 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0167 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19058 | hp1 | a0001 | c0002 | t0002 | g0134 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19058 | hp2 | a0001 | c0001 | t0004 | g0064 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19082 | hp1 | a0001 | c0001 | t0012 | g0079 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19082 | hp2 | a0001 | c0002 | t0002 | g0121 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19084 | hp1 | a0001 | c0002 | t0002 | g0120 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19084 | hp2 | a0001 | c0001 | t0012 | g0074 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19090 | hp1 | a0001 | c0002 | t0002 | g0102 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19090 | hp2 | a0001 | c0001 | t0004 | g0069 | EAS | JPT | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0028 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0050 | AFR | YRI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20129 | hp1 | a0001 | c0002 | t0001 | g0174 | AFR | ASW | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | ASW | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20805 | hp1 | a0002 | c0003 | t0006 | g0096 | EUR | TSI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20805 | hp2 | a0001 | c0002 | t0016 | g0148 | EUR | TSI | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0085 | SAS | GIH | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA20905 | hp2 | a0001 | c0002 | t0001 | g0111 | SAS | GIH | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01123 | hp1 | a0001 | c0001 | t0014 | g0027 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG01123 | hp2 | a0001 | c0001 | t0003 | g0086 | AMR | CLM | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02109 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02109 | hp2 | a0001 | c0001 | t0025 | g0056 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02486 | hp2 | a0001 | c0002 | t0001 | g0133 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0180 | AFR | ACB | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03471 | hp1 | a0001 | c0001 | t0010 | g0164 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| NA21309 | hp2 | a0002 | c0003 | t0006 | g0088 | AFR | LWK | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0003 | g0098 | REF | REF | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| homoSapiens | grch38p0 | a0001 | c0002 | t0003 | g0077 | REF | REF | INVS_chr9_100094243_100307175 | INVS | chr9 | 100094243 | 100307175 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100126394 | C | G | 1 | a0005 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.118C>G | p.Leu40Val | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/17 | 316/4897 | 118/3198 | 40/1065 | chr9 | 100126394 | |||
| chr9:100240112 | C | CCAACAAA others(990): Show |
1 | a0005 | 1 | HG02056.hp2 | frameshift_variant&stop_gained | HIGH | c.668_669insCAACAAAG others(989): Show |
p.Pro224fs | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/17 | 867/4897 | 669/3198 | 223/1065 | chr9 | 100240112 | |||
| chr9:100240114 | C | A | 1 | a0005 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.670C>A | p.Pro224Thr | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/17 | 868/4897 | 670/3198 | 224/1065 | chr9 | 100240114 | |||
| chr9:100240169 | C | T | 1 | a0004 | 1 | HG01496.hp2 | missense_variant | MODERATE | c.725C>T | p.Ser242Leu | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/17 | 923/4897 | 725/3198 | 242/1065 | chr9 | 100240169 | |||
| chr9:100284480 | G | A | 1 | a0007 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1945G>A | p.Val649Met | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/17 | 2143/4897 | 1945/3198 | 649/1065 | chr9 | 100284480 | |||
| chr9:100292373 | A | G | 1 | a0003 | 2 | HG00733.hp2 HG03098.hp1 |
missense_variant | MODERATE | c.2116A>G | p.Arg706Gly | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/17 | 2314/4897 | 2116/3198 | 706/1065 | chr9 | 100292373 | |||
| chr9:100292659 | G | A | 1 | a0002 | 7 | HG00735.hp1 HG00738.hp1 HG01175.hp1 others(4): Show |
missense_variant | MODERATE | c.2402G>A | p.Gly801Glu | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/17 | 2600/4897 | 2402/3198 | 801/1065 | chr9 | 100292659 | |||
| chr9:100292743 | G | A | 1 | a0006 | 1 | HG03209.hp2 | missense_variant | MODERATE | c.2486G>A | p.Arg829His | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/17 | 2684/4897 | 2486/3198 | 829/1065 | chr9 | 100292743 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100104623 | C | T | 1 | a0001c0004 | 2 | HG03225.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.102C>T | p.Ile34Ile | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/17 | 300/4897 | 102/3198 | 34/1065 | chr9 | 100104623 | |||
| chr9:100229827 | G | C | 1 | a0003c0005 | 1 | HG03098.hp1 | splice_region_variant&synonymous_variant | LOW | c.615G>C | p.Leu205Leu | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/17 | 813/4897 | 615/3198 | 205/1065 | chr9 | 100229827 | |||
| chr9:100240113 | T | A | 1 | a0005c0011 | 1 | HG02056.hp2 | synonymous_variant | LOW | c.669T>A | p.Thr223Thr | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/17 | 867/4897 | 669/3198 | 223/1065 | chr9 | 100240113 | |||
| chr9:100284536 | C | T | 1 | a0001c0009 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.2001C>T | p.Gly667Gly | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/17 | 2199/4897 | 2001/3198 | 667/1065 | chr9 | 100284536 | |||
| chr9:100292669 | T | C | 8 | a0001c0001 a0001c0009 a0002c0003 others(5): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
synonymous_variant | LOW | c.2412T>C | p.Ser804Ser | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/17 | 2610/4897 | 2412/3198 | 804/1065 | chr9 | 100292669 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100099249 | A | T | 1 | a0001c0001t0028 | 1 | HG00423.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-192A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/17 | chr9 | 100099249 | |||||||
| chr9:100099286 | C | T | 1 | a0001c0002t0016 | 2 | HG01516.hp1 NA20805.hp2 |
5_prime_UTR_variant | MODIFIER | c.-155C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/17 | 5236 | chr9 | 100099286 | ||||||
| chr9:100099312 | C | A | 1 | a0001c0001t0017 | 1 | HG02451.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-129C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/17 | chr9 | 100099312 | |||||||
| chr9:100099331 | T | G | 5 | a0001c0001t0008 a0001c0002t0002 a0001c0002t0008 others(2): Show |
36 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(33): Show |
5_prime_UTR_variant | MODIFIER | c.-110T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/17 | 5191 | chr9 | 100099331 | ||||||
| chr9:100099390 | G | T | 1 | a0001c0002t0027 | 1 | HG03490.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-51G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/17 | chr9 | 100099390 | |||||||
| chr9:100301002 | G | A | 2 | a0001c0001t0012 a0001c0001t0028 |
4 | HG00423.hp2 HG00621.hp1 NA19082.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*328G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 328 | chr9 | 100301002 | ||||||
| chr9:100301138 | A | ATC | 1 | a0001c0001t0005 | 7 | HG02451.hp2 HG02717.hp2 HG02922.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*465_*466dupTC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301138 | |||||
| chr9:100301139 | T | TCACA | 2 | a0001c0001t0017 a0002c0003t0006 |
7 | HG00735.hp1 HG00738.hp1 HG01175.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*502_*505dupCACA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 506 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | T | TCACACAC others(1): Show |
2 | a0002c0003t0021 a0003c0005t0020 |
2 | HG02055.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*498_*505dupCACACA others(2): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 506 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | T | TCACACAC others(3): Show |
1 | a0003c0008t0019 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*496_*505dupCACACA others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 506 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | T | TCACACAC others(9): Show |
1 | a0007c0006t0018 | 1 | NA19030.hp2 | 3_prime_UTR_variant | MODIFIER | c.*490_*505dupCACACA others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 506 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | T | TCTCA | 1 | a0001c0001t0015 | 2 | HG00642.hp2 HG00738.hp2 |
3_prime_UTR_variant | MODIFIER | c.*466_*467insTCAC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | T | TCTCACA | 1 | a0001c0001t0011 | 4 | HG00323.hp1 HG01106.hp1 HG03669.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | T | TCTCACAC others(1): Show |
1 | a0001c0001t0014 | 2 | HG01123.hp1 HG02280.hp2 |
3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC others(2): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | T | TCTCACAC others(3): Show |
1 | a0001c0001t0026 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | T | TCTCACAC others(5): Show |
1 | a0001c0001t0013 | 3 | HG00741.hp2 HG01168.hp1 HG02602.hp1 |
3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | T | TCTCACAC others(9): Show |
1 | a0001c0001t0025 | 1 | HG02109.hp2 | 3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | T | TCTCACAC others(11): Show |
1 | a0001c0001t0024 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*466_*467insTCACAC others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 467 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | TCA | T | 6 | a0001c0001t0004 a0001c0001t0008 a0001c0001t0012 others(3): Show |
28 | HG00280.hp2 HG00323.hp2 HG00423.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*504_*505delCA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 504 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | TCACA | T | 2 | a0001c0001t0007 a0001c0009t0007 |
6 | HG02647.hp1 HG02809.hp1 HG02897.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*502_*505delCACA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 502 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | TCACACAC others(9): Show |
T | 2 | a0001c0001t0009 a0006c0007t0009 |
4 | HG03098.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*490_*505delCACACA others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 490 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301139 | TCACACAC others(11): Show |
T | 1 | a0001c0001t0010 | 4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*488_*505delCACACA others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 488 | INFO_REALIGN_3_PRIME | chr9 | 100301139 | |||||
| chr9:100301170 | CACACACA others(3): Show |
C | 1 | a0001c0001t0023 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*498_*507delCACACA others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 498 | INFO_REALIGN_3_PRIME | chr9 | 100301170 | |||||
| chr9:100301172 | CACACACA others(1): Show |
C | 4 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0027 others(1): Show |
49 | HG00280.hp1 HG00642.hp1 HG00741.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*500_*507delCACACA others(2): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 500 | INFO_REALIGN_3_PRIME | chr9 | 100301172 | |||||
| chr9:100301174 | CACACAT | C | 5 | a0001c0001t0001 a0001c0002t0001 a0001c0002t0002 others(2): Show |
33 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*502_*507delCACATA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 502 | INFO_REALIGN_3_PRIME | chr9 | 100301174 | |||||
| chr9:100301176 | CACAT | C | 2 | a0001c0002t0001 a0001c0002t0002 |
6 | HG00609.hp2 HG00735.hp2 HG01192.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*504_*507delCATA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 504 | INFO_REALIGN_3_PRIME | chr9 | 100301176 | |||||
| chr9:100301180 | T | C | 8 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0013 others(5): Show |
21 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*506T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 506 | chr9 | 100301180 | ||||||
| chr9:100301363 | G | A | 8 | a0001c0001t0001 a0001c0001t0023 a0001c0002t0001 others(5): Show |
89 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*689G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 689 | chr9 | 100301363 | ||||||
| chr9:100301438 | T | C | 2 | a0003c0005t0020 a0003c0008t0019 |
2 | HG00733.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*764T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 764 | chr9 | 100301438 | ||||||
| chr9:100301544 | G | T | 8 | a0001c0001t0001 a0001c0001t0023 a0001c0002t0001 others(5): Show |
89 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*870G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 870 | chr9 | 100301544 | ||||||
| chr9:100301709 | T | G | 1 | a0001c0001t0022 | 1 | HG01081.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1035T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 1035 | chr9 | 100301709 | ||||||
| chr9:100301752 | G | GAGAT | 8 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0013 others(5): Show |
21 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1082_*1085dupTAGA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 1086 | INFO_REALIGN_3_PRIME | chr9 | 100301752 | |||||
| chr9:100301778 | T | C | 3 | a0001c0001t0009 a0001c0001t0010 a0006c0007t0009 |
8 | HG02280.hp1 HG02970.hp2 HG03098.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1104T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 1104 | chr9 | 100301778 | ||||||
| chr9:100301871 | A | G | 19 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0011 others(16): Show |
113 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1197A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 17/17 | 1197 | chr9 | 100301871 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:100099732 | T | C | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-25+316T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100099732 | |||||||
| chr9:100099948 | C | T | 2 | a0001c0001t0022g0182 a0006c0007t0009g0181 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-25+532C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100099948 | |||||||
| chr9:100100001 | C | T | 1 | a0001c0002t0001g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-25+585C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100001 | |||||||
| chr9:100100073 | T | C | 1 | a0001c0002t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-25+657T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100073 | |||||||
| chr9:100100239 | A | G | 4 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0003g0178 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+823A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100239 | |||||||
| chr9:100100257 | T | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-25+841T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100257 | |||||||
| chr9:100100361 | T | G | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-25+945T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100361 | |||||||
| chr9:100100569 | T | C | 2 | a0001c0001t0022g0182 a0006c0007t0009g0181 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-25+1153T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100569 | |||||||
| chr9:100100575 | T | TATATAAT others(17): Show |
1 | a0001c0001t0003g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-25+1183_-25+1206d others(26): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100575 | ||||||
| chr9:100100599 | C | T | 120 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0021 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.-25+1183C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100599 | |||||||
| chr9:100100617 | T | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1201T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100617 | |||||||
| chr9:100100628 | AAT | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1221_-25+1222d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100628 | ||||||
| chr9:100100634 | T | C | 9 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1218T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100634 | |||||||
| chr9:100100637 | ATT | A | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+1222_-25+1223d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100637 | |||||||
| chr9:100100638 | T | A | 2 | a0001c0001t0022g0182 a0006c0007t0009g0181 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.-25+1222T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100638 | |||||||
| chr9:100100638 | TTA | T | 2 | a0001c0002t0001g0082 a0001c0002t0001g0168 |
2 | HG03453.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.-25+1228_-25+1229d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100638 | ||||||
| chr9:100100638 | TTATATAT others(47): Show |
T | 1 | a0001c0002t0002g0173 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-25+1228_-25+1281d others(56): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100638 | ||||||
| chr9:100100639 | T | A | 11 | a0001c0001t0003g0083 a0001c0001t0005g0005 a0001c0001t0005g0006 others(8): Show |
11 | HG01516.hp2 HG02280.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+1223T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100639 | |||||||
| chr9:100100640 | A | ATATGTAT others(133): Show |
1 | a0006c0007t0009g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-25+1227_-25+1228i others(142): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100640 | ||||||
| chr9:100100640 | A | ATATGTAT others(157): Show |
1 | a0001c0001t0022g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-25+1227_-25+1228i others(166): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100640 | ||||||
| chr9:100100641 | T | C | 1 | a0001c0002t0001g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-25+1225T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100641 | |||||||
| chr9:100100649 | T | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.-25+1233T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100649 | |||||||
| chr9:100100649 | T | TATATATA others(68): Show |
9 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1238_-25+1239i others(77): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100649 | ||||||
| chr9:100100654 | AAT | A | 19 | a0001c0001t0003g0042 a0001c0001t0003g0085 a0001c0001t0003g0086 others(16): Show |
19 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.-25+1247_-25+1248d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100654 | ||||||
| chr9:100100663 | ATT | A | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+1248_-25+1249d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100663 | |||||||
| chr9:100100664 | TTA | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(37): Show |
40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.-25+1254_-25+1255d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100664 | ||||||
| chr9:100100665 | T | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1249T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100665 | |||||||
| chr9:100100671 | TGTAC | T | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-25+1256_-25+1259d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100671 | |||||||
| chr9:100100672 | G | A | 1 | a0001c0002t0027g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-25+1256G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100672 | |||||||
| chr9:100100673 | T | C | 1 | a0001c0002t0027g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-25+1257T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100673 | |||||||
| chr9:100100675 | C | CATATAAT others(113): Show |
3 | a0002c0003t0006g0094 a0002c0003t0006g0095 a0002c0003t0006g0096 |
3 | HG00735.hp1 HG01975.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-25+1271_-25+1272i others(122): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100675 | ||||||
| chr9:100100675 | C | CATATAAT others(117): Show |
2 | a0001c0001t0003g0042 a0001c0001t0003g0085 |
2 | HG01106.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.-25+1279_-25+1280i others(126): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100675 | ||||||
| chr9:100100675 | C | T | 86 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(83): Show |
86 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.-25+1259C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100675 | |||||||
| chr9:100100688 | TATTA | T | 9 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1273_-25+1276d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100688 | |||||||
| chr9:100100690 | TTA | T | 69 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(66): Show |
69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.-25+1280_-25+1281d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100690 | ||||||
| chr9:100100692 | A | ATATGTAC others(141): Show |
1 | a0001c0001t0003g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-25+1279_-25+1280i others(150): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100692 | ||||||
| chr9:100100692 | A | ATATGTAC others(141): Show |
11 | a0001c0001t0003g0086 a0001c0001t0003g0089 a0001c0001t0003g0090 others(8): Show |
11 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(8): Show |
intron_variant | MODIFIER | c.-25+1279_-25+1280i others(150): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100692 | ||||||
| chr9:100100692 | A | ATATGTAC others(37): Show |
1 | a0001c0001t0001g0032 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-25+1279_-25+1280i others(46): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100692 | ||||||
| chr9:100100692 | A | ATATGTAT others(109): Show |
1 | a0001c0001t0009g0100 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-25+1279_-25+1280i others(118): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100692 | ||||||
| chr9:100100692 | A | ATATGTAT others(109): Show |
1 | a0001c0001t0009g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-25+1279_-25+1280i others(118): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100692 | ||||||
| chr9:100100696 | A | G | 4 | a0001c0001t0003g0084 a0001c0002t0001g0174 a0003c0005t0020g0002 others(1): Show |
4 | HG00733.hp2 HG02083.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+1280A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100696 | |||||||
| chr9:100100698 | G | A | 80 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(77): Show |
80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-25+1282G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100698 | |||||||
| chr9:100100699 | T | C | 78 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(75): Show |
78 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.-25+1283T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100699 | |||||||
| chr9:100100701 | C | T | 91 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(88): Show |
91 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(88): Show |
intron_variant | MODIFIER | c.-25+1285C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100701 | |||||||
| chr9:100100707 | A | ATATATGT others(29): Show |
1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1296_-25+1297i others(38): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100707 | ||||||
| chr9:100100716 | T | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1300T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100716 | |||||||
| chr9:100100722 | G | A | 31 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(28): Show |
31 | HG00140.hp1 HG00280.hp2 HG01069.hp2 others(28): Show |
intron_variant | MODIFIER | c.-25+1306G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100722 | |||||||
| chr9:100100723 | TAC | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(25): Show |
28 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.-25+1309_-25+1310d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100723 | ||||||
| chr9:100100725 | C | CAT | 122 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(119): Show |
122 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(119): Show |
intron_variant | MODIFIER | c.-25+1313_-25+1314d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100725 | ||||||
| chr9:100100725 | C | CATATATA others(21): Show |
3 | a0002c0003t0006g0094 a0002c0003t0006g0095 a0002c0003t0006g0096 |
3 | HG00735.hp1 HG01975.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.-25+1314_-25+1315i others(30): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100725 | ||||||
| chr9:100100725 | C | CATATATA others(147): Show |
2 | a0002c0003t0006g0093 a0002c0003t0006g0097 |
2 | HG00738.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-25+1314_-25+1315i others(156): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100725 | ||||||
| chr9:100100725 | C | T | 17 | a0001c0001t0001g0032 a0001c0001t0003g0177 a0001c0001t0003g0178 others(14): Show |
17 | HG00733.hp2 HG01069.hp2 HG01071.hp2 others(14): Show |
intron_variant | MODIFIER | c.-25+1309C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100725 | |||||||
| chr9:100100730 | AAT | A | 10 | a0001c0001t0001g0032 a0001c0001t0005g0005 a0001c0001t0005g0006 others(7): Show |
10 | HG01109.hp1 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+1323_-25+1324d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100730 | ||||||
| chr9:100100731 | A | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(25): Show |
28 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.-25+1315A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100731 | |||||||
| chr9:100100740 | T | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1324T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100740 | |||||||
| chr9:100100749 | C | T | 92 | a0001c0001t0001g0032 a0001c0001t0001g0107 a0001c0001t0001g0146 others(89): Show |
92 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.-25+1333C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100749 | |||||||
| chr9:100100754 | A | AATATATA others(118): Show |
1 | a0001c0001t0014g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-25+1347_-25+1348i others(127): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100754 | ||||||
| chr9:100100754 | A | ATAATATA others(52): Show |
1 | a0001c0001t0003g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.-25+1338_-25+1339i others(61): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100754 | |||||||
| chr9:100100763 | A | ATTATATG others(78): Show |
1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-25+1347_-25+1348i others(87): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100763 | |||||||
| chr9:100100763 | A | ATTATATG others(87): Show |
2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.-25+1347_-25+1348i others(96): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100763 | |||||||
| chr9:100100763 | A | ATTATATG others(85): Show |
9 | a0001c0001t0001g0037 a0001c0001t0001g0038 a0001c0001t0001g0039 others(6): Show |
9 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1347_-25+1348i others(94): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100763 | |||||||
| chr9:100100763 | A | T | 14 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(11): Show |
14 | HG01081.hp2 HG01975.hp1 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25+1347A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100763 | |||||||
| chr9:100100764 | A | T | 93 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(90): Show |
93 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.-25+1348A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100764 | |||||||
| chr9:100100765 | T | C | 1 | a0001c0002t0027g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-25+1349T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100765 | |||||||
| chr9:100100773 | T | C | 16 | a0001c0001t0001g0015 a0001c0001t0001g0034 a0001c0001t0004g0061 others(13): Show |
16 | HG00609.hp1 HG00609.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25+1357T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100773 | |||||||
| chr9:100100778 | A | AAT | 4 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0027g0113 others(1): Show |
4 | HG02523.hp1 HG03490.hp1 HG03669.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+1369_-25+1370d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100778 | ||||||
| chr9:100100778 | AATATATA others(2): Show |
A | 2 | a0001c0001t0001g0015 a0001c0002t0002g0125 |
2 | HG01192.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-25+1371_-25+1379d others(11): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100778 | ||||||
| chr9:100100779 | A | ATATATAT others(8): Show |
69 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(66): Show |
intron_variant | MODIFIER | c.-25+1370_-25+1371i others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100779 | ||||||
| chr9:100100779 | A | ATATATAT others(32): Show |
1 | a0001c0002t0008g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-25+1370_-25+1371i others(41): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100779 | ||||||
| chr9:100100783 | ATATTATA others(12): Show |
A | 1 | a0001c0002t0002g0173 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-25+1368_-25+1386d others(21): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100783 | |||||||
| chr9:100100784 | T | TA | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.-25+1369dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100784 | ||||||
| chr9:100100786 | T | TATTATAT others(5): Show |
1 | a0001c0002t0001g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-25+1370_-25+1371i others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100786 | |||||||
| chr9:100100786 | T | TTATATGT others(111): Show |
1 | a0001c0001t0001g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-25+1375_-25+1376i others(120): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100786 | ||||||
| chr9:100100786 | TTATATAT others(4): Show |
T | 8 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+1376_-25+1386d others(13): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100786 | ||||||
| chr9:100100787 | T | A | 70 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.-25+1371T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100787 | |||||||
| chr9:100100787 | T | TATATGTA others(255): Show |
3 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 |
3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-25+1375_-25+1376i others(264): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100787 | ||||||
| chr9:100100787 | T | TATATGTA others(329): Show |
2 | a0001c0002t0001g0003 a0001c0002t0001g0028 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-25+1375_-25+1376i others(338): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100787 | ||||||
| chr9:100100788 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1372A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100788 | |||||||
| chr9:100100791 | T | TGTAC | 5 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0027g0113 others(2): Show |
5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1375_-25+1376i others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100791 | |||||||
| chr9:100100796 | A | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+1380A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100796 | |||||||
| chr9:100100796 | A | T | 6 | a0001c0001t0001g0033 a0001c0001t0007g0029 a0001c0001t0023g0030 others(3): Show |
6 | HG02145.hp2 HG02647.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+1380A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100796 | |||||||
| chr9:100100797 | A | T | 73 | a0001c0001t0001g0015 a0001c0001t0001g0107 a0001c0001t0001g0146 others(70): Show |
73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.-25+1381A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100797 | |||||||
| chr9:100100802 | T | TA | 5 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0027g0113 others(2): Show |
5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1386_-25+1387i others(3): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100802 | |||||||
| chr9:100100803 | G | A | 20 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(17): Show |
20 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(17): Show |
intron_variant | MODIFIER | c.-25+1387G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100803 | |||||||
| chr9:100100803 | G | T | 5 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0027g0113 others(2): Show |
5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1387G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100803 | |||||||
| chr9:100100804 | T | C | 15 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(12): Show |
15 | HG01109.hp1 HG01123.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.-25+1388T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100804 | |||||||
| chr9:100100806 | T | C | 71 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(68): Show |
71 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.-25+1390T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100806 | |||||||
| chr9:100100810 | T | A | 18 | a0001c0001t0003g0042 a0001c0001t0003g0085 a0001c0001t0003g0086 others(15): Show |
18 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-25+1394T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100810 | |||||||
| chr9:100100810 | TA | T | 5 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0027g0113 others(2): Show |
5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1396delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100810 | ||||||
| chr9:100100811 | A | AAT | 29 | a0001c0001t0003g0045 a0001c0001t0004g0051 a0001c0001t0004g0052 others(26): Show |
29 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(26): Show |
intron_variant | MODIFIER | c.-25+1403_-25+1404d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100811 | ||||||
| chr9:100100811 | A | AATATATA others(21): Show |
2 | a0001c0001t0004g0046 a0001c0001t0004g0047 |
2 | HG03239.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-25+1404_-25+1405i others(30): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100811 | ||||||
| chr9:100100811 | A | T | 18 | a0001c0001t0003g0042 a0001c0001t0003g0085 a0001c0001t0003g0086 others(15): Show |
18 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.-25+1395A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100811 | |||||||
| chr9:100100812 | A | ATATATAT others(4): Show |
1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1404_-25+1405i others(13): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100812 | ||||||
| chr9:100100812 | A | G | 5 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0027g0113 others(2): Show |
5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1396A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100812 | |||||||
| chr9:100100820 | A | ATG | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+1404_-25+1405i others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100820 | |||||||
| chr9:100100820 | A | ATT | 6 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(3): Show |
6 | HG01109.hp1 HG01123.hp1 HG02055.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+1404_-25+1405i others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100820 | |||||||
| chr9:100100820 | A | T | 80 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0039 others(77): Show |
80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.-25+1404A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100820 | |||||||
| chr9:100100821 | A | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(6): Show |
9 | HG01192.hp1 HG02109.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1405A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100821 | |||||||
| chr9:100100825 | AT | A | 9 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0001c0002t0001g0129 others(6): Show |
9 | HG00280.hp1 HG00741.hp1 HG01069.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1410delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100825 | |||||||
| chr9:100100825 | ATGT | A | 5 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0027g0113 others(2): Show |
5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1410_-25+1412d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100825 | |||||||
| chr9:100100828 | T | C | 14 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0001g0035 others(11): Show |
14 | HG01109.hp1 HG01123.hp1 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.-25+1412T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100828 | |||||||
| chr9:100100830 | T | C | 1 | a0001c0002t0002g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-25+1414T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100830 | |||||||
| chr9:100100835 | AAT | A | 8 | a0001c0001t0007g0029 a0001c0001t0022g0182 a0001c0001t0023g0030 others(5): Show |
8 | HG01081.hp2 HG01192.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.-25+1429_-25+1430d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100835 | ||||||
| chr9:100100836 | A | T | 5 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0027g0113 others(2): Show |
5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1420A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100836 | |||||||
| chr9:100100837 | T | A | 5 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0027g0113 others(2): Show |
5 | HG00733.hp2 HG02523.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1421T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100837 | |||||||
| chr9:100100837 | T | TATAAATA others(6): Show |
2 | a0001c0002t0002g0117 a0001c0002t0002g0119 |
2 | HG02080.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.-25+1424_-25+1425i others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100837 | ||||||
| chr9:100100837 | T | TATAATAT others(5): Show |
69 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-25+1424_-25+1425i others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100837 | ||||||
| chr9:100100837 | T | TATATATT others(63): Show |
2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+1427_-25+1428i others(72): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100837 | ||||||
| chr9:100100843 | T | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1427T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100843 | |||||||
| chr9:100100843 | TATAA | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1428_-25+1431d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100843 | |||||||
| chr9:100100844 | A | G | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-25+1428A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100844 | |||||||
| chr9:100100846 | A | T | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
23 | HG01109.hp1 HG01123.hp1 HG01192.hp1 others(20): Show |
intron_variant | MODIFIER | c.-25+1430A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100846 | |||||||
| chr9:100100853 | G | A | 1 | a0001c0002t0002g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-25+1437G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100853 | |||||||
| chr9:100100854 | T | C | 23 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(20): Show |
23 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(20): Show |
intron_variant | MODIFIER | c.-25+1438T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100854 | |||||||
| chr9:100100861 | AAT | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(14): Show |
17 | HG01346.hp2 HG02109.hp1 HG02145.hp1 others(14): Show |
intron_variant | MODIFIER | c.-25+1454_-25+1455d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100861 | ||||||
| chr9:100100862 | A | ATATATAA others(6): Show |
75 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(72): Show |
75 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.-25+1452_-25+1453i others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100862 | ||||||
| chr9:100100863 | T | TATAAATT others(346): Show |
1 | a0001c0001t0005g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-25+1450_-25+1451i others(355): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | ||||||
| chr9:100100863 | T | TATAAATT others(348): Show |
1 | a0001c0001t0005g0006 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-25+1450_-25+1451i others(357): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | ||||||
| chr9:100100863 | T | TATAAATT others(324): Show |
3 | a0001c0001t0005g0012 a0001c0001t0005g0013 a0001c0001t0014g0011 |
3 | HG02280.hp2 HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-25+1450_-25+1451i others(333): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | ||||||
| chr9:100100863 | T | TATAAATT others(348): Show |
4 | a0001c0001t0005g0007 a0001c0001t0005g0009 a0001c0001t0005g0010 others(1): Show |
4 | HG02717.hp2 HG02922.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+1450_-25+1451i others(357): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | ||||||
| chr9:100100863 | T | TATAATAT others(5): Show |
1 | a0001c0002t0002g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-25+1450_-25+1451i others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | ||||||
| chr9:100100863 | T | TATATAGA others(167): Show |
1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1452_-25+1453i others(176): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | ||||||
| chr9:100100863 | T | TATATATA others(115): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0037 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-25+1479_-25+1480i others(124): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | ||||||
| chr9:100100863 | T | TATATATT others(63): Show |
1 | a0006c0007t0009g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-25+1453_-25+1454i others(72): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | ||||||
| chr9:100100863 | T | TATATATT others(87): Show |
1 | a0001c0001t0022g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-25+1453_-25+1454i others(96): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100863 | ||||||
| chr9:100100872 | T | A | 1 | a0001c0002t0002g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-25+1456T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100872 | |||||||
| chr9:100100880 | T | C | 7 | a0001c0001t0001g0033 a0001c0001t0011g0022 a0001c0001t0013g0025 others(4): Show |
7 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.-25+1464T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100880 | |||||||
| chr9:100100887 | A | AAT | 14 | a0001c0001t0001g0035 a0001c0001t0001g0036 a0001c0001t0001g0038 others(11): Show |
14 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(11): Show |
intron_variant | MODIFIER | c.-25+1478_-25+1479d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100887 | ||||||
| chr9:100100897 | ATATATG | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1487_-25+1492d others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100897 | ||||||
| chr9:100100904 | T | C | 7 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
7 | HG01123.hp1 HG02055.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.-25+1488T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100904 | |||||||
| chr9:100100904 | T | TATATATA | 9 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1489_-25+1495d others(9): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100904 | ||||||
| chr9:100100905 | A | ATATATAT | 2 | a0001c0001t0001g0032 a0001c0001t0001g0037 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-25+1495_-25+1501d others(9): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100905 | ||||||
| chr9:100100907 | A | G | 4 | a0001c0002t0001g0168 a0001c0002t0001g0169 a0001c0002t0001g0170 others(1): Show |
4 | HG00423.hp1 HG00544.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+1491A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100907 | |||||||
| chr9:100100912 | T | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(31): Show |
34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.-25+1496T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100912 | |||||||
| chr9:100100917 | T | TA | 2 | a0001c0001t0001g0033 a0001c0001t0014g0027 |
2 | HG01123.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-25+1501_-25+1502i others(3): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100917 | |||||||
| chr9:100100918 | G | A | 16 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0036 others(13): Show |
16 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(13): Show |
intron_variant | MODIFIER | c.-25+1502G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100918 | |||||||
| chr9:100100918 | G | T | 2 | a0001c0001t0001g0033 a0001c0001t0014g0027 |
2 | HG01123.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-25+1502G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100918 | |||||||
| chr9:100100918 | GTA | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1511_-25+1512d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100918 | ||||||
| chr9:100100919 | TA | T | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1504delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100919 | |||||||
| chr9:100100920 | A | ATTATATA others(136): Show |
1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-25+1505_-25+1506i others(145): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100920 | ||||||
| chr9:100100921 | TA | T | 10 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(7): Show |
10 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+1506delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100921 | |||||||
| chr9:100100922 | A | ATATAATA others(5): Show |
2 | a0001c0001t0001g0032 a0001c0001t0001g0037 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-25+1510_-25+1511i others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100922 | ||||||
| chr9:100100926 | A | G | 2 | a0001c0001t0001g0033 a0001c0001t0014g0027 |
2 | HG01123.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-25+1510A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100926 | |||||||
| chr9:100100927 | T | A | 10 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(7): Show |
10 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-25+1511T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100927 | |||||||
| chr9:100100927 | T | TG | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.-25+1511_-25+1512i others(3): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100927 | |||||||
| chr9:100100928 | A | ATATATAA others(38): Show |
2 | a0001c0001t0001g0033 a0001c0001t0014g0027 |
2 | HG01123.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-25+1512_-25+1513i others(47): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100928 | |||||||
| chr9:100100928 | A | ATGCATAT others(138): Show |
5 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0001g0038 others(2): Show |
5 | HG02055.hp1 HG02559.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+1512_-25+1513i others(147): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100928 | |||||||
| chr9:100100928 | A | ATGCATAT others(90): Show |
5 | a0001c0001t0011g0022 a0001c0001t0013g0025 a0001c0001t0013g0026 others(2): Show |
5 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+1512_-25+1513i others(99): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100928 | |||||||
| chr9:100100928 | A | ATGT | 2 | a0001c0001t0001g0032 a0001c0001t0001g0037 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.-25+1512_-25+1513i others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100928 | |||||||
| chr9:100100928 | A | T | 15 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(12): Show |
15 | HG02145.hp2 HG02280.hp2 HG02451.hp2 others(12): Show |
intron_variant | MODIFIER | c.-25+1512A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100928 | |||||||
| chr9:100100929 | A | ATATATTA others(6): Show |
9 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.-25+1518_-25+1519i others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100929 | ||||||
| chr9:100100929 | A | ATATATTA others(80): Show |
1 | a0001c0001t0005g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-25+1518_-25+1519i others(89): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100929 | ||||||
| chr9:100100929 | A | G | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-25+1513A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100929 | |||||||
| chr9:100100938 | A | T | 15 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(12): Show |
15 | HG01081.hp2 HG02109.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.-25+1522A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100938 | |||||||
| chr9:100100946 | A | G | 9 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1530A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100946 | |||||||
| chr9:100100946 | AC | A | 6 | a0001c0001t0004g0061 a0001c0001t0004g0062 a0001c0001t0004g0064 others(3): Show |
6 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.-25+1531delC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100946 | |||||||
| chr9:100100947 | CA | C | 2 | a0001c0001t0004g0059 a0001c0002t0001g0167 |
2 | HG02080.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-25+1532delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100947 | |||||||
| chr9:100100955 | T | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1539T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100955 | |||||||
| chr9:100100957 | A | ATATATAT others(28): Show |
1 | a0001c0001t0004g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-25+1558_-25+1592d others(37): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100957 | ||||||
| chr9:100100964 | TAA | T | 69 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0004g0116 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.-25+1549_-25+1550d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100964 | |||||||
| chr9:100100965 | A | T | 16 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(13): Show |
16 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-25+1549A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100965 | |||||||
| chr9:100100967 | T | TATATGC | 9 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1555_-25+1556i others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100967 | ||||||
| chr9:100100968 | ATATAT | A | 3 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 |
3 | HG02622.hp1 HG03130.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-25+1558_-25+1562d others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100968 | ||||||
| chr9:100100970 | ATAT | A | 4 | a0001c0001t0001g0107 a0001c0002t0001g0108 a0001c0002t0001g0135 others(1): Show |
4 | HG02886.hp1 HG02886.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-25+1558_-25+1560d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100100970 | ||||||
| chr9:100100972 | A | G | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-25+1556A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100972 | |||||||
| chr9:100100974 | T | A | 9 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1558T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100974 | |||||||
| chr9:100100978 | T | C | 11 | a0001c0001t0004g0116 a0001c0002t0002g0102 a0001c0002t0002g0114 others(8): Show |
11 | HG00609.hp2 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.-25+1562T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100978 | |||||||
| chr9:100100984 | A | T | 9 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+1568A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100100984 | |||||||
| chr9:100101000 | A | ATAATGCA others(3): Show |
1 | a0001c0001t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-25+1584_-25+1585i others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101000 | |||||||
| chr9:100101000 | A | ATAATGCA others(5): Show |
8 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.-25+1584_-25+1585i others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101000 | |||||||
| chr9:100101010 | T | TTATATAT others(92): Show |
1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1599_-25+1600i others(101): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100101010 | ||||||
| chr9:100101073 | TACAC | T | 3 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 |
3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-25+1667_-25+1670d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100101073 | ||||||
| chr9:100101098 | C | T | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+1682C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101098 | |||||||
| chr9:100101133 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-25+1717A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101133 | |||||||
| chr9:100101475 | C | T | 9 | a0001c0001t0004g0055 a0001c0001t0007g0048 a0001c0001t0007g0050 others(6): Show |
9 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.-25+2059C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101475 | |||||||
| chr9:100101539 | C | A | 76 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(73): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.-25+2123C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101539 | |||||||
| chr9:100101546 | T | A | 5 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.-25+2130T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101546 | |||||||
| chr9:100101885 | T | C | 2 | a0001c0002t0002g0102 a0001c0002t0002g0114 |
2 | NA18964.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-25+2469T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101885 | |||||||
| chr9:100101908 | G | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-25+2492G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100101908 | |||||||
| chr9:100102053 | G | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-24-2445G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100102053 | |||||||
| chr9:100102131 | G | GT | 155 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(152): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.-24-2366dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chr9 | 100102131 | ||||||
| chr9:100102287 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-24-2211C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100102287 | |||||||
| chr9:100102576 | A | G | 1 | a0001c0001t0011g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-24-1922A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100102576 | |||||||
| chr9:100102772 | G | A | 3 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 |
3 | HG02280.hp1 HG02970.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.-24-1726G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100102772 | |||||||
| chr9:100103429 | C | G | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-24-1069C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 1/16 | chr9 | 100103429 | |||||||
| chr9:100104687 | G | T | 1 | a0001c0001t0017g0063 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.106+60G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100104687 | |||||||
| chr9:100104839 | T | A | 1 | a0001c0001t0007g0054 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.106+212T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100104839 | |||||||
| chr9:100105545 | G | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+918G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100105545 | |||||||
| chr9:100105850 | C | CT | 48 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0037 others(45): Show |
48 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(45): Show |
intron_variant | MODIFIER | c.106+1248dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100105850 | ||||||
| chr9:100105850 | C | CTT | 39 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0159 others(36): Show |
39 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.106+1247_106+1248d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100105850 | ||||||
| chr9:100105850 | CT | C | 5 | a0001c0001t0003g0085 a0001c0001t0004g0064 a0001c0001t0004g0067 others(2): Show |
5 | HG00323.hp1 NA18522.hp1 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.106+1248delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100105850 | ||||||
| chr9:100106193 | C | T | 72 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(69): Show |
72 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.106+1566C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106193 | |||||||
| chr9:100106357 | C | G | 9 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.106+1730C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106357 | |||||||
| chr9:100106389 | C | T | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.106+1762C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106389 | |||||||
| chr9:100106402 | C | A | 36 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0159 others(33): Show |
36 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(33): Show |
intron_variant | MODIFIER | c.106+1775C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106402 | |||||||
| chr9:100106487 | A | G | 34 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(31): Show |
34 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.106+1860A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106487 | |||||||
| chr9:100106809 | A | G | 1 | a0001c0002t0001g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.106+2182A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106809 | |||||||
| chr9:100106945 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+2318T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100106945 | |||||||
| chr9:100106949 | AAAG | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.106+2328_106+2330d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100106949 | ||||||
| chr9:100107047 | C | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.106+2420C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100107047 | |||||||
| chr9:100107246 | T | C | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.106+2619T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100107246 | |||||||
| chr9:100107564 | G | A | 77 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.106+2937G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100107564 | |||||||
| chr9:100108023 | C | A | 2 | a0001c0001t0004g0068 a0001c0001t0004g0069 |
2 | NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.106+3396C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100108023 | |||||||
| chr9:100108378 | C | A | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.106+3751C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100108378 | |||||||
| chr9:100108434 | T | C | 1 | a0001c0001t0011g0078 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.106+3807T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100108434 | |||||||
| chr9:100108556 | T | C | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.106+3929T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100108556 | |||||||
| chr9:100108619 | C | T | 1 | a0001c0002t0002g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.106+3992C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100108619 | |||||||
| chr9:100109246 | C | T | 1 | a0001c0001t0003g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.106+4619C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109246 | |||||||
| chr9:100109304 | A | G | 79 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(76): Show |
79 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(76): Show |
intron_variant | MODIFIER | c.106+4677A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109304 | |||||||
| chr9:100109553 | C | T | 78 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(75): Show |
78 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(75): Show |
intron_variant | MODIFIER | c.106+4926C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109553 | |||||||
| chr9:100109856 | G | A | 1 | a0001c0002t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.106+5229G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109856 | |||||||
| chr9:100109913 | C | T | 1 | a0001c0002t0001g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.106+5286C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109913 | |||||||
| chr9:100109959 | G | A | 77 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.106+5332G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100109959 | |||||||
| chr9:100110168 | C | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+5541C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100110168 | |||||||
| chr9:100110175 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.106+5548A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100110175 | |||||||
| chr9:100110441 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.106+5814T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100110441 | |||||||
| chr9:100110483 | G | A | 2 | a0001c0001t0003g0070 a0001c0001t0003g0083 |
2 | HG01074.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.106+5856G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100110483 | |||||||
| chr9:100110775 | T | A | 120 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+6148T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100110775 | |||||||
| chr9:100111027 | T | G | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.106+6400T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111027 | |||||||
| chr9:100111178 | A | G | 2 | a0001c0001t0001g0107 a0001c0002t0001g0112 |
2 | HG02886.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.106+6551A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111178 | |||||||
| chr9:100111302 | G | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+6675G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111302 | |||||||
| chr9:100111487 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+6860T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111487 | |||||||
| chr9:100111741 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+7114G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111741 | |||||||
| chr9:100111742 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+7115C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111742 | |||||||
| chr9:100111808 | G | C | 1 | a0001c0002t0001g0108 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.106+7181G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111808 | |||||||
| chr9:100111960 | T | C | 1 | a0006c0007t0009g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.106+7333T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100111960 | |||||||
| chr9:100111977 | A | ACTTT | 11 | a0001c0001t0004g0055 a0001c0001t0007g0048 a0001c0001t0007g0050 others(8): Show |
11 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.106+7371_106+7374d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100111977 | ||||||
| chr9:100112028 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+7401C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100112028 | |||||||
| chr9:100112171 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+7544T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100112171 | |||||||
| chr9:100112444 | T | A | 1 | a0001c0002t0016g0148 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.106+7817T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100112444 | |||||||
| chr9:100112665 | T | TA | 7 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(4): Show |
7 | HG00621.hp2 HG01081.hp2 HG03209.hp2 others(4): Show |
intron_variant | MODIFIER | c.106+8052dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100112665 | ||||||
| chr9:100112945 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+8318T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100112945 | |||||||
| chr9:100112961 | C | A | 1 | a0001c0001t0007g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.106+8334C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100112961 | |||||||
| chr9:100113261 | GTTA | G | 77 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.106+8639_106+8641d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100113261 | ||||||
| chr9:100113461 | A | G | 1 | a0001c0001t0003g0092 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.106+8834A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100113461 | |||||||
| chr9:100113542 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+8915A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100113542 | |||||||
| chr9:100113558 | TTTTG | T | 17 | a0001c0001t0001g0147 a0001c0001t0003g0090 a0001c0001t0003g0091 others(14): Show |
17 | HG00140.hp2 HG00733.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.106+8963_106+8966d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100113558 | ||||||
| chr9:100113826 | T | C | 1 | a0001c0002t0001g0128 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.106+9199T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100113826 | |||||||
| chr9:100113899 | T | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+9272T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100113899 | |||||||
| chr9:100114026 | A | C | 25 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0001t0008g0159 others(22): Show |
25 | HG00609.hp2 HG00621.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.106+9399A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114026 | |||||||
| chr9:100114114 | A | G | 1 | a0001c0001t0011g0078 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.106+9487A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114114 | |||||||
| chr9:100114143 | G | A | 1 | a0001c0002t0002g0150 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.106+9516G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114143 | |||||||
| chr9:100114204 | A | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+9577A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114204 | |||||||
| chr9:100114391 | CT | C | 63 | a0001c0001t0001g0020 a0001c0001t0001g0034 a0001c0001t0001g0107 others(60): Show |
63 | HG00140.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.106+9792delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100114391 | ||||||
| chr9:100114391 | CTT | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0021 others(95): Show |
98 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.106+9791_106+9792d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100114391 | ||||||
| chr9:100114391 | CTTT | C | 7 | a0001c0001t0001g0032 a0001c0001t0022g0182 a0001c0002t0002g0149 others(4): Show |
7 | HG01074.hp2 HG01081.hp2 HG01109.hp1 others(4): Show |
intron_variant | MODIFIER | c.106+9790_106+9792d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100114391 | ||||||
| chr9:100114537 | G | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+9910G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114537 | |||||||
| chr9:100114686 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+10059G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114686 | |||||||
| chr9:100114839 | G | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.106+10212G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114839 | |||||||
| chr9:100114955 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.106+10328G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100114955 | |||||||
| chr9:100115267 | G | A | 1 | a0001c0002t0001g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.106+10640G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115267 | |||||||
| chr9:100115300 | TTA | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.106+10685_106+1068 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100115300 | ||||||
| chr9:100115351 | A | G | 77 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.106+10724A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115351 | |||||||
| chr9:100115353 | G | A | 2 | a0001c0001t0003g0090 a0001c0001t0003g0091 |
2 | HG01243.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.106+10726G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115353 | |||||||
| chr9:100115453 | C | T | 1 | a0001c0002t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.106+10826C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115453 | |||||||
| chr9:100115605 | C | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.107-10778C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115605 | |||||||
| chr9:100115789 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-10594A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115789 | |||||||
| chr9:100115792 | A | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-10591A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115792 | |||||||
| chr9:100115806 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-10577C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115806 | |||||||
| chr9:100115858 | C | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-10525C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115858 | |||||||
| chr9:100115869 | A | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-10514A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100115869 | |||||||
| chr9:100116001 | G | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.107-10382G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116001 | |||||||
| chr9:100116094 | CTTTCTTT others(2): Show |
C | 2 | a0001c0001t0004g0053 a0001c0001t0004g0059 |
2 | HG02080.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.107-10276_107-1026 others(13): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100116094 | ||||||
| chr9:100116107 | CT | C | 117 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(114): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.107-10262delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100116107 | ||||||
| chr9:100116190 | G | A | 9 | a0001c0001t0004g0055 a0001c0001t0007g0048 a0001c0001t0007g0050 others(6): Show |
9 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.107-10193G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116190 | |||||||
| chr9:100116239 | G | C | 1 | a0001c0001t0004g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.107-10144G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116239 | |||||||
| chr9:100116327 | T | G | 3 | a0001c0002t0001g0142 a0001c0002t0001g0167 a0001c0002t0001g0180 |
3 | HG01071.hp1 HG02559.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.107-10056T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116327 | |||||||
| chr9:100116368 | C | A | 1 | a0001c0002t0001g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.107-10015C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116368 | |||||||
| chr9:100116460 | G | C | 75 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(72): Show |
75 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.107-9923G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116460 | |||||||
| chr9:100116477 | C | G | 1 | a0001c0002t0001g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.107-9906C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116477 | |||||||
| chr9:100116540 | T | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.107-9843T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100116540 | |||||||
| chr9:100117054 | A | G | 120 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-9329A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117054 | |||||||
| chr9:100117097 | G | A | 119 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(116): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.107-9286G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117097 | |||||||
| chr9:100117232 | G | A | 1 | a0001c0001t0001g0040 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.107-9151G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117232 | |||||||
| chr9:100117334 | G | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-9049G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117334 | |||||||
| chr9:100117477 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.107-8906C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117477 | |||||||
| chr9:100117522 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-8861A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117522 | |||||||
| chr9:100117564 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.107-8819C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100117564 | |||||||
| chr9:100117609 | G | GC | 45 | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0033 others(42): Show |
45 | HG00140.hp2 HG00544.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.107-8766dupC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100117609 | ||||||
| chr9:100118302 | G | A | 3 | a0001c0002t0001g0104 a0001c0002t0001g0106 a0001c0002t0001g0108 |
3 | HG02622.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.107-8081G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100118302 | |||||||
| chr9:100118661 | G | T | 1 | a0005c0011t0002g0103 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.107-7722G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100118661 | |||||||
| chr9:100119173 | T | A | 77 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.107-7210T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100119173 | |||||||
| chr9:100119189 | C | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-7194C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100119189 | |||||||
| chr9:100119435 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-6948T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100119435 | |||||||
| chr9:100119495 | C | G | 76 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(73): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.107-6888C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100119495 | |||||||
| chr9:100120260 | A | T | 1 | a0001c0001t0014g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.107-6123A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100120260 | |||||||
| chr9:100120263 | C | A | 1 | a0001c0001t0014g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.107-6120C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100120263 | |||||||
| chr9:100120458 | C | G | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.107-5925C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100120458 | |||||||
| chr9:100121051 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.107-5332A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100121051 | |||||||
| chr9:100121709 | T | TC | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.107-4673dupC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100121709 | ||||||
| chr9:100121894 | C | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.107-4489C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100121894 | |||||||
| chr9:100122133 | T | C | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.107-4250T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100122133 | |||||||
| chr9:100122168 | T | C | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.107-4215T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100122168 | |||||||
| chr9:100122576 | C | CT | 72 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(69): Show |
72 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.107-3782dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100122576 | ||||||
| chr9:100122576 | C | CTT | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.107-3783_107-3782d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100122576 | ||||||
| chr9:100122576 | C | CTTT | 10 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0035 others(7): Show |
10 | HG02055.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.107-3784_107-3782d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100122576 | ||||||
| chr9:100122657 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.107-3726T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100122657 | |||||||
| chr9:100122864 | G | A | 152 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(149): Show |
152 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(149): Show |
intron_variant | MODIFIER | c.107-3519G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100122864 | |||||||
| chr9:100122880 | A | G | 117 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(114): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.107-3503A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100122880 | |||||||
| chr9:100123149 | T | C | 1 | a0001c0002t0001g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.107-3234T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100123149 | |||||||
| chr9:100123449 | T | C | 1 | a0001c0001t0003g0086 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.107-2934T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100123449 | |||||||
| chr9:100123629 | G | A | 76 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0001g0147 others(73): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.107-2754G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100123629 | |||||||
| chr9:100123997 | C | G | 34 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(31): Show |
34 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.107-2386C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100123997 | |||||||
| chr9:100124177 | A | AGT | 37 | a0001c0001t0001g0040 a0001c0001t0003g0085 a0001c0001t0003g0177 others(34): Show |
37 | HG00280.hp2 HG00735.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.107-2169_107-2168d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | ||||||
| chr9:100124177 | A | AGTGT | 20 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(17): Show |
20 | HG00140.hp1 HG00323.hp1 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.107-2171_107-2168d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | ||||||
| chr9:100124177 | A | AGTGTGT | 5 | a0001c0001t0001g0015 a0001c0001t0003g0089 a0001c0001t0004g0047 others(2): Show |
5 | HG01346.hp2 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.107-2173_107-2168d others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | ||||||
| chr9:100124177 | A | AGTGTGTG others(1): Show |
3 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0001c0002t0001g0019 |
3 | HG01243.hp1 HG02630.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.107-2175_107-2168d others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | ||||||
| chr9:100124177 | AGT | A | 50 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0004g0065 others(47): Show |
50 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.107-2169_107-2168d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | ||||||
| chr9:100124177 | AGTGT | A | 34 | a0001c0001t0001g0034 a0001c0001t0001g0035 a0001c0001t0003g0070 others(31): Show |
34 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(31): Show |
intron_variant | MODIFIER | c.107-2171_107-2168d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | ||||||
| chr9:100124177 | AGTGTGTG others(3): Show |
A | 2 | a0001c0004t0001g0109 a0001c0004t0001g0110 |
2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.107-2177_107-2168d others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124177 | ||||||
| chr9:100124312 | C | G | 2 | a0001c0002t0016g0148 a0001c0002t0016g0151 |
2 | HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.107-2071C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100124312 | |||||||
| chr9:100124526 | C | A | 1 | a0001c0002t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.107-1857C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100124526 | |||||||
| chr9:100124546 | T | TA | 19 | a0001c0001t0003g0042 a0001c0001t0003g0085 a0001c0001t0003g0086 others(16): Show |
19 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(16): Show |
intron_variant | MODIFIER | c.107-1821dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124546 | ||||||
| chr9:100124546 | T | TAA | 41 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(38): Show |
41 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.107-1822_107-1821d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100124546 | ||||||
| chr9:100124654 | T | A | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.107-1729T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100124654 | |||||||
| chr9:100124666 | G | A | 117 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(114): Show |
117 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.107-1717G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100124666 | |||||||
| chr9:100125018 | G | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.107-1365G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100125018 | |||||||
| chr9:100125147 | G | T | 2 | a0001c0002t0002g0161 a0001c0002t0002g0162 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.107-1236G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100125147 | |||||||
| chr9:100125309 | T | C | 1 | a0001c0002t0001g0170 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.107-1074T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100125309 | |||||||
| chr9:100125321 | G | A | 1 | a0001c0002t0002g0118 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.107-1062G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100125321 | |||||||
| chr9:100125681 | AT | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0021 others(101): Show |
104 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.107-681delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chr9 | 100125681 | ||||||
| chr9:100125742 | A | G | 1 | a0001c0002t0002g0160 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.107-641A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100125742 | |||||||
| chr9:100126039 | T | C | 73 | a0001c0001t0001g0107 a0001c0001t0004g0116 a0001c0001t0008g0123 others(70): Show |
73 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.107-344T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100126039 | |||||||
| chr9:100126156 | C | G | 1 | a0001c0002t0001g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.107-227C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 2/16 | chr9 | 100126156 | |||||||
| chr9:100126595 | C | T | 1 | a0001c0001t0011g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+46C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100126595 | |||||||
| chr9:100127087 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+538T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100127087 | |||||||
| chr9:100127577 | G | A | 1 | a0001c0002t0002g0173 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.273+1028G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100127577 | |||||||
| chr9:100127696 | T | C | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.273+1147T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100127696 | |||||||
| chr9:100127775 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+1226G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100127775 | |||||||
| chr9:100127797 | T | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+1248T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100127797 | |||||||
| chr9:100128432 | C | A | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.273+1883C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100128432 | |||||||
| chr9:100128729 | G | T | 1 | a0001c0002t0008g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.273+2180G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100128729 | |||||||
| chr9:100128854 | A | G | 4 | a0001c0001t0001g0107 a0001c0002t0001g0112 a0001c0004t0001g0109 others(1): Show |
4 | HG02886.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+2305A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100128854 | |||||||
| chr9:100129124 | A | C | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.273+2575A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100129124 | |||||||
| chr9:100129239 | T | C | 1 | a0001c0002t0001g0105 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.273+2690T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100129239 | |||||||
| chr9:100129551 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+3002A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100129551 | |||||||
| chr9:100129659 | A | G | 1 | a0001c0001t0004g0064 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.273+3110A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100129659 | |||||||
| chr9:100130278 | G | A | 1 | a0001c0001t0004g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.273+3729G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130278 | |||||||
| chr9:100130320 | A | G | 1 | a0001c0001t0017g0063 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.273+3771A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130320 | |||||||
| chr9:100130460 | C | T | 118 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+3911C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130460 | |||||||
| chr9:100130574 | C | G | 3 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 |
3 | HG01081.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+4025C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130574 | |||||||
| chr9:100130593 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+4044A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130593 | |||||||
| chr9:100130595 | T | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+4046T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130595 | |||||||
| chr9:100130647 | C | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+4098C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130647 | |||||||
| chr9:100130709 | T | C | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+4160T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100130709 | |||||||
| chr9:100131433 | A | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+4884A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131433 | |||||||
| chr9:100131473 | C | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+4924C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131473 | |||||||
| chr9:100131674 | G | A | 1 | a0001c0001t0022g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.273+5125G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131674 | |||||||
| chr9:100131763 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+5214A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131763 | |||||||
| chr9:100131964 | T | C | 1 | a0001c0001t0008g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.273+5415T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131964 | |||||||
| chr9:100131973 | C | T | 70 | a0001c0001t0001g0107 a0001c0001t0008g0123 a0001c0001t0008g0124 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.273+5424C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100131973 | |||||||
| chr9:100132117 | G | A | 1 | a0001c0002t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.273+5568G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100132117 | |||||||
| chr9:100132226 | CATGA | C | 95 | a0001c0001t0001g0107 a0001c0001t0003g0086 a0001c0001t0003g0089 others(92): Show |
95 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(92): Show |
intron_variant | MODIFIER | c.273+5712_273+5715d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100132226 | ||||||
| chr9:100132226 | CATGAATG others(1): Show |
C | 57 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(54): Show |
57 | HG00140.hp1 HG00323.hp1 HG00642.hp2 others(54): Show |
intron_variant | MODIFIER | c.273+5708_273+5715d others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100132226 | ||||||
| chr9:100132226 | CATGAATG others(5): Show |
C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+5704_273+5715d others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100132226 | ||||||
| chr9:100132403 | G | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+5854G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100132403 | |||||||
| chr9:100132436 | T | C | 118 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+5887T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100132436 | |||||||
| chr9:100132777 | A | AT | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+6240dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100132777 | ||||||
| chr9:100132777 | AT | A | 72 | a0001c0001t0001g0107 a0001c0001t0008g0123 a0001c0001t0008g0124 others(69): Show |
72 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(69): Show |
intron_variant | MODIFIER | c.273+6240delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100132777 | ||||||
| chr9:100132964 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+6415G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100132964 | |||||||
| chr9:100132975 | C | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+6426C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100132975 | |||||||
| chr9:100133008 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+6459G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100133008 | |||||||
| chr9:100133065 | A | G | 1 | a0001c0002t0002g0173 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.273+6516A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100133065 | |||||||
| chr9:100133338 | A | ATG | 13 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(10): Show |
13 | HG00140.hp1 HG01071.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.273+6813_273+6814d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133338 | ||||||
| chr9:100133338 | A | ATGTG | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+6811_273+6814d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133338 | ||||||
| chr9:100133338 | ATG | A | 6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0009g0100 others(3): Show |
6 | HG01081.hp1 HG01081.hp2 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+6813_273+6814d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133338 | ||||||
| chr9:100133423 | T | C | 1 | a0001c0001t0008g0159 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.273+6874T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100133423 | |||||||
| chr9:100133477 | T | TGAAACTT others(307): Show |
1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+6938_273+6939i others(316): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133477 | ||||||
| chr9:100133764 | T | TAC | 17 | a0001c0001t0003g0045 a0001c0001t0003g0084 a0001c0001t0003g0086 others(14): Show |
17 | HG00140.hp1 HG00423.hp2 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.273+7255_273+7256d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACAC | 2 | a0001c0001t0007g0054 a0007c0006t0018g0099 |
2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.273+7253_273+7256d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACACAC | 6 | a0001c0001t0001g0146 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
6 | HG01081.hp1 HG02280.hp1 HG02602.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+7251_273+7256d others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACACACA others(1): Show |
5 | a0001c0001t0001g0147 a0001c0002t0001g0144 a0001c0002t0001g0163 others(2): Show |
5 | HG01243.hp2 HG01952.hp1 HG02155.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+7249_273+7256d others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACACACA others(3): Show |
3 | a0001c0002t0002g0160 a0001c0002t0016g0148 a0001c0004t0001g0110 |
3 | HG03540.hp1 HG03927.hp2 NA20805.hp2 |
intron_variant | MODIFIER | c.273+7247_273+7256d others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACACACA others(5): Show |
10 | a0001c0002t0001g0111 a0001c0002t0001g0143 a0001c0002t0001g0145 others(7): Show |
10 | HG00323.hp2 HG00609.hp2 HG00642.hp1 others(7): Show |
intron_variant | MODIFIER | c.273+7245_273+7256d others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACACACA others(7): Show |
14 | a0001c0002t0001g0105 a0001c0002t0001g0131 a0001c0002t0001g0132 others(11): Show |
14 | HG00735.hp2 HG01069.hp1 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.273+7243_273+7256d others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACACACA others(9): Show |
12 | a0001c0001t0008g0124 a0001c0002t0001g0104 a0001c0002t0001g0106 others(9): Show |
12 | HG00140.hp2 HG00621.hp2 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+7241_273+7256d others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACACACA others(11): Show |
12 | a0001c0001t0008g0123 a0001c0002t0001g0127 a0001c0002t0001g0128 others(9): Show |
12 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(9): Show |
intron_variant | MODIFIER | c.273+7239_273+7256d others(20): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACACACA others(13): Show |
10 | a0001c0001t0001g0107 a0001c0001t0008g0159 a0001c0002t0001g0112 others(7): Show |
10 | HG00733.hp2 HG01109.hp2 HG02056.hp2 others(7): Show |
intron_variant | MODIFIER | c.273+7237_273+7256d others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACACACA others(15): Show |
3 | a0001c0002t0001g0129 a0001c0002t0001g0174 a0001c0002t0001g0180 |
3 | HG02559.hp2 HG03239.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.273+7235_273+7256d others(24): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | T | TACACACA others(17): Show |
2 | a0001c0002t0001g0170 a0001c0002t0002g0173 |
2 | HG01975.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.273+7233_273+7256d others(26): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | TAC | T | 5 | a0001c0001t0003g0042 a0001c0001t0003g0085 a0001c0001t0009g0100 others(2): Show |
5 | HG01106.hp2 HG02055.hp2 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+7255_273+7256d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133764 | TACACACA others(3): Show |
T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.273+7247_273+7256d others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133764 | ||||||
| chr9:100133796 | CACACACA others(3): Show |
C | 3 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 |
3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+7255_273+7264d others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100133796 | ||||||
| chr9:100133806 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+7257T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100133806 | |||||||
| chr9:100133956 | A | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+7407A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100133956 | |||||||
| chr9:100134015 | T | C | 2 | a0001c0001t0022g0182 a0006c0007t0009g0181 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.273+7466T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134015 | |||||||
| chr9:100134126 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+7577G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134126 | |||||||
| chr9:100134182 | C | T | 2 | a0001c0002t0001g0003 a0001c0002t0001g0028 |
2 | HG03041.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.273+7633C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134182 | |||||||
| chr9:100134339 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+7790G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134339 | |||||||
| chr9:100134639 | T | TA | 18 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(15): Show |
18 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.273+8091dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100134639 | ||||||
| chr9:100134862 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+8313G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134862 | |||||||
| chr9:100134922 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+8373T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100134922 | |||||||
| chr9:100135072 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.273+8523C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100135072 | |||||||
| chr9:100135146 | T | C | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.273+8597T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100135146 | |||||||
| chr9:100135730 | C | T | 2 | a0001c0002t0002g0120 a0001c0002t0002g0121 |
2 | NA19082.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.273+9181C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100135730 | |||||||
| chr9:100135797 | T | C | 1 | a0001c0001t0003g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.273+9248T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100135797 | |||||||
| chr9:100135965 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.273+9416T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100135965 | |||||||
| chr9:100136443 | C | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+9894C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136443 | |||||||
| chr9:100136462 | C | T | 4 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+9913C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136462 | |||||||
| chr9:100136505 | A | G | 3 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 |
3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+9956A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136505 | |||||||
| chr9:100136600 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+10051G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136600 | |||||||
| chr9:100136717 | A | G | 1 | a0001c0002t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.273+10168A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136717 | |||||||
| chr9:100136725 | C | T | 1 | a0001c0002t0001g0028 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.273+10176C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136725 | |||||||
| chr9:100136789 | C | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+10240C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136789 | |||||||
| chr9:100136933 | G | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+10384G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100136933 | |||||||
| chr9:100137234 | T | G | 1 | a0001c0002t0002g0149 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.273+10685T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100137234 | |||||||
| chr9:100137357 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+10808A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100137357 | |||||||
| chr9:100137560 | C | CACTAGAT | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+11011_273+1101 others(11): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100137560 | |||||||
| chr9:100138212 | C | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+11663C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138212 | |||||||
| chr9:100138283 | A | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+11734A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138283 | |||||||
| chr9:100138384 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+11835T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138384 | |||||||
| chr9:100138401 | C | T | 11 | a0001c0002t0002g0102 a0001c0002t0002g0114 a0001c0002t0002g0115 others(8): Show |
11 | HG00609.hp2 HG01192.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.273+11852C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138401 | |||||||
| chr9:100138561 | G | A | 1 | a0001c0002t0002g0121 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.273+12012G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138561 | |||||||
| chr9:100138631 | AAG | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+12085_273+1208 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100138631 | ||||||
| chr9:100138700 | C | CT | 11 | a0001c0001t0005g0013 a0001c0001t0010g0136 a0001c0001t0010g0137 others(8): Show |
11 | HG00733.hp2 HG02083.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.273+12169dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100138700 | ||||||
| chr9:100138700 | C | CTT | 64 | a0001c0001t0001g0107 a0001c0001t0008g0123 a0001c0001t0008g0124 others(61): Show |
64 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(61): Show |
intron_variant | MODIFIER | c.273+12168_273+1216 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100138700 | ||||||
| chr9:100138809 | C | T | 2 | a0001c0001t0003g0084 a0001c0001t0004g0067 |
2 | HG02083.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.273+12260C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138809 | |||||||
| chr9:100138895 | T | TG | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+12349dupG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100138895 | ||||||
| chr9:100138996 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+12447G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100138996 | |||||||
| chr9:100139002 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+12453G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139002 | |||||||
| chr9:100139333 | C | A | 1 | a0001c0002t0001g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.273+12784C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139333 | |||||||
| chr9:100139423 | C | T | 6 | a0001c0001t0003g0086 a0001c0001t0003g0092 a0001c0001t0003g0176 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+12874C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139423 | |||||||
| chr9:100139458 | A | G | 1 | a0001c0002t0002g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.273+12909A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139458 | |||||||
| chr9:100139720 | G | A | 1 | a0001c0001t0004g0065 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.273+13171G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139720 | |||||||
| chr9:100139942 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+13393C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100139942 | |||||||
| chr9:100140198 | A | G | 1 | a0001c0001t0003g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.273+13649A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140198 | |||||||
| chr9:100140260 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+13711C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140260 | |||||||
| chr9:100140382 | C | T | 4 | a0001c0002t0002g0154 a0001c0002t0002g0156 a0001c0002t0002g0157 others(1): Show |
4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+13833C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140382 | |||||||
| chr9:100140517 | G | A | 1 | a0001c0002t0001g0142 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.273+13968G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140517 | |||||||
| chr9:100140650 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+14101A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140650 | |||||||
| chr9:100140673 | C | T | 2 | a0001c0001t0004g0053 a0001c0001t0004g0059 |
2 | HG02080.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.273+14124C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140673 | |||||||
| chr9:100140814 | G | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+14265G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100140814 | |||||||
| chr9:100141029 | T | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+14480T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100141029 | |||||||
| chr9:100141547 | C | T | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+14998C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100141547 | |||||||
| chr9:100141884 | G | A | 1 | a0001c0002t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.273+15335G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100141884 | |||||||
| chr9:100142582 | C | T | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.273+16033C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100142582 | |||||||
| chr9:100142709 | T | C | 70 | a0001c0001t0001g0107 a0001c0001t0004g0116 a0001c0001t0008g0123 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.273+16160T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100142709 | |||||||
| chr9:100142956 | A | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+16407A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100142956 | |||||||
| chr9:100143045 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.273+16496G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143045 | |||||||
| chr9:100143127 | G | A | 1 | a0001c0001t0003g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.273+16578G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143127 | |||||||
| chr9:100143166 | C | G | 118 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+16617C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143166 | |||||||
| chr9:100143291 | C | T | 1 | a0001c0001t0008g0159 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.273+16742C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143291 | |||||||
| chr9:100143334 | A | G | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+16785A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143334 | |||||||
| chr9:100143612 | G | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+17063G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143612 | |||||||
| chr9:100143757 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.273+17208G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143757 | |||||||
| chr9:100143827 | T | C | 1 | a0001c0002t0002g0149 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.273+17278T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143827 | |||||||
| chr9:100143853 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+17304C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143853 | |||||||
| chr9:100143911 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+17362C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143911 | |||||||
| chr9:100143971 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+17422G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100143971 | |||||||
| chr9:100144167 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+17618T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144167 | |||||||
| chr9:100144226 | G | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+17677G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144226 | |||||||
| chr9:100144310 | G | A | 1 | a0001c0002t0002g0155 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.273+17761G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144310 | |||||||
| chr9:100144345 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.273+17796C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144345 | |||||||
| chr9:100144824 | C | T | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+18275C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144824 | |||||||
| chr9:100144922 | G | T | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+18373G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144922 | |||||||
| chr9:100144927 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+18378A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100144927 | |||||||
| chr9:100145366 | C | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+18817C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145366 | |||||||
| chr9:100145367 | G | A | 33 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.273+18818G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145367 | |||||||
| chr9:100145385 | G | A | 2 | a0001c0001t0007g0029 a0001c0001t0023g0030 |
2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+18836G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145385 | |||||||
| chr9:100145429 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+18880G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145429 | |||||||
| chr9:100145690 | G | A | 1 | a0001c0001t0003g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.273+19141G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145690 | |||||||
| chr9:100145794 | G | T | 69 | a0001c0001t0001g0107 a0001c0001t0008g0123 a0001c0001t0008g0124 others(66): Show |
69 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(66): Show |
intron_variant | MODIFIER | c.273+19245G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145794 | |||||||
| chr9:100145823 | C | T | 1 | a0001c0001t0004g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.273+19274C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100145823 | |||||||
| chr9:100146017 | G | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+19468G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146017 | |||||||
| chr9:100146086 | T | TC | 11 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0001g0127 others(8): Show |
11 | HG00280.hp1 HG00741.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.273+19543dupC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100146086 | ||||||
| chr9:100146086 | TC | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+19543delC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100146086 | ||||||
| chr9:100146121 | C | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+19572C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146121 | |||||||
| chr9:100146232 | G | C | 6 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0051 others(3): Show |
6 | HG00280.hp2 HG02080.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+19683G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146232 | |||||||
| chr9:100146298 | T | TGGCG | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+19752_273+1975 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100146298 | ||||||
| chr9:100146439 | G | A | 71 | a0001c0001t0001g0107 a0001c0001t0008g0123 a0001c0001t0008g0124 others(68): Show |
71 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.273+19890G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146439 | |||||||
| chr9:100146750 | T | C | 9 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(6): Show |
9 | HG02109.hp1 HG02145.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+20201T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146750 | |||||||
| chr9:100146790 | A | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+20241A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146790 | |||||||
| chr9:100146921 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+20372G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100146921 | |||||||
| chr9:100146956 | CT | C | 29 | a0001c0001t0001g0107 a0001c0002t0001g0111 a0001c0002t0001g0112 others(26): Show |
29 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.273+20409delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100146956 | ||||||
| chr9:100147069 | T | G | 2 | a0001c0001t0022g0182 a0006c0007t0009g0181 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.273+20520T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100147069 | |||||||
| chr9:100147479 | T | C | 1 | a0001c0001t0008g0124 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.273+20930T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100147479 | |||||||
| chr9:100147491 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+20942G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100147491 | |||||||
| chr9:100147662 | G | A | 1 | a0001c0001t0001g0036 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.273+21113G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100147662 | |||||||
| chr9:100147949 | C | T | 1 | a0001c0002t0002g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.273+21400C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100147949 | |||||||
| chr9:100148020 | C | CA | 16 | a0001c0001t0001g0107 a0001c0001t0004g0047 a0001c0001t0004g0068 others(13): Show |
16 | HG00735.hp1 HG01175.hp1 HG02280.hp1 others(13): Show |
intron_variant | MODIFIER | c.273+21492dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100148020 | ||||||
| chr9:100148020 | CAAAAAA | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+21487_273+2149 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100148020 | ||||||
| chr9:100148382 | G | A | 1 | a0001c0001t0003g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.273+21833G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100148382 | |||||||
| chr9:100148611 | G | A | 2 | a0001c0002t0002g0152 a0001c0002t0002g0153 |
2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.273+22062G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100148611 | |||||||
| chr9:100148820 | A | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+22271A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100148820 | |||||||
| chr9:100148941 | T | C | 4 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+22392T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100148941 | |||||||
| chr9:100149043 | C | T | 120 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.273+22494C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100149043 | |||||||
| chr9:100149049 | CA | C | 70 | a0001c0001t0001g0107 a0001c0001t0008g0123 a0001c0001t0008g0124 others(67): Show |
70 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(67): Show |
intron_variant | MODIFIER | c.273+22514delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100149049 | ||||||
| chr9:100149306 | GC | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+22760delC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100149306 | ||||||
| chr9:100149385 | G | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+22836G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100149385 | |||||||
| chr9:100149402 | C | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+22853C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100149402 | |||||||
| chr9:100149424 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+22875T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100149424 | |||||||
| chr9:100150194 | C | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+23645C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150194 | |||||||
| chr9:100150248 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+23699T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150248 | |||||||
| chr9:100150438 | G | A | 80 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(77): Show |
80 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(77): Show |
intron_variant | MODIFIER | c.273+23889G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150438 | |||||||
| chr9:100150476 | G | T | 1 | a0001c0001t0013g0026 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.273+23927G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150476 | |||||||
| chr9:100150775 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+24226G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150775 | |||||||
| chr9:100150978 | A | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+24429A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100150978 | |||||||
| chr9:100151117 | C | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+24568C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151117 | |||||||
| chr9:100151132 | A | T | 1 | a0001c0002t0002g0175 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.273+24583A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151132 | |||||||
| chr9:100151154 | T | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+24605T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151154 | |||||||
| chr9:100151532 | C | T | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.273+24983C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151532 | |||||||
| chr9:100151644 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25095A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151644 | |||||||
| chr9:100151664 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25115T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151664 | |||||||
| chr9:100151869 | A | T | 1 | a0001c0001t0003g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.273+25320A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151869 | |||||||
| chr9:100151987 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25438G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100151987 | |||||||
| chr9:100152035 | A | C | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+25486A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152035 | |||||||
| chr9:100152079 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25530T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152079 | |||||||
| chr9:100152132 | T | C | 1 | a0001c0002t0001g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.273+25583T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152132 | |||||||
| chr9:100152168 | C | T | 1 | a0001c0001t0004g0072 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.273+25619C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152168 | |||||||
| chr9:100152214 | T | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25665T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152214 | |||||||
| chr9:100152226 | C | CTTTT | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25679_273+2568 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100152226 | ||||||
| chr9:100152387 | A | T | 4 | a0001c0001t0012g0074 a0001c0001t0012g0079 a0001c0001t0012g0080 others(1): Show |
4 | HG00423.hp2 HG00621.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+25838A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152387 | |||||||
| chr9:100152409 | A | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+25860A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152409 | |||||||
| chr9:100152739 | T | A | 2 | a0001c0001t0003g0176 a0001c0001t0003g0179 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.273+26190T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152739 | |||||||
| chr9:100152774 | C | T | 2 | a0001c0001t0013g0025 a0001c0001t0013g0026 |
2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.273+26225C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152774 | |||||||
| chr9:100152885 | T | C | 2 | a0001c0001t0022g0182 a0006c0007t0009g0181 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.273+26336T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100152885 | |||||||
| chr9:100153005 | T | TTG | 6 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(3): Show |
6 | HG01081.hp2 HG03209.hp2 HG03225.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+26482_273+2648 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | ||||||
| chr9:100153005 | T | TTGTG | 8 | a0001c0002t0001g0003 a0001c0002t0001g0014 a0001c0002t0001g0016 others(5): Show |
8 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.273+26480_273+2648 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | ||||||
| chr9:100153005 | T | TTGTGTG | 20 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(17): Show |
20 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(17): Show |
intron_variant | MODIFIER | c.273+26478_273+2648 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | ||||||
| chr9:100153005 | T | TTGTGTGT others(1): Show |
7 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(4): Show |
7 | HG01109.hp1 HG02559.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+26476_273+2648 others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | ||||||
| chr9:100153005 | T | TTGTGTGT others(3): Show |
2 | a0001c0001t0001g0033 a0001c0001t0001g0034 |
2 | HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.273+26474_273+2648 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | ||||||
| chr9:100153005 | TTG | T | 36 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(33): Show |
36 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.273+26482_273+2648 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153005 | ||||||
| chr9:100153013 | G | GTGTA | 3 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 |
3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+26467_273+2646 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153013 | ||||||
| chr9:100153044 | C | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+26495C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100153044 | |||||||
| chr9:100153141 | G | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+26592G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100153141 | |||||||
| chr9:100153263 | TA | T | 76 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0008g0123 others(73): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.273+26727delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100153263 | ||||||
| chr9:100153718 | G | A | 1 | a0001c0001t0011g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.273+27169G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100153718 | |||||||
| chr9:100153897 | G | C | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+27348G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100153897 | |||||||
| chr9:100154088 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+27539C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100154088 | |||||||
| chr9:100154256 | TTGGGCTT others(33): Show |
T | 1 | a0002c0003t0006g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273+27712_273+2775 others(44): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154256 | ||||||
| chr9:100154331 | A | AT | 42 | a0001c0001t0001g0107 a0001c0001t0003g0086 a0001c0001t0004g0047 others(39): Show |
42 | HG00280.hp1 HG00423.hp2 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.273+27810dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATT | 9 | a0001c0002t0001g0112 a0001c0002t0001g0127 a0001c0002t0001g0133 others(6): Show |
9 | HG00423.hp1 HG00741.hp1 HG01109.hp2 others(6): Show |
intron_variant | MODIFIER | c.273+27809_273+2781 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTT | 6 | a0001c0001t0001g0032 a0001c0001t0001g0035 a0001c0001t0001g0036 others(3): Show |
6 | HG01109.hp1 HG02559.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+27808_273+2781 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTT | 6 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0040 others(3): Show |
6 | HG01081.hp2 HG02055.hp1 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+27807_273+2781 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTTTTT others(4): Show |
3 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0021 |
3 | HG02486.hp1 HG02809.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.273+27800_273+2781 others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTTTTT others(6): Show |
1 | a0001c0002t0001g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.273+27798_273+2781 others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTTTTT others(7): Show |
2 | a0001c0002t0001g0017 a0001c0002t0001g0018 |
2 | HG02109.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.273+27797_273+2781 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTTTTT others(8): Show |
5 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(2): Show |
5 | HG02451.hp2 HG02897.hp1 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+27796_273+2781 others(19): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTTTTT others(9): Show |
4 | a0001c0001t0001g0004 a0001c0001t0005g0009 a0001c0001t0013g0025 others(1): Show |
4 | HG01168.hp1 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+27795_273+2781 others(20): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTTTTT others(10): Show |
7 | a0001c0001t0005g0013 a0001c0001t0011g0022 a0001c0001t0013g0026 others(4): Show |
7 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(4): Show |
intron_variant | MODIFIER | c.273+27794_273+2781 others(21): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTTTTT others(11): Show |
1 | a0001c0001t0005g0010 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.273+27793_273+2781 others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTTTTT others(13): Show |
1 | a0001c0002t0001g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.273+27791_273+2781 others(24): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTTTTT others(15): Show |
2 | a0001c0001t0007g0029 a0001c0001t0023g0030 |
2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.273+27789_273+2781 others(26): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | A | ATTTTTTT others(17): Show |
1 | a0001c0001t0024g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.273+27787_273+2781 others(28): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154331 | ATTTTTTT others(3): Show |
A | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+27801_273+2781 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154331 | ||||||
| chr9:100154978 | C | CA | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+28431dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100154978 | ||||||
| chr9:100155135 | C | T | 4 | a0001c0001t0011g0076 a0001c0001t0011g0078 a0001c0001t0011g0081 others(1): Show |
4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+28586C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155135 | |||||||
| chr9:100155162 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+28613G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155162 | |||||||
| chr9:100155254 | A | C | 178 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(175): Show |
178 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(175): Show |
intron_variant | MODIFIER | c.273+28705A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155254 | |||||||
| chr9:100155368 | G | A | 5 | a0001c0002t0002g0041 a0001c0002t0002g0140 a0001c0002t0002g0141 others(2): Show |
5 | HG00140.hp2 HG00323.hp2 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+28819G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155368 | |||||||
| chr9:100155404 | T | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+28855T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155404 | |||||||
| chr9:100155813 | G | A | 1 | a0001c0002t0016g0151 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.273+29264G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100155813 | |||||||
| chr9:100156024 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+29475T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100156024 | |||||||
| chr9:100156257 | C | CT | 12 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0164 others(9): Show |
12 | HG00323.hp1 HG00733.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+29729dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156257 | ||||||
| chr9:100156257 | C | CTT | 34 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(31): Show |
34 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.273+29728_273+2972 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156257 | ||||||
| chr9:100156499 | A | G | 119 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(116): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.273+29950A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100156499 | |||||||
| chr9:100156574 | T | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+30025T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100156574 | |||||||
| chr9:100156723 | T | C | 2 | a0001c0001t0007g0060 a0001c0002t0001g0057 |
2 | HG02647.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.273+30174T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100156723 | |||||||
| chr9:100156823 | TA | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+30280delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156823 | ||||||
| chr9:100156931 | C | CAT | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+30394_273+3039 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156931 | ||||||
| chr9:100156941 | T | TAC | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+30393_273+3039 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156941 | ||||||
| chr9:100156943 | T | C | 6 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(3): Show |
6 | HG00733.hp2 HG01081.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+30394T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100156943 | |||||||
| chr9:100156943 | T | TAC | 71 | a0001c0001t0001g0107 a0001c0001t0004g0116 a0001c0001t0008g0123 others(68): Show |
71 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(68): Show |
intron_variant | MODIFIER | c.273+30406_273+3040 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156943 | ||||||
| chr9:100156943 | T | TACAC | 37 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(34): Show |
37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.273+30404_273+3040 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156943 | ||||||
| chr9:100156971 | TATTC | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+30429_273+3043 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100156971 | ||||||
| chr9:100157156 | A | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+30607A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157156 | |||||||
| chr9:100157251 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+30702A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157251 | |||||||
| chr9:100157267 | C | CTTTTTTT others(3): Show |
34 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(31): Show |
34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.273+30724_273+3073 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100157267 | ||||||
| chr9:100157267 | C | CTTTTTTT others(4): Show |
6 | a0001c0001t0001g0032 a0001c0001t0001g0034 a0001c0001t0023g0030 others(3): Show |
6 | HG01109.hp1 HG02055.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+30723_273+3073 others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100157267 | ||||||
| chr9:100157267 | C | CTTTTTTT others(5): Show |
2 | a0001c0001t0007g0029 a0001c0001t0024g0031 |
2 | HG02145.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.273+30722_273+3073 others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100157267 | ||||||
| chr9:100157273 | T | C | 38 | a0001c0001t0004g0116 a0001c0001t0008g0123 a0001c0001t0008g0124 others(35): Show |
38 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+30724T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157273 | |||||||
| chr9:100157380 | T | G | 2 | a0001c0002t0001g0169 a0001c0002t0001g0171 |
2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.273+30831T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157380 | |||||||
| chr9:100157410 | G | A | 6 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0051 others(3): Show |
6 | HG00280.hp2 HG02080.hp2 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+30861G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157410 | |||||||
| chr9:100157509 | G | A | 1 | a0002c0003t0021g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.273+30960G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157509 | |||||||
| chr9:100157561 | G | A | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+31012G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157561 | |||||||
| chr9:100157779 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+31230T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100157779 | |||||||
| chr9:100158072 | T | G | 2 | a0001c0001t0013g0025 a0001c0001t0013g0026 |
2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.273+31523T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158072 | |||||||
| chr9:100158091 | T | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+31542T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158091 | |||||||
| chr9:100158226 | T | C | 1 | a0001c0002t0002g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.273+31677T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158226 | |||||||
| chr9:100158314 | G | GA | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+31772dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100158314 | ||||||
| chr9:100158524 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+31975A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158524 | |||||||
| chr9:100158754 | C | T | 118 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+32205C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158754 | |||||||
| chr9:100158758 | G | A | 1 | a0002c0003t0006g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273+32209G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158758 | |||||||
| chr9:100158874 | A | G | 1 | a0005c0011t0002g0103 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.273+32325A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158874 | |||||||
| chr9:100158964 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+32415A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100158964 | |||||||
| chr9:100159005 | G | T | 1 | a0001c0002t0002g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.273+32456G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100159005 | |||||||
| chr9:100159108 | C | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+32559C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100159108 | |||||||
| chr9:100160025 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+33476T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160025 | |||||||
| chr9:100160069 | T | C | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+33520T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160069 | |||||||
| chr9:100160182 | C | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+33633C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160182 | |||||||
| chr9:100160505 | G | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+33956G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160505 | |||||||
| chr9:100160574 | G | A | 4 | a0001c0002t0002g0154 a0001c0002t0002g0156 a0001c0002t0002g0157 others(1): Show |
4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+34025G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160574 | |||||||
| chr9:100160689 | TC | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+34144delC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100160689 | ||||||
| chr9:100160702 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+34153G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160702 | |||||||
| chr9:100160836 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+34287C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160836 | |||||||
| chr9:100160880 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+34331G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160880 | |||||||
| chr9:100160939 | A | C | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+34390A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160939 | |||||||
| chr9:100160940 | G | C | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+34391G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160940 | |||||||
| chr9:100160943 | A | G | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+34394A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160943 | |||||||
| chr9:100160944 | GACTC | G | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+34396_273+3439 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100160944 | |||||||
| chr9:100160954 | C | CA | 6 | a0001c0001t0004g0047 a0001c0001t0004g0065 a0001c0001t0009g0058 others(3): Show |
6 | HG01175.hp1 HG02055.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.273+34427dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100160954 | ||||||
| chr9:100160954 | CA | C | 68 | a0001c0001t0001g0107 a0001c0001t0001g0146 a0001c0001t0003g0089 others(65): Show |
68 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(65): Show |
intron_variant | MODIFIER | c.273+34427delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100160954 | ||||||
| chr9:100160954 | CAAA | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+34425_273+3442 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100160954 | ||||||
| chr9:100161069 | G | C | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+34520G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161069 | |||||||
| chr9:100161141 | C | T | 33 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(30): Show |
33 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.273+34592C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161141 | |||||||
| chr9:100161204 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.273+34655T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161204 | |||||||
| chr9:100161326 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+34777T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161326 | |||||||
| chr9:100161364 | C | CA | 31 | a0001c0001t0001g0107 a0001c0001t0003g0042 a0001c0001t0003g0070 others(28): Show |
31 | HG00423.hp1 HG00423.hp2 HG00621.hp1 others(28): Show |
intron_variant | MODIFIER | c.273+34843dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161364 | ||||||
| chr9:100161364 | C | CAAAAAAA others(6): Show |
1 | a0001c0001t0022g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.273+34823_273+3482 others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161364 | ||||||
| chr9:100161364 | C | CAAAAAAA others(7): Show |
1 | a0006c0007t0009g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.273+34823_273+3482 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161364 | ||||||
| chr9:100161364 | CA | C | 12 | a0001c0001t0001g0146 a0001c0001t0003g0176 a0001c0001t0004g0055 others(9): Show |
12 | HG01081.hp1 HG01167.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.273+34843delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161364 | ||||||
| chr9:100161366 | A | AAACAAAA others(7): Show |
1 | a0001c0001t0023g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.273+34819_273+3482 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161366 | ||||||
| chr9:100161373 | A | C | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+34824A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161373 | |||||||
| chr9:100161376 | A | AAAACAAA others(8): Show |
1 | a0001c0002t0001g0028 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.273+34830_273+3483 others(19): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161376 | ||||||
| chr9:100161377 | A | AAACAAAA others(7): Show |
36 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(33): Show |
36 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(33): Show |
intron_variant | MODIFIER | c.273+34830_273+3483 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161377 | ||||||
| chr9:100161377 | A | AAACAAAA others(6): Show |
1 | a0001c0001t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.273+34830_273+3483 others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161377 | ||||||
| chr9:100161377 | A | C | 1 | a0001c0001t0023g0030 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.273+34828A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161377 | |||||||
| chr9:100161380 | A | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+34831A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161380 | |||||||
| chr9:100161388 | A | AACAAAAA others(6): Show |
2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.273+34840_273+3484 others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161388 | ||||||
| chr9:100161388 | A | C | 40 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(37): Show |
40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.273+34839A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161388 | |||||||
| chr9:100161436 | T | G | 5 | a0001c0001t0004g0061 a0001c0001t0004g0062 a0001c0001t0004g0064 others(2): Show |
5 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+34887T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161436 | |||||||
| chr9:100161481 | G | A | 118 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+34932G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161481 | |||||||
| chr9:100161613 | A | AGATG | 2 | a0001c0004t0001g0110 a0007c0006t0018g0099 |
2 | HG03540.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.273+35094_273+3509 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100161613 | ||||||
| chr9:100161696 | T | C | 1 | a0001c0002t0002g0150 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.273+35147T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100161696 | |||||||
| chr9:100162081 | G | A | 2 | a0001c0001t0003g0070 a0001c0001t0003g0083 |
2 | HG01074.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.273+35532G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162081 | |||||||
| chr9:100162150 | G | T | 1 | a0001c0001t0007g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.273+35601G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162150 | |||||||
| chr9:100162418 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+35869C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162418 | |||||||
| chr9:100162583 | A | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+36034A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162583 | |||||||
| chr9:100162783 | T | C | 1 | a0001c0001t0015g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.273+36234T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162783 | |||||||
| chr9:100162826 | C | CA | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+36290dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100162826 | ||||||
| chr9:100162984 | G | A | 1 | a0002c0003t0006g0088 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.273+36435G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100162984 | |||||||
| chr9:100163003 | A | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+36454A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163003 | |||||||
| chr9:100163140 | G | T | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.273+36591G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163140 | |||||||
| chr9:100163186 | A | AT | 75 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0107 others(72): Show |
75 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(72): Show |
intron_variant | MODIFIER | c.273+36656dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100163186 | ||||||
| chr9:100163186 | A | ATT | 31 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(28): Show |
31 | HG00140.hp2 HG00323.hp1 HG00642.hp2 others(28): Show |
intron_variant | MODIFIER | c.273+36655_273+3665 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100163186 | ||||||
| chr9:100163186 | A | ATTT | 6 | a0001c0001t0005g0005 a0001c0001t0009g0100 a0001c0001t0009g0101 others(3): Show |
6 | HG01081.hp2 HG02451.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.273+36654_273+3665 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100163186 | ||||||
| chr9:100163322 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(37): Show |
40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.273+36773C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163322 | |||||||
| chr9:100163354 | A | C | 2 | a0001c0002t0002g0152 a0001c0002t0002g0153 |
2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.273+36805A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163354 | |||||||
| chr9:100163524 | T | A | 9 | a0001c0001t0003g0090 a0001c0001t0003g0091 a0002c0003t0006g0088 others(6): Show |
9 | HG00735.hp1 HG00738.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+36975T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163524 | |||||||
| chr9:100163554 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+37005G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163554 | |||||||
| chr9:100163822 | G | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+37273G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100163822 | |||||||
| chr9:100163929 | G | GCA | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.273+37383_273+3738 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100163929 | ||||||
| chr9:100164135 | G | A | 1 | a0001c0002t0002g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.273+37586G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100164135 | |||||||
| chr9:100164337 | A | G | 76 | a0001c0001t0001g0107 a0001c0001t0008g0123 a0001c0001t0008g0124 others(73): Show |
76 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(73): Show |
intron_variant | MODIFIER | c.273+37788A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100164337 | |||||||
| chr9:100164407 | GT | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+37868delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100164407 | ||||||
| chr9:100164495 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+37946T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100164495 | |||||||
| chr9:100164569 | T | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+38020T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100164569 | |||||||
| chr9:100164615 | T | C | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+38066T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100164615 | |||||||
| chr9:100164896 | C | CT | 22 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(19): Show |
22 | HG00609.hp2 HG00741.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.273+38364dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100164896 | ||||||
| chr9:100165229 | A | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+38680A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100165229 | |||||||
| chr9:100165254 | T | A | 118 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+38705T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100165254 | |||||||
| chr9:100165508 | A | G | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+38959A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100165508 | |||||||
| chr9:100165724 | G | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+39175G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100165724 | |||||||
| chr9:100166096 | C | G | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+39547C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100166096 | |||||||
| chr9:100166164 | A | G | 119 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(116): Show |
119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.273+39615A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100166164 | |||||||
| chr9:100166330 | A | G | 1 | a0001c0002t0001g0144 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.273+39781A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100166330 | |||||||
| chr9:100166772 | A | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+40223A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100166772 | |||||||
| chr9:100166965 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+40416C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100166965 | |||||||
| chr9:100167047 | A | G | 2 | a0001c0001t0003g0090 a0001c0001t0003g0091 |
2 | HG01243.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.273+40498A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167047 | |||||||
| chr9:100167050 | G | A | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.273+40501G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167050 | |||||||
| chr9:100167141 | G | T | 1 | a0001c0002t0001g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.273+40592G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167141 | |||||||
| chr9:100167173 | G | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+40624G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167173 | |||||||
| chr9:100167583 | C | T | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+41034C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167583 | |||||||
| chr9:100167655 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.273+41106C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167655 | |||||||
| chr9:100167660 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.273+41111T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167660 | |||||||
| chr9:100167823 | C | T | 3 | a0001c0001t0014g0027 a0001c0001t0015g0023 a0001c0001t0015g0024 |
3 | HG00642.hp2 HG00738.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.273+41274C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167823 | |||||||
| chr9:100167975 | C | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+41426C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100167975 | |||||||
| chr9:100168180 | G | A | 1 | a0001c0002t0002g0118 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.273+41631G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100168180 | |||||||
| chr9:100168493 | G | A | 4 | a0001c0002t0001g0104 a0001c0002t0001g0105 a0001c0002t0001g0106 others(1): Show |
4 | HG02622.hp1 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+41944G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100168493 | |||||||
| chr9:100168828 | C | T | 2 | a0001c0001t0012g0074 a0001c0001t0012g0080 |
2 | HG00621.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.273+42279C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100168828 | |||||||
| chr9:100168904 | G | A | 1 | a0001c0002t0002g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.273+42355G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100168904 | |||||||
| chr9:100169033 | C | A | 1 | a0001c0002t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.273+42484C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169033 | |||||||
| chr9:100169145 | T | C | 1 | a0001c0001t0014g0011 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.273+42596T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169145 | |||||||
| chr9:100169213 | T | C | 1 | a0001c0001t0011g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.273+42664T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169213 | |||||||
| chr9:100169297 | A | G | 1 | a0001c0001t0007g0048 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.273+42748A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169297 | |||||||
| chr9:100169341 | T | C | 72 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(69): Show |
72 | HG00280.hp1 HG00323.hp1 HG00423.hp1 others(69): Show |
intron_variant | MODIFIER | c.273+42792T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169341 | |||||||
| chr9:100169913 | T | G | 1 | a0001c0002t0002g0155 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.273+43364T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169913 | |||||||
| chr9:100169978 | A | T | 29 | a0001c0001t0001g0107 a0001c0001t0008g0159 a0001c0002t0001g0111 others(26): Show |
29 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.273+43429A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100169978 | |||||||
| chr9:100170108 | C | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+43559C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100170108 | |||||||
| chr9:100170276 | G | C | 1 | a0001c0002t0027g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.273+43727G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100170276 | |||||||
| chr9:100170323 | A | G | 1 | a0001c0002t0002g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.273+43774A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100170323 | |||||||
| chr9:100170393 | CAAA | C | 116 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(113): Show |
116 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(113): Show |
intron_variant | MODIFIER | c.273+43860_273+4386 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100170393 | ||||||
| chr9:100170564 | C | CA | 5 | a0001c0001t0001g0004 a0001c0001t0001g0107 a0001c0002t0001g0112 others(2): Show |
5 | HG02886.hp1 HG03225.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+44025dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100170564 | ||||||
| chr9:100170580 | TA | T | 5 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(2): Show |
5 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.273+44037delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100170580 | ||||||
| chr9:100170950 | T | C | 1 | a0001c0002t0001g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.273+44401T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100170950 | |||||||
| chr9:100170999 | T | G | 1 | a0001c0001t0005g0005 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.273+44450T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100170999 | |||||||
| chr9:100171059 | G | A | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.273+44510G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171059 | |||||||
| chr9:100171244 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+44695T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171244 | |||||||
| chr9:100171354 | T | A | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+44805T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171354 | |||||||
| chr9:100171365 | C | CA | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.273+44817dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100171365 | ||||||
| chr9:100171385 | T | G | 2 | a0001c0001t0022g0182 a0006c0007t0009g0181 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.273+44836T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171385 | |||||||
| chr9:100171654 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+45105A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171654 | |||||||
| chr9:100171829 | T | A | 118 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(115): Show |
118 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.273+45280T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171829 | |||||||
| chr9:100171902 | C | T | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.273+45353C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100171902 | |||||||
| chr9:100172008 | T | G | 121 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(118): Show |
121 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(118): Show |
intron_variant | MODIFIER | c.273+45459T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100172008 | |||||||
| chr9:100172498 | A | G | 37 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(34): Show |
37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.273+45949A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100172498 | |||||||
| chr9:100172838 | G | C | 120 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(117): Show |
120 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(117): Show |
intron_variant | MODIFIER | c.273+46289G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100172838 | |||||||
| chr9:100173170 | G | C | 1 | a0001c0002t0001g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.273+46621G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173170 | |||||||
| chr9:100173301 | C | T | 2 | a0001c0001t0004g0053 a0001c0001t0004g0059 |
2 | HG02080.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.273+46752C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173301 | |||||||
| chr9:100173460 | G | A | 1 | a0001c0002t0002g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.273+46911G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173460 | |||||||
| chr9:100173544 | A | G | 2 | a0001c0002t0002g0155 a0001c0002t0002g0160 |
2 | HG02602.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.273+46995A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173544 | |||||||
| chr9:100173557 | G | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+47008G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173557 | |||||||
| chr9:100173687 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+47138T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173687 | |||||||
| chr9:100173867 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.273+47318G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173867 | |||||||
| chr9:100173888 | T | C | 1 | a0001c0001t0014g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.273+47339T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100173888 | |||||||
| chr9:100174100 | A | C | 4 | a0001c0001t0008g0159 a0001c0002t0001g0169 a0001c0002t0001g0170 others(1): Show |
4 | HG00423.hp1 HG00544.hp1 NA18983.hp1 others(1): Show |
intron_variant | MODIFIER | c.273+47551A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100174100 | |||||||
| chr9:100174223 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.273+47674C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100174223 | |||||||
| chr9:100174593 | C | T | 1 | a0001c0001t0003g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.273+48044C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100174593 | |||||||
| chr9:100174895 | G | C | 4 | a0001c0001t0011g0076 a0001c0001t0011g0078 a0001c0001t0011g0081 others(1): Show |
4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+48346G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100174895 | |||||||
| chr9:100175251 | T | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.273+48702T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175251 | |||||||
| chr9:100175287 | C | G | 1 | a0001c0002t0002g0153 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.273+48738C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175287 | |||||||
| chr9:100175575 | C | G | 2 | a0001c0001t0022g0182 a0006c0007t0009g0181 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.273+49026C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175575 | |||||||
| chr9:100175699 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.273+49150C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175699 | |||||||
| chr9:100175925 | T | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+49376T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175925 | |||||||
| chr9:100175969 | A | G | 4 | a0001c0001t0011g0076 a0001c0001t0011g0078 a0001c0001t0011g0081 others(1): Show |
4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.273+49420A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100175969 | |||||||
| chr9:100176392 | G | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.274-49670G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100176392 | |||||||
| chr9:100176455 | T | C | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.274-49607T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100176455 | |||||||
| chr9:100176569 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.274-49493C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100176569 | |||||||
| chr9:100176705 | T | C | 1 | a0001c0002t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.274-49357T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100176705 | |||||||
| chr9:100176911 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(34): Show |
37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.274-49151G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100176911 | |||||||
| chr9:100177038 | C | T | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-49024C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100177038 | |||||||
| chr9:100177088 | C | T | 1 | a0001c0002t0001g0133 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.274-48974C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100177088 | |||||||
| chr9:100177150 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-48912G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100177150 | |||||||
| chr9:100177575 | G | C | 1 | a0001c0002t0002g0120 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.274-48487G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100177575 | |||||||
| chr9:100177767 | C | T | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-48295C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100177767 | |||||||
| chr9:100178109 | A | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-47953A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178109 | |||||||
| chr9:100178275 | T | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-47787T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178275 | |||||||
| chr9:100178293 | A | C | 77 | a0001c0001t0001g0107 a0001c0001t0004g0116 a0001c0001t0008g0123 others(74): Show |
77 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.274-47769A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178293 | |||||||
| chr9:100178315 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-47747G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178315 | |||||||
| chr9:100178458 | C | G | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.274-47604C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178458 | |||||||
| chr9:100178495 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-47567G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178495 | |||||||
| chr9:100178702 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-47360A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178702 | |||||||
| chr9:100178707 | A | G | 4 | a0001c0002t0002g0154 a0001c0002t0002g0156 a0001c0002t0002g0157 others(1): Show |
4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-47355A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178707 | |||||||
| chr9:100178937 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.274-47125C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178937 | |||||||
| chr9:100178994 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-47068G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100178994 | |||||||
| chr9:100179023 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-47039A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179023 | |||||||
| chr9:100179128 | C | A | 2 | a0001c0001t0022g0182 a0006c0007t0009g0181 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.274-46934C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179128 | |||||||
| chr9:100179176 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-46886G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179176 | |||||||
| chr9:100179202 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-46860C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179202 | |||||||
| chr9:100179230 | C | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-46832C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179230 | |||||||
| chr9:100179260 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-46802A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179260 | |||||||
| chr9:100179309 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-46753G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179309 | |||||||
| chr9:100179437 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-46625A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179437 | |||||||
| chr9:100179515 | T | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-46547T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179515 | |||||||
| chr9:100179656 | A | C | 1 | a0001c0002t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.274-46406A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179656 | |||||||
| chr9:100179687 | A | C | 1 | a0001c0002t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.274-46375A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179687 | |||||||
| chr9:100179792 | C | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-46270C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179792 | |||||||
| chr9:100179881 | A | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-46181A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100179881 | |||||||
| chr9:100180203 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-45859G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100180203 | |||||||
| chr9:100180344 | GT | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.274-45709delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100180344 | ||||||
| chr9:100180605 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-45457A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100180605 | |||||||
| chr9:100180916 | A | T | 2 | a0001c0001t0003g0176 a0001c0001t0003g0179 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.274-45146A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100180916 | |||||||
| chr9:100181057 | G | T | 3 | a0001c0001t0014g0027 a0001c0001t0015g0023 a0001c0001t0015g0024 |
3 | HG00642.hp2 HG00738.hp2 HG01123.hp1 |
intron_variant | MODIFIER | c.274-45005G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181057 | |||||||
| chr9:100181375 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-44687A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181375 | |||||||
| chr9:100181508 | A | C | 62 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(59): Show |
62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.274-44554A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181508 | |||||||
| chr9:100181560 | G | A | 1 | a0001c0002t0027g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.274-44502G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181560 | |||||||
| chr9:100181776 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-44286G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181776 | |||||||
| chr9:100181866 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-44196C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181866 | |||||||
| chr9:100181953 | A | G | 2 | a0001c0001t0004g0073 a0004c0010t0003g0044 |
2 | HG01496.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.274-44109A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100181953 | |||||||
| chr9:100182114 | T | C | 1 | a0001c0002t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274-43948T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182114 | |||||||
| chr9:100182137 | C | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-43925C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182137 | |||||||
| chr9:100182233 | A | T | 1 | a0001c0002t0002g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.274-43829A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182233 | |||||||
| chr9:100182357 | A | G | 2 | a0001c0002t0002g0152 a0001c0002t0002g0153 |
2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.274-43705A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182357 | |||||||
| chr9:100182494 | C | T | 59 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(56): Show |
59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.274-43568C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182494 | |||||||
| chr9:100182574 | C | T | 40 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(37): Show |
40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.274-43488C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182574 | |||||||
| chr9:100182645 | G | A | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.274-43417G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182645 | |||||||
| chr9:100182753 | A | G | 5 | a0001c0002t0001g0143 a0001c0002t0001g0144 a0001c0002t0001g0163 others(2): Show |
5 | HG00642.hp1 HG01175.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-43309A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182753 | |||||||
| chr9:100182811 | G | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-43251G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100182811 | |||||||
| chr9:100183017 | C | G | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-43045C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183017 | |||||||
| chr9:100183248 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-42814A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183248 | |||||||
| chr9:100183720 | G | A | 2 | a0001c0001t0022g0182 a0006c0007t0009g0181 |
2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.274-42342G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183720 | |||||||
| chr9:100183794 | G | GA | 21 | a0001c0001t0003g0042 a0001c0001t0003g0086 a0001c0001t0004g0055 others(18): Show |
21 | HG00735.hp2 HG01106.hp1 HG01106.hp2 others(18): Show |
intron_variant | MODIFIER | c.274-42246dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100183794 | ||||||
| chr9:100183794 | GA | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-42246delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100183794 | ||||||
| chr9:100183795 | A | G | 2 | a0001c0001t0003g0176 a0001c0001t0003g0179 |
2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.274-42267A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183795 | |||||||
| chr9:100183852 | C | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-42210C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183852 | |||||||
| chr9:100183940 | G | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-42122G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183940 | |||||||
| chr9:100183955 | A | G | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.274-42107A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100183955 | |||||||
| chr9:100184314 | A | G | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.274-41748A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184314 | |||||||
| chr9:100184437 | C | T | 9 | a0001c0001t0004g0055 a0001c0001t0007g0048 a0001c0001t0007g0050 others(6): Show |
9 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-41625C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184437 | |||||||
| chr9:100184460 | T | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-41602T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184460 | |||||||
| chr9:100184463 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-41599G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184463 | |||||||
| chr9:100184520 | T | C | 1 | a0001c0002t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274-41542T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184520 | |||||||
| chr9:100184793 | A | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-41269A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184793 | |||||||
| chr9:100184842 | A | G | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.274-41220A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184842 | |||||||
| chr9:100184891 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-41171C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100184891 | |||||||
| chr9:100185022 | G | A | 2 | a0001c0001t0003g0042 a0001c0001t0003g0085 |
2 | HG01106.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.274-41040G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185022 | |||||||
| chr9:100185220 | GATT | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-40832_274-4083 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185220 | ||||||
| chr9:100185474 | T | G | 1 | a0001c0001t0011g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.274-40588T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185474 | |||||||
| chr9:100185489 | A | G | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-40573A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185489 | |||||||
| chr9:100185516 | A | AAT | 3 | a0001c0002t0001g0168 a0001c0002t0002g0121 a0001c0002t0002g0139 |
3 | HG00621.hp2 NA18983.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.274-40505_274-4050 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | A | AATAT | 8 | a0001c0001t0008g0123 a0001c0001t0008g0124 a0001c0002t0001g0105 others(5): Show |
8 | HG00733.hp1 HG00733.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.274-40507_274-4050 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | A | AATATAT | 8 | a0001c0002t0001g0112 a0001c0002t0001g0132 a0001c0002t0001g0135 others(5): Show |
8 | HG01069.hp1 HG01975.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-40509_274-4050 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | A | AATATATA others(1): Show |
8 | a0001c0002t0001g0106 a0001c0002t0001g0133 a0001c0002t0001g0143 others(5): Show |
8 | HG00323.hp2 HG00642.hp1 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-40511_274-4050 others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | A | AATATATA others(3): Show |
10 | a0001c0002t0001g0108 a0001c0002t0001g0127 a0001c0002t0001g0169 others(7): Show |
10 | HG00423.hp1 HG00544.hp1 HG00735.hp2 others(7): Show |
intron_variant | MODIFIER | c.274-40513_274-4050 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | A | AATATATA others(5): Show |
4 | a0001c0002t0001g0172 a0001c0002t0002g0041 a0001c0002t0002g0134 others(1): Show |
4 | HG00140.hp2 HG01109.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-40515_274-4050 others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | A | AATATATA others(7): Show |
1 | a0001c0002t0002g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.274-40517_274-4050 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | A | AATATATA others(11): Show |
2 | a0001c0002t0002g0115 a0001c0002t0002g0160 |
2 | HG03927.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.274-40521_274-4050 others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AAT | A | 10 | a0001c0001t0001g0107 a0001c0002t0001g0128 a0001c0002t0001g0129 others(7): Show |
10 | HG00280.hp1 HG01168.hp2 HG01169.hp1 others(7): Show |
intron_variant | MODIFIER | c.274-40505_274-4050 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AATAT | A | 3 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0002t0002g0118 |
3 | HG00609.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-40507_274-4050 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AATATATA others(1): Show |
A | 4 | a0001c0001t0014g0011 a0001c0001t0022g0182 a0001c0002t0001g0017 others(1): Show |
4 | HG01081.hp2 HG02109.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-40511_274-4050 others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AATATATA others(3): Show |
A | 3 | a0001c0001t0005g0013 a0001c0001t0026g0008 a0001c0002t0001g0018 |
3 | HG02970.hp1 HG03209.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.274-40513_274-4050 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AATATATA others(5): Show |
A | 9 | a0001c0001t0004g0064 a0001c0001t0005g0005 a0001c0001t0005g0006 others(6): Show |
9 | HG02451.hp2 HG02630.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-40515_274-4050 others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AATATATA others(7): Show |
A | 19 | a0001c0001t0001g0020 a0001c0001t0001g0146 a0001c0001t0001g0147 others(16): Show |
19 | HG00609.hp1 HG01081.hp1 HG01106.hp1 others(16): Show |
intron_variant | MODIFIER | c.274-40517_274-4050 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AATATATA others(9): Show |
A | 57 | a0001c0001t0001g0015 a0001c0001t0003g0042 a0001c0001t0003g0045 others(54): Show |
57 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.274-40519_274-4050 others(20): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AATATATA others(11): Show |
A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0032 others(12): Show |
15 | HG01074.hp1 HG01109.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.274-40521_274-4050 others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AATATATA others(17): Show |
A | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.274-40527_274-4050 others(28): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AATATATA others(19): Show |
A | 5 | a0001c0001t0008g0159 a0001c0002t0001g0142 a0001c0002t0001g0145 others(2): Show |
5 | HG01071.hp1 HG02559.hp2 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-40529_274-4050 others(30): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185516 | AATATATA others(25): Show |
A | 1 | a0001c0002t0002g0140 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.274-40535_274-4050 others(36): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100185516 | ||||||
| chr9:100185560 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.274-40502C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185560 | |||||||
| chr9:100185695 | G | A | 1 | a0001c0001t0017g0063 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.274-40367G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185695 | |||||||
| chr9:100185735 | A | G | 60 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.274-40327A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185735 | |||||||
| chr9:100185774 | G | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-40288G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100185774 | |||||||
| chr9:100186186 | G | A | 62 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(59): Show |
62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.274-39876G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100186186 | |||||||
| chr9:100186198 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.274-39864G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100186198 | |||||||
| chr9:100186384 | A | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-39678A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100186384 | |||||||
| chr9:100186938 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-39124A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100186938 | |||||||
| chr9:100187004 | G | A | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.274-39058G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187004 | |||||||
| chr9:100187005 | T | G | 1 | a0001c0001t0004g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.274-39057T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187005 | |||||||
| chr9:100187078 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-38984G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187078 | |||||||
| chr9:100187163 | T | C | 1 | a0001c0002t0008g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.274-38899T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187163 | |||||||
| chr9:100187515 | T | C | 1 | a0001c0002t0002g0175 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.274-38547T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187515 | |||||||
| chr9:100187525 | C | CT | 63 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(60): Show |
63 | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
intron_variant | MODIFIER | c.274-38518dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100187525 | ||||||
| chr9:100187525 | C | CTTTTTTT others(3): Show |
6 | a0001c0001t0001g0038 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG01168.hp1 HG02622.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-38527_274-3851 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100187525 | ||||||
| chr9:100187525 | C | CTTTTTTT others(4): Show |
19 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0021 others(16): Show |
19 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.274-38528_274-3851 others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100187525 | ||||||
| chr9:100187525 | C | CTTTTTTT others(5): Show |
11 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(8): Show |
11 | HG00642.hp2 HG01081.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-38529_274-3851 others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100187525 | ||||||
| chr9:100187525 | C | CTTTTTTT others(7): Show |
1 | a0001c0001t0014g0011 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.274-38531_274-3851 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100187525 | ||||||
| chr9:100187712 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-38350G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187712 | |||||||
| chr9:100187755 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-38307A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100187755 | |||||||
| chr9:100188033 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-38029C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188033 | |||||||
| chr9:100188178 | G | A | 1 | a0001c0002t0002g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.274-37884G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188178 | |||||||
| chr9:100188255 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-37807G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188255 | |||||||
| chr9:100188268 | A | C | 1 | a0001c0001t0014g0027 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.274-37794A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188268 | |||||||
| chr9:100188307 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.274-37755G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188307 | |||||||
| chr9:100188444 | T | G | 104 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.274-37618T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188444 | |||||||
| chr9:100188635 | CT | C | 39 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(36): Show |
39 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(36): Show |
intron_variant | MODIFIER | c.274-37411delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100188635 | ||||||
| chr9:100188941 | G | A | 62 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(59): Show |
62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.274-37121G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100188941 | |||||||
| chr9:100189106 | C | CT | 28 | a0001c0001t0001g0147 a0001c0001t0003g0070 a0001c0001t0003g0083 others(25): Show |
28 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.274-36935dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100189106 | ||||||
| chr9:100189106 | C | CTTTTTTT | 29 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(26): Show |
29 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.274-36941_274-3693 others(11): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100189106 | ||||||
| chr9:100189106 | CT | C | 11 | a0001c0001t0003g0045 a0001c0001t0010g0136 a0001c0001t0010g0137 others(8): Show |
11 | HG00140.hp1 HG02280.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-36935delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100189106 | ||||||
| chr9:100189106 | CTTTTTTT others(3): Show |
C | 2 | a0001c0002t0001g0169 a0001c0002t0001g0171 |
2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.274-36944_274-3693 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100189106 | ||||||
| chr9:100189346 | T | C | 4 | a0001c0001t0001g0107 a0001c0002t0001g0112 a0001c0004t0001g0109 others(1): Show |
4 | HG02886.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-36716T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189346 | |||||||
| chr9:100189420 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-36642C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189420 | |||||||
| chr9:100189422 | T | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-36640T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189422 | |||||||
| chr9:100189440 | T | C | 1 | a0001c0002t0002g0150 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.274-36622T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189440 | |||||||
| chr9:100189493 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-36569G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189493 | |||||||
| chr9:100189777 | C | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-36285C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100189777 | |||||||
| chr9:100190456 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.274-35606G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100190456 | |||||||
| chr9:100190484 | C | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-35578C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100190484 | |||||||
| chr9:100190606 | T | C | 60 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.274-35456T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100190606 | |||||||
| chr9:100190649 | T | C | 1 | a0001c0002t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.274-35413T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100190649 | |||||||
| chr9:100190674 | G | A | 1 | a0001c0002t0002g0115 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.274-35388G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100190674 | |||||||
| chr9:100191044 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-35018A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100191044 | |||||||
| chr9:100191110 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.274-34952C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100191110 | |||||||
| chr9:100191113 | G | A | 3 | a0001c0002t0001g0169 a0001c0002t0001g0170 a0001c0002t0001g0171 |
3 | HG00423.hp1 HG00544.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.274-34949G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100191113 | |||||||
| chr9:100191719 | A | G | 3 | a0001c0001t0003g0084 a0001c0001t0004g0067 a0001c0001t0004g0072 |
3 | HG00544.hp2 HG02083.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.274-34343A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100191719 | |||||||
| chr9:100192248 | A | AGT | 28 | a0001c0001t0003g0042 a0001c0001t0003g0085 a0001c0001t0003g0090 others(25): Show |
28 | HG00280.hp1 HG00642.hp1 HG01069.hp2 others(25): Show |
intron_variant | MODIFIER | c.274-33779_274-3377 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | ||||||
| chr9:100192248 | A | AGTGT | 33 | a0001c0001t0003g0045 a0001c0001t0003g0070 a0001c0001t0003g0083 others(30): Show |
33 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.274-33781_274-3377 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | ||||||
| chr9:100192248 | A | AGTGTGT | 14 | a0001c0001t0001g0036 a0001c0001t0001g0038 a0001c0001t0001g0040 others(11): Show |
14 | HG00280.hp2 HG00423.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.274-33783_274-3377 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | ||||||
| chr9:100192248 | A | AGTGTGTG others(1): Show |
21 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0021 others(18): Show |
21 | HG00741.hp2 HG01109.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.274-33785_274-3377 others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | ||||||
| chr9:100192248 | A | AGTGTGTG others(3): Show |
9 | a0001c0001t0001g0020 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG00323.hp1 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-33787_274-3377 others(14): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | ||||||
| chr9:100192248 | AGT | A | 3 | a0001c0002t0001g0016 a0001c0002t0001g0104 a0004c0010t0003g0044 |
3 | HG01496.hp2 HG02897.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.274-33779_274-3377 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | ||||||
| chr9:100192248 | AGTGT | A | 5 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0002t0001g0105 others(2): Show |
5 | HG01081.hp1 HG01243.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-33781_274-3377 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192248 | ||||||
| chr9:100192407 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-33655G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100192407 | |||||||
| chr9:100192814 | A | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-33248A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100192814 | |||||||
| chr9:100192830 | T | A | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.274-33232T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100192830 | |||||||
| chr9:100192956 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-33106A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100192956 | |||||||
| chr9:100192978 | C | CTT | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.274-33069_274-3306 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100192978 | ||||||
| chr9:100193081 | A | T | 1 | a0001c0001t0008g0159 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.274-32981A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100193081 | |||||||
| chr9:100193305 | A | T | 4 | a0001c0001t0001g0107 a0001c0002t0001g0112 a0001c0004t0001g0109 others(1): Show |
4 | HG02886.hp1 HG03225.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-32757A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100193305 | |||||||
| chr9:100193307 | A | G | 4 | a0001c0001t0012g0074 a0001c0001t0012g0079 a0001c0001t0012g0080 others(1): Show |
4 | HG00423.hp2 HG00621.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.274-32755A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100193307 | |||||||
| chr9:100193776 | A | G | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.274-32286A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100193776 | |||||||
| chr9:100193931 | A | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-32131A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100193931 | |||||||
| chr9:100194109 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.274-31953G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194109 | |||||||
| chr9:100194116 | T | A | 1 | a0001c0002t0001g0105 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.274-31946T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194116 | |||||||
| chr9:100194453 | T | C | 2 | a0001c0002t0002g0120 a0001c0002t0002g0121 |
2 | NA19082.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.274-31609T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194453 | |||||||
| chr9:100194475 | ATCGTCTT others(10): Show |
A | 2 | a0001c0002t0001g0169 a0001c0002t0001g0171 |
2 | HG00423.hp1 HG00544.hp1 |
intron_variant | MODIFIER | c.274-31585_274-3156 others(21): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100194475 | ||||||
| chr9:100194503 | GT | G | 67 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(64): Show |
67 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.274-31549delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100194503 | ||||||
| chr9:100194505 | T | G | 7 | a0001c0001t0004g0046 a0001c0001t0004g0047 a0001c0001t0004g0051 others(4): Show |
7 | HG00280.hp2 HG02080.hp2 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-31557T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194505 | |||||||
| chr9:100194616 | G | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-31446G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194616 | |||||||
| chr9:100194964 | C | G | 1 | a0001c0001t0014g0011 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.274-31098C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194964 | |||||||
| chr9:100194987 | C | T | 2 | a0001c0002t0001g0135 a0001c0002t0001g0174 |
2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.274-31075C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100194987 | |||||||
| chr9:100195251 | C | T | 1 | a0001c0002t0002g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.274-30811C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195251 | |||||||
| chr9:100195423 | A | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(103): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.274-30639A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195423 | |||||||
| chr9:100195493 | A | AT | 105 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.274-30558dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100195493 | ||||||
| chr9:100195542 | C | T | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-30520C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195542 | |||||||
| chr9:100195557 | G | A | 11 | a0001c0002t0002g0102 a0001c0002t0002g0114 a0001c0002t0002g0115 others(8): Show |
11 | HG00609.hp2 HG01192.hp1 HG02056.hp2 others(8): Show |
intron_variant | MODIFIER | c.274-30505G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195557 | |||||||
| chr9:100195601 | G | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-30461G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195601 | |||||||
| chr9:100195708 | G | A | 60 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.274-30354G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195708 | |||||||
| chr9:100195725 | T | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-30337T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195725 | |||||||
| chr9:100195824 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-30238A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195824 | |||||||
| chr9:100195886 | A | T | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-30176A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195886 | |||||||
| chr9:100195957 | G | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-30105G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195957 | |||||||
| chr9:100195962 | G | A | 9 | a0001c0001t0004g0055 a0001c0001t0007g0048 a0001c0001t0007g0050 others(6): Show |
9 | HG02109.hp2 HG02647.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-30100G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195962 | |||||||
| chr9:100195970 | A | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-30092A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100195970 | |||||||
| chr9:100196317 | G | A | 157 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(154): Show |
157 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(154): Show |
intron_variant | MODIFIER | c.274-29745G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100196317 | |||||||
| chr9:100196454 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-29608G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100196454 | |||||||
| chr9:100196888 | GT | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-29167delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100196888 | ||||||
| chr9:100197093 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.274-28969G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197093 | |||||||
| chr9:100197587 | C | G | 60 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.274-28475C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197587 | |||||||
| chr9:100197636 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-28426A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197636 | |||||||
| chr9:100197715 | G | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-28347G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197715 | |||||||
| chr9:100197791 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-28271G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197791 | |||||||
| chr9:100197817 | G | C | 2 | a0001c0002t0016g0148 a0001c0002t0016g0151 |
2 | HG01516.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.274-28245G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197817 | |||||||
| chr9:100197969 | C | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-28093C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100197969 | |||||||
| chr9:100198244 | T | C | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.274-27818T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198244 | |||||||
| chr9:100198264 | A | AT | 5 | a0001c0001t0001g0021 a0001c0002t0001g0163 a0001c0002t0001g0168 others(2): Show |
5 | HG01952.hp1 HG03471.hp2 HG03490.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-27747dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | A | ATTTTTTT others(7): Show |
1 | a0001c0002t0001g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.274-27760_274-2774 others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | AT | A | 7 | a0001c0001t0009g0100 a0001c0002t0001g0127 a0001c0002t0001g0128 others(4): Show |
7 | HG00280.hp1 HG00741.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-27747delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTT | A | 7 | a0001c0001t0001g0036 a0001c0002t0002g0102 a0001c0002t0002g0134 others(4): Show |
7 | HG00323.hp2 HG01074.hp2 HG01346.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-27750_274-2774 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTT | A | 15 | a0001c0001t0007g0029 a0001c0001t0008g0124 a0001c0001t0024g0031 others(12): Show |
15 | HG00733.hp1 HG01167.hp2 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.274-27751_274-2774 others(9): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTT | A | 15 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0039 others(12): Show |
15 | HG00642.hp2 HG01168.hp2 HG01169.hp1 others(12): Show |
intron_variant | MODIFIER | c.274-27752_274-2774 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT | A | 11 | a0001c0001t0001g0020 a0001c0001t0001g0032 a0001c0001t0001g0034 others(8): Show |
11 | HG00735.hp2 HG01109.hp1 HG01123.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-27753_274-2774 others(11): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(1): Show |
A | 7 | a0001c0001t0001g0037 a0001c0001t0013g0025 a0001c0001t0015g0024 others(4): Show |
7 | HG00738.hp2 HG01168.hp1 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-27754_274-2774 others(12): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(6): Show |
A | 1 | a0001c0002t0001g0170 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.274-27759_274-2774 others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(8): Show |
A | 7 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(4): Show |
7 | HG00140.hp2 HG00733.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.274-27761_274-2774 others(19): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(11): Show |
A | 1 | a0001c0002t0002g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.274-27764_274-2774 others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(13): Show |
A | 2 | a0001c0001t0022g0182 a0001c0002t0001g0106 |
2 | HG01081.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.274-27766_274-2774 others(24): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(14): Show |
A | 5 | a0001c0001t0001g0147 a0001c0002t0001g0104 a0001c0002t0001g0105 others(2): Show |
5 | HG01243.hp2 HG02886.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-27767_274-2774 others(25): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(15): Show |
A | 2 | a0001c0001t0001g0146 a0001c0002t0002g0119 |
2 | HG01081.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.274-27768_274-2774 others(26): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(17): Show |
A | 11 | a0001c0001t0003g0042 a0001c0001t0003g0085 a0001c0001t0003g0090 others(8): Show |
11 | HG01106.hp1 HG01106.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.274-27770_274-2774 others(28): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(18): Show |
A | 50 | a0001c0001t0003g0045 a0001c0001t0003g0070 a0001c0001t0003g0083 others(47): Show |
50 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(47): Show |
intron_variant | MODIFIER | c.274-27771_274-2774 others(29): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(19): Show |
A | 1 | a0001c0001t0011g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.274-27772_274-2774 others(30): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(20): Show |
A | 8 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(5): Show |
8 | HG00741.hp2 HG02451.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.274-27773_274-2774 others(31): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198264 | ATTTTTTT others(21): Show |
A | 1 | a0001c0002t0002g0160 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.274-27774_274-2774 others(32): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100198264 | ||||||
| chr9:100198591 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-27471C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198591 | |||||||
| chr9:100198713 | C | G | 1 | a0001c0002t0002g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.274-27349C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198713 | |||||||
| chr9:100198718 | G | A | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-27344G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198718 | |||||||
| chr9:100198724 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-27338C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198724 | |||||||
| chr9:100198803 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-27259G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198803 | |||||||
| chr9:100198833 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-27229C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100198833 | |||||||
| chr9:100199389 | G | T | 1 | a0001c0001t0007g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.274-26673G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199389 | |||||||
| chr9:100199434 | T | C | 1 | a0001c0002t0002g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.274-26628T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199434 | |||||||
| chr9:100199656 | C | T | 1 | a0001c0002t0002g0173 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.274-26406C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199656 | |||||||
| chr9:100199657 | G | A | 1 | a0001c0002t0001g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.274-26405G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199657 | |||||||
| chr9:100199662 | C | T | 1 | a0001c0002t0001g0131 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.274-26400C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199662 | |||||||
| chr9:100199678 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-26384A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199678 | |||||||
| chr9:100199830 | T | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-26232T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199830 | |||||||
| chr9:100199830 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-26232T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199830 | |||||||
| chr9:100199859 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-26203C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100199859 | |||||||
| chr9:100200136 | A | G | 1 | a0001c0001t0003g0083 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.274-25926A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100200136 | |||||||
| chr9:100200299 | G | T | 1 | a0001c0002t0002g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.274-25763G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100200299 | |||||||
| chr9:100200347 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.274-25715G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100200347 | |||||||
| chr9:100200545 | A | C | 1 | a0002c0003t0006g0094 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.274-25517A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100200545 | |||||||
| chr9:100200585 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-25477G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100200585 | |||||||
| chr9:100201196 | C | T | 1 | a0001c0001t0004g0072 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.274-24866C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100201196 | |||||||
| chr9:100201379 | T | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-24683T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100201379 | |||||||
| chr9:100201547 | T | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-24515T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100201547 | |||||||
| chr9:100201865 | C | T | 1 | a0001c0001t0003g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.274-24197C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100201865 | |||||||
| chr9:100201958 | G | A | 2 | a0001c0002t0001g0135 a0001c0002t0001g0174 |
2 | HG02976.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.274-24104G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100201958 | |||||||
| chr9:100202086 | A | G | 2 | a0001c0001t0013g0025 a0001c0001t0013g0026 |
2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.274-23976A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100202086 | |||||||
| chr9:100202092 | G | GT | 99 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(96): Show |
99 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.274-23957dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100202092 | ||||||
| chr9:100202624 | C | T | 1 | a0001c0001t0003g0086 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.274-23438C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100202624 | |||||||
| chr9:100203100 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(31): Show |
34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.274-22962G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203100 | |||||||
| chr9:100203341 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-22721C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203341 | |||||||
| chr9:100203501 | C | CT | 67 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(64): Show |
67 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.274-22542dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100203501 | ||||||
| chr9:100203501 | C | CTTT | 28 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(25): Show |
28 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(25): Show |
intron_variant | MODIFIER | c.274-22544_274-2254 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100203501 | ||||||
| chr9:100203501 | C | CTTTT | 6 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(3): Show |
6 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.274-22545_274-2254 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100203501 | ||||||
| chr9:100203521 | G | T | 27 | a0001c0001t0003g0070 a0001c0001t0003g0083 a0001c0001t0003g0084 others(24): Show |
27 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.274-22541G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203521 | |||||||
| chr9:100203662 | G | A | 34 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(31): Show |
34 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.274-22400G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203662 | |||||||
| chr9:100203774 | C | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-22288C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203774 | |||||||
| chr9:100203785 | C | G | 1 | a0001c0001t0009g0100 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.274-22277C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203785 | |||||||
| chr9:100203819 | A | G | 2 | a0001c0001t0003g0042 a0001c0001t0003g0085 |
2 | HG01106.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.274-22243A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203819 | |||||||
| chr9:100203841 | C | T | 2 | a0001c0001t0003g0090 a0001c0001t0003g0091 |
2 | HG01243.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.274-22221C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203841 | |||||||
| chr9:100203988 | A | G | 62 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(59): Show |
62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.274-22074A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100203988 | |||||||
| chr9:100204029 | A | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-22033A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204029 | |||||||
| chr9:100204083 | A | G | 1 | a0001c0001t0011g0076 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.274-21979A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204083 | |||||||
| chr9:100204104 | A | T | 3 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 |
3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.274-21958A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204104 | |||||||
| chr9:100204681 | G | C | 1 | a0001c0001t0007g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.274-21381G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204681 | |||||||
| chr9:100204744 | A | C | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-21318A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204744 | |||||||
| chr9:100204786 | A | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-21276A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204786 | |||||||
| chr9:100204938 | G | A | 2 | a0001c0001t0004g0073 a0004c0010t0003g0044 |
2 | HG01496.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.274-21124G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100204938 | |||||||
| chr9:100205093 | CTG | C | 2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.274-20966_274-2096 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100205093 | ||||||
| chr9:100205159 | T | C | 2 | a0001c0001t0007g0029 a0001c0001t0023g0030 |
2 | HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.274-20903T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100205159 | |||||||
| chr9:100205310 | A | T | 1 | a0001c0002t0001g0003 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.274-20752A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100205310 | |||||||
| chr9:100205491 | CAGTT | C | 5 | a0001c0001t0001g0107 a0001c0002t0001g0104 a0001c0002t0001g0105 others(2): Show |
5 | HG02622.hp1 HG02886.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-20569_274-2056 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100205491 | ||||||
| chr9:100205611 | G | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-20451G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100205611 | |||||||
| chr9:100205721 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-20341C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100205721 | |||||||
| chr9:100206031 | A | G | 6 | a0001c0001t0011g0022 a0001c0001t0013g0025 a0001c0001t0013g0026 others(3): Show |
6 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-20031A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206031 | |||||||
| chr9:100206112 | C | T | 1 | a0001c0001t0003g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.274-19950C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206112 | |||||||
| chr9:100206240 | G | A | 1 | a0001c0002t0002g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.274-19822G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206240 | |||||||
| chr9:100206341 | T | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-19721T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206341 | |||||||
| chr9:100206430 | C | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-19632C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206430 | |||||||
| chr9:100206468 | C | T | 1 | a0001c0002t0002g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.274-19594C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206468 | |||||||
| chr9:100206524 | T | A | 9 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0136 others(6): Show |
9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-19538T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206524 | |||||||
| chr9:100206565 | G | T | 5 | a0001c0001t0004g0061 a0001c0001t0004g0062 a0001c0001t0004g0064 others(2): Show |
5 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-19497G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100206565 | |||||||
| chr9:100207177 | A | AC | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-18883dupC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100207177 | ||||||
| chr9:100207180 | G | A | 1 | a0001c0001t0012g0074 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.274-18882G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207180 | |||||||
| chr9:100207180 | G | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-18882G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207180 | |||||||
| chr9:100207280 | A | AT | 4 | a0001c0001t0011g0076 a0001c0001t0011g0078 a0001c0001t0011g0081 others(1): Show |
4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-18776dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100207280 | ||||||
| chr9:100207577 | C | T | 42 | a0001c0001t0004g0116 a0001c0001t0008g0123 a0001c0001t0008g0124 others(39): Show |
42 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-18485C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207577 | |||||||
| chr9:100207650 | A | C | 1 | a0001c0001t0001g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.274-18412A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207650 | |||||||
| chr9:100207650 | A | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(38): Show |
41 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.274-18412A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207650 | |||||||
| chr9:100207971 | GATTAC | G | 6 | a0001c0001t0011g0022 a0001c0001t0013g0025 a0001c0001t0013g0026 others(3): Show |
6 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-18089_274-1808 others(9): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100207971 | ||||||
| chr9:100207976 | C | G | 36 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(33): Show |
36 | HG01081.hp2 HG01109.hp1 HG02055.hp1 others(33): Show |
intron_variant | MODIFIER | c.274-18086C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100207976 | |||||||
| chr9:100208031 | T | TG | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-18030dupG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100208031 | ||||||
| chr9:100208080 | A | G | 1 | a0001c0001t0015g0024 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.274-17982A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100208080 | |||||||
| chr9:100208169 | A | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-17893A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100208169 | |||||||
| chr9:100208484 | G | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-17578G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100208484 | |||||||
| chr9:100208830 | T | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-17232T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100208830 | |||||||
| chr9:100209508 | T | C | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-16554T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100209508 | |||||||
| chr9:100209769 | C | CA | 7 | a0001c0001t0008g0159 a0001c0002t0001g0163 a0001c0002t0001g0165 others(4): Show |
7 | HG00423.hp1 HG01109.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-16267dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100209769 | ||||||
| chr9:100209769 | CA | C | 89 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0045 others(86): Show |
89 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(86): Show |
intron_variant | MODIFIER | c.274-16267delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100209769 | ||||||
| chr9:100209769 | CAAAAA | C | 29 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(26): Show |
29 | HG00642.hp2 HG00738.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.274-16271_274-1626 others(9): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100209769 | ||||||
| chr9:100209769 | CAAAAAA | C | 12 | a0001c0001t0001g0033 a0001c0001t0007g0029 a0001c0001t0009g0100 others(9): Show |
12 | HG00323.hp1 HG01081.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.274-16272_274-1626 others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100209769 | ||||||
| chr9:100209808 | G | A | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-16254G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100209808 | |||||||
| chr9:100209908 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-16154G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100209908 | |||||||
| chr9:100210035 | A | G | 1 | a0001c0001t0003g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.274-16027A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210035 | |||||||
| chr9:100210054 | C | G | 60 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.274-16008C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210054 | |||||||
| chr9:100210061 | T | G | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-16001T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210061 | |||||||
| chr9:100210355 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-15707G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210355 | |||||||
| chr9:100210426 | A | G | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-15636A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210426 | |||||||
| chr9:100210719 | C | T | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.274-15343C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210719 | |||||||
| chr9:100210779 | A | G | 1 | a0001c0001t0004g0066 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.274-15283A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210779 | |||||||
| chr9:100210834 | C | G | 1 | a0001c0001t0001g0039 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.274-15228C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100210834 | |||||||
| chr9:100211096 | C | T | 2 | a0001c0004t0001g0109 a0001c0004t0001g0110 |
2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.274-14966C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100211096 | |||||||
| chr9:100211437 | C | A | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.274-14625C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100211437 | |||||||
| chr9:100211638 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.274-14424T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100211638 | |||||||
| chr9:100211716 | A | G | 2 | a0001c0001t0003g0084 a0001c0001t0004g0067 |
2 | HG02083.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.274-14346A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100211716 | |||||||
| chr9:100212455 | CTCT | C | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-13603_274-1360 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100212455 | ||||||
| chr9:100212465 | G | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-13597G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100212465 | |||||||
| chr9:100212745 | C | T | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-13317C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100212745 | |||||||
| chr9:100213037 | T | C | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-13025T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213037 | |||||||
| chr9:100213116 | G | A | 2 | a0001c0002t0002g0152 a0001c0002t0002g0153 |
2 | HG00735.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.274-12946G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213116 | |||||||
| chr9:100213200 | T | TG | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.274-12855dupG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100213200 | ||||||
| chr9:100213378 | T | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-12684T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213378 | |||||||
| chr9:100213637 | C | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-12425C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213637 | |||||||
| chr9:100213692 | C | T | 9 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0136 others(6): Show |
9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-12370C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213692 | |||||||
| chr9:100213720 | C | T | 9 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0136 others(6): Show |
9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-12342C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213720 | |||||||
| chr9:100213814 | A | C | 9 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0136 others(6): Show |
9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-12248A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213814 | |||||||
| chr9:100213886 | A | G | 9 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0136 others(6): Show |
9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-12176A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100213886 | |||||||
| chr9:100214089 | G | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-11973G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214089 | |||||||
| chr9:100214135 | A | T | 58 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.274-11927A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214135 | |||||||
| chr9:100214259 | T | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-11803T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214259 | |||||||
| chr9:100214271 | A | C | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-11791A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214271 | |||||||
| chr9:100214362 | G | A | 100 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(97): Show |
100 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(97): Show |
intron_variant | MODIFIER | c.274-11700G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214362 | |||||||
| chr9:100214541 | T | C | 1 | a0001c0002t0001g0167 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.274-11521T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214541 | |||||||
| chr9:100214568 | A | C | 9 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0136 others(6): Show |
9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-11494A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214568 | |||||||
| chr9:100214846 | C | G | 9 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0136 others(6): Show |
9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-11216C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100214846 | |||||||
| chr9:100215013 | C | T | 28 | a0001c0001t0004g0116 a0001c0001t0008g0123 a0001c0001t0008g0124 others(25): Show |
28 | HG00609.hp2 HG00621.hp2 HG00733.hp1 others(25): Show |
intron_variant | MODIFIER | c.274-11049C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100215013 | |||||||
| chr9:100215179 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.274-10883T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100215179 | |||||||
| chr9:100215645 | A | G | 1 | a0001c0002t0002g0160 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.274-10417A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100215645 | |||||||
| chr9:100215791 | G | A | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-10271G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100215791 | |||||||
| chr9:100216115 | A | G | 1 | a0001c0001t0004g0072 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.274-9947A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216115 | |||||||
| chr9:100216329 | AC | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-9731delC | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100216329 | ||||||
| chr9:100216358 | G | C | 1 | a0001c0002t0002g0160 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.274-9704G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216358 | |||||||
| chr9:100216374 | C | T | 9 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-9688C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216374 | |||||||
| chr9:100216452 | G | A | 4 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(1): Show |
4 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-9610G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216452 | |||||||
| chr9:100216752 | C | T | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.274-9310C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216752 | |||||||
| chr9:100216766 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-9296C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216766 | |||||||
| chr9:100216962 | A | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.274-9100A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100216962 | |||||||
| chr9:100217016 | T | C | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.274-9046T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217016 | |||||||
| chr9:100217064 | G | A | 1 | a0001c0001t0007g0060 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.274-8998G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217064 | |||||||
| chr9:100217230 | A | G | 3 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0116 |
3 | NA19005.hp1 NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.274-8832A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217230 | |||||||
| chr9:100217274 | A | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.274-8788A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217274 | |||||||
| chr9:100217447 | C | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-8615C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217447 | |||||||
| chr9:100217632 | C | T | 5 | a0001c0001t0004g0061 a0001c0001t0004g0062 a0001c0001t0004g0064 others(2): Show |
5 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-8430C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217632 | |||||||
| chr9:100217836 | C | T | 1 | a0001c0002t0002g0122 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.274-8226C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217836 | |||||||
| chr9:100217918 | G | A | 1 | a0001c0002t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.274-8144G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100217918 | |||||||
| chr9:100218077 | A | G | 2 | a0001c0001t0004g0068 a0001c0001t0004g0069 |
2 | NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.274-7985A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100218077 | |||||||
| chr9:100218387 | C | T | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.274-7675C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100218387 | |||||||
| chr9:100218391 | G | A | 9 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0136 others(6): Show |
9 | HG01081.hp2 HG02280.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.274-7671G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100218391 | |||||||
| chr9:100218550 | C | G | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-7512C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100218550 | |||||||
| chr9:100218985 | A | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-7077A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100218985 | |||||||
| chr9:100219266 | G | A | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-6796G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100219266 | |||||||
| chr9:100219274 | A | G | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(39): Show |
intron_variant | MODIFIER | c.274-6788A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100219274 | |||||||
| chr9:100219290 | T | C | 59 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(56): Show |
59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.274-6772T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100219290 | |||||||
| chr9:100219881 | G | GATATATA others(23): Show |
1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.274-6163_274-6162i others(32): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100219881 | ||||||
| chr9:100219881 | GATATATA others(1): Show |
G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-6170_274-6163d others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100219881 | ||||||
| chr9:100220136 | T | A | 63 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(60): Show |
63 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.274-5926T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220136 | |||||||
| chr9:100220137 | T | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.274-5925T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220137 | |||||||
| chr9:100220421 | T | G | 1 | a0001c0001t0004g0046 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.274-5641T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220421 | |||||||
| chr9:100220598 | T | G | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.274-5464T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220598 | |||||||
| chr9:100220783 | G | T | 1 | a0001c0002t0001g0174 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.274-5279G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220783 | |||||||
| chr9:100220803 | C | T | 1 | a0001c0001t0009g0100 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.274-5259C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220803 | |||||||
| chr9:100220814 | T | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.274-5248T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100220814 | |||||||
| chr9:100220974 | C | CA | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-5074dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100220974 | ||||||
| chr9:100220974 | C | CAA | 57 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(54): Show |
57 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.274-5075_274-5074d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100220974 | ||||||
| chr9:100220974 | C | CAAA | 7 | a0001c0001t0004g0053 a0001c0001t0010g0136 a0001c0001t0010g0137 others(4): Show |
7 | HG01175.hp1 HG02280.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.274-5076_274-5074d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100220974 | ||||||
| chr9:100221047 | A | G | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-5015A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221047 | |||||||
| chr9:100221052 | A | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-5010A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221052 | |||||||
| chr9:100221305 | A | AT | 66 | a0001c0001t0001g0015 a0001c0001t0003g0042 a0001c0001t0003g0045 others(63): Show |
66 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.274-4741dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100221305 | ||||||
| chr9:100221305 | A | ATT | 30 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(27): Show |
30 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.274-4742_274-4741d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100221305 | ||||||
| chr9:100221399 | C | G | 1 | a0001c0002t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.274-4663C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221399 | |||||||
| chr9:100221588 | C | CCTTATCA others(9): Show |
38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-4472_274-4471i others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100221588 | ||||||
| chr9:100221621 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.274-4441G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221621 | |||||||
| chr9:100221762 | G | A | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-4300G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221762 | |||||||
| chr9:100221934 | GA | G | 5 | a0001c0001t0004g0046 a0001c0001t0004g0051 a0001c0001t0004g0052 others(2): Show |
5 | HG00280.hp2 HG02080.hp2 HG02523.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-4121delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100221934 | ||||||
| chr9:100221937 | A | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-4125A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221937 | |||||||
| chr9:100221981 | A | C | 1 | a0001c0001t0004g0047 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.274-4081A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100221981 | |||||||
| chr9:100222302 | A | G | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-3760A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100222302 | |||||||
| chr9:100222475 | T | C | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3587T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100222475 | |||||||
| chr9:100222605 | G | A | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3457G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100222605 | |||||||
| chr9:100222685 | G | A | 103 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.274-3377G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100222685 | |||||||
| chr9:100222730 | C | T | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3332C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100222730 | |||||||
| chr9:100222819 | CT | C | 19 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(16): Show |
19 | HG01109.hp1 HG02055.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.274-3226delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100222819 | ||||||
| chr9:100223020 | G | C | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-3042G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223020 | |||||||
| chr9:100223078 | CATTT | C | 2 | a0001c0001t0001g0032 a0001c0001t0001g0037 |
2 | HG01109.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.274-2967_274-2964d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100223078 | ||||||
| chr9:100223088 | T | G | 1 | a0001c0002t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.274-2974T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223088 | |||||||
| chr9:100223490 | C | CACCT | 6 | a0001c0001t0003g0086 a0001c0001t0003g0092 a0001c0001t0003g0176 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.274-2570_274-2567d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100223490 | ||||||
| chr9:100223608 | A | G | 1 | a0001c0001t0004g0116 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.274-2454A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223608 | |||||||
| chr9:100223639 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-2423G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223639 | |||||||
| chr9:100223957 | T | C | 1 | a0001c0002t0002g0118 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.274-2105T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223957 | |||||||
| chr9:100223975 | A | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-2087A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100223975 | |||||||
| chr9:100224071 | A | G | 1 | a0001c0002t0001g0129 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.274-1991A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100224071 | |||||||
| chr9:100224078 | A | C | 5 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 others(2): Show |
5 | HG02145.hp2 HG02717.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.274-1984A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100224078 | |||||||
| chr9:100224610 | T | C | 2 | a0001c0002t0002g0161 a0001c0002t0002g0162 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.274-1452T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100224610 | |||||||
| chr9:100224984 | A | C | 18 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(15): Show |
18 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.274-1078A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100224984 | |||||||
| chr9:100225054 | G | T | 1 | a0001c0002t0016g0151 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.274-1008G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225054 | |||||||
| chr9:100225062 | G | GT | 13 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0005g0005 others(10): Show |
13 | HG01081.hp1 HG01243.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.274-987dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100225062 | ||||||
| chr9:100225062 | GT | G | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-987delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100225062 | ||||||
| chr9:100225158 | C | T | 3 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0006c0007t0009g0181 |
3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.274-904C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225158 | |||||||
| chr9:100225178 | C | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.274-884C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225178 | |||||||
| chr9:100225182 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-880C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225182 | |||||||
| chr9:100225203 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-859G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225203 | |||||||
| chr9:100225218 | C | A | 1 | a0001c0001t0004g0052 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.274-844C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225218 | |||||||
| chr9:100225253 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-809C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225253 | |||||||
| chr9:100225339 | CG | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-722delG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225339 | |||||||
| chr9:100225341 | C | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.274-721C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225341 | |||||||
| chr9:100225459 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-603G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225459 | |||||||
| chr9:100225500 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-562G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225500 | |||||||
| chr9:100225731 | T | C | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.274-331T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225731 | |||||||
| chr9:100225746 | A | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-316A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225746 | |||||||
| chr9:100225750 | CA | C | 5 | a0001c0001t0001g0107 a0001c0002t0001g0108 a0001c0002t0001g0112 others(2): Show |
5 | HG02886.hp1 HG02886.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.274-304delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100225750 | ||||||
| chr9:100225754 | A | AG | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-308_274-307ins others(1): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225754 | |||||||
| chr9:100225908 | T | TATCTC | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-153_274-152ins others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chr9 | 100225908 | ||||||
| chr9:100225952 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-110G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100225952 | |||||||
| chr9:100226046 | CTT | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.274-15_274-14delTT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 3/16 | chr9 | 100226046 | |||||||
| chr9:100226600 | T | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.447+365T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100226600 | |||||||
| chr9:100226612 | A | C | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.447+377A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100226612 | |||||||
| chr9:100226706 | G | A | 60 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.447+471G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100226706 | |||||||
| chr9:100226810 | C | CA | 55 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.447+600dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100226810 | ||||||
| chr9:100226810 | C | CAA | 8 | a0001c0001t0004g0051 a0001c0001t0004g0064 a0001c0001t0004g0072 others(5): Show |
8 | HG00544.hp2 HG01175.hp1 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.447+599_447+600dup others(2): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100226810 | ||||||
| chr9:100226810 | CAAAA | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(27): Show |
30 | HG00323.hp1 HG00738.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.447+597_447+600del others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100226810 | ||||||
| chr9:100226935 | C | T | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.447+700C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100226935 | |||||||
| chr9:100226963 | C | T | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.447+728C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100226963 | |||||||
| chr9:100227264 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.447+1029G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100227264 | |||||||
| chr9:100227360 | G | T | 1 | a0001c0001t0001g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.447+1125G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100227360 | |||||||
| chr9:100227514 | ACAG | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.447+1283_447+1285d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100227514 | ||||||
| chr9:100227610 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.447+1375G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100227610 | |||||||
| chr9:100227700 | T | TAA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.447+1478_447+1479d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100227700 | ||||||
| chr9:100227991 | C | CT | 6 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0002t0001g0003 others(3): Show |
6 | HG00735.hp2 HG01081.hp1 HG01243.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-1652dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100227991 | ||||||
| chr9:100227991 | C | CTT | 94 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(91): Show |
94 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.448-1653_448-1652d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100227991 | ||||||
| chr9:100227991 | CT | C | 6 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0022g0182 others(3): Show |
6 | HG01081.hp2 HG03209.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.448-1652delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | INFO_REALIGN_3_PRIME | chr9 | 100227991 | ||||||
| chr9:100228032 | C | A | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.448-1628C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228032 | |||||||
| chr9:100228159 | T | C | 1 | a0001c0001t0001g0035 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.448-1501T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228159 | |||||||
| chr9:100228175 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.448-1485G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228175 | |||||||
| chr9:100228300 | T | C | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.448-1360T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228300 | |||||||
| chr9:100228413 | T | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.448-1247T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228413 | |||||||
| chr9:100228513 | G | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(38): Show |
41 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.448-1147G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228513 | |||||||
| chr9:100228530 | C | G | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.448-1130C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228530 | |||||||
| chr9:100228530 | C | T | 1 | a0001c0002t0001g0112 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.448-1130C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228530 | |||||||
| chr9:100228913 | A | T | 1 | a0001c0002t0001g0142 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.448-747A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100228913 | |||||||
| chr9:100229032 | G | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.448-628G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100229032 | |||||||
| chr9:100229132 | T | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.448-528T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100229132 | |||||||
| chr9:100229301 | A | G | 1 | a0001c0001t0009g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.448-359A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100229301 | |||||||
| chr9:100229402 | G | A | 3 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0006c0007t0009g0181 |
3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.448-258G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100229402 | |||||||
| chr9:100229557 | C | T | 1 | a0001c0002t0002g0114 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.448-103C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 4/16 | chr9 | 100229557 | |||||||
| chr9:100230048 | C | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+221C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230048 | |||||||
| chr9:100230054 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.615+227C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230054 | |||||||
| chr9:100230119 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+292A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230119 | |||||||
| chr9:100230267 | CCT | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+443_615+444del others(2): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 100230267 | ||||||
| chr9:100230276 | G | A | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+449G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230276 | |||||||
| chr9:100230362 | A | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+535A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230362 | |||||||
| chr9:100230405 | A | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+578A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230405 | |||||||
| chr9:100230440 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.615+613T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230440 | |||||||
| chr9:100230444 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+617G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230444 | |||||||
| chr9:100230469 | TG | T | 6 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG02451.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+643delG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230469 | |||||||
| chr9:100230532 | A | T | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+705A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230532 | |||||||
| chr9:100230674 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.615+847G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230674 | |||||||
| chr9:100230688 | T | C | 4 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0003g0178 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.615+861T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230688 | |||||||
| chr9:100230893 | G | A | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.615+1066G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100230893 | |||||||
| chr9:100231018 | T | C | 3 | a0001c0001t0004g0068 a0001c0001t0004g0069 a0001c0001t0004g0116 |
3 | NA19005.hp1 NA19012.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.615+1191T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231018 | |||||||
| chr9:100231213 | TTAAAG | T | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+1389_615+1393d others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 100231213 | ||||||
| chr9:100231293 | AT | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.615+1474delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 100231293 | ||||||
| chr9:100231337 | C | T | 1 | a0001c0002t0001g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.615+1510C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231337 | |||||||
| chr9:100231359 | AT | A | 5 | a0001c0002t0001g0143 a0001c0002t0001g0144 a0001c0002t0001g0163 others(2): Show |
5 | HG00642.hp1 HG01175.hp2 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.615+1540delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 100231359 | ||||||
| chr9:100231379 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+1552G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231379 | |||||||
| chr9:100231457 | A | G | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.615+1630A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231457 | |||||||
| chr9:100231582 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+1755C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231582 | |||||||
| chr9:100231664 | C | G | 2 | a0001c0002t0001g0143 a0001c0002t0001g0165 |
2 | HG00642.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.615+1837C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231664 | |||||||
| chr9:100231900 | C | G | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.615+2073C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231900 | |||||||
| chr9:100231927 | G | A | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+2100G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100231927 | |||||||
| chr9:100232192 | T | C | 1 | a0001c0001t0004g0067 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.615+2365T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100232192 | |||||||
| chr9:100232199 | GT | G | 6 | a0001c0001t0003g0086 a0001c0001t0003g0092 a0001c0001t0003g0176 others(3): Show |
6 | HG01069.hp2 HG01071.hp2 HG01123.hp2 others(3): Show |
intron_variant | MODIFIER | c.615+2382delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chr9 | 100232199 | ||||||
| chr9:100232567 | C | T | 3 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0006c0007t0009g0181 |
3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.615+2740C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100232567 | |||||||
| chr9:100232989 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+3162G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100232989 | |||||||
| chr9:100233131 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.615+3304G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100233131 | |||||||
| chr9:100233781 | A | G | 4 | a0001c0002t0002g0154 a0001c0002t0002g0156 a0001c0002t0002g0157 others(1): Show |
4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.615+3954A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100233781 | |||||||
| chr9:100234074 | T | C | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.615+4247T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100234074 | |||||||
| chr9:100234588 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.615+4761G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100234588 | |||||||
| chr9:100234689 | T | G | 1 | a0001c0001t0022g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.615+4862T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100234689 | |||||||
| chr9:100235215 | C | G | 1 | a0001c0001t0005g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.616-4845C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100235215 | |||||||
| chr9:100235272 | G | C | 3 | a0001c0002t0001g0144 a0001c0002t0001g0163 a0001c0002t0001g0166 |
3 | HG01952.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.616-4788G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100235272 | |||||||
| chr9:100235278 | T | C | 1 | a0001c0001t0025g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.616-4782T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100235278 | |||||||
| chr9:100235535 | C | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-4525C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100235535 | |||||||
| chr9:100236149 | G | A | 1 | a0005c0011t0002g0103 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.616-3911G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236149 | |||||||
| chr9:100236299 | T | G | 104 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.616-3761T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236299 | |||||||
| chr9:100236403 | A | G | 9 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.616-3657A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236403 | |||||||
| chr9:100236489 | G | A | 2 | a0001c0001t0005g0005 a0001c0001t0005g0010 |
2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.616-3571G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236489 | |||||||
| chr9:100236564 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.616-3496G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236564 | |||||||
| chr9:100236669 | G | A | 47 | a0001c0001t0001g0107 a0001c0001t0008g0123 a0001c0001t0008g0124 others(44): Show |
47 | HG00140.hp2 HG00323.hp2 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.616-3391G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236669 | |||||||
| chr9:100236690 | T | A | 1 | a0001c0002t0002g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.616-3370T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236690 | |||||||
| chr9:100236746 | G | T | 1 | a0001c0001t0015g0023 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.616-3314G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236746 | |||||||
| chr9:100236750 | A | C | 110 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(107): Show |
110 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.616-3310A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100236750 | |||||||
| chr9:100237105 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.616-2955C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100237105 | |||||||
| chr9:100237267 | A | C | 3 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 |
3 | HG02109.hp1 HG02897.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.616-2793A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100237267 | |||||||
| chr9:100237823 | T | C | 59 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(56): Show |
59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.616-2237T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100237823 | |||||||
| chr9:100238026 | A | G | 1 | a0001c0001t0011g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.616-2034A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238026 | |||||||
| chr9:100238035 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.616-2025C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238035 | |||||||
| chr9:100238068 | G | A | 2 | a0001c0001t0004g0073 a0004c0010t0003g0044 |
2 | HG01496.hp2 HG01952.hp2 |
intron_variant | MODIFIER | c.616-1992G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238068 | |||||||
| chr9:100238323 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.616-1737G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238323 | |||||||
| chr9:100238377 | G | A | 4 | a0001c0001t0003g0176 a0001c0001t0003g0177 a0001c0001t0003g0178 others(1): Show |
4 | HG01069.hp2 HG01071.hp2 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.616-1683G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238377 | |||||||
| chr9:100238832 | A | G | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.616-1228A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238832 | |||||||
| chr9:100238946 | C | A | 2 | a0001c0001t0013g0025 a0001c0001t0013g0026 |
2 | HG00741.hp2 HG01168.hp1 |
intron_variant | MODIFIER | c.616-1114C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100238946 | |||||||
| chr9:100239183 | G | T | 1 | a0001c0001t0007g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.616-877G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100239183 | |||||||
| chr9:100239605 | T | G | 59 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(56): Show |
59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.616-455T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100239605 | |||||||
| chr9:100239736 | C | T | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.616-324C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100239736 | |||||||
| chr9:100239770 | A | G | 7 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(4): Show |
7 | HG00733.hp2 HG02280.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.616-290A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100239770 | |||||||
| chr9:100239787 | C | T | 58 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.616-273C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100239787 | |||||||
| chr9:100240041 | T | C | 6 | a0001c0002t0001g0014 a0001c0002t0001g0016 a0001c0002t0001g0017 others(3): Show |
6 | HG02109.hp1 HG02145.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.616-19T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 5/16 | chr9 | 100240041 | |||||||
| chr9:100240264 | G | A | 1 | a0001c0002t0002g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.796+24G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240264 | |||||||
| chr9:100240474 | A | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.796+234A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240474 | |||||||
| chr9:100240756 | A | T | 1 | a0001c0002t0001g0018 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.796+516A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240756 | |||||||
| chr9:100240794 | T | C | 3 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0006c0007t0009g0181 |
3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.796+554T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240794 | |||||||
| chr9:100240834 | G | A | 1 | a0001c0001t0004g0059 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.796+594G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240834 | |||||||
| chr9:100240944 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.796+704G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100240944 | |||||||
| chr9:100241151 | T | G | 7 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(4): Show |
7 | HG00733.hp2 HG02280.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.796+911T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100241151 | |||||||
| chr9:100241350 | C | A | 104 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.796+1110C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100241350 | |||||||
| chr9:100241682 | G | A | 1 | a0001c0002t0001g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.797-888G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100241682 | |||||||
| chr9:100241996 | A | G | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.797-574A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100241996 | |||||||
| chr9:100242264 | T | C | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.797-306T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100242264 | |||||||
| chr9:100242285 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.797-285G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 6/16 | chr9 | 100242285 | |||||||
| chr9:100243437 | A | G | 1 | a0001c0002t0002g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.906+758A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243437 | |||||||
| chr9:100243487 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+808G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243487 | |||||||
| chr9:100243533 | T | C | 104 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.906+854T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243533 | |||||||
| chr9:100243604 | G | A | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.906+925G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243604 | |||||||
| chr9:100243677 | G | T | 2 | a0001c0004t0001g0109 a0001c0004t0001g0110 |
2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.906+998G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243677 | |||||||
| chr9:100243741 | A | G | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+1062A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243741 | |||||||
| chr9:100243747 | C | T | 3 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 |
3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.906+1068C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243747 | |||||||
| chr9:100243768 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.906+1089G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243768 | |||||||
| chr9:100243840 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.906+1161G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243840 | |||||||
| chr9:100243874 | A | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.906+1195A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100243874 | |||||||
| chr9:100244049 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+1370G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100244049 | |||||||
| chr9:100244304 | C | T | 1 | a0001c0002t0001g0105 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.906+1625C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100244304 | |||||||
| chr9:100244364 | A | G | 1 | a0001c0002t0001g0131 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.906+1685A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100244364 | |||||||
| chr9:100244824 | A | C | 1 | a0001c0002t0001g0057 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.907-1792A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100244824 | |||||||
| chr9:100244859 | C | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.907-1757C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100244859 | |||||||
| chr9:100245132 | C | T | 58 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.907-1484C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100245132 | |||||||
| chr9:100245208 | A | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.907-1408A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100245208 | |||||||
| chr9:100245558 | G | T | 1 | a0001c0001t0008g0123 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.907-1058G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100245558 | |||||||
| chr9:100245955 | T | A | 41 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(38): Show |
41 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(38): Show |
intron_variant | MODIFIER | c.907-661T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100245955 | |||||||
| chr9:100246106 | T | C | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.907-510T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246106 | |||||||
| chr9:100246156 | AAAAAAAG others(6): Show |
A | 1 | a0001c0002t0001g0132 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.907-448_907-436del others(13): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chr9 | 100246156 | ||||||
| chr9:100246163 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(34): Show |
37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.907-453G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246163 | |||||||
| chr9:100246182 | A | G | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.907-434A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246182 | |||||||
| chr9:100246209 | A | T | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.907-407A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246209 | |||||||
| chr9:100246378 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-238G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246378 | |||||||
| chr9:100246578 | T | C | 1 | a0001c0002t0008g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.907-38T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 7/16 | chr9 | 100246578 | |||||||
| chr9:100247029 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1078+242C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100247029 | |||||||
| chr9:100247133 | G | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1078+346G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100247133 | |||||||
| chr9:100247672 | TAAA | T | 103 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1078+890_1078+892d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr9 | 100247672 | ||||||
| chr9:100247832 | G | A | 33 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(30): Show |
33 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.1078+1045G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100247832 | |||||||
| chr9:100247910 | G | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1078+1123G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100247910 | |||||||
| chr9:100247965 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1078+1178C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100247965 | |||||||
| chr9:100248007 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1078+1220G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100248007 | |||||||
| chr9:100248390 | A | G | 1 | a0004c0010t0003g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1078+1603A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100248390 | |||||||
| chr9:100248635 | C | T | 1 | a0001c0002t0001g0016 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1078+1848C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100248635 | |||||||
| chr9:100248665 | A | C | 32 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(29): Show |
32 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(29): Show |
intron_variant | MODIFIER | c.1078+1878A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100248665 | |||||||
| chr9:100248993 | GCTT | G | 101 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1078+2211_1078+221 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr9 | 100248993 | ||||||
| chr9:100249031 | G | A | 58 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1078+2244G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249031 | |||||||
| chr9:100249305 | C | G | 38 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(35): Show |
38 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.1078+2518C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249305 | |||||||
| chr9:100249401 | A | T | 1 | a0001c0002t0027g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1078+2614A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249401 | |||||||
| chr9:100249408 | T | A | 1 | a0001c0002t0001g0142 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.1078+2621T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249408 | |||||||
| chr9:100249421 | T | G | 9 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(6): Show |
9 | HG02280.hp2 HG02451.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.1078+2634T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249421 | |||||||
| chr9:100249589 | G | C | 1 | a0001c0002t0002g0125 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1079-2694G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249589 | |||||||
| chr9:100249826 | C | T | 1 | a0001c0002t0002g0156 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1079-2457C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249826 | |||||||
| chr9:100249853 | C | G | 1 | a0001c0001t0014g0011 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1079-2430C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249853 | |||||||
| chr9:100249963 | G | T | 3 | a0001c0001t0007g0029 a0001c0001t0023g0030 a0001c0001t0024g0031 |
3 | HG02145.hp2 HG02717.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1079-2320G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100249963 | |||||||
| chr9:100250546 | G | GTGTT | 104 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(101): Show |
104 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(101): Show |
intron_variant | MODIFIER | c.1079-1735_1079-173 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chr9 | 100250546 | ||||||
| chr9:100250848 | T | C | 1 | a0006c0007t0009g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1079-1435T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100250848 | |||||||
| chr9:100250849 | C | T | 1 | a0006c0007t0009g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1079-1434C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100250849 | |||||||
| chr9:100251564 | T | G | 1 | a0001c0001t0004g0055 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1079-719T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100251564 | |||||||
| chr9:100251704 | G | A | 24 | a0001c0001t0003g0070 a0001c0001t0003g0083 a0001c0001t0003g0084 others(21): Show |
24 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(21): Show |
intron_variant | MODIFIER | c.1079-579G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100251704 | |||||||
| chr9:100251832 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1079-451T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100251832 | |||||||
| chr9:100251915 | T | C | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1079-368T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100251915 | |||||||
| chr9:100252075 | T | G | 1 | a0001c0002t0002g0121 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1079-208T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100252075 | |||||||
| chr9:100252257 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1079-26A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 8/16 | chr9 | 100252257 | |||||||
| chr9:100252736 | C | T | 101 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(98): Show |
101 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.1235-171C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 9/16 | chr9 | 100252736 | |||||||
| chr9:100252902 | T | C | 55 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(52): Show |
splice_region_variant&intron_variant | LOW | c.1235-5T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 9/16 | chr9 | 100252902 | |||||||
| chr9:100253415 | CT | C | 98 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(95): Show |
98 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(95): Show |
intron_variant | MODIFIER | c.1464+290delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100253415 | ||||||
| chr9:100253426 | T | A | 1 | a0001c0002t0002g0119 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1464+290T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253426 | |||||||
| chr9:100253588 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1464+452C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253588 | |||||||
| chr9:100253618 | A | G | 1 | a0001c0002t0001g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1464+482A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253618 | |||||||
| chr9:100253680 | T | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1464+544T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253680 | |||||||
| chr9:100253865 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1464+729G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253865 | |||||||
| chr9:100253986 | G | A | 56 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(53): Show |
56 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.1464+850G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100253986 | |||||||
| chr9:100254045 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1464+909G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254045 | |||||||
| chr9:100254117 | A | G | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1464+981A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254117 | |||||||
| chr9:100254234 | A | G | 3 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0006c0007t0009g0181 |
3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1464+1098A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254234 | |||||||
| chr9:100254376 | C | T | 1 | a0001c0002t0002g0141 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1464+1240C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254376 | |||||||
| chr9:100254556 | C | T | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1464+1420C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254556 | |||||||
| chr9:100254657 | T | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1464+1521T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254657 | |||||||
| chr9:100254658 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1464+1522G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254658 | |||||||
| chr9:100254824 | A | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1464+1688A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100254824 | |||||||
| chr9:100255256 | A | C | 4 | a0001c0001t0011g0076 a0001c0001t0011g0078 a0001c0001t0011g0081 others(1): Show |
4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1464+2120A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255256 | |||||||
| chr9:100255390 | A | G | 1 | a0003c0008t0019g0001 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1464+2254A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255390 | |||||||
| chr9:100255407 | C | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1464+2271C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255407 | |||||||
| chr9:100255487 | G | C | 1 | a0001c0002t0002g0149 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1464+2351G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255487 | |||||||
| chr9:100255536 | C | T | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1464+2400C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255536 | |||||||
| chr9:100255633 | G | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1464+2497G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255633 | |||||||
| chr9:100255899 | G | A | 6 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(3): Show |
6 | HG02451.hp2 HG02922.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1464+2763G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100255899 | |||||||
| chr9:100256095 | T | G | 9 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0034 others(6): Show |
9 | HG01109.hp1 HG02055.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.1464+2959T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256095 | |||||||
| chr9:100256113 | G | C | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1464+2977G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256113 | |||||||
| chr9:100256171 | A | C | 2 | a0001c0004t0001g0109 a0001c0004t0001g0110 |
2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1464+3035A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256171 | |||||||
| chr9:100256201 | T | C | 1 | a0001c0001t0004g0067 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1464+3065T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256201 | |||||||
| chr9:100256363 | C | A | 2 | a0001c0001t0001g0036 a0007c0006t0018g0099 |
2 | HG03130.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1464+3227C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256363 | |||||||
| chr9:100256559 | A | G | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1464+3423A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100256559 | |||||||
| chr9:100257641 | G | C | 1 | a0001c0002t0001g0131 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1464+4505G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100257641 | |||||||
| chr9:100257783 | A | C | 3 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0006c0007t0009g0181 |
3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1464+4647A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100257783 | |||||||
| chr9:100257817 | C | T | 1 | a0001c0002t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1464+4681C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100257817 | |||||||
| chr9:100258342 | G | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1464+5206G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258342 | |||||||
| chr9:100258355 | C | T | 55 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1464+5219C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258355 | |||||||
| chr9:100258413 | G | A | 3 | a0001c0001t0009g0058 a0001c0001t0024g0031 a0001c0001t0025g0056 |
3 | HG02109.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1464+5277G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258413 | |||||||
| chr9:100258477 | G | A | 1 | a0001c0002t0001g0019 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1464+5341G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258477 | |||||||
| chr9:100258715 | G | A | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1464+5579G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258715 | |||||||
| chr9:100258860 | G | C | 60 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1464+5724G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100258860 | |||||||
| chr9:100259053 | G | A | 1 | a0001c0002t0002g0158 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1465-5769G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259053 | |||||||
| chr9:100259088 | C | T | 7 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0136 others(4): Show |
7 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1465-5734C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259088 | |||||||
| chr9:100259121 | C | T | 1 | a0001c0002t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1465-5701C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259121 | |||||||
| chr9:100259252 | C | T | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1465-5570C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259252 | |||||||
| chr9:100259312 | C | G | 1 | a0001c0002t0002g0155 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1465-5510C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259312 | |||||||
| chr9:100259365 | A | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1465-5457A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259365 | |||||||
| chr9:100259557 | C | CT | 95 | a0001c0001t0001g0015 a0001c0001t0001g0020 a0001c0001t0001g0021 others(92): Show |
95 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1465-5248dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100259557 | ||||||
| chr9:100259557 | C | CTT | 6 | a0001c0001t0004g0072 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
6 | HG00544.hp2 HG02280.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-5249_1465-524 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100259557 | ||||||
| chr9:100259581 | A | T | 5 | a0001c0001t0004g0061 a0001c0001t0004g0062 a0001c0001t0004g0064 others(2): Show |
5 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.1465-5241A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259581 | |||||||
| chr9:100259802 | G | A | 1 | a0001c0002t0001g0135 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1465-5020G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259802 | |||||||
| chr9:100259903 | G | A | 4 | a0001c0001t0012g0074 a0001c0001t0012g0079 a0001c0001t0012g0080 others(1): Show |
4 | HG00423.hp2 HG00621.hp1 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.1465-4919G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100259903 | |||||||
| chr9:100260113 | G | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1465-4709G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260113 | |||||||
| chr9:100260171 | A | G | 3 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0006c0007t0009g0181 |
3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1465-4651A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260171 | |||||||
| chr9:100260186 | C | CT | 19 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(16): Show |
19 | HG00140.hp1 HG00323.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.1465-4616dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100260186 | ||||||
| chr9:100260186 | C | CTT | 15 | a0001c0001t0003g0086 a0001c0001t0003g0090 a0001c0001t0003g0091 others(12): Show |
15 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.1465-4617_1465-461 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100260186 | ||||||
| chr9:100260186 | CT | C | 6 | a0001c0001t0004g0055 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
6 | HG02280.hp1 HG02970.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.1465-4616delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100260186 | ||||||
| chr9:100260193 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1465-4629T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260193 | |||||||
| chr9:100260198 | T | C | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1465-4624T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260198 | |||||||
| chr9:100260312 | C | T | 1 | a0001c0002t0001g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1465-4510C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260312 | |||||||
| chr9:100260357 | T | C | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1465-4465T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260357 | |||||||
| chr9:100260709 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1465-4113A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100260709 | |||||||
| chr9:100261069 | A | G | 1 | a0006c0007t0009g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1465-3753A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261069 | |||||||
| chr9:100261095 | A | G | 1 | a0001c0002t0001g0169 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1465-3727A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261095 | |||||||
| chr9:100261117 | T | G | 3 | a0001c0002t0001g0127 a0001c0002t0001g0132 a0001c0002t0003g0130 |
3 | HG00741.hp1 HG01069.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.1465-3705T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261117 | |||||||
| chr9:100261299 | T | C | 3 | a0001c0001t0009g0058 a0001c0001t0024g0031 a0001c0001t0025g0056 |
3 | HG02109.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1465-3523T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261299 | |||||||
| chr9:100261896 | T | A | 1 | a0006c0007t0009g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1465-2926T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261896 | |||||||
| chr9:100261950 | GT | G | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1465-2870delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100261950 | ||||||
| chr9:100261997 | T | G | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1465-2825T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100261997 | |||||||
| chr9:100262038 | A | AT | 41 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(38): Show |
41 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(38): Show |
intron_variant | MODIFIER | c.1465-2774dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262038 | ||||||
| chr9:100262088 | T | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1465-2734T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100262088 | |||||||
| chr9:100262197 | A | G | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465-2625A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100262197 | |||||||
| chr9:100262238 | CA | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1465-2573delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262238 | ||||||
| chr9:100262638 | TA | T | 30 | a0001c0001t0001g0020 a0001c0001t0001g0107 a0001c0001t0009g0058 others(27): Show |
30 | HG00280.hp1 HG00423.hp1 HG00544.hp1 others(27): Show |
intron_variant | MODIFIER | c.1465-2161delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262638 | ||||||
| chr9:100262638 | TAA | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0021 others(34): Show |
37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.1465-2162_1465-216 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262638 | ||||||
| chr9:100262638 | TAAA | T | 52 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(49): Show |
52 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(49): Show |
intron_variant | MODIFIER | c.1465-2163_1465-216 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262638 | ||||||
| chr9:100262742 | CTTGT | C | 55 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1465-2065_1465-206 others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100262742 | ||||||
| chr9:100262942 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1465-1880T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100262942 | |||||||
| chr9:100262960 | G | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1465-1862G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100262960 | |||||||
| chr9:100263167 | T | TAGAAGTG others(320): Show |
4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1465-1639_1465-163 others(331): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100263167 | ||||||
| chr9:100263297 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1465-1525T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100263297 | |||||||
| chr9:100263511 | T | C | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465-1311T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100263511 | |||||||
| chr9:100263552 | C | T | 60 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1465-1270C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100263552 | |||||||
| chr9:100263656 | T | A | 1 | a0001c0001t0028g0075 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1465-1166T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100263656 | |||||||
| chr9:100264275 | T | G | 1 | a0001c0002t0027g0113 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1465-547T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100264275 | |||||||
| chr9:100264496 | T | C | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1465-326T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100264496 | |||||||
| chr9:100264618 | C | CA | 40 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(37): Show |
40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1465-188dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100264618 | ||||||
| chr9:100264618 | CA | C | 60 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1465-188delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chr9 | 100264618 | ||||||
| chr9:100264731 | G | A | 2 | a0001c0001t0009g0100 a0001c0001t0009g0101 |
2 | HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1465-91G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 10/16 | chr9 | 100264731 | |||||||
| chr9:100264944 | C | CT | 7 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0001c0001t0010g0136 others(4): Show |
7 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(4): Show |
intron_variant | MODIFIER | c.1571+32dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100264944 | ||||||
| chr9:100265165 | G | A | 7 | a0002c0003t0006g0088 a0002c0003t0006g0093 a0002c0003t0006g0094 others(4): Show |
7 | HG00735.hp1 HG00738.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.1571+237G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265165 | |||||||
| chr9:100265225 | G | A | 1 | a0001c0002t0002g0160 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1571+297G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265225 | |||||||
| chr9:100265408 | A | C | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1571+480A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265408 | |||||||
| chr9:100265573 | C | G | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1571+645C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265573 | |||||||
| chr9:100265710 | G | A | 1 | a0001c0002t0001g0108 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1571+782G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265710 | |||||||
| chr9:100265923 | A | T | 42 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(39): Show |
42 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(39): Show |
intron_variant | MODIFIER | c.1571+995A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100265923 | |||||||
| chr9:100266040 | A | G | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1571+1112A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100266040 | |||||||
| chr9:100266281 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1571+1353C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100266281 | |||||||
| chr9:100266770 | G | C | 1 | a0001c0001t0003g0085 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1571+1842G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100266770 | |||||||
| chr9:100266957 | C | G | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1571+2029C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100266957 | |||||||
| chr9:100267019 | T | TA | 75 | a0001c0001t0001g0034 a0001c0001t0001g0107 a0001c0001t0001g0147 others(72): Show |
75 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(72): Show |
intron_variant | MODIFIER | c.1571+2115dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100267019 | ||||||
| chr9:100267019 | T | TAA | 57 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(54): Show |
57 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1571+2114_1571+211 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100267019 | ||||||
| chr9:100267019 | TA | T | 39 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(36): Show |
39 | HG00642.hp2 HG00733.hp2 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.1571+2115delA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100267019 | ||||||
| chr9:100267121 | C | T | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1571+2193C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100267121 | |||||||
| chr9:100267421 | A | G | 58 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.1571+2493A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100267421 | |||||||
| chr9:100267557 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1571+2629A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100267557 | |||||||
| chr9:100267806 | G | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1571+2878G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100267806 | |||||||
| chr9:100267885 | G | A | 1 | a0001c0002t0001g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1571+2957G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100267885 | |||||||
| chr9:100268037 | C | T | 1 | a0001c0001t0001g0004 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1571+3109C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100268037 | |||||||
| chr9:100269173 | T | C | 2 | a0001c0004t0001g0109 a0001c0004t0001g0110 |
2 | HG03225.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1572-3691T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100269173 | |||||||
| chr9:100269371 | AT | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1572-3485delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100269371 | ||||||
| chr9:100269790 | G | A | 1 | a0001c0002t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1572-3074G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100269790 | |||||||
| chr9:100269805 | T | C | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1572-3059T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100269805 | |||||||
| chr9:100270042 | AT | A | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1572-2821delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100270042 | |||||||
| chr9:100270048 | T | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1572-2816T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100270048 | |||||||
| chr9:100270050 | A | G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1572-2814A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100270050 | |||||||
| chr9:100270121 | A | AT | 59 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(56): Show |
59 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(56): Show |
intron_variant | MODIFIER | c.1572-2733dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100270121 | ||||||
| chr9:100270609 | G | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1572-2255G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100270609 | |||||||
| chr9:100270748 | C | CA | 26 | a0001c0001t0004g0047 a0001c0001t0004g0059 a0001c0001t0004g0065 others(23): Show |
26 | HG00609.hp2 HG00621.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.1572-2092dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100270748 | ||||||
| chr9:100270748 | C | CAA | 25 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(22): Show |
25 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.1572-2093_1572-209 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100270748 | ||||||
| chr9:100270748 | C | CAAA | 11 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0035 others(8): Show |
11 | HG00741.hp2 HG01106.hp1 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.1572-2094_1572-209 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | INFO_REALIGN_3_PRIME | chr9 | 100270748 | ||||||
| chr9:100270853 | A | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1572-2011A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100270853 | |||||||
| chr9:100271070 | A | G | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1572-1794A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271070 | |||||||
| chr9:100271136 | G | C | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1572-1728G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271136 | |||||||
| chr9:100271557 | T | C | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1572-1307T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271557 | |||||||
| chr9:100271648 | C | T | 1 | a0002c0003t0021g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1572-1216C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271648 | |||||||
| chr9:100271800 | C | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1572-1064C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271800 | |||||||
| chr9:100271907 | C | T | 1 | a0001c0001t0007g0050 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1572-957C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271907 | |||||||
| chr9:100271908 | A | G | 103 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(100): Show |
103 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(100): Show |
intron_variant | MODIFIER | c.1572-956A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100271908 | |||||||
| chr9:100272059 | G | T | 1 | a0001c0001t0001g0146 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1572-805G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272059 | |||||||
| chr9:100272090 | A | G | 1 | a0001c0002t0001g0111 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1572-774A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272090 | |||||||
| chr9:100272160 | G | T | 1 | a0001c0001t0025g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1572-704G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272160 | |||||||
| chr9:100272429 | A | G | 1 | a0001c0002t0002g0160 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1572-435A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272429 | |||||||
| chr9:100272546 | G | A | 55 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1572-318G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 11/16 | chr9 | 100272546 | |||||||
| chr9:100273180 | T | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784+104T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273180 | |||||||
| chr9:100273219 | T | G | 1 | a0001c0002t0002g0041 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1784+143T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273219 | |||||||
| chr9:100273473 | G | C | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784+397G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273473 | |||||||
| chr9:100273527 | C | CT | 42 | a0001c0001t0001g0107 a0001c0001t0004g0116 a0001c0002t0001g0003 others(39): Show |
42 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(39): Show |
intron_variant | MODIFIER | c.1784+478dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100273527 | ||||||
| chr9:100273527 | C | CTT | 5 | a0001c0002t0001g0014 a0001c0002t0002g0041 a0001c0002t0002g0125 others(2): Show |
5 | HG00140.hp2 HG01192.hp1 HG02056.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784+477_1784+478d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100273527 | ||||||
| chr9:100273527 | CT | C | 12 | a0001c0001t0001g0034 a0001c0001t0005g0013 a0001c0001t0009g0058 others(9): Show |
12 | HG02055.hp1 HG02145.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1784+478delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100273527 | ||||||
| chr9:100273527 | CTT | C | 26 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(23): Show |
26 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.1784+477_1784+478d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100273527 | ||||||
| chr9:100273527 | CTTTTTTT others(8): Show |
C | 60 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1784+464_1784+478d others(17): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100273527 | ||||||
| chr9:100273682 | C | T | 1 | a0001c0002t0001g0169 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1784+606C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273682 | |||||||
| chr9:100273694 | C | T | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1784+618C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273694 | |||||||
| chr9:100273728 | G | C | 1 | a0001c0001t0004g0055 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1784+652G>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273728 | |||||||
| chr9:100273787 | C | T | 57 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(54): Show |
57 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1784+711C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273787 | |||||||
| chr9:100273975 | C | T | 11 | a0001c0001t0004g0116 a0001c0002t0002g0102 a0001c0002t0002g0114 others(8): Show |
11 | HG00609.hp2 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1784+899C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100273975 | |||||||
| chr9:100274122 | C | T | 1 | a0001c0001t0004g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1784+1046C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100274122 | |||||||
| chr9:100274345 | C | CA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1784+1270dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100274345 | ||||||
| chr9:100274515 | C | CT | 7 | a0001c0002t0001g0127 a0001c0002t0001g0128 a0001c0002t0001g0129 others(4): Show |
7 | HG00280.hp1 HG00741.hp1 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.1784+1448dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100274515 | ||||||
| chr9:100274566 | A | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1784+1490A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100274566 | |||||||
| chr9:100274597 | C | T | 60 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(57): Show |
60 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.1784+1521C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100274597 | |||||||
| chr9:100275007 | C | T | 3 | a0001c0002t0001g0144 a0001c0002t0001g0163 a0001c0002t0001g0166 |
3 | HG01952.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1784+1931C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100275007 | |||||||
| chr9:100275666 | T | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784+2590T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100275666 | |||||||
| chr9:100275763 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1784+2687G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100275763 | |||||||
| chr9:100275840 | A | G | 1 | a0001c0001t0007g0029 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1784+2764A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100275840 | |||||||
| chr9:100275911 | C | T | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.1784+2835C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100275911 | |||||||
| chr9:100276371 | C | G | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1784+3295C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276371 | |||||||
| chr9:100276374 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1784+3298G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276374 | |||||||
| chr9:100276438 | T | C | 55 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.1784+3362T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276438 | |||||||
| chr9:100276489 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1784+3413C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276489 | |||||||
| chr9:100276554 | G | A | 1 | a0001c0001t0004g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1784+3478G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276554 | |||||||
| chr9:100276915 | T | C | 102 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(99): Show |
102 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(99): Show |
intron_variant | MODIFIER | c.1784+3839T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100276915 | |||||||
| chr9:100277015 | G | A | 3 | a0001c0001t0009g0058 a0001c0001t0024g0031 a0001c0001t0025g0056 |
3 | HG02109.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1784+3939G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100277015 | |||||||
| chr9:100277821 | C | T | 1 | a0001c0001t0024g0031 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1784+4745C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100277821 | |||||||
| chr9:100278231 | C | CA | 7 | a0001c0001t0005g0007 a0001c0001t0005g0009 a0001c0002t0002g0140 others(4): Show |
7 | HG01167.hp2 HG01975.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.1784+5179dupA | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100278231 | ||||||
| chr9:100278231 | C | CAA | 95 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(92): Show |
95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.1784+5178_1784+517 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100278231 | ||||||
| chr9:100278231 | C | CAAA | 12 | a0001c0001t0001g0034 a0001c0001t0001g0040 a0001c0001t0001g0107 others(9): Show |
12 | HG00735.hp2 HG02055.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.1784+5177_1784+517 others(7): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100278231 | ||||||
| chr9:100278231 | C | CAAAAAAA others(4): Show |
4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1784+5169_1784+517 others(15): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100278231 | ||||||
| chr9:100278381 | G | A | 63 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(60): Show |
63 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1784+5305G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278381 | |||||||
| chr9:100278646 | T | C | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1784+5570T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278646 | |||||||
| chr9:100278667 | T | C | 1 | a0001c0001t0009g0101 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1784+5591T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278667 | |||||||
| chr9:100278729 | T | C | 1 | a0001c0001t0003g0089 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1785-5591T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278729 | |||||||
| chr9:100278837 | A | C | 62 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(59): Show |
62 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.1785-5483A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278837 | |||||||
| chr9:100278867 | C | G | 63 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(60): Show |
63 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.1785-5453C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100278867 | |||||||
| chr9:100279062 | G | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(37): Show |
40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1785-5258G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100279062 | |||||||
| chr9:100279156 | G | A | 3 | a0001c0002t0001g0144 a0001c0002t0001g0163 a0001c0002t0001g0166 |
3 | HG01952.hp1 HG02922.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1785-5164G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100279156 | |||||||
| chr9:100279524 | A | G | 1 | a0001c0001t0004g0051 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1785-4796A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100279524 | |||||||
| chr9:100279987 | C | G | 1 | a0001c0001t0001g0033 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1785-4333C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100279987 | |||||||
| chr9:100280129 | T | G | 3 | a0001c0001t0009g0100 a0001c0001t0009g0101 a0006c0007t0009g0181 |
3 | HG03209.hp2 HG03453.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1785-4191T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100280129 | |||||||
| chr9:100280808 | C | G | 40 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(37): Show |
40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.1785-3512C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100280808 | |||||||
| chr9:100280999 | T | C | 57 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(54): Show |
57 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1785-3321T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100280999 | |||||||
| chr9:100281037 | T | C | 57 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(54): Show |
57 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(54): Show |
intron_variant | MODIFIER | c.1785-3283T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100281037 | |||||||
| chr9:100281061 | T | G | 1 | a0001c0001t0022g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1785-3259T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100281061 | |||||||
| chr9:100281689 | T | C | 18 | a0001c0001t0003g0042 a0001c0001t0003g0085 a0001c0001t0003g0086 others(15): Show |
18 | HG00735.hp1 HG00738.hp1 HG01069.hp2 others(15): Show |
intron_variant | MODIFIER | c.1785-2631T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100281689 | |||||||
| chr9:100281733 | A | C | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.1785-2587A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100281733 | |||||||
| chr9:100281740 | T | C | 1 | a0001c0001t0003g0086 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1785-2580T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100281740 | |||||||
| chr9:100282017 | G | T | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1785-2303G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282017 | |||||||
| chr9:100282075 | A | G | 1 | a0001c0001t0022g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1785-2245A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282075 | |||||||
| chr9:100282103 | C | G | 3 | a0001c0001t0009g0058 a0001c0001t0024g0031 a0001c0001t0025g0056 |
3 | HG02109.hp2 HG02145.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1785-2217C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282103 | |||||||
| chr9:100282170 | C | A | 31 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(28): Show |
31 | HG00140.hp1 HG00280.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.1785-2150C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282170 | |||||||
| chr9:100282546 | T | C | 4 | a0001c0001t0011g0076 a0001c0001t0011g0078 a0001c0001t0011g0081 others(1): Show |
4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1785-1774T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282546 | |||||||
| chr9:100282813 | G | GTA | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.1785-1504_1785-150 others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chr9 | 100282813 | ||||||
| chr9:100282927 | T | C | 1 | a0001c0001t0004g0055 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1785-1393T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100282927 | |||||||
| chr9:100283196 | C | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1785-1124C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100283196 | |||||||
| chr9:100283324 | A | G | 6 | a0001c0001t0009g0058 a0001c0001t0009g0100 a0001c0001t0009g0101 others(3): Show |
6 | HG00733.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1785-996A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100283324 | |||||||
| chr9:100283582 | C | T | 3 | a0001c0002t0001g0016 a0001c0002t0001g0017 a0001c0002t0001g0018 |
3 | HG02109.hp1 HG02897.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1785-738C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100283582 | |||||||
| chr9:100283799 | C | T | 105 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.1785-521C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100283799 | |||||||
| chr9:100283870 | T | C | 1 | a0001c0001t0010g0137 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1785-450T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100283870 | |||||||
| chr9:100284026 | G | A | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1785-294G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 12/16 | chr9 | 100284026 | |||||||
| chr9:100284634 | G | A | 37 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(34): Show |
37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2068+31G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100284634 | |||||||
| chr9:100284889 | T | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(103): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2068+286T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100284889 | |||||||
| chr9:100284928 | G | T | 1 | a0001c0001t0017g0063 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2068+325G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100284928 | |||||||
| chr9:100285097 | A | G | 4 | a0001c0001t0009g0058 a0001c0001t0009g0100 a0001c0001t0009g0101 others(1): Show |
4 | HG03098.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+494A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285097 | |||||||
| chr9:100285358 | C | G | 56 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(53): Show |
56 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.2068+755C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285358 | |||||||
| chr9:100285467 | C | A | 6 | a0001c0001t0009g0058 a0001c0001t0009g0100 a0001c0001t0009g0101 others(3): Show |
6 | HG00733.hp2 HG03098.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.2068+864C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285467 | |||||||
| chr9:100285634 | G | A | 2 | a0001c0001t0011g0076 a0001c0001t0013g0071 |
2 | HG02602.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.2068+1031G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285634 | |||||||
| chr9:100285673 | C | T | 1 | a0001c0001t0004g0051 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.2068+1070C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285673 | |||||||
| chr9:100285918 | T | C | 1 | a0001c0002t0001g0082 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2068+1315T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100285918 | |||||||
| chr9:100286057 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2068+1454G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286057 | |||||||
| chr9:100286067 | A | G | 58 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.2068+1464A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286067 | |||||||
| chr9:100286071 | G | A | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2068+1468G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286071 | |||||||
| chr9:100286118 | T | C | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2068+1515T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286118 | |||||||
| chr9:100286169 | T | C | 1 | a0001c0001t0022g0182 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2068+1566T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286169 | |||||||
| chr9:100286395 | A | C | 25 | a0001c0001t0003g0070 a0001c0001t0003g0083 a0001c0001t0003g0084 others(22): Show |
25 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.2068+1792A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286395 | |||||||
| chr9:100286730 | T | C | 1 | a0001c0002t0001g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2068+2127T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286730 | |||||||
| chr9:100286962 | T | C | 58 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.2068+2359T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286962 | |||||||
| chr9:100286975 | C | G | 1 | a0001c0002t0008g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2068+2372C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100286975 | |||||||
| chr9:100287174 | A | G | 1 | a0001c0002t0002g0154 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2068+2571A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287174 | |||||||
| chr9:100287204 | G | A | 1 | a0001c0001t0003g0042 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2068+2601G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287204 | |||||||
| chr9:100287276 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2068+2673G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287276 | |||||||
| chr9:100287351 | C | T | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2068+2748C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287351 | |||||||
| chr9:100287582 | T | C | 4 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(1): Show |
4 | HG02486.hp1 HG02809.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+2979T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287582 | |||||||
| chr9:100287827 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+3224G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287827 | |||||||
| chr9:100287846 | T | C | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+3243T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287846 | |||||||
| chr9:100287939 | G | T | 2 | a0001c0001t0024g0031 a0001c0001t0025g0056 |
2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2068+3336G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100287939 | |||||||
| chr9:100288065 | C | T | 4 | a0001c0002t0002g0154 a0001c0002t0002g0156 a0001c0002t0002g0157 others(1): Show |
4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.2068+3462C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288065 | |||||||
| chr9:100288125 | C | T | 63 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(60): Show |
63 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(60): Show |
intron_variant | MODIFIER | c.2068+3522C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288125 | |||||||
| chr9:100288255 | C | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2068+3652C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288255 | |||||||
| chr9:100288669 | G | A | 1 | a0001c0002t0002g0139 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2069-3657G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288669 | |||||||
| chr9:100288855 | G | A | 55 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(52): Show |
55 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.2069-3471G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288855 | |||||||
| chr9:100288896 | G | A | 1 | a0001c0002t0008g0126 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2069-3430G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288896 | |||||||
| chr9:100288923 | C | T | 43 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(40): Show |
43 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(40): Show |
intron_variant | MODIFIER | c.2069-3403C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288923 | |||||||
| chr9:100288968 | TG | T | 37 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(34): Show |
37 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(34): Show |
intron_variant | MODIFIER | c.2069-3356delG | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 100288968 | ||||||
| chr9:100288973 | G | A | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-3353G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100288973 | |||||||
| chr9:100289046 | A | G | 1 | a0001c0001t0015g0024 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2069-3280A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100289046 | |||||||
| chr9:100289995 | G | A | 2 | a0001c0001t0001g0034 a0001c0001t0001g0035 |
2 | HG02055.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2069-2331G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100289995 | |||||||
| chr9:100290086 | G | GT | 64 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(61): Show |
64 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.2069-2230dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 100290086 | ||||||
| chr9:100290317 | A | C | 1 | a0001c0001t0003g0045 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.2069-2009A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290317 | |||||||
| chr9:100290389 | G | A | 35 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(32): Show |
35 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.2069-1937G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290389 | |||||||
| chr9:100290516 | A | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(103): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2069-1810A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290516 | |||||||
| chr9:100290632 | G | A | 2 | a0001c0002t0002g0102 a0001c0002t0002g0114 |
2 | NA18964.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.2069-1694G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290632 | |||||||
| chr9:100290903 | A | G | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2069-1423A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290903 | |||||||
| chr9:100290913 | A | T | 1 | a0001c0001t0004g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2069-1413A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100290913 | |||||||
| chr9:100291071 | AT | A | 40 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(37): Show |
40 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(37): Show |
intron_variant | MODIFIER | c.2069-1243delT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 100291071 | ||||||
| chr9:100291224 | C | T | 1 | a0001c0002t0003g0130 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.2069-1102C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291224 | |||||||
| chr9:100291256 | A | G | 154 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(151): Show |
154 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.2069-1070A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291256 | |||||||
| chr9:100291317 | C | A | 1 | a0001c0002t0002g0134 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.2069-1009C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291317 | |||||||
| chr9:100291461 | TGA | T | 4 | a0001c0001t0009g0058 a0001c0001t0009g0100 a0001c0001t0009g0101 others(1): Show |
4 | HG03098.hp2 HG03209.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-860_2069-859d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 100291461 | ||||||
| chr9:100291562 | C | T | 1 | a0004c0010t0003g0044 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2069-764C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291562 | |||||||
| chr9:100291579 | T | G | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2069-747T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291579 | |||||||
| chr9:100291795 | C | CT | 2 | a0001c0001t0024g0031 a0001c0001t0025g0056 |
2 | HG02109.hp2 HG02145.hp2 |
intron_variant | MODIFIER | c.2069-530dupT | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chr9 | 100291795 | ||||||
| chr9:100291908 | A | C | 106 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(103): Show |
106 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.2069-418A>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100291908 | |||||||
| chr9:100292048 | C | A | 1 | a0001c0002t0001g0172 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2069-278C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100292048 | |||||||
| chr9:100292286 | C | A | 1 | a0001c0001t0005g0006 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2069-40C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 13/16 | chr9 | 100292286 | |||||||
| chr9:100293554 | T | C | 1 | a0001c0001t0001g0034 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2786+511T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100293554 | |||||||
| chr9:100293656 | G | A | 64 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(61): Show |
64 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.2786+613G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100293656 | |||||||
| chr9:100293715 | G | T | 61 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(58): Show |
61 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(58): Show |
intron_variant | MODIFIER | c.2786+672G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100293715 | |||||||
| chr9:100293885 | G | A | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2786+842G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100293885 | |||||||
| chr9:100293985 | C | T | 105 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(102): Show |
105 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.2786+942C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100293985 | |||||||
| chr9:100294011 | TACA | T | 5 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2786+973_2786+975d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chr9 | 100294011 | ||||||
| chr9:100294337 | T | C | 1 | a0001c0002t0002g0118 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.2786+1294T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100294337 | |||||||
| chr9:100294707 | G | A | 1 | a0001c0009t0007g0049 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2786+1664G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100294707 | |||||||
| chr9:100294808 | T | A | 1 | a0001c0002t0001g0145 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.2786+1765T>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100294808 | |||||||
| chr9:100294879 | C | T | 2 | a0001c0002t0001g0082 a0001c0002t0001g0174 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2786+1836C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100294879 | |||||||
| chr9:100295235 | A | T | 58 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(55): Show |
58 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(55): Show |
intron_variant | MODIFIER | c.2787-1682A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295235 | |||||||
| chr9:100295268 | T | C | 1 | a0001c0002t0001g0169 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.2787-1649T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295268 | |||||||
| chr9:100295439 | A | G | 25 | a0001c0001t0003g0070 a0001c0001t0003g0083 a0001c0001t0003g0084 others(22): Show |
25 | HG00423.hp2 HG00544.hp2 HG00609.hp1 others(22): Show |
intron_variant | MODIFIER | c.2787-1478A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295439 | |||||||
| chr9:100295649 | C | A | 2 | a0003c0005t0020g0002 a0003c0008t0019g0001 |
2 | HG00733.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.2787-1268C>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295649 | |||||||
| chr9:100295811 | C | G | 56 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0070 others(53): Show |
56 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.2787-1106C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295811 | |||||||
| chr9:100295943 | C | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2787-974C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100295943 | |||||||
| chr9:100296204 | A | G | 2 | a0001c0002t0001g0082 a0001c0002t0001g0174 |
2 | HG03453.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2787-713A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296204 | |||||||
| chr9:100296389 | C | T | 4 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(1): Show |
4 | HG02280.hp1 HG02970.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.2787-528C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296389 | |||||||
| chr9:100296417 | G | T | 89 | a0001c0001t0001g0146 a0001c0001t0001g0147 a0001c0001t0003g0042 others(86): Show |
89 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(86): Show |
intron_variant | MODIFIER | c.2787-500G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296417 | |||||||
| chr9:100296487 | G | A | 4 | a0001c0001t0011g0076 a0001c0001t0011g0078 a0001c0001t0011g0081 others(1): Show |
4 | HG01106.hp1 HG02602.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.2787-430G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296487 | |||||||
| chr9:100296506 | C | T | 8 | a0001c0001t0009g0058 a0001c0001t0009g0100 a0001c0001t0009g0101 others(5): Show |
8 | HG02280.hp1 HG02970.hp2 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.2787-411C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296506 | |||||||
| chr9:100296649 | C | T | 19 | a0001c0001t0005g0006 a0001c0001t0005g0007 a0001c0001t0005g0009 others(16): Show |
19 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(16): Show |
intron_variant | MODIFIER | c.2787-268C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296649 | |||||||
| chr9:100296894 | C | G | 21 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(18): Show |
21 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.2787-23C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 14/16 | chr9 | 100296894 | |||||||
| chr9:100297194 | A | G | 115 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(112): Show |
115 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(112): Show |
intron_variant | MODIFIER | c.3016+48A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 15/16 | chr9 | 100297194 | |||||||
| chr9:100297553 | G | A | 4 | a0001c0002t0002g0154 a0001c0002t0002g0156 a0001c0002t0002g0157 others(1): Show |
4 | HG00733.hp1 HG01074.hp2 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.3017-383G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 15/16 | chr9 | 100297553 | |||||||
| chr9:100297931 | T | G | 1 | a0001c0001t0011g0081 | 1 | HG03831.hp1 | splice_region_variant&intron_variant | LOW | c.3017-5T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 15/16 | chr9 | 100297931 | |||||||
| chr9:100298104 | T | G | 124 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(121): Show |
124 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.3091+94T>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298104 | |||||||
| chr9:100298350 | A | G | 2 | a0001c0002t0001g0108 a0001c0002t0001g0135 |
2 | HG02886.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.3091+340A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298350 | |||||||
| chr9:100298389 | A | G | 1 | a0001c0001t0003g0070 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.3091+379A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298389 | |||||||
| chr9:100298437 | G | A | 24 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(21): Show |
24 | HG00323.hp1 HG00642.hp2 HG00733.hp2 others(21): Show |
intron_variant | MODIFIER | c.3091+427G>A | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298437 | |||||||
| chr9:100298597 | G | T | 1 | a0001c0002t0001g0168 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.3091+587G>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298597 | |||||||
| chr9:100298636 | C | T | 21 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(18): Show |
21 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.3091+626C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100298636 | |||||||
| chr9:100298874 | AAAAC | A | 25 | a0001c0001t0005g0005 a0001c0001t0005g0006 a0001c0001t0005g0007 others(22): Show |
25 | HG00323.hp1 HG00642.hp2 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.3091+876_3091+879d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100298874 | ||||||
| chr9:100299084 | A | G | 92 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(89): Show |
92 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(89): Show |
intron_variant | MODIFIER | c.3091+1074A>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100299084 | |||||||
| chr9:100299207 | T | C | 1 | a0001c0001t0011g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3091+1197T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100299207 | |||||||
| chr9:100299501 | CCAGCCTT others(80): Show |
C | 2 | a0001c0002t0002g0119 a0001c0002t0002g0152 |
2 | HG00735.hp2 HG02080.hp1 |
intron_variant | MODIFIER | c.3092-1012_3092-926 others(90): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299501 | ||||||
| chr9:100299554 | C | CAACACAC others(93): Show |
2 | a0001c0001t0005g0005 a0001c0001t0005g0010 |
2 | HG02451.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3092-978_3092-977i others(102): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299554 | ||||||
| chr9:100299554 | C | CAACACAC others(91): Show |
1 | a0001c0001t0005g0006 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.3092-978_3092-977i others(100): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299554 | ||||||
| chr9:100299554 | C | CAACACAC others(75): Show |
1 | a0001c0001t0025g0056 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3092-980_3092-979i others(84): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299554 | ||||||
| chr9:100299555 | A | AAC | 13 | a0001c0001t0004g0043 a0001c0001t0004g0055 a0001c0001t0004g0062 others(10): Show |
13 | HG01496.hp2 HG02056.hp1 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.3092-979_3092-978d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | ||||||
| chr9:100299555 | A | AACACACA others(9): Show |
1 | a0003c0005t0020g0002 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3092-993_3092-978d others(18): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | ||||||
| chr9:100299555 | A | AACACACA others(11): Show |
1 | a0003c0008t0019g0001 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.3092-995_3092-978d others(20): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | ||||||
| chr9:100299555 | A | AACACACA others(13): Show |
1 | a0001c0001t0001g0147 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.3092-997_3092-978d others(22): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | ||||||
| chr9:100299555 | A | AACACACA others(19): Show |
1 | a0001c0001t0001g0146 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.3092-1003_3092-978 others(29): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | ||||||
| chr9:100299555 | AAC | A | 8 | a0001c0001t0004g0064 a0001c0001t0009g0058 a0001c0001t0009g0100 others(5): Show |
8 | HG02145.hp2 HG02280.hp1 HG03098.hp2 others(5): Show |
intron_variant | MODIFIER | c.3092-979_3092-978d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | ||||||
| chr9:100299555 | AACAC | A | 11 | a0001c0001t0003g0045 a0001c0001t0003g0090 a0001c0001t0003g0091 others(8): Show |
11 | HG00140.hp1 HG00735.hp1 HG00738.hp1 others(8): Show |
intron_variant | MODIFIER | c.3092-981_3092-978d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | ||||||
| chr9:100299555 | AACACACA others(15): Show |
A | 86 | a0001c0001t0001g0004 a0001c0001t0001g0020 a0001c0001t0001g0021 others(83): Show |
86 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(83): Show |
intron_variant | MODIFIER | c.3092-999_3092-978d others(24): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299555 | ||||||
| chr9:100299557 | C | CACACACA others(93): Show |
2 | a0001c0001t0005g0012 a0001c0001t0005g0013 |
2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3092-978_3092-977i others(102): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299557 | ||||||
| chr9:100299557 | C | CACACACA others(85): Show |
1 | a0001c0001t0005g0009 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3092-978_3092-977i others(94): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299557 | ||||||
| chr9:100299557 | C | CACACACA others(83): Show |
2 | a0001c0001t0005g0007 a0001c0001t0014g0011 |
2 | HG02280.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3092-978_3092-977i others(92): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299557 | ||||||
| chr9:100299557 | C | CACACACA others(79): Show |
7 | a0001c0001t0011g0076 a0001c0001t0011g0078 a0001c0001t0011g0081 others(4): Show |
7 | HG00741.hp2 HG01106.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.3092-978_3092-977i others(88): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299557 | ||||||
| chr9:100299557 | C | CACACACA others(73): Show |
1 | a0001c0001t0026g0008 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3092-980_3092-979i others(82): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299557 | ||||||
| chr9:100299568 | A | AGCCTTGC others(37): Show |
1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3092-1000_3092-999 others(47): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100299568 | |||||||
| chr9:100299569 | C | G | 1 | a0001c0001t0001g0015 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.3092-999C>G | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100299569 | |||||||
| chr9:100299604 | CCCA | C | 6 | a0001c0001t0004g0061 a0001c0001t0004g0062 a0001c0001t0004g0064 others(3): Show |
6 | HG00609.hp1 HG02056.hp1 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.3092-960_3092-958d others(5): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299604 | ||||||
| chr9:100299635 | G | GAC | 11 | a0001c0001t0004g0046 a0001c0001t0004g0051 a0001c0001t0004g0052 others(8): Show |
11 | HG00280.hp2 HG00741.hp2 HG01168.hp1 others(8): Show |
intron_variant | MODIFIER | c.3092-888_3092-887d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | ||||||
| chr9:100299635 | G | GACAAACA others(77): Show |
1 | a0001c0001t0011g0022 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3092-930_3092-929i others(86): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | ||||||
| chr9:100299635 | G | GACAC | 2 | a0001c0001t0008g0123 a0001c0001t0008g0124 |
2 | HG02523.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.3092-890_3092-887d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | ||||||
| chr9:100299635 | GAC | G | 21 | a0001c0001t0003g0070 a0001c0001t0003g0083 a0001c0001t0003g0089 others(18): Show |
21 | HG00609.hp1 HG01074.hp1 HG01346.hp2 others(18): Show |
intron_variant | MODIFIER | c.3092-888_3092-887d others(4): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | ||||||
| chr9:100299635 | GACAC | G | 8 | a0001c0001t0003g0177 a0001c0001t0003g0178 a0001c0001t0004g0116 others(5): Show |
8 | HG00642.hp2 HG00738.hp1 HG00738.hp2 others(5): Show |
intron_variant | MODIFIER | c.3092-890_3092-887d others(6): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | ||||||
| chr9:100299635 | GACACAC | G | 19 | a0001c0001t0003g0042 a0001c0001t0003g0045 a0001c0001t0003g0085 others(16): Show |
19 | HG00140.hp1 HG00735.hp1 HG01081.hp2 others(16): Show |
intron_variant | MODIFIER | c.3092-892_3092-887d others(8): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | ||||||
| chr9:100299635 | GACACACA others(1): Show |
G | 7 | a0001c0001t0004g0047 a0001c0001t0009g0058 a0001c0001t0009g0100 others(4): Show |
7 | HG00733.hp2 HG02280.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.3092-894_3092-887d others(10): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | ||||||
| chr9:100299635 | GACACACA others(7): Show |
G | 1 | a0006c0007t0009g0181 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.3092-900_3092-887d others(16): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | ||||||
| chr9:100299635 | GACACACA others(15): Show |
G | 2 | a0001c0001t0001g0146 a0001c0001t0001g0147 |
2 | HG01081.hp1 HG01243.hp2 |
intron_variant | MODIFIER | c.3092-908_3092-887d others(24): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | ||||||
| chr9:100299635 | GACACACA others(19): Show |
G | 90 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(87): Show |
90 | HG00140.hp2 HG00280.hp1 HG00323.hp2 others(87): Show |
intron_variant | MODIFIER | c.3092-912_3092-887d others(28): Show |
INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | INFO_REALIGN_3_PRIME | chr9 | 100299635 | ||||||
| chr9:100299987 | A | T | 1 | a0007c0006t0018g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3092-581A>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100299987 | |||||||
| chr9:100300094 | C | T | 87 | a0001c0001t0001g0004 a0001c0001t0001g0015 a0001c0001t0001g0020 others(84): Show |
87 | HG00140.hp2 HG00280.hp1 HG00423.hp1 others(84): Show |
intron_variant | MODIFIER | c.3092-474C>T | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100300094 | |||||||
| chr9:100300430 | T | C | 1 | a0001c0001t0017g0063 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3092-138T>C | INVS | ENSG00000119509.13 | transcript | ENST00000262457.7 | protein_coding | 16/16 | chr9 | 100300430 |