Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 445 |
| ensemblid | ENSG00000130707.18 |
| hgncid | 758 |
| symbol | ASS1 |
| name | argininosuccinate synthase 1 |
| refseq_nuc | NM_054012.4 |
| refseq_prot | NP_446464.1 |
| ensembl_nuc | ENST00000352480.10 |
| ensembl_prot | ENSP00000253004.6 |
| mane_status | MANE Select |
| chr | chr9 |
| start | 130444961 |
| end | 130501274 |
| strand | + |
| ver | v1.2 |
| region | chr9:130444961-130501274 |
| region5000 | chr9:130439961-130506274 |
| regionname0 | ASS1_chr9_130444961_130501274 |
| regionname5000 | ASS1_chr9_130439961_130506274 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 412 | 357 | 87 | 70 | 142 | 18 | 38 | 103 | ASS1_chr9_130439961_130506274 | ASS1 | MSSKG others(407): Show |
chr9 | 130439961 | 130506274 |
| a0002 | 0/0 | 412 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | MSSKG others(407): Show |
chr9 | 130439961 | 130506274 |
| a0003 | 0/0 | 412 | 5 | 2 | 3 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | MSSKG others(407): Show |
chr9 | 130439961 | 130506274 |
| a0004 | 0/0 | 412 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | MSSKG others(407): Show |
chr9 | 130439961 | 130506274 |
| a0005 | 0/0 | 412 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | MSSKG others(407): Show |
chr9 | 130439961 | 130506274 |
| a0006 | 0/0 | 412 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | MSSKG others(407): Show |
chr9 | 130439961 | 130506274 |
| a0007 | 0/0 | 412 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | MSSKG others(407): Show |
chr9 | 130439961 | 130506274 |
| a0008 | 0/0 | 412 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | MTSKG others(407): Show |
chr9 | 130439961 | 130506274 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1236 | 297 | 66 | 58 | 127 | 14 | 30 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0001c0002 | 0/0 | 1236 | 31 | 6 | 6 | 10 | 2 | 7 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0001c0003 | 0/0 | 1236 | 23 | 14 | 6 | 0 | 2 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0001c0005 | 0/0 | 1236 | 3 | 0 | 0 | 3 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0001c0007 | 0/0 | 1236 | 2 | 0 | 0 | 2 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0001c0014 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0002c0004 | 0/0 | 1236 | 6 | 5 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0003c0008 | 0/0 | 1236 | 2 | 1 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0003c0009 | 0/0 | 1236 | 2 | 0 | 2 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0003c0015 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0004c0006 | 0/0 | 1236 | 2 | 1 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0005c0013 | 0/0 | 1236 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0006c0012 | 0/0 | 1236 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0007c0011 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGTC others(1231): Show |
chr9 | 130439961 | 130506274 | ||
| a0008c0010 | 0/0 | 1236 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | ATGAC others(1231): Show |
chr9 | 130439961 | 130506274 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1532 | 296 | 66 | 58 | 126 | 14 | 30 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0001c0001t0003 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0001c0002t0001 | 0/0 | 1532 | 30 | 6 | 6 | 9 | 2 | 7 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0001c0002t0002 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0001c0003t0001 | 0/0 | 1532 | 23 | 14 | 6 | 0 | 2 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0001c0005t0001 | 0/0 | 1532 | 3 | 0 | 0 | 3 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0001c0007t0001 | 0/0 | 1532 | 2 | 0 | 0 | 2 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0001c0014t0001 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0002c0004t0001 | 0/0 | 1532 | 6 | 5 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0003c0008t0001 | 0/0 | 1532 | 2 | 1 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0003c0009t0001 | 0/0 | 1532 | 2 | 0 | 2 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0003c0015t0001 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0004c0006t0001 | 0/0 | 1532 | 2 | 1 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0005c0013t0001 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0006c0012t0001 | 0/0 | 1532 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0007c0011t0001 | 0/0 | 1532 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| a0008c0010t0001 | 0/0 | 1532 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | CCTGC others(1527): Show |
chr9 | 130439961 | 130506274 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0004 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0017 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0045 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0295 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0330 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0339 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0352 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0353 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0001g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0002 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0002t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0003t0001g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0005t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0005t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0005t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0007t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0007t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0001c0014t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0002c0004t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0002c0004t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0002c0004t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0002c0004t0001g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0002c0004t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0003c0008t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0003c0008t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0003c0009t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0003c0009t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0003c0015t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0004c0006t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0004c0006t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0005c0013t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0006c0012t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0007c0011t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| a0008c0010t0001g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | GBR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00099 | hp2 | a0001 | c0002 | t0001 | g0185 | EUR | GBR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0028 | EUR | GBR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0110 | EUR | GBR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0058 | EUR | FIN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0241 | EUR | FIN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00323 | hp1 | a0001 | c0001 | t0001 | g0316 | EUR | FIN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0174 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0114 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00738 | hp2 | a0001 | c0003 | t0001 | g0296 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0002 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0340 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01070 | hp2 | a0001 | c0003 | t0001 | g0299 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01071 | hp1 | a0001 | c0003 | t0001 | g0298 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01071 | hp2 | a0001 | c0002 | t0001 | g0010 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0059 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01099 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0327 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01167 | hp2 | a0002 | c0004 | t0001 | g0218 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0318 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01192 | hp1 | a0001 | c0003 | t0001 | g0300 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01255 | hp2 | a0003 | c0009 | t0001 | g0306 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01258 | hp1 | a0003 | c0009 | t0001 | g0307 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01261 | hp2 | a0001 | c0003 | t0001 | g0319 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0302 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0295 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0272 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0038 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01361 | hp2 | a0001 | c0003 | t0001 | g0048 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01433 | hp1 | a0003 | c0008 | t0001 | g0201 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0333 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0284 | EUR | IBS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0182 | EUR | IBS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0176 | EUR | IBS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0280 | EUR | IBS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0175 | EUR | IBS | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01884 | hp1 | a0004 | c0006 | t0001 | g0141 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01891 | hp2 | a0001 | c0003 | t0001 | g0345 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0339 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01943 | hp2 | a0004 | c0006 | t0001 | g0142 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0190 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01952 | hp2 | a0001 | c0001 | t0001 | g0150 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0057 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0312 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02040 | hp1 | a0005 | c0013 | t0001 | g0083 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02055 | hp1 | a0001 | c0003 | t0001 | g0135 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0332 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0352 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02148 | hp2 | a0006 | c0012 | t0001 | g0261 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02257 | hp1 | a0001 | c0003 | t0001 | g0131 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02258 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02273 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0344 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02280 | hp2 | a0002 | c0004 | t0001 | g0217 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0203 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02523 | hp2 | a0001 | c0002 | t0001 | g0053 | EAS | KHV | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02602 | hp1 | a0001 | c0003 | t0001 | g0149 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02602 | hp2 | a0001 | c0002 | t0001 | g0187 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0331 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02647 | hp1 | a0001 | c0003 | t0001 | g0282 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02683 | hp2 | a0001 | c0002 | t0001 | g0225 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0304 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0347 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02723 | hp1 | a0001 | c0001 | t0001 | g0342 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02723 | hp2 | a0001 | c0001 | t0001 | g0164 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0183 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0186 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0337 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02895 | hp1 | a0001 | c0003 | t0001 | g0321 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0213 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02897 | hp2 | a0001 | c0003 | t0001 | g0322 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02922 | hp1 | a0001 | c0003 | t0001 | g0292 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02922 | hp2 | a0002 | c0004 | t0001 | g0216 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02965 | hp2 | a0001 | c0003 | t0001 | g0227 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02970 | hp1 | a0001 | c0003 | t0001 | g0199 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0326 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0349 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03098 | hp1 | a0001 | c0003 | t0001 | g0215 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03098 | hp2 | a0007 | c0011 | t0001 | g0168 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0334 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0348 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0146 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03225 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0330 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03492 | hp1 | a0001 | c0002 | t0001 | g0002 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03516 | hp1 | a0001 | c0002 | t0001 | g0191 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03540 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0350 | AFR | GWD | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0161 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0317 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03669 | hp2 | a0001 | c0002 | t0001 | g0184 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0088 | SAS | STU | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0113 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0035 | SAS | PJL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | BEB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | BEB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | STU | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | STU | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | BEB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0020 | SAS | BEB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | STU | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | STU | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0002 | SAS | STU | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0346 | AFR | YRI | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18522 | hp2 | a0002 | c0004 | t0001 | g0011 | AFR | YRI | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | CHB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | CHB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18906 | hp1 | a0001 | c0003 | t0001 | g0343 | AFR | YRI | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0177 | AFR | YRI | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18940 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18943 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18950 | hp1 | a0001 | c0002 | t0001 | g0005 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0354 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18961 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18964 | hp1 | a0001 | c0005 | t0001 | g0251 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18964 | hp2 | a0001 | c0007 | t0001 | g0003 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18965 | hp1 | a0001 | c0005 | t0001 | g0031 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18970 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18980 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18986 | hp1 | a0001 | c0002 | t0001 | g0189 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18993 | hp2 | a0001 | c0005 | t0001 | g0291 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19004 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0192 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19030 | hp1 | a0003 | c0015 | t0001 | g0211 | AFR | LWK | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19030 | hp2 | a0003 | c0008 | t0001 | g0200 | AFR | LWK | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0323 | AFR | LWK | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19043 | hp2 | a0001 | c0002 | t0001 | g0136 | AFR | LWK | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0181 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19063 | hp2 | a0001 | c0007 | t0001 | g0093 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19064 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19065 | hp1 | a0001 | c0002 | t0001 | g0178 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19065 | hp2 | a0008 | c0010 | t0001 | g0003 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19067 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19070 | hp1 | a0001 | c0002 | t0001 | g0180 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19070 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19074 | hp1 | a0001 | c0001 | t0001 | g0353 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19078 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19086 | hp1 | a0001 | c0002 | t0002 | g0179 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19086 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19240 | hp1 | a0001 | c0014 | t0001 | g0171 | AFR | YRI | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA19240 | hp2 | a0001 | c0003 | t0001 | g0336 | AFR | YRI | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA20129 | hp1 | a0002 | c0004 | t0001 | g0351 | AFR | ASW | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA20129 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ASW | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0281 | EUR | TSI | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA20752 | hp2 | a0001 | c0003 | t0001 | g0297 | EUR | TSI | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA20805 | hp1 | a0001 | c0003 | t0001 | g0310 | EUR | TSI | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0152 | SAS | GIH | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | GIH | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02486 | hp2 | a0002 | c0004 | t0001 | g0011 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG02559 | hp2 | a0001 | c0003 | t0001 | g0188 | AFR | ACB | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0019 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | MSL | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0329 | AFR | USA | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | USA | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA20300 | hp1 | a0001 | c0003 | t0001 | g0228 | AFR | USA | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | USA | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | LWK | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0017 | REF | REF | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0045 | REF | REF | ASS1_chr9_130439961_130506274 | ASS1 | chr9 | 130439961 | 130506274 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130444994 | C | G | 1 | a0001 | 1 | NA19070.hp2 | splice_region_variant | LOW | c.-7C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/15 | chr9 | 130444994 | |||||||
| chr9:130452232 | T | A | 1 | a0008 | 1 | NA19065.hp2 | missense_variant | MODERATE | c.4T>A | p.Ser2Thr | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/15 | 44/1532 | 4/1239 | 2/412 | chr9 | 130452232 | |||
| chr9:130458471 | T | C | 1 | a0007 | 1 | HG03098.hp2 | missense_variant | MODERATE | c.245T>C | p.Leu82Pro | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/15 | 285/1532 | 245/1239 | 82/412 | chr9 | 130458471 | |||
| chr9:130458548 | C | T | 1 | a0003 | 2 | HG01255.hp2 HG01258.hp1 |
missense_variant | MODERATE | c.322C>T | p.Arg108Trp | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/15 | 362/1532 | 322/1239 | 108/412 | chr9 | 130458548 | |||
| chr9:130458549 | G | T | 1 | a0003 | 3 | HG01433.hp1 NA19030.hp1 NA19030.hp2 |
missense_variant | MODERATE | c.323G>T | p.Arg108Leu | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/15 | 363/1532 | 323/1239 | 108/412 | chr9 | 130458549 | |||
| chr9:130471492 | G | A | 1 | a0006 | 1 | HG02148.hp2 | missense_variant | MODERATE | c.574G>A | p.Ala192Thr | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/15 | 614/1532 | 574/1239 | 192/412 | chr9 | 130471492 | |||
| chr9:130476895 | A | G | 1 | a0004 | 2 | HG01884.hp1 HG01943.hp2 |
missense_variant | MODERATE | c.622A>G | p.Thr208Ala | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/15 | 662/1532 | 622/1239 | 208/412 | chr9 | 130476895 | |||
| chr9:130479793 | G | A | 1 | a0002 | 6 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
missense_variant | MODERATE | c.766G>A | p.Glu256Lys | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 10/15 | 806/1532 | 766/1239 | 256/412 | chr9 | 130479793 | |||
| chr9:130494911 | G | A | 1 | a0005 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.1015G>A | p.Ala339Thr | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/15 | 1055/1532 | 1015/1239 | 339/412 | chr9 | 130494911 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130470839 | C | T | 3 | a0001c0002 a0002c0004 a0003c0015 |
38 | HG00099.hp2 HG00733.hp1 HG00738.hp1 others(35): Show |
synonymous_variant | LOW | c.501C>T | p.His167His | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 7/15 | 541/1532 | 501/1239 | 167/412 | chr9 | 130470839 | |||
| chr9:130470902 | C | T | 2 | a0001c0007 a0008c0010 |
3 | NA18964.hp2 NA19063.hp2 NA19065.hp2 |
splice_region_variant&synonymous_variant | LOW | c.564C>T | p.Ile188Ile | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 7/15 | 604/1532 | 564/1239 | 188/412 | chr9 | 130470902 | |||
| chr9:130476948 | C | T | 1 | a0001c0014 | 1 | NA19240.hp1 | synonymous_variant | LOW | c.675C>T | p.Ile225Ile | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/15 | 715/1532 | 675/1239 | 225/412 | chr9 | 130476948 | |||
| chr9:130489370 | T | C | 1 | a0001c0003 | 23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
synonymous_variant | LOW | c.876T>C | p.His292His | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/15 | 916/1532 | 876/1239 | 292/412 | chr9 | 130489370 | |||
| chr9:130494979 | C | T | 1 | a0001c0005 | 3 | NA18964.hp1 NA18965.hp1 NA18993.hp2 |
synonymous_variant | LOW | c.1083C>T | p.Leu361Leu | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/15 | 1123/1532 | 1083/1239 | 361/412 | chr9 | 130494979 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130501135 | G | T | 1 | a0001c0002t0002 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*114G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 15/15 | 114 | chr9 | 130501135 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr9:130445062 | A | C | 201 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(198): Show |
212 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(209): Show |
intron_variant | MODIFIER | c.-6+67A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130445062 | |||||||
| chr9:130445222 | G | GCGGGGGC others(9): Show |
1 | a0001c0002t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-6+248_-6+263dupGG others(14): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130445222 | ||||||
| chr9:130445222 | GCGGGGGC others(9): Show |
G | 318 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(315): Show |
336 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(333): Show |
intron_variant | MODIFIER | c.-6+248_-6+263delGG others(14): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130445222 | ||||||
| chr9:130445224 | GGGGGCGC others(8): Show |
G | 1 | a0001c0001t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-6+234_-6+248delCG others(13): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130445224 | ||||||
| chr9:130445259 | T | C | 1 | a0001c0001t0001g0018 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-6+264T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130445259 | |||||||
| chr9:130445458 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-6+463G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130445458 | |||||||
| chr9:130445490 | G | A | 1 | a0001c0001t0001g0020 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-6+495G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130445490 | |||||||
| chr9:130445512 | A | G | 3 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 |
3 | HG02071.hp2 NA18950.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.-6+517A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130445512 | |||||||
| chr9:130445648 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-6+653G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130445648 | |||||||
| chr9:130445711 | A | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0342 others(9): Show |
14 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6+716A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130445711 | |||||||
| chr9:130445849 | A | G | 1 | a0001c0001t0001g0163 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-6+854A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130445849 | |||||||
| chr9:130446148 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(309): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(326): Show |
intron_variant | MODIFIER | c.-6+1153T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130446148 | |||||||
| chr9:130446167 | A | T | 1 | a0001c0001t0001g0155 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-6+1172A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130446167 | |||||||
| chr9:130446232 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-6+1237G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130446232 | |||||||
| chr9:130446282 | TGTG | T | 3 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 |
3 | HG00597.hp2 NA18945.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-6+1288_-6+1290del others(3): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130446282 | |||||||
| chr9:130446391 | C | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0326 a0001c0001t0001g0327 others(11): Show |
15 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-6+1396C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130446391 | |||||||
| chr9:130446711 | C | G | 1 | a0001c0001t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-6+1716C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130446711 | |||||||
| chr9:130446790 | T | C | 24 | a0001c0001t0001g0054 a0001c0001t0001g0175 a0001c0001t0001g0176 others(21): Show |
28 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.-6+1795T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130446790 | |||||||
| chr9:130446857 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-6+1862G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130446857 | |||||||
| chr9:130446886 | T | G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0342 others(9): Show |
14 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-6+1891T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130446886 | |||||||
| chr9:130447015 | C | T | 1 | a0001c0001t0001g0154 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-6+2020C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447015 | |||||||
| chr9:130447033 | C | A | 3 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0002t0001g0174 |
3 | HG00733.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.-6+2038C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447033 | |||||||
| chr9:130447054 | G | A | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.-6+2059G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447054 | |||||||
| chr9:130447085 | G | A | 1 | a0001c0001t0001g0022 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-6+2090G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447085 | |||||||
| chr9:130447151 | G | A | 31 | a0001c0001t0001g0009 a0001c0001t0001g0020 a0001c0001t0001g0022 others(28): Show |
32 | HG00140.hp1 HG00323.hp2 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.-6+2156G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447151 | |||||||
| chr9:130447388 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-6+2393G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447388 | |||||||
| chr9:130447429 | G | T | 1 | a0001c0001t0001g0008 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.-6+2434G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447429 | |||||||
| chr9:130447458 | A | G | 1 | a0001c0001t0001g0324 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-6+2463A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447458 | |||||||
| chr9:130447589 | C | T | 1 | a0001c0001t0001g0323 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-6+2594C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447589 | |||||||
| chr9:130447627 | G | A | 1 | a0001c0002t0001g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.-6+2632G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447627 | |||||||
| chr9:130447784 | G | A | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-6+2789G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447784 | |||||||
| chr9:130447842 | T | C | 3 | a0001c0003t0001g0199 a0003c0008t0001g0200 a0003c0008t0001g0201 |
3 | HG01433.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-6+2847T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447842 | |||||||
| chr9:130447940 | T | G | 13 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0056 others(10): Show |
14 | HG00280.hp1 HG00735.hp1 HG01099.hp1 others(11): Show |
intron_variant | MODIFIER | c.-6+2945T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130447940 | |||||||
| chr9:130448151 | A | G | 4 | a0001c0001t0001g0170 a0001c0001t0001g0197 a0001c0001t0001g0198 others(1): Show |
4 | HG02145.hp1 HG02970.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6+3156A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448151 | |||||||
| chr9:130448288 | T | C | 109 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(106): Show |
113 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-6+3293T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448288 | |||||||
| chr9:130448339 | C | T | 3 | a0001c0003t0001g0199 a0003c0008t0001g0200 a0003c0008t0001g0201 |
3 | HG01433.hp1 HG02970.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-6+3344C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448339 | |||||||
| chr9:130448364 | C | T | 2 | a0001c0003t0001g0321 a0001c0003t0001g0322 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-6+3369C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448364 | |||||||
| chr9:130448409 | G | GGT | 3 | a0001c0001t0001g0170 a0001c0001t0001g0198 a0001c0001t0001g0323 |
3 | HG02145.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-6+3420_-6+3421dup others(2): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448409 | ||||||
| chr9:130448415 | T | TGTGCGC | 6 | a0001c0001t0001g0315 a0001c0001t0001g0316 a0001c0001t0001g0317 others(3): Show |
6 | HG00323.hp1 HG01175.hp2 HG01261.hp1 others(3): Show |
intron_variant | MODIFIER | c.-6+3421_-6+3422ins others(6): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448415 | ||||||
| chr9:130448417 | C | T | 3 | a0001c0001t0001g0172 a0001c0001t0001g0314 a0001c0014t0001g0171 |
3 | HG01891.hp1 HG02148.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-6+3422C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448417 | |||||||
| chr9:130448420 | GCGCACA | G | 16 | a0001c0001t0001g0016 a0001c0001t0001g0326 a0001c0001t0001g0327 others(13): Show |
17 | HG01109.hp1 HG01433.hp1 HG01496.hp1 others(14): Show |
intron_variant | MODIFIER | c.-6+3427_-6+3432del others(6): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448420 | ||||||
| chr9:130448422 | G | A | 8 | a0001c0001t0001g0197 a0001c0001t0001g0219 a0001c0001t0001g0315 others(5): Show |
8 | HG00323.hp1 HG00642.hp2 HG01175.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+3427G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448422 | |||||||
| chr9:130448422 | G | GCACACAC others(19): Show |
1 | a0001c0001t0001g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-6+3450_-6+3451ins others(26): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | G | GCGCA | 5 | a0001c0001t0001g0008 a0001c0001t0001g0143 a0001c0001t0001g0144 others(2): Show |
6 | HG01884.hp1 HG01943.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-6+3428_-6+3429ins others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | G | GCGCACAC others(1): Show |
5 | a0001c0001t0001g0352 a0001c0001t0001g0353 a0001c0001t0001g0354 others(2): Show |
5 | HG00738.hp2 HG02071.hp2 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+3428_-6+3429ins others(8): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | G | GCGCACAC others(3): Show |
109 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(106): Show |
115 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.-6+3428_-6+3429ins others(10): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | G | GCGCACAC others(5): Show |
8 | a0001c0001t0001g0229 a0001c0001t0001g0237 a0001c0001t0001g0272 others(5): Show |
8 | HG01358.hp2 HG02293.hp1 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.-6+3428_-6+3429ins others(12): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | G | GCGCACAC others(7): Show |
7 | a0001c0001t0001g0342 a0001c0001t0001g0346 a0001c0001t0001g0347 others(4): Show |
7 | HG01891.hp2 HG02717.hp1 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.-6+3428_-6+3429ins others(14): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | G | GCGCACAC others(13): Show |
1 | a0007c0011t0001g0168 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-6+3428_-6+3429ins others(20): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | G | GCGCACAC others(15): Show |
3 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0166 |
3 | HG02895.hp2 HG02896.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.-6+3428_-6+3429ins others(22): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | G | GCGCACAC others(17): Show |
2 | a0001c0001t0001g0021 a0001c0001t0001g0169 |
2 | HG02258.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-6+3428_-6+3429ins others(24): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | G | GCGCGCA | 23 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0224 others(20): Show |
27 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.-6+3428_-6+3429ins others(6): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | G | GCGCGCAC others(3): Show |
2 | a0001c0001t0001g0259 a0001c0001t0001g0277 |
2 | NA18945.hp1 NA18957.hp2 |
intron_variant | MODIFIER | c.-6+3428_-6+3429ins others(10): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448422 | GCA | G | 106 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0007 others(103): Show |
110 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(107): Show |
intron_variant | MODIFIER | c.-6+3449_-6+3450del others(2): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448422 | ||||||
| chr9:130448424 | A | G | 4 | a0002c0004t0001g0011 a0002c0004t0001g0216 a0002c0004t0001g0217 others(1): Show |
5 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-6+3429A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448424 | |||||||
| chr9:130448426 | A | ACG | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02145.hp2 HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-6+3432_-6+3433ins others(2): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130448426 | ||||||
| chr9:130448426 | A | G | 25 | a0001c0001t0001g0090 a0001c0001t0001g0106 a0001c0001t0001g0107 others(22): Show |
25 | HG00099.hp1 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-6+3431A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448426 | |||||||
| chr9:130448667 | G | A | 1 | a0001c0001t0001g0166 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-5-3557G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448667 | |||||||
| chr9:130448753 | G | A | 1 | a0001c0001t0001g0065 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-5-3471G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448753 | |||||||
| chr9:130448907 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.-5-3317C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448907 | |||||||
| chr9:130448909 | T | A | 4 | a0002c0004t0001g0011 a0002c0004t0001g0216 a0002c0004t0001g0217 others(1): Show |
5 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-3315T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448909 | |||||||
| chr9:130448915 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-5-3309T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448915 | |||||||
| chr9:130448916 | G | C | 1 | a0001c0001t0001g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-5-3308G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448916 | |||||||
| chr9:130448917 | C | G | 1 | a0001c0001t0001g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-5-3307C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448917 | |||||||
| chr9:130448943 | G | A | 3 | a0001c0001t0001g0021 a0001c0001t0001g0166 a0001c0001t0001g0167 |
3 | HG02809.hp2 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.-5-3281G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130448943 | |||||||
| chr9:130449013 | A | G | 175 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(172): Show |
185 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(182): Show |
intron_variant | MODIFIER | c.-5-3211A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449013 | |||||||
| chr9:130449029 | C | T | 14 | a0001c0001t0001g0016 a0001c0001t0001g0326 a0001c0001t0001g0327 others(11): Show |
15 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.-5-3195C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449029 | |||||||
| chr9:130449115 | A | G | 315 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(312): Show |
332 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(329): Show |
intron_variant | MODIFIER | c.-5-3109A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449115 | |||||||
| chr9:130449222 | T | G | 4 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0204 others(1): Show |
4 | HG01884.hp2 HG02451.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.-5-3002T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449222 | |||||||
| chr9:130449284 | GGT | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0198 a0001c0001t0001g0323 |
3 | HG02145.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-5-2938_-5-2937del others(2): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130449284 | ||||||
| chr9:130449342 | G | GA | 57 | a0001c0001t0001g0006 a0001c0001t0001g0051 a0001c0001t0001g0057 others(54): Show |
58 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(55): Show |
intron_variant | MODIFIER | c.-5-2861dupA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130449342 | ||||||
| chr9:130449342 | G | GAA | 48 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(45): Show |
51 | HG00673.hp2 HG00735.hp1 HG01168.hp2 others(48): Show |
intron_variant | MODIFIER | c.-5-2862_-5-2861dup others(2): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130449342 | ||||||
| chr9:130449342 | GA | G | 134 | a0001c0001t0001g0003 a0001c0001t0001g0012 a0001c0001t0001g0013 others(131): Show |
139 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(136): Show |
intron_variant | MODIFIER | c.-5-2861delA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130449342 | ||||||
| chr9:130449407 | C | T | 1 | a0001c0001t0001g0038 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-5-2817C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449407 | |||||||
| chr9:130449447 | C | T | 4 | a0002c0004t0001g0011 a0002c0004t0001g0216 a0002c0004t0001g0217 others(1): Show |
5 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-2777C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449447 | |||||||
| chr9:130449574 | T | C | 12 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0342 others(9): Show |
14 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.-5-2650T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449574 | |||||||
| chr9:130449617 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02145.hp2 HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-5-2607G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449617 | |||||||
| chr9:130449766 | A | G | 3 | a0001c0001t0001g0170 a0001c0001t0001g0198 a0001c0001t0001g0323 |
3 | HG02145.hp1 HG02970.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-5-2458A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449766 | |||||||
| chr9:130449800 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-5-2424A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449800 | |||||||
| chr9:130449841 | A | C | 1 | a0001c0001t0001g0313 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.-5-2383A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449841 | |||||||
| chr9:130449850 | G | A | 1 | a0007c0011t0001g0168 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-5-2374G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130449850 | |||||||
| chr9:130450046 | A | C | 1 | a0001c0001t0001g0312 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-5-2178A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450046 | |||||||
| chr9:130450085 | T | C | 299 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(296): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.-5-2139T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450085 | |||||||
| chr9:130450120 | G | T | 1 | a0001c0001t0001g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.-5-2104G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450120 | |||||||
| chr9:130450169 | A | G | 1 | a0001c0003t0001g0131 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-5-2055A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450169 | |||||||
| chr9:130450327 | A | G | 1 | a0001c0001t0001g0130 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.-5-1897A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450327 | |||||||
| chr9:130450341 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
7 | HG02258.hp2 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-1883C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450341 | |||||||
| chr9:130450348 | A | G | 1 | a0001c0001t0003g0311 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.-5-1876A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450348 | |||||||
| chr9:130450481 | G | A | 1 | a0001c0003t0001g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-5-1743G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450481 | |||||||
| chr9:130450601 | C | T | 181 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0012 others(178): Show |
192 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.-5-1623C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450601 | |||||||
| chr9:130450605 | G | A | 1 | a0001c0001t0001g0012 | 2 | HG00735.hp2 HG01243.hp1 |
intron_variant | MODIFIER | c.-5-1619G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450605 | |||||||
| chr9:130450638 | C | T | 4 | a0002c0004t0001g0011 a0002c0004t0001g0216 a0002c0004t0001g0217 others(1): Show |
5 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-1586C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450638 | |||||||
| chr9:130450756 | C | T | 4 | a0002c0004t0001g0011 a0002c0004t0001g0216 a0002c0004t0001g0217 others(1): Show |
5 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-1468C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450756 | |||||||
| chr9:130450784 | C | T | 1 | a0001c0002t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-5-1440C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450784 | |||||||
| chr9:130450826 | A | G | 293 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(290): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.-5-1398A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450826 | |||||||
| chr9:130450839 | T | G | 1 | a0001c0002t0001g0178 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-5-1385T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450839 | |||||||
| chr9:130450933 | T | C | 9 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0069 others(6): Show |
9 | HG01884.hp2 HG02109.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-5-1291T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130450933 | |||||||
| chr9:130451123 | G | A | 1 | a0001c0003t0001g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-5-1101G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130451123 | |||||||
| chr9:130451275 | G | A | 4 | a0002c0004t0001g0011 a0002c0004t0001g0216 a0002c0004t0001g0217 others(1): Show |
5 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.-5-949G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130451275 | |||||||
| chr9:130451306 | TG | T | 208 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
217 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(214): Show |
intron_variant | MODIFIER | c.-5-917delG | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130451306 | |||||||
| chr9:130451348 | G | A | 91 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(88): Show |
94 | HG00099.hp1 HG00140.hp2 HG00597.hp2 others(91): Show |
intron_variant | MODIFIER | c.-5-876G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130451348 | |||||||
| chr9:130451461 | AT | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02145.hp2 HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.-5-761delT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr9 | 130451461 | ||||||
| chr9:130451607 | C | T | 1 | a0001c0002t0001g0136 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-5-617C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130451607 | |||||||
| chr9:130451617 | G | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0147 a0001c0001t0001g0148 others(4): Show |
7 | HG02258.hp2 HG02809.hp2 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.-5-607G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130451617 | |||||||
| chr9:130451791 | G | C | 1 | a0001c0001t0001g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-5-433G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130451791 | |||||||
| chr9:130451799 | C | A | 4 | a0001c0001t0001g0327 a0001c0001t0001g0328 a0001c0001t0001g0329 others(1): Show |
4 | HG01109.hp1 HG02559.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-425C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130451799 | |||||||
| chr9:130451924 | G | A | 3 | a0001c0001t0001g0008 a0004c0006t0001g0141 a0004c0006t0001g0142 |
4 | HG01884.hp1 HG01943.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.-5-300G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130451924 | |||||||
| chr9:130452052 | T | C | 343 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(340): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-5-172T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130452052 | |||||||
| chr9:130452131 | C | T | 2 | a0001c0001t0001g0172 a0001c0014t0001g0171 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-5-93C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130452131 | |||||||
| chr9:130452144 | G | A | 1 | a0001c0001t0001g0220 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-5-80G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130452144 | |||||||
| chr9:130452183 | C | T | 1 | a0001c0014t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-5-41C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130452183 | |||||||
| chr9:130452219 | G | A | 1 | a0001c0001t0001g0021 | 1 | HG03540.hp1 | splice_region_variant&intron_variant | LOW | c.-5-5G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 1/14 | chr9 | 130452219 | |||||||
| chr9:130452407 | G | C | 12 | a0001c0001t0001g0016 a0001c0001t0001g0327 a0001c0001t0001g0328 others(9): Show |
13 | HG01109.hp1 HG01496.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.105+74G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130452407 | |||||||
| chr9:130452448 | G | A | 204 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(201): Show |
214 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.105+115G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130452448 | |||||||
| chr9:130452579 | C | T | 3 | a0001c0001t0001g0212 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG02258.hp1 HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.105+246C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130452579 | |||||||
| chr9:130452623 | C | T | 2 | a0001c0001t0001g0049 a0001c0003t0001g0048 |
2 | HG01361.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.105+290C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130452623 | |||||||
| chr9:130452846 | T | A | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.105+513T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130452846 | |||||||
| chr9:130452950 | G | C | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(339): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.105+617G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130452950 | |||||||
| chr9:130453015 | C | G | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(339): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.105+682C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453015 | |||||||
| chr9:130453378 | G | T | 1 | a0001c0001t0001g0152 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.106-927G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453378 | |||||||
| chr9:130453391 | C | T | 2 | a0001c0001t0001g0128 a0001c0002t0001g0192 |
2 | NA19007.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.106-914C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453391 | |||||||
| chr9:130453395 | A | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0205 |
2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.106-910A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453395 | |||||||
| chr9:130453582 | G | A | 193 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(190): Show |
203 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.106-723G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453582 | |||||||
| chr9:130453593 | C | A | 5 | a0001c0001t0001g0224 a0001c0001t0001g0326 a0001c0001t0001g0337 others(2): Show |
5 | HG02818.hp1 HG02976.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.106-712C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453593 | |||||||
| chr9:130453685 | C | T | 1 | a0001c0001t0001g0037 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.106-620C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453685 | |||||||
| chr9:130453757 | C | A | 4 | a0001c0003t0001g0199 a0003c0008t0001g0200 a0003c0008t0001g0201 others(1): Show |
4 | HG01433.hp1 HG02970.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.106-548C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453757 | |||||||
| chr9:130453786 | G | A | 1 | a0001c0001t0001g0130 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.106-519G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453786 | |||||||
| chr9:130453811 | C | T | 2 | a0001c0002t0001g0177 a0001c0002t0001g0191 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.106-494C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453811 | |||||||
| chr9:130453812 | G | A | 1 | a0001c0001t0001g0197 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.106-493G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453812 | |||||||
| chr9:130453833 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.106-472C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130453833 | |||||||
| chr9:130454021 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0342 others(9): Show |
14 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.106-284G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130454021 | |||||||
| chr9:130454159 | C | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0342 others(9): Show |
14 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.106-146C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130454159 | |||||||
| chr9:130454289 | C | T | 1 | a0001c0003t0001g0199 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.106-16C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130454289 | |||||||
| chr9:130454290 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.106-15G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130454290 | |||||||
| chr9:130454295 | T | G | 2 | a0001c0001t0001g0172 a0001c0014t0001g0171 |
2 | HG01891.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.106-10T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 2/14 | chr9 | 130454295 | |||||||
| chr9:130454394 | A | G | 24 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0138 others(21): Show |
25 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.174+21A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130454394 | |||||||
| chr9:130454411 | G | A | 1 | a0001c0001t0001g0023 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.174+38G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130454411 | |||||||
| chr9:130454655 | C | T | 1 | a0001c0001t0001g0068 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.174+282C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130454655 | |||||||
| chr9:130454720 | C | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0323 a0001c0001t0001g0330 others(7): Show |
11 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+347C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130454720 | |||||||
| chr9:130454747 | GCCATCCA others(39): Show |
G | 12 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0342 others(9): Show |
14 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.174+433_174+478del others(46): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr9 | 130454747 | ||||||
| chr9:130454786 | TCATCCAT others(1): Show |
T | 11 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(8): Show |
11 | HG02145.hp1 HG02258.hp2 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+430_174+437del others(8): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr9 | 130454786 | ||||||
| chr9:130454794 | C | CCATCCAT others(23): Show |
3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02145.hp2 HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.174+429_174+430ins others(30): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr9 | 130454794 | ||||||
| chr9:130454848 | C | CCATTCAT others(5): Show |
1 | a0001c0001t0003g0311 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.174+479_174+490dup others(12): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr9 | 130454848 | ||||||
| chr9:130454924 | T | C | 10 | a0001c0001t0001g0016 a0001c0001t0001g0323 a0001c0001t0001g0330 others(7): Show |
11 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+551T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130454924 | |||||||
| chr9:130454981 | G | A | 232 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(229): Show |
244 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(241): Show |
intron_variant | MODIFIER | c.174+608G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130454981 | |||||||
| chr9:130455025 | C | A | 10 | a0001c0001t0001g0016 a0001c0001t0001g0323 a0001c0001t0001g0330 others(7): Show |
11 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.174+652C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455025 | |||||||
| chr9:130455034 | A | C | 1 | a0001c0002t0001g0190 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.174+661A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455034 | |||||||
| chr9:130455042 | A | C | 1 | a0001c0001t0001g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.174+669A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455042 | |||||||
| chr9:130455043 | T | A | 1 | a0001c0001t0001g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.174+670T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455043 | |||||||
| chr9:130455051 | TCATC | T | 22 | a0001c0001t0001g0175 a0001c0001t0001g0176 a0001c0001t0001g0326 others(19): Show |
26 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.174+694_174+697del others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr9 | 130455051 | ||||||
| chr9:130455103 | G | A | 230 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(227): Show |
242 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(239): Show |
intron_variant | MODIFIER | c.174+730G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455103 | |||||||
| chr9:130455128 | T | TCATCCAT others(4): Show |
24 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0138 others(21): Show |
25 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.174+764_174+774dup others(11): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr9 | 130455128 | ||||||
| chr9:130455153 | A | C | 24 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0138 others(21): Show |
25 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(22): Show |
intron_variant | MODIFIER | c.174+780A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455153 | |||||||
| chr9:130455417 | C | G | 199 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(196): Show |
209 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.174+1044C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455417 | |||||||
| chr9:130455698 | G | C | 3 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02040.hp2 NA18944.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.174+1325G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455698 | |||||||
| chr9:130455744 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0342 others(9): Show |
14 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.174+1371G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455744 | |||||||
| chr9:130455839 | A | G | 111 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(108): Show |
114 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.174+1466A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455839 | |||||||
| chr9:130455895 | A | G | 7 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(4): Show |
7 | NA18963.hp2 NA18971.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.174+1522A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455895 | |||||||
| chr9:130455963 | G | C | 1 | a0001c0001t0001g0226 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.174+1590G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130455963 | |||||||
| chr9:130456059 | C | T | 1 | a0001c0002t0001g0136 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.174+1686C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456059 | |||||||
| chr9:130456103 | A | C | 337 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(334): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.174+1730A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456103 | |||||||
| chr9:130456103 | A | T | 7 | a0001c0001t0001g0224 a0001c0001t0001g0326 a0001c0001t0001g0328 others(4): Show |
7 | HG02559.hp1 HG02818.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.174+1730A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456103 | |||||||
| chr9:130456203 | C | T | 4 | a0001c0003t0001g0199 a0003c0008t0001g0200 a0003c0008t0001g0201 others(1): Show |
4 | HG01433.hp1 HG02970.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.174+1830C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456203 | |||||||
| chr9:130456322 | T | C | 2 | a0001c0001t0001g0073 a0001c0001t0001g0219 |
2 | HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.174+1949T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456322 | |||||||
| chr9:130456323 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0219 |
2 | HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.174+1950G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456323 | |||||||
| chr9:130456324 | G | A | 1 | a0001c0003t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.174+1951G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456324 | |||||||
| chr9:130456484 | C | A | 1 | a0001c0001t0001g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.175-1917C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456484 | |||||||
| chr9:130456532 | T | C | 1 | a0003c0015t0001g0211 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.175-1869T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456532 | |||||||
| chr9:130456580 | A | G | 1 | a0001c0001t0001g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.175-1821A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456580 | |||||||
| chr9:130456582 | G | A | 1 | a0001c0001t0001g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.175-1819G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456582 | |||||||
| chr9:130456583 | A | T | 1 | a0001c0001t0001g0066 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.175-1818A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456583 | |||||||
| chr9:130456819 | G | A | 2 | a0004c0006t0001g0141 a0004c0006t0001g0142 |
2 | HG01884.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.175-1582G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456819 | |||||||
| chr9:130456821 | G | A | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.175-1580G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456821 | |||||||
| chr9:130456850 | C | T | 94 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(91): Show |
97 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(94): Show |
intron_variant | MODIFIER | c.175-1551C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456850 | |||||||
| chr9:130456883 | A | C | 1 | a0001c0001t0001g0036 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.175-1518A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456883 | |||||||
| chr9:130456921 | C | CA | 23 | a0001c0001t0001g0004 a0001c0001t0001g0075 a0001c0001t0001g0132 others(20): Show |
25 | HG00609.hp2 HG01106.hp2 HG01891.hp2 others(22): Show |
intron_variant | MODIFIER | c.175-1473dupA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr9 | 130456921 | ||||||
| chr9:130456929 | T | A | 343 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(340): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.175-1472T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130456929 | |||||||
| chr9:130457140 | T | G | 1 | a0001c0001t0001g0076 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.175-1261T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130457140 | |||||||
| chr9:130457168 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(146): Show |
155 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.175-1233G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130457168 | |||||||
| chr9:130457272 | A | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0330 a0001c0001t0001g0331 others(6): Show |
10 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.175-1129A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130457272 | |||||||
| chr9:130457402 | T | C | 162 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(159): Show |
168 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.175-999T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130457402 | |||||||
| chr9:130457452 | C | T | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02145.hp2 HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.175-949C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130457452 | |||||||
| chr9:130457722 | T | G | 4 | a0001c0001t0001g0049 a0001c0001t0001g0175 a0001c0001t0001g0176 others(1): Show |
4 | HG01361.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.175-679T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130457722 | |||||||
| chr9:130457887 | G | A | 9 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(6): Show |
9 | HG02258.hp2 HG02809.hp2 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.175-514G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130457887 | |||||||
| chr9:130458031 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.175-370C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130458031 | |||||||
| chr9:130458032 | G | A | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.175-369G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130458032 | |||||||
| chr9:130458158 | C | CA | 7 | a0001c0001t0001g0285 a0001c0001t0001g0286 a0001c0001t0001g0287 others(4): Show |
7 | NA18963.hp2 NA18971.hp1 NA18980.hp2 others(4): Show |
intron_variant | MODIFIER | c.175-226dupA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr9 | 130458158 | ||||||
| chr9:130458158 | CA | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(104): Show |
110 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.175-226delA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr9 | 130458158 | ||||||
| chr9:130458174 | A | G | 1 | a0001c0001t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.175-227A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130458174 | |||||||
| chr9:130458397 | G | A | 1 | a0001c0001t0001g0111 | 1 | NA19090.hp2 | splice_region_variant&intron_variant | LOW | c.175-4G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 3/14 | chr9 | 130458397 | |||||||
| chr9:130458605 | A | G | 3 | a0001c0001t0001g0223 a0001c0001t0001g0273 a0001c0001t0001g0274 |
3 | HG00408.hp2 HG02135.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.363+16A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130458605 | |||||||
| chr9:130458610 | C | G | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.363+21C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130458610 | |||||||
| chr9:130458784 | C | T | 148 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(145): Show |
154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.363+195C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130458784 | |||||||
| chr9:130458902 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.363+313G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130458902 | |||||||
| chr9:130459082 | C | T | 2 | a0001c0001t0001g0008 a0001c0014t0001g0171 |
3 | HG03486.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.363+493C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459082 | |||||||
| chr9:130459181 | G | A | 1 | a0001c0001t0001g0008 | 2 | HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.363+592G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459181 | |||||||
| chr9:130459185 | C | A | 1 | a0001c0003t0001g0292 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.363+596C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459185 | |||||||
| chr9:130459186 | G | A | 3 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 |
3 | HG02145.hp2 HG02615.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.363+597G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459186 | |||||||
| chr9:130459441 | T | G | 2 | a0001c0001t0001g0330 a0001c0001t0001g0331 |
2 | HG02622.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.363+852T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459441 | |||||||
| chr9:130459479 | T | C | 1 | a0001c0001t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.363+890T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459479 | |||||||
| chr9:130459594 | C | T | 1 | a0001c0001t0001g0035 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.363+1005C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459594 | |||||||
| chr9:130459762 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0219 |
2 | HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.363+1173C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459762 | |||||||
| chr9:130459783 | A | G | 1 | a0001c0001t0001g0054 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.363+1194A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459783 | |||||||
| chr9:130459829 | A | T | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.363+1240A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459829 | |||||||
| chr9:130459845 | T | C | 1 | a0001c0001t0001g0342 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.363+1256T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459845 | |||||||
| chr9:130459853 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.363+1264G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459853 | |||||||
| chr9:130459884 | C | A | 4 | a0001c0001t0001g0150 a0001c0001t0001g0229 a0001c0001t0001g0230 others(1): Show |
4 | HG01928.hp1 HG01934.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.363+1295C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459884 | |||||||
| chr9:130459928 | G | A | 21 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0010 others(18): Show |
25 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.363+1339G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130459928 | |||||||
| chr9:130460022 | G | A | 9 | a0001c0001t0001g0054 a0001c0001t0001g0065 a0001c0001t0001g0066 others(6): Show |
9 | HG00673.hp2 HG02040.hp2 NA18944.hp2 others(6): Show |
intron_variant | MODIFIER | c.363+1433G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460022 | |||||||
| chr9:130460028 | C | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(248): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.363+1439C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460028 | |||||||
| chr9:130460038 | G | A | 12 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0198 others(9): Show |
14 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.363+1449G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460038 | |||||||
| chr9:130460116 | C | T | 1 | a0001c0001t0001g0272 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.363+1527C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460116 | |||||||
| chr9:130460321 | C | G | 9 | a0001c0001t0001g0016 a0001c0001t0001g0330 a0001c0001t0001g0331 others(6): Show |
10 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.363+1732C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460321 | |||||||
| chr9:130460429 | C | T | 2 | a0004c0006t0001g0141 a0004c0006t0001g0142 |
2 | HG01884.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.363+1840C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460429 | |||||||
| chr9:130460508 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(249): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.363+1919C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460508 | |||||||
| chr9:130460593 | T | C | 1 | a0001c0001t0001g0024 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.363+2004T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460593 | |||||||
| chr9:130460665 | G | A | 251 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(248): Show |
260 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(257): Show |
intron_variant | MODIFIER | c.363+2076G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460665 | |||||||
| chr9:130460764 | G | T | 1 | a0001c0001t0001g0051 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.363+2175G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460764 | |||||||
| chr9:130460784 | A | G | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.363+2195A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460784 | |||||||
| chr9:130460804 | A | G | 5 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(2): Show |
5 | HG02145.hp2 HG02615.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.363+2215A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460804 | |||||||
| chr9:130460835 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.363+2246G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460835 | |||||||
| chr9:130460949 | T | C | 1 | a0001c0003t0001g0215 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.363+2360T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130460949 | |||||||
| chr9:130461021 | C | CA | 64 | a0001c0001t0001g0016 a0001c0001t0001g0020 a0001c0001t0001g0042 others(61): Show |
69 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.363+2442dupA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 130461021 | ||||||
| chr9:130461078 | C | T | 1 | a0001c0001t0001g0024 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.363+2489C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461078 | |||||||
| chr9:130461201 | C | CATGGGTG others(11): Show |
68 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0042 others(65): Show |
73 | HG00099.hp2 HG00597.hp1 HG00733.hp1 others(70): Show |
intron_variant | MODIFIER | c.363+2623_363+2640d others(20): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 130461201 | ||||||
| chr9:130461272 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.363+2683C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461272 | |||||||
| chr9:130461278 | G | T | 1 | a0001c0001t0001g0323 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.363+2689G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461278 | |||||||
| chr9:130461384 | CG | C | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(94): Show |
100 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.364-2726delG | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461384 | |||||||
| chr9:130461385 | G | A | 153 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(150): Show |
159 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.364-2726G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461385 | |||||||
| chr9:130461387 | C | A | 97 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(94): Show |
100 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(97): Show |
intron_variant | MODIFIER | c.364-2724C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461387 | |||||||
| chr9:130461409 | C | T | 1 | a0001c0001t0001g0198 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.364-2702C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461409 | |||||||
| chr9:130461468 | G | GC | 23 | a0001c0001t0001g0198 a0001c0002t0001g0002 a0001c0002t0001g0005 others(20): Show |
27 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.364-2637dupC | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr9 | 130461468 | ||||||
| chr9:130461468 | G | T | 4 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0328 others(1): Show |
4 | HG02559.hp1 HG02615.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.364-2643G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461468 | |||||||
| chr9:130461473 | C | CG | 148 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(145): Show |
154 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(151): Show |
intron_variant | MODIFIER | c.364-2638_364-2637i others(3): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461473 | |||||||
| chr9:130461473 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.364-2638C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461473 | |||||||
| chr9:130461481 | G | C | 5 | a0002c0004t0001g0011 a0002c0004t0001g0216 a0002c0004t0001g0217 others(2): Show |
6 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-2630G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461481 | |||||||
| chr9:130461495 | C | T | 2 | a0004c0006t0001g0141 a0004c0006t0001g0142 |
2 | HG01884.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.364-2616C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461495 | |||||||
| chr9:130461497 | G | A | 2 | a0001c0001t0001g0008 a0001c0014t0001g0171 |
3 | HG03486.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.364-2614G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461497 | |||||||
| chr9:130461561 | G | A | 223 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(220): Show |
235 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(232): Show |
intron_variant | MODIFIER | c.364-2550G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461561 | |||||||
| chr9:130461567 | T | A | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.364-2544T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461567 | |||||||
| chr9:130461702 | A | G | 64 | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0001g0043 others(61): Show |
69 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(66): Show |
intron_variant | MODIFIER | c.364-2409A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461702 | |||||||
| chr9:130461783 | C | G | 2 | a0004c0006t0001g0141 a0004c0006t0001g0142 |
2 | HG01884.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.364-2328C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461783 | |||||||
| chr9:130461862 | G | A | 253 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(250): Show |
262 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(259): Show |
intron_variant | MODIFIER | c.364-2249G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461862 | |||||||
| chr9:130461914 | G | C | 1 | a0001c0001t0001g0025 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.364-2197G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461914 | |||||||
| chr9:130461920 | A | C | 265 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(262): Show |
275 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(272): Show |
intron_variant | MODIFIER | c.364-2191A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461920 | |||||||
| chr9:130461922 | C | T | 3 | a0001c0001t0001g0015 a0001c0001t0001g0269 a0001c0001t0001g0270 |
4 | HG00438.hp1 NA18966.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-2189C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130461922 | |||||||
| chr9:130462057 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.364-2054C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462057 | |||||||
| chr9:130462199 | A | G | 346 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(343): Show |
364 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(361): Show |
intron_variant | MODIFIER | c.364-1912A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462199 | |||||||
| chr9:130462202 | C | T | 8 | a0001c0001t0001g0016 a0001c0001t0001g0330 a0001c0001t0001g0331 others(5): Show |
9 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.364-1909C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462202 | |||||||
| chr9:130462203 | G | A | 6 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(3): Show |
6 | HG02145.hp2 HG02615.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.364-1908G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462203 | |||||||
| chr9:130462210 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0219 |
2 | HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.364-1901G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462210 | |||||||
| chr9:130462280 | C | T | 2 | a0001c0001t0001g0280 a0001c0001t0001g0284 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.364-1831C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462280 | |||||||
| chr9:130462288 | A | C | 3 | a0001c0001t0001g0155 a0004c0006t0001g0141 a0004c0006t0001g0142 |
3 | HG01884.hp1 HG01943.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.364-1823A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462288 | |||||||
| chr9:130462435 | A | G | 3 | a0001c0001t0001g0155 a0004c0006t0001g0141 a0004c0006t0001g0142 |
3 | HG01884.hp1 HG01943.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.364-1676A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462435 | |||||||
| chr9:130462713 | C | T | 5 | a0001c0001t0001g0111 a0001c0001t0001g0125 a0001c0001t0001g0130 others(2): Show |
5 | HG02056.hp1 NA18980.hp1 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.364-1398C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462713 | |||||||
| chr9:130462723 | T | C | 3 | a0001c0001t0001g0155 a0004c0006t0001g0141 a0004c0006t0001g0142 |
3 | HG01884.hp1 HG01943.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.364-1388T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462723 | |||||||
| chr9:130462759 | A | G | 2 | a0001c0001t0001g0079 a0001c0001t0001g0080 |
2 | HG00673.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.364-1352A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462759 | |||||||
| chr9:130462769 | T | C | 1 | a0001c0001t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.364-1342T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462769 | |||||||
| chr9:130462964 | C | T | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-1147C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130462964 | |||||||
| chr9:130463006 | T | C | 250 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(247): Show |
259 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(256): Show |
intron_variant | MODIFIER | c.364-1105T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463006 | |||||||
| chr9:130463281 | C | T | 9 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0056 others(6): Show |
10 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(7): Show |
intron_variant | MODIFIER | c.364-830C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463281 | |||||||
| chr9:130463288 | C | G | 1 | a0001c0001t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.364-823C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463288 | |||||||
| chr9:130463369 | C | T | 2 | a0001c0001t0001g0008 a0001c0014t0001g0171 |
3 | HG03486.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.364-742C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463369 | |||||||
| chr9:130463374 | G | T | 1 | a0001c0001t0001g0072 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.364-737G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463374 | |||||||
| chr9:130463654 | C | T | 1 | a0001c0001t0001g0309 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.364-457C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463654 | |||||||
| chr9:130463667 | G | A | 1 | a0001c0001t0001g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.364-444G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463667 | |||||||
| chr9:130463746 | G | T | 1 | a0001c0001t0001g0047 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.364-365G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463746 | |||||||
| chr9:130463789 | C | G | 4 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.364-322C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463789 | |||||||
| chr9:130463803 | G | A | 1 | a0001c0003t0001g0310 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.364-308G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463803 | |||||||
| chr9:130463975 | C | T | 1 | a0001c0014t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.364-136C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463975 | |||||||
| chr9:130463978 | T | G | 1 | a0001c0003t0001g0310 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.364-133T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130463978 | |||||||
| chr9:130464001 | G | A | 1 | a0001c0001t0001g0275 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.364-110G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130464001 | |||||||
| chr9:130464105 | T | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG02258.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.364-6T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 4/14 | chr9 | 130464105 | |||||||
| chr9:130464489 | G | C | 1 | a0001c0002t0001g0136 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.420+322G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130464489 | |||||||
| chr9:130464539 | C | T | 1 | a0001c0001t0001g0023 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.420+372C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130464539 | |||||||
| chr9:130464681 | C | T | 21 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0010 others(18): Show |
25 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.420+514C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130464681 | |||||||
| chr9:130464865 | C | T | 1 | a0001c0001t0001g0208 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.420+698C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130464865 | |||||||
| chr9:130464945 | C | T | 2 | a0001c0001t0001g0172 a0001c0001t0001g0212 |
2 | HG01891.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.420+778C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130464945 | |||||||
| chr9:130465034 | T | TTA | 5 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0064 others(2): Show |
5 | HG00438.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.420+889_420+890dup others(2): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr9 | 130465034 | ||||||
| chr9:130465034 | TTA | T | 14 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0065 others(11): Show |
14 | HG00639.hp2 HG01243.hp2 HG01261.hp1 others(11): Show |
intron_variant | MODIFIER | c.420+889_420+890del others(2): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr9 | 130465034 | ||||||
| chr9:130465034 | TTATA | T | 27 | a0001c0001t0001g0021 a0001c0001t0001g0167 a0001c0001t0001g0169 others(24): Show |
30 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(27): Show |
intron_variant | MODIFIER | c.420+887_420+890del others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr9 | 130465034 | ||||||
| chr9:130465034 | TTATATA | T | 11 | a0001c0001t0001g0004 a0001c0001t0001g0344 a0001c0001t0001g0346 others(8): Show |
13 | HG01891.hp2 HG02280.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.420+885_420+890del others(6): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr9 | 130465034 | ||||||
| chr9:130465036 | A | T | 4 | a0001c0001t0001g0028 a0001c0001t0001g0138 a0001c0001t0001g0139 others(1): Show |
4 | HG00140.hp1 HG02145.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+869A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465036 | |||||||
| chr9:130465044 | A | G | 4 | a0001c0001t0001g0268 a0001c0001t0001g0278 a0001c0001t0001g0312 others(1): Show |
4 | HG01255.hp1 HG01993.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+877A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465044 | |||||||
| chr9:130465047 | TATATATA | T | 5 | a0002c0004t0001g0011 a0002c0004t0001g0216 a0002c0004t0001g0217 others(2): Show |
6 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+881_420+887del others(7): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465047 | |||||||
| chr9:130465049 | TATA | T | 6 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0003t0001g0298 others(3): Show |
6 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+883_420+885del others(3): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465049 | |||||||
| chr9:130465049 | TATATA | T | 6 | a0001c0002t0001g0053 a0001c0002t0001g0192 a0001c0002t0002g0179 others(3): Show |
6 | HG01433.hp1 HG02523.hp2 HG02922.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+883_420+887del others(5): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465049 | |||||||
| chr9:130465050 | A | T | 1 | a0001c0001t0001g0303 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.420+883A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465050 | |||||||
| chr9:130465051 | TATA | T | 8 | a0001c0001t0001g0043 a0001c0001t0001g0166 a0001c0001t0001g0172 others(5): Show |
8 | HG01891.hp1 HG02559.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.420+885_420+887del others(3): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465051 | |||||||
| chr9:130465051 | TATATA | T | 9 | a0001c0001t0001g0138 a0001c0001t0001g0139 a0001c0001t0001g0140 others(6): Show |
10 | HG02145.hp2 HG02615.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.420+885_420+889del others(5): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465051 | |||||||
| chr9:130465052 | A | T | 2 | a0001c0001t0001g0303 a0001c0001t0001g0305 |
2 | HG01074.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.420+885A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465052 | |||||||
| chr9:130465053 | TA | T | 36 | a0001c0001t0001g0023 a0001c0001t0001g0028 a0001c0001t0001g0044 others(33): Show |
36 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(33): Show |
intron_variant | MODIFIER | c.420+887delA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465053 | |||||||
| chr9:130465053 | TATA | T | 5 | a0001c0001t0001g0018 a0001c0001t0001g0042 a0001c0001t0001g0212 others(2): Show |
5 | HG02258.hp1 HG02559.hp1 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.420+887_420+889del others(3): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465053 | |||||||
| chr9:130465054 | A | AT | 5 | a0001c0001t0001g0109 a0001c0001t0001g0161 a0001c0001t0001g0223 others(2): Show |
5 | HG01106.hp1 HG01943.hp1 HG02135.hp1 others(2): Show |
intron_variant | MODIFIER | c.420+888dupT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr9 | 130465054 | ||||||
| chr9:130465054 | A | T | 32 | a0001c0001t0001g0022 a0001c0001t0001g0025 a0001c0001t0001g0029 others(29): Show |
32 | HG00408.hp1 HG00639.hp2 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.420+887A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465054 | |||||||
| chr9:130465055 | TA | T | 51 | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0033 others(48): Show |
53 | HG00323.hp1 HG00408.hp2 HG00597.hp2 others(50): Show |
intron_variant | MODIFIER | c.420+889delA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465055 | |||||||
| chr9:130465056 | A | ATATATAT others(27): Show |
1 | a0001c0001t0001g0155 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.420+890_420+891ins others(34): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr9 | 130465056 | ||||||
| chr9:130465056 | A | ATATATAT others(23): Show |
1 | a0004c0006t0001g0141 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.420+890_420+891ins others(30): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr9 | 130465056 | ||||||
| chr9:130465056 | A | ATATATAT others(20): Show |
1 | a0004c0006t0001g0142 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.420+890_420+891ins others(27): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr9 | 130465056 | ||||||
| chr9:130465056 | A | T | 153 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0015 others(150): Show |
159 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(156): Show |
intron_variant | MODIFIER | c.420+889A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465056 | |||||||
| chr9:130465056 | AT | A | 14 | a0001c0001t0001g0007 a0001c0001t0001g0037 a0001c0001t0001g0081 others(11): Show |
15 | HG00140.hp2 HG00323.hp2 HG00642.hp2 others(12): Show |
intron_variant | MODIFIER | c.420+901delT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr9 | 130465056 | ||||||
| chr9:130465058 | T | A | 16 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0056 others(13): Show |
17 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+891T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465058 | |||||||
| chr9:130465059 | T | A | 2 | a0001c0001t0001g0113 a0001c0001t0001g0238 |
2 | HG03704.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.420+892T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465059 | |||||||
| chr9:130465060 | T | A | 9 | a0001c0001t0001g0006 a0001c0001t0001g0057 a0001c0001t0001g0058 others(6): Show |
10 | HG00280.hp1 HG00741.hp1 HG01099.hp1 others(7): Show |
intron_variant | MODIFIER | c.420+893T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465060 | |||||||
| chr9:130465315 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(249): Show |
261 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(258): Show |
intron_variant | MODIFIER | c.420+1148G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465315 | |||||||
| chr9:130465404 | A | G | 338 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(335): Show |
355 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(352): Show |
intron_variant | MODIFIER | c.420+1237A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465404 | |||||||
| chr9:130465466 | T | C | 8 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG02258.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-1259T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465466 | |||||||
| chr9:130465516 | G | A | 4 | a0001c0001t0001g0095 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
4 | HG01168.hp2 HG01169.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-1209G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465516 | |||||||
| chr9:130465526 | T | C | 27 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(24): Show |
30 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.421-1199T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465526 | |||||||
| chr9:130465602 | T | C | 1 | a0001c0001t0001g0352 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.421-1123T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465602 | |||||||
| chr9:130465610 | G | A | 1 | a0001c0001t0001g0156 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.421-1115G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465610 | |||||||
| chr9:130465649 | GC | G | 12 | a0001c0001t0001g0009 a0001c0001t0001g0239 a0001c0001t0001g0240 others(9): Show |
13 | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(10): Show |
intron_variant | MODIFIER | c.421-1071delC | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr9 | 130465649 | ||||||
| chr9:130465650 | C | T | 27 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(24): Show |
30 | HG01167.hp2 HG01884.hp1 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.421-1075C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465650 | |||||||
| chr9:130465916 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.421-809G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465916 | |||||||
| chr9:130465997 | G | A | 301 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(298): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.421-728G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130465997 | |||||||
| chr9:130466105 | C | T | 1 | a0001c0001t0001g0210 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.421-620C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466105 | |||||||
| chr9:130466109 | C | T | 1 | a0001c0001t0001g0231 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.421-616C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466109 | |||||||
| chr9:130466140 | G | A | 1 | a0001c0001t0001g0246 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.421-585G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466140 | |||||||
| chr9:130466206 | C | G | 1 | a0001c0001t0001g0154 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.421-519C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466206 | |||||||
| chr9:130466210 | G | T | 24 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(21): Show |
27 | HG01167.hp2 HG01891.hp2 HG02145.hp2 others(24): Show |
intron_variant | MODIFIER | c.421-515G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466210 | |||||||
| chr9:130466310 | G | A | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.421-415G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466310 | |||||||
| chr9:130466315 | C | T | 28 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(25): Show |
31 | HG01109.hp1 HG01167.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.421-410C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466315 | |||||||
| chr9:130466324 | G | A | 25 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(22): Show |
28 | HG01109.hp1 HG01167.hp2 HG01891.hp2 others(25): Show |
intron_variant | MODIFIER | c.421-401G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466324 | |||||||
| chr9:130466348 | C | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0276 |
2 | NA18961.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.421-377C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466348 | |||||||
| chr9:130466372 | G | A | 1 | a0001c0001t0001g0328 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.421-353G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466372 | |||||||
| chr9:130466414 | C | T | 10 | a0001c0001t0001g0008 a0001c0001t0001g0021 a0001c0001t0001g0143 others(7): Show |
11 | HG02258.hp2 HG02809.hp2 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.421-311C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466414 | |||||||
| chr9:130466491 | C | A | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.421-234C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466491 | |||||||
| chr9:130466537 | C | T | 8 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG02258.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-188C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466537 | |||||||
| chr9:130466697 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0151 a0001c0001t0001g0220 others(4): Show |
8 | HG00438.hp1 NA18747.hp2 NA18961.hp1 others(5): Show |
intron_variant | MODIFIER | c.421-28C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466697 | |||||||
| chr9:130466706 | C | T | 3 | a0001c0001t0001g0155 a0004c0006t0001g0141 a0004c0006t0001g0142 |
3 | HG01884.hp1 HG01943.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.421-19C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 5/14 | chr9 | 130466706 | |||||||
| chr9:130466883 | A | C | 55 | a0001c0001t0001g0004 a0001c0001t0001g0138 a0001c0001t0001g0139 others(52): Show |
62 | HG00099.hp2 HG00733.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.495+84A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130466883 | |||||||
| chr9:130467248 | C | T | 21 | a0001c0002t0001g0002 a0001c0002t0001g0005 a0001c0002t0001g0010 others(18): Show |
25 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.495+449C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130467248 | |||||||
| chr9:130467378 | C | T | 3 | a0001c0001t0001g0155 a0004c0006t0001g0141 a0004c0006t0001g0142 |
3 | HG01884.hp1 HG01943.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.495+579C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130467378 | |||||||
| chr9:130467437 | C | G | 2 | a0001c0001t0001g0022 a0001c0001t0001g0035 |
2 | HG03239.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.495+638C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130467437 | |||||||
| chr9:130467866 | C | G | 1 | a0001c0001t0001g0155 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.495+1067C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130467866 | |||||||
| chr9:130468272 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(266): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.495+1473C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468272 | |||||||
| chr9:130468286 | A | G | 1 | a0001c0002t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.495+1487A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468286 | |||||||
| chr9:130468287 | G | A | 1 | a0001c0001t0001g0018 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.495+1488G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468287 | |||||||
| chr9:130468331 | C | T | 2 | a0001c0001t0001g0163 a0001c0003t0001g0199 |
2 | HG02698.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.495+1532C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468331 | |||||||
| chr9:130468357 | G | A | 14 | a0001c0001t0001g0196 a0001c0001t0001g0327 a0001c0003t0001g0149 others(11): Show |
14 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(11): Show |
intron_variant | MODIFIER | c.495+1558G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468357 | |||||||
| chr9:130468411 | TA | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(88): Show |
94 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.495+1621delA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr9 | 130468411 | ||||||
| chr9:130468557 | G | A | 287 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(284): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.495+1758G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468557 | |||||||
| chr9:130468590 | C | T | 327 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(324): Show |
343 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(340): Show |
intron_variant | MODIFIER | c.495+1791C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468590 | |||||||
| chr9:130468597 | T | G | 17 | a0001c0001t0001g0155 a0001c0001t0001g0170 a0001c0001t0001g0196 others(14): Show |
17 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.495+1798T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468597 | |||||||
| chr9:130468607 | A | T | 1 | a0001c0002t0001g0077 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.495+1808A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468607 | |||||||
| chr9:130468611 | T | A | 3 | a0001c0001t0001g0074 a0001c0001t0001g0248 a0001c0001t0001g0285 |
3 | NA18954.hp1 NA18963.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.495+1812T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468611 | |||||||
| chr9:130468676 | C | G | 7 | a0001c0002t0001g0136 a0002c0004t0001g0011 a0002c0004t0001g0216 others(4): Show |
8 | HG01167.hp2 HG02280.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.495+1877C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468676 | |||||||
| chr9:130468740 | A | C | 1 | a0001c0001t0001g0337 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.495+1941A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468740 | |||||||
| chr9:130468903 | A | G | 19 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0138 others(16): Show |
19 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.496-1931A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130468903 | |||||||
| chr9:130469070 | C | T | 2 | a0001c0001t0001g0155 a0003c0008t0001g0200 |
2 | HG03516.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.496-1764C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130469070 | |||||||
| chr9:130469148 | G | A | 1 | a0001c0001t0001g0249 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.496-1686G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130469148 | |||||||
| chr9:130469190 | G | A | 3 | a0001c0001t0001g0213 a0001c0001t0001g0214 a0001c0003t0001g0199 |
3 | HG02896.hp1 HG02897.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.496-1644G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130469190 | |||||||
| chr9:130469251 | C | T | 2 | a0001c0003t0001g0227 a0001c0003t0001g0228 |
2 | HG02965.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.496-1583C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130469251 | |||||||
| chr9:130469352 | T | C | 1 | a0001c0001t0001g0057 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.496-1482T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130469352 | |||||||
| chr9:130469754 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.496-1080G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130469754 | |||||||
| chr9:130469828 | A | G | 2 | a0001c0001t0001g0015 a0001c0001t0001g0270 |
3 | NA18966.hp1 NA19005.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.496-1006A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130469828 | |||||||
| chr9:130469868 | C | T | 21 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(18): Show |
21 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.496-966C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130469868 | |||||||
| chr9:130469985 | G | A | 21 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(18): Show |
21 | HG01891.hp1 HG02145.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.496-849G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130469985 | |||||||
| chr9:130470112 | ATCT | A | 8 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG02258.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.496-716_496-714del others(3): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr9 | 130470112 | ||||||
| chr9:130470156 | C | T | 17 | a0001c0001t0001g0021 a0001c0001t0001g0042 a0001c0001t0001g0043 others(14): Show |
17 | HG01891.hp1 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.496-678C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130470156 | |||||||
| chr9:130470191 | G | A | 12 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(9): Show |
12 | HG01106.hp2 HG01109.hp2 HG01358.hp1 others(9): Show |
intron_variant | MODIFIER | c.496-643G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130470191 | |||||||
| chr9:130470337 | C | T | 6 | a0001c0001t0001g0150 a0001c0001t0001g0229 a0001c0001t0001g0230 others(3): Show |
6 | HG01928.hp1 HG01934.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.496-497C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130470337 | |||||||
| chr9:130470448 | C | T | 2 | a0004c0006t0001g0141 a0004c0006t0001g0142 |
2 | HG01884.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.496-386C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130470448 | |||||||
| chr9:130470459 | G | C | 1 | a0001c0001t0001g0081 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.496-375G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130470459 | |||||||
| chr9:130470580 | T | C | 1 | a0001c0001t0001g0167 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.496-254T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130470580 | |||||||
| chr9:130470776 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.496-58G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130470776 | |||||||
| chr9:130470784 | C | T | 1 | a0001c0002t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.496-50C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130470784 | |||||||
| chr9:130470798 | C | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0342 others(18): Show |
24 | HG01167.hp2 HG01891.hp2 HG02280.hp1 others(21): Show |
intron_variant | MODIFIER | c.496-36C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 6/14 | chr9 | 130470798 | |||||||
| chr9:130470958 | G | A | 2 | a0001c0002t0001g0177 a0001c0002t0001g0191 |
2 | HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.566+54G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 7/14 | chr9 | 130470958 | |||||||
| chr9:130470964 | G | A | 2 | a0001c0001t0001g0111 a0001c0001t0001g0239 |
2 | HG00558.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.566+60G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 7/14 | chr9 | 130470964 | |||||||
| chr9:130470992 | C | T | 235 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(232): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.566+88C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 7/14 | chr9 | 130470992 | |||||||
| chr9:130471076 | A | G | 2 | a0004c0006t0001g0141 a0004c0006t0001g0142 |
2 | HG01884.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.566+172A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 7/14 | chr9 | 130471076 | |||||||
| chr9:130471316 | C | T | 3 | a0001c0002t0001g0180 a0001c0002t0001g0192 a0001c0002t0002g0179 |
3 | NA19007.hp2 NA19070.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.567-169C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 7/14 | chr9 | 130471316 | |||||||
| chr9:130471385 | G | A | 2 | a0001c0003t0001g0321 a0001c0003t0001g0322 |
2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.567-100G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 7/14 | chr9 | 130471385 | |||||||
| chr9:130471410 | G | A | 1 | a0001c0001t0001g0041 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.567-75G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 7/14 | chr9 | 130471410 | |||||||
| chr9:130471523 | C | T | 14 | a0001c0001t0001g0043 a0001c0001t0001g0172 a0001c0001t0001g0212 others(11): Show |
15 | HG01167.hp2 HG01891.hp1 HG02258.hp1 others(12): Show |
splice_region_variant&intron_variant | LOW | c.597+8C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471523 | |||||||
| chr9:130471533 | A | G | 284 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(281): Show |
297 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(294): Show |
intron_variant | MODIFIER | c.597+18A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471533 | |||||||
| chr9:130471575 | C | T | 2 | a0001c0001t0001g0223 a0001c0001t0001g0274 |
2 | HG02135.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.597+60C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471575 | |||||||
| chr9:130471596 | A | G | 329 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(326): Show |
346 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(343): Show |
intron_variant | MODIFIER | c.597+81A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471596 | |||||||
| chr9:130471682 | C | A | 5 | a0001c0001t0001g0067 a0001c0001t0001g0068 a0001c0001t0001g0103 others(2): Show |
5 | HG01884.hp2 HG02451.hp1 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+167C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471682 | |||||||
| chr9:130471693 | G | A | 222 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(219): Show |
230 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(227): Show |
intron_variant | MODIFIER | c.597+178G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471693 | |||||||
| chr9:130471721 | C | T | 1 | a0001c0001t0001g0106 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.597+206C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471721 | |||||||
| chr9:130471801 | T | A | 1 | a0001c0001t0001g0040 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.597+286T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471801 | |||||||
| chr9:130471907 | T | C | 281 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(278): Show |
294 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(291): Show |
intron_variant | MODIFIER | c.597+392T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471907 | |||||||
| chr9:130471912 | G | A | 1 | a0001c0001t0001g0096 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.597+397G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471912 | |||||||
| chr9:130471919 | T | C | 1 | a0001c0001t0001g0323 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.597+404T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130471919 | |||||||
| chr9:130472044 | C | T | 2 | a0001c0001t0001g0243 a0001c0001t0001g0244 |
2 | HG00558.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.597+529C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130472044 | |||||||
| chr9:130472045 | G | T | 1 | a0001c0001t0001g0035 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.597+530G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130472045 | |||||||
| chr9:130472197 | C | G | 1 | a0001c0003t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.597+682C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130472197 | |||||||
| chr9:130472293 | C | T | 3 | a0001c0001t0001g0018 a0001c0001t0001g0100 a0001c0001t0001g0101 |
3 | NA18612.hp1 NA18940.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.597+778C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130472293 | |||||||
| chr9:130472386 | C | T | 16 | a0001c0001t0001g0196 a0001c0001t0001g0327 a0001c0003t0001g0135 others(13): Show |
16 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.597+871C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130472386 | |||||||
| chr9:130472389 | G | T | 1 | a0001c0002t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.597+874G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130472389 | |||||||
| chr9:130472425 | A | G | 16 | a0001c0001t0001g0042 a0001c0001t0001g0043 a0001c0001t0001g0172 others(13): Show |
17 | HG01167.hp2 HG01891.hp1 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.597+910A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130472425 | |||||||
| chr9:130472600 | G | A | 2 | a0001c0001t0001g0123 a0001c0001t0001g0320 |
2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.597+1085G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130472600 | |||||||
| chr9:130472800 | G | A | 322 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(319): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.597+1285G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130472800 | |||||||
| chr9:130472908 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.597+1393G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130472908 | |||||||
| chr9:130473009 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.597+1494C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473009 | |||||||
| chr9:130473068 | C | T | 7 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0331 others(4): Show |
8 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.597+1553C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473068 | |||||||
| chr9:130473299 | G | A | 1 | a0001c0003t0001g0149 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.597+1784G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473299 | |||||||
| chr9:130473467 | GGGCACCC others(13): Show |
G | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.597+1987_597+2006d others(22): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr9 | 130473467 | ||||||
| chr9:130473507 | A | G | 8 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(5): Show |
8 | HG02258.hp2 HG02809.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.597+1992A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473507 | |||||||
| chr9:130473518 | G | A | 1 | a0001c0002t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.597+2003G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473518 | |||||||
| chr9:130473602 | C | T | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.597+2087C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473602 | |||||||
| chr9:130473845 | G | A | 1 | a0001c0003t0001g0188 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.597+2330G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473845 | |||||||
| chr9:130473850 | A | G | 3 | a0001c0001t0001g0349 a0001c0001t0001g0350 a0001c0002t0001g0136 |
3 | HG03041.hp1 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.597+2335A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473850 | |||||||
| chr9:130473923 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.597+2408C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473923 | |||||||
| chr9:130473993 | C | T | 44 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0076 others(41): Show |
45 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(42): Show |
intron_variant | MODIFIER | c.597+2478C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473993 | |||||||
| chr9:130473997 | C | T | 58 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0022 others(55): Show |
60 | HG00140.hp1 HG00280.hp1 HG00558.hp1 others(57): Show |
intron_variant | MODIFIER | c.597+2482C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473997 | |||||||
| chr9:130473999 | C | G | 64 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0018 others(61): Show |
67 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(64): Show |
intron_variant | MODIFIER | c.597+2484C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130473999 | |||||||
| chr9:130474005 | CT | C | 46 | a0001c0001t0001g0014 a0001c0001t0001g0034 a0001c0001t0001g0076 others(43): Show |
47 | HG00099.hp1 HG00609.hp2 HG00733.hp2 others(44): Show |
intron_variant | MODIFIER | c.597+2491delT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474005 | |||||||
| chr9:130474048 | C | T | 2 | a0001c0002t0001g0181 a0001c0002t0001g0189 |
2 | NA18986.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.597+2533C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474048 | |||||||
| chr9:130474062 | AC | A | 69 | a0001c0001t0001g0016 a0001c0001t0001g0021 a0001c0001t0001g0022 others(66): Show |
70 | HG00597.hp1 HG00738.hp1 HG01167.hp2 others(67): Show |
intron_variant | MODIFIER | c.597+2560delC | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr9 | 130474062 | ||||||
| chr9:130474062 | ACC | A | 240 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(237): Show |
257 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(254): Show |
intron_variant | MODIFIER | c.597+2559_597+2560d others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr9 | 130474062 | ||||||
| chr9:130474063 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.597+2548C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474063 | |||||||
| chr9:130474069 | C | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.597+2554C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474069 | |||||||
| chr9:130474076 | A | G | 15 | a0001c0001t0001g0006 a0001c0001t0001g0055 a0001c0001t0001g0056 others(12): Show |
16 | HG00280.hp1 HG00735.hp1 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.597+2561A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474076 | |||||||
| chr9:130474104 | G | A | 1 | a0001c0002t0001g0180 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.597+2589G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474104 | |||||||
| chr9:130474284 | C | T | 1 | a0001c0001t0001g0039 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.598-2587C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474284 | |||||||
| chr9:130474305 | G | A | 1 | a0001c0001t0001g0338 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.598-2566G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474305 | |||||||
| chr9:130474383 | C | T | 1 | a0001c0001t0001g0260 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.598-2488C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474383 | |||||||
| chr9:130474457 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.598-2414G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474457 | |||||||
| chr9:130474463 | G | T | 110 | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0013 others(107): Show |
118 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.598-2408G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474463 | |||||||
| chr9:130474513 | G | T | 1 | a0001c0014t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.598-2358G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474513 | |||||||
| chr9:130474640 | C | A | 1 | a0001c0001t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.598-2231C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474640 | |||||||
| chr9:130474695 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(254): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.598-2176A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474695 | |||||||
| chr9:130474715 | C | T | 1 | a0001c0001t0001g0221 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.598-2156C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474715 | |||||||
| chr9:130474716 | T | G | 1 | a0001c0001t0001g0221 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.598-2155T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474716 | |||||||
| chr9:130474717 | G | C | 1 | a0001c0001t0001g0221 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.598-2154G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474717 | |||||||
| chr9:130474798 | T | A | 1 | a0001c0001t0001g0221 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.598-2073T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474798 | |||||||
| chr9:130474887 | G | T | 1 | a0001c0001t0001g0339 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.598-1984G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474887 | |||||||
| chr9:130474898 | C | G | 1 | a0001c0001t0001g0341 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.598-1973C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474898 | |||||||
| chr9:130474932 | G | A | 330 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(327): Show |
347 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(344): Show |
intron_variant | MODIFIER | c.598-1939G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130474932 | |||||||
| chr9:130475020 | G | A | 1 | a0001c0001t0001g0267 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.598-1851G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475020 | |||||||
| chr9:130475221 | G | A | 226 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(223): Show |
239 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(236): Show |
intron_variant | MODIFIER | c.598-1650G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475221 | |||||||
| chr9:130475246 | A | G | 2 | a0001c0001t0001g0041 a0001c0002t0001g0019 |
2 | HG03471.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.598-1625A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475246 | |||||||
| chr9:130475454 | A | T | 3 | a0001c0001t0001g0106 a0001c0001t0001g0280 a0001c0001t0001g0284 |
3 | HG00733.hp2 HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.598-1417A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475454 | |||||||
| chr9:130475481 | T | A | 1 | a0001c0001t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.598-1390T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475481 | |||||||
| chr9:130475490 | G | A | 2 | a0003c0009t0001g0306 a0003c0009t0001g0307 |
2 | HG01255.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.598-1381G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475490 | |||||||
| chr9:130475541 | G | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0197 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.598-1330G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475541 | |||||||
| chr9:130475598 | TC | T | 3 | a0001c0001t0001g0041 a0001c0002t0001g0019 a0001c0014t0001g0171 |
3 | HG03471.hp1 HG04115.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.598-1272delC | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475598 | |||||||
| chr9:130475652 | T | TGGGGTAA others(26): Show |
1 | a0001c0001t0001g0156 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.598-1216_598-1184d others(35): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr9 | 130475652 | ||||||
| chr9:130475719 | A | G | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0006 others(252): Show |
269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.598-1152A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475719 | |||||||
| chr9:130475741 | G | GT | 86 | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0009 others(83): Show |
90 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.598-1110dupT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr9 | 130475741 | ||||||
| chr9:130475741 | G | GTT | 7 | a0001c0001t0001g0020 a0001c0001t0001g0207 a0001c0001t0001g0244 others(4): Show |
7 | HG01169.hp1 HG01358.hp2 HG04184.hp2 others(4): Show |
intron_variant | MODIFIER | c.598-1111_598-1110d others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr9 | 130475741 | ||||||
| chr9:130475741 | G | T | 1 | a0001c0001t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.598-1130G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475741 | |||||||
| chr9:130475741 | GT | G | 9 | a0001c0001t0001g0041 a0001c0001t0001g0090 a0001c0001t0001g0156 others(6): Show |
9 | HG01975.hp2 HG02683.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.598-1110delT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | INFO_REALIGN_3_PRIME | chr9 | 130475741 | ||||||
| chr9:130475766 | G | T | 1 | a0001c0014t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.598-1105G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475766 | |||||||
| chr9:130475770 | G | T | 1 | a0001c0001t0001g0323 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.598-1101G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475770 | |||||||
| chr9:130475773 | G | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0283 a0004c0006t0001g0141 others(1): Show |
5 | HG01884.hp1 HG01943.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.598-1098G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475773 | |||||||
| chr9:130475821 | A | G | 9 | a0001c0001t0001g0140 a0001c0001t0001g0326 a0001c0001t0001g0337 others(6): Show |
9 | HG02145.hp2 HG02818.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.598-1050A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475821 | |||||||
| chr9:130475842 | C | T | 1 | a0002c0004t0001g0217 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.598-1029C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475842 | |||||||
| chr9:130475894 | C | T | 1 | a0001c0001t0001g0326 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.598-977C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475894 | |||||||
| chr9:130475902 | G | A | 1 | a0001c0001t0001g0196 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.598-969G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475902 | |||||||
| chr9:130475908 | C | T | 7 | a0001c0001t0001g0008 a0001c0001t0001g0041 a0001c0001t0001g0283 others(4): Show |
8 | HG01884.hp1 HG01943.hp2 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.598-963C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130475908 | |||||||
| chr9:130476072 | T | G | 1 | a0001c0001t0001g0325 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.598-799T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130476072 | |||||||
| chr9:130476159 | A | G | 2 | a0001c0001t0001g0041 a0001c0002t0001g0019 |
2 | HG03471.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.598-712A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130476159 | |||||||
| chr9:130476269 | G | A | 1 | a0001c0002t0001g0053 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.598-602G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130476269 | |||||||
| chr9:130476280 | A | G | 5 | a0001c0003t0001g0135 a0001c0003t0001g0297 a0001c0003t0001g0298 others(2): Show |
5 | HG01070.hp2 HG01071.hp1 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.598-591A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130476280 | |||||||
| chr9:130476334 | A | G | 2 | a0003c0008t0001g0200 a0003c0008t0001g0201 |
2 | HG01433.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.598-537A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130476334 | |||||||
| chr9:130476420 | G | A | 1 | a0001c0001t0001g0038 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.598-451G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130476420 | |||||||
| chr9:130476517 | G | C | 1 | a0001c0001t0001g0220 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.598-354G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130476517 | |||||||
| chr9:130476547 | G | A | 3 | a0001c0001t0001g0117 a0001c0001t0001g0120 a0001c0001t0001g0122 |
3 | HG01192.hp2 HG02683.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.598-324G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130476547 | |||||||
| chr9:130476718 | A | T | 1 | a0001c0001t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.598-153A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130476718 | |||||||
| chr9:130476797 | C | T | 1 | a0001c0001t0001g0285 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.598-74C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 8/14 | chr9 | 130476797 | |||||||
| chr9:130476965 | T | C | 7 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0331 others(4): Show |
8 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(5): Show |
splice_region_variant&intron_variant | LOW | c.688+4T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130476965 | |||||||
| chr9:130477065 | A | G | 2 | a0001c0001t0001g0107 a0001c0001t0001g0108 |
2 | HG01099.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.688+104A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130477065 | |||||||
| chr9:130477167 | G | A | 18 | a0001c0001t0001g0196 a0001c0001t0001g0327 a0001c0003t0001g0131 others(15): Show |
18 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(15): Show |
intron_variant | MODIFIER | c.688+206G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130477167 | |||||||
| chr9:130477360 | C | T | 4 | a0001c0001t0001g0008 a0001c0001t0001g0283 a0004c0006t0001g0141 others(1): Show |
5 | HG01884.hp1 HG01943.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.688+399C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130477360 | |||||||
| chr9:130477394 | C | T | 1 | a0001c0001t0001g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.688+433C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130477394 | |||||||
| chr9:130477425 | C | CA | 4 | a0001c0001t0001g0008 a0001c0001t0001g0283 a0004c0006t0001g0141 others(1): Show |
5 | HG01884.hp1 HG01943.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.688+465dupA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr9 | 130477425 | ||||||
| chr9:130477457 | G | A | 1 | a0001c0001t0001g0064 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.688+496G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130477457 | |||||||
| chr9:130477692 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.688+731G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130477692 | |||||||
| chr9:130477695 | C | T | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.688+734C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130477695 | |||||||
| chr9:130477717 | C | T | 3 | a0001c0001t0001g0041 a0001c0002t0001g0019 a0001c0014t0001g0171 |
3 | HG03471.hp1 HG04115.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.688+756C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130477717 | |||||||
| chr9:130477799 | G | A | 23 | a0001c0001t0001g0026 a0001c0001t0001g0348 a0001c0002t0001g0002 others(20): Show |
27 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.688+838G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130477799 | |||||||
| chr9:130477880 | C | T | 32 | a0001c0001t0001g0026 a0001c0001t0001g0140 a0001c0001t0001g0326 others(29): Show |
36 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.688+919C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130477880 | |||||||
| chr9:130478022 | G | A | 2 | a0001c0001t0001g0073 a0001c0001t0001g0219 |
2 | HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.688+1061G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130478022 | |||||||
| chr9:130478497 | C | A | 7 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0249 others(4): Show |
9 | HG02280.hp1 HG02630.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.689-1219C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130478497 | |||||||
| chr9:130478696 | C | T | 2 | a0001c0001t0001g0328 a0007c0011t0001g0168 |
2 | HG02559.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.689-1020C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130478696 | |||||||
| chr9:130478744 | G | A | 1 | a0001c0003t0001g0131 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.689-972G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130478744 | |||||||
| chr9:130478846 | C | G | 1 | a0001c0001t0001g0317 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.689-870C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130478846 | |||||||
| chr9:130478955 | T | A | 1 | a0001c0001t0001g0240 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.689-761T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130478955 | |||||||
| chr9:130479032 | T | A | 4 | a0001c0001t0001g0281 a0001c0001t0001g0293 a0001c0001t0001g0294 others(1): Show |
4 | HG01106.hp2 HG01109.hp2 HG01358.hp1 others(1): Show |
intron_variant | MODIFIER | c.689-684T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130479032 | |||||||
| chr9:130479106 | C | T | 1 | a0001c0001t0001g0156 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.689-610C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130479106 | |||||||
| chr9:130479107 | CA | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.689-608delA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130479107 | |||||||
| chr9:130479108 | A | C | 320 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(317): Show |
337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.689-608A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130479108 | |||||||
| chr9:130479110 | C | G | 6 | a0001c0001t0001g0020 a0001c0001t0001g0057 a0001c0001t0001g0095 others(3): Show |
6 | HG01168.hp2 HG01169.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.689-606C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130479110 | |||||||
| chr9:130479250 | G | A | 21 | a0001c0001t0001g0035 a0001c0001t0001g0196 a0001c0001t0001g0327 others(18): Show |
21 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.689-466G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130479250 | |||||||
| chr9:130479281 | C | CTG | 5 | a0001c0001t0001g0148 a0001c0001t0001g0170 a0001c0001t0001g0213 others(2): Show |
5 | HG02145.hp1 HG02896.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.689-412_689-411dup others(2): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr9 | 130479281 | ||||||
| chr9:130479281 | CTGTG | C | 3 | a0001c0001t0001g0046 a0001c0003t0001g0188 a0001c0003t0001g0345 |
3 | HG01891.hp2 HG02559.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.689-414_689-411del others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr9 | 130479281 | ||||||
| chr9:130479281 | CTGTGTGT others(5): Show |
C | 1 | a0001c0001t0001g0317 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.689-422_689-411del others(12): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr9 | 130479281 | ||||||
| chr9:130479349 | C | T | 1 | a0001c0001t0001g0316 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.689-367C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130479349 | |||||||
| chr9:130479425 | A | G | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.689-291A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130479425 | |||||||
| chr9:130479524 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.689-192G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130479524 | |||||||
| chr9:130479678 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.689-38C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 9/14 | chr9 | 130479678 | |||||||
| chr9:130479856 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.773+56G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 10/14 | chr9 | 130479856 | |||||||
| chr9:130479984 | G | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0015 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.773+184G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 10/14 | chr9 | 130479984 | |||||||
| chr9:130480355 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.774-30C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 10/14 | chr9 | 130480355 | |||||||
| chr9:130480357 | GAACCTAA others(5): Show |
G | 1 | a0001c0001t0001g0289 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.774-27_774-16delAA others(10): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 10/14 | chr9 | 130480357 | |||||||
| chr9:130480487 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(319): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.838+38A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480487 | |||||||
| chr9:130480515 | C | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(96): Show |
104 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(101): Show |
intron_variant | MODIFIER | c.838+66C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480515 | |||||||
| chr9:130480541 | C | T | 3 | a0001c0001t0001g0139 a0001c0001t0001g0198 a0001c0001t0001g0330 |
3 | HG02615.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.838+92C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480541 | |||||||
| chr9:130480567 | C | T | 1 | a0001c0014t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.838+118C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480567 | |||||||
| chr9:130480578 | C | G | 66 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0015 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.838+129C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480578 | |||||||
| chr9:130480593 | C | T | 186 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(183): Show |
196 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(193): Show |
intron_variant | MODIFIER | c.838+144C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480593 | |||||||
| chr9:130480806 | C | A | 66 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0015 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.838+357C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480806 | |||||||
| chr9:130480849 | G | A | 1 | a0001c0001t0001g0308 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.838+400G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480849 | |||||||
| chr9:130480886 | G | A | 1 | a0001c0002t0001g0182 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.838+437G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480886 | |||||||
| chr9:130480901 | C | A | 1 | a0001c0001t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.838+452C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480901 | |||||||
| chr9:130480904 | G | A | 4 | a0001c0001t0001g0163 a0001c0001t0001g0249 a0001c0001t0001g0252 others(1): Show |
4 | HG02698.hp2 HG02735.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+455G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130480904 | |||||||
| chr9:130481015 | C | G | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+566C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481015 | |||||||
| chr9:130481016 | A | C | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+567A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481016 | |||||||
| chr9:130481026 | C | A | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+577C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481026 | |||||||
| chr9:130481026 | C | G | 21 | a0001c0001t0001g0196 a0001c0003t0001g0131 a0001c0003t0001g0135 others(18): Show |
21 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.838+577C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481026 | |||||||
| chr9:130481038 | T | A | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+589T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481038 | |||||||
| chr9:130481049 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+600T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481049 | |||||||
| chr9:130481051 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+602G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481051 | |||||||
| chr9:130481058 | A | T | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+609A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481058 | |||||||
| chr9:130481059 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+610T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481059 | |||||||
| chr9:130481061 | C | G | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+612C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481061 | |||||||
| chr9:130481064 | C | A | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+615C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481064 | |||||||
| chr9:130481064 | C | G | 1 | a0001c0001t0001g0025 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.838+615C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481064 | |||||||
| chr9:130481065 | T | C | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+616T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481065 | |||||||
| chr9:130481066 | G | A | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+617G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481066 | |||||||
| chr9:130481067 | T | G | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+618T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481067 | |||||||
| chr9:130481083 | C | A | 1 | a0001c0001t0001g0290 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.838+634C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481083 | |||||||
| chr9:130481236 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0242 a0001c0001t0001g0262 others(1): Show |
5 | NA18952.hp2 NA18957.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.838+787C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481236 | |||||||
| chr9:130481377 | T | C | 322 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(319): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.838+928T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481377 | |||||||
| chr9:130481418 | T | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(319): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.838+969T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481418 | |||||||
| chr9:130481557 | G | A | 100 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(97): Show |
105 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(102): Show |
intron_variant | MODIFIER | c.838+1108G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481557 | |||||||
| chr9:130481584 | C | G | 1 | a0001c0001t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.838+1135C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481584 | |||||||
| chr9:130481630 | G | A | 1 | a0001c0003t0001g0296 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.838+1181G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481630 | |||||||
| chr9:130481740 | G | A | 2 | a0001c0003t0001g0336 a0001c0003t0001g0343 |
2 | NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.838+1291G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481740 | |||||||
| chr9:130481786 | A | G | 322 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(319): Show |
339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.838+1337A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481786 | |||||||
| chr9:130481906 | C | T | 9 | a0001c0001t0001g0037 a0001c0001t0001g0049 a0001c0001t0001g0073 others(6): Show |
9 | HG00140.hp2 HG00323.hp2 HG00639.hp1 others(6): Show |
intron_variant | MODIFIER | c.838+1457C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481906 | |||||||
| chr9:130481907 | G | T | 66 | a0001c0001t0001g0006 a0001c0001t0001g0012 a0001c0001t0001g0015 others(63): Show |
69 | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(66): Show |
intron_variant | MODIFIER | c.838+1458G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130481907 | |||||||
| chr9:130482185 | G | A | 10 | a0001c0003t0001g0149 a0001c0003t0001g0199 a0001c0003t0001g0227 others(7): Show |
10 | HG02602.hp1 HG02647.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.838+1736G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130482185 | |||||||
| chr9:130482326 | GGGGGGT | G | 22 | a0001c0001t0001g0196 a0001c0003t0001g0131 a0001c0003t0001g0135 others(19): Show |
22 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.838+1882_838+1887d others(8): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130482326 | ||||||
| chr9:130482343 | C | T | 2 | a0001c0001t0001g0263 a0001c0001t0001g0325 |
2 | HG02083.hp2 NA19009.hp1 |
intron_variant | MODIFIER | c.838+1894C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130482343 | |||||||
| chr9:130482582 | G | T | 1 | a0001c0001t0001g0335 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.838+2133G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130482582 | |||||||
| chr9:130482639 | A | G | 30 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(27): Show |
30 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.838+2190A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130482639 | |||||||
| chr9:130482812 | G | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0164 others(38): Show |
47 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.838+2363G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130482812 | |||||||
| chr9:130482818 | C | G | 2 | a0001c0001t0001g0041 a0001c0001t0001g0043 |
2 | HG04115.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.838+2369C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130482818 | |||||||
| chr9:130483139 | A | G | 1 | a0001c0001t0001g0285 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.838+2690A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130483139 | |||||||
| chr9:130483221 | G | A | 2 | a0001c0001t0001g0249 a0001c0001t0001g0252 |
2 | HG02735.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.838+2772G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130483221 | |||||||
| chr9:130483269 | G | T | 41 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0164 others(38): Show |
47 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.838+2820G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130483269 | |||||||
| chr9:130483284 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.838+2835C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130483284 | |||||||
| chr9:130483361 | G | C | 1 | a0001c0001t0001g0156 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.838+2912G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130483361 | |||||||
| chr9:130483362 | C | G | 1 | a0001c0001t0001g0156 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.838+2913C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130483362 | |||||||
| chr9:130483569 | G | T | 3 | a0001c0001t0001g0041 a0001c0001t0001g0043 a0001c0002t0001g0019 |
3 | HG03471.hp1 HG04115.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.838+3120G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130483569 | |||||||
| chr9:130483620 | G | A | 3 | a0001c0001t0001g0204 a0001c0001t0001g0205 a0001c0001t0001g0328 |
3 | HG02451.hp1 HG02559.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.838+3171G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130483620 | |||||||
| chr9:130483758 | T | TCCTTTCC others(13): Show |
248 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(245): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.838+3343_838+3362d others(22): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130483758 | ||||||
| chr9:130483758 | T | TCCTTTCC others(33): Show |
2 | a0001c0001t0001g0172 a0007c0011t0001g0168 |
2 | HG01891.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.838+3323_838+3362d others(42): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130483758 | ||||||
| chr9:130483758 | T | TCCTTTCC others(53): Show |
10 | a0001c0001t0001g0021 a0001c0001t0001g0139 a0001c0001t0001g0143 others(7): Show |
10 | HG02615.hp2 HG02818.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.838+3362_838+3363i others(62): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130483758 | ||||||
| chr9:130483775 | T | TCTCCCTT others(14): Show |
1 | a0001c0001t0001g0250 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.838+3327_838+3347d others(23): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130483775 | ||||||
| chr9:130483801 | T | TTTCCTCC others(12): Show |
1 | a0001c0001t0001g0156 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.838+3362_838+3363i others(21): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130483801 | ||||||
| chr9:130483814 | C | CTCCCTTT others(10): Show |
1 | a0001c0001t0001g0289 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.838+3365_838+3366i others(19): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130483814 | |||||||
| chr9:130484095 | T | C | 334 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(331): Show |
351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.838+3646T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484095 | |||||||
| chr9:130484109 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.838+3660C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484109 | |||||||
| chr9:130484310 | T | C | 225 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(222): Show |
237 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(234): Show |
intron_variant | MODIFIER | c.838+3861T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484310 | |||||||
| chr9:130484338 | T | C | 345 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(342): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
intron_variant | MODIFIER | c.838+3889T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484338 | |||||||
| chr9:130484369 | G | C | 42 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0164 others(39): Show |
48 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(45): Show |
intron_variant | MODIFIER | c.838+3920G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484369 | |||||||
| chr9:130484689 | A | G | 1 | a0001c0001t0001g0097 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.838+4240A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484689 | |||||||
| chr9:130484707 | G | A | 7 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.838+4258G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484707 | |||||||
| chr9:130484799 | G | GCA | 20 | a0001c0001t0001g0016 a0001c0001t0001g0046 a0001c0001t0001g0047 others(17): Show |
21 | HG01891.hp2 HG01981.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.838+4380_838+4381d others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130484799 | ||||||
| chr9:130484799 | G | GCACACAC others(1): Show |
4 | a0001c0001t0001g0139 a0001c0001t0001g0140 a0001c0001t0001g0198 others(1): Show |
4 | HG02145.hp2 HG02615.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.838+4374_838+4381d others(10): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130484799 | ||||||
| chr9:130484799 | GCA | G | 203 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
215 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(212): Show |
intron_variant | MODIFIER | c.838+4380_838+4381d others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130484799 | ||||||
| chr9:130484799 | GCACA | G | 5 | a0001c0001t0001g0043 a0001c0001t0001g0065 a0001c0001t0001g0260 others(2): Show |
6 | HG01069.hp2 HG01071.hp2 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.838+4378_838+4381d others(6): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130484799 | ||||||
| chr9:130484799 | GCACACA | G | 25 | a0001c0001t0001g0026 a0001c0001t0001g0170 a0001c0001t0001g0280 others(22): Show |
28 | HG00099.hp2 HG00738.hp1 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.838+4376_838+4381d others(8): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130484799 | ||||||
| chr9:130484829 | A | G | 5 | a0001c0001t0001g0042 a0001c0001t0001g0084 a0001c0001t0001g0155 others(2): Show |
5 | HG02615.hp1 HG03516.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.838+4380A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484829 | |||||||
| chr9:130484830 | C | T | 4 | a0001c0001t0001g0084 a0001c0001t0001g0155 a0001c0001t0001g0234 others(1): Show |
4 | HG03516.hp2 HG03927.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+4381C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484830 | |||||||
| chr9:130484832 | T | C | 4 | a0001c0001t0001g0084 a0001c0001t0001g0155 a0001c0001t0001g0234 others(1): Show |
4 | HG03516.hp2 HG03927.hp2 HG04204.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+4383T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484832 | |||||||
| chr9:130484844 | C | T | 3 | a0001c0001t0001g0008 a0001c0001t0001g0167 a0001c0001t0001g0283 |
4 | HG02809.hp2 HG03471.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.838+4395C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484844 | |||||||
| chr9:130484985 | G | A | 1 | a0001c0001t0001g0340 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.839-4348G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130484985 | |||||||
| chr9:130485156 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.839-4177G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485156 | |||||||
| chr9:130485202 | GGCGATGC others(9): Show |
G | 1 | a0001c0001t0001g0075 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.839-4129_839-4114d others(18): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130485202 | ||||||
| chr9:130485216 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.839-4117C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485216 | |||||||
| chr9:130485228 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.839-4105C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485228 | |||||||
| chr9:130485307 | T | A | 1 | a0001c0001t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.839-4026T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485307 | |||||||
| chr9:130485408 | AGCCAAGC others(18): Show |
A | 3 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0344 |
5 | HG02280.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-3910_839-3886d others(27): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130485408 | ||||||
| chr9:130485505 | G | A | 151 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(148): Show |
157 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.839-3828G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485505 | |||||||
| chr9:130485506 | T | C | 22 | a0001c0001t0001g0196 a0001c0003t0001g0131 a0001c0003t0001g0135 others(19): Show |
22 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.839-3827T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485506 | |||||||
| chr9:130485536 | G | C | 1 | a0001c0014t0001g0171 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.839-3797G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485536 | |||||||
| chr9:130485571 | G | C | 22 | a0001c0001t0001g0196 a0001c0003t0001g0131 a0001c0003t0001g0135 others(19): Show |
22 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.839-3762G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485571 | |||||||
| chr9:130485585 | G | A | 2 | a0001c0001t0001g0280 a0001c0001t0001g0284 |
2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.839-3748G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485585 | |||||||
| chr9:130485623 | T | C | 64 | a0001c0001t0001g0004 a0001c0001t0001g0026 a0001c0001t0001g0164 others(61): Show |
70 | HG00099.hp2 HG00738.hp1 HG00738.hp2 others(67): Show |
intron_variant | MODIFIER | c.839-3710T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485623 | |||||||
| chr9:130485627 | G | A | 1 | a0001c0001t0001g0169 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.839-3706G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485627 | |||||||
| chr9:130485704 | G | A | 4 | a0001c0001t0001g0013 a0001c0001t0001g0236 a0001c0001t0001g0250 others(1): Show |
5 | HG00438.hp2 HG02074.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.839-3629G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485704 | |||||||
| chr9:130485780 | G | A | 3 | a0001c0001t0001g0035 a0001c0001t0001g0085 a0001c0001t0001g0234 |
3 | HG03710.hp2 HG03927.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.839-3553G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485780 | |||||||
| chr9:130485804 | T | A | 22 | a0001c0001t0001g0196 a0001c0003t0001g0131 a0001c0003t0001g0135 others(19): Show |
22 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.839-3529T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485804 | |||||||
| chr9:130485805 | C | G | 10 | a0001c0003t0001g0149 a0001c0003t0001g0199 a0001c0003t0001g0227 others(7): Show |
10 | HG02602.hp1 HG02647.hp1 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.839-3528C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485805 | |||||||
| chr9:130485958 | A | G | 324 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(321): Show |
341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.839-3375A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130485958 | |||||||
| chr9:130486141 | T | G | 1 | a0001c0001t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.839-3192T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130486141 | |||||||
| chr9:130486445 | A | C | 2 | a0001c0003t0001g0188 a0001c0003t0001g0345 |
2 | HG01891.hp2 HG02559.hp2 |
intron_variant | MODIFIER | c.839-2888A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130486445 | |||||||
| chr9:130486509 | A | G | 158 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(155): Show |
164 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.839-2824A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130486509 | |||||||
| chr9:130486529 | G | A | 149 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(146): Show |
155 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.839-2804G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130486529 | |||||||
| chr9:130486579 | C | T | 2 | a0001c0001t0001g0123 a0001c0001t0001g0320 |
2 | HG01261.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.839-2754C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130486579 | |||||||
| chr9:130486627 | A | G | 159 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(156): Show |
165 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(162): Show |
intron_variant | MODIFIER | c.839-2706A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130486627 | |||||||
| chr9:130486668 | A | G | 195 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(192): Show |
203 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(200): Show |
intron_variant | MODIFIER | c.839-2665A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130486668 | |||||||
| chr9:130486956 | G | A | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.839-2377G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130486956 | |||||||
| chr9:130487016 | C | CT | 40 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0326 others(37): Show |
42 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(39): Show |
intron_variant | MODIFIER | c.839-2316dupT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130487016 | ||||||
| chr9:130487051 | G | C | 152 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(149): Show |
157 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.839-2282G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130487051 | |||||||
| chr9:130487223 | A | G | 23 | a0001c0003t0001g0048 a0001c0003t0001g0131 a0001c0003t0001g0135 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.839-2110A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130487223 | |||||||
| chr9:130487263 | G | A | 7 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.839-2070G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130487263 | |||||||
| chr9:130487330 | C | T | 1 | a0001c0001t0001g0196 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.839-2003C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130487330 | |||||||
| chr9:130487400 | G | GT | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.839-1918dupT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130487400 | ||||||
| chr9:130487400 | GT | G | 177 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0006 others(174): Show |
185 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(182): Show |
intron_variant | MODIFIER | c.839-1918delT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130487400 | ||||||
| chr9:130487418 | T | A | 1 | a0001c0002t0002g0179 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.839-1915T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130487418 | |||||||
| chr9:130487504 | C | G | 10 | a0001c0001t0001g0006 a0001c0001t0001g0056 a0001c0001t0001g0061 others(7): Show |
11 | HG00735.hp1 HG01167.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.839-1829C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130487504 | |||||||
| chr9:130487581 | A | AAC | 177 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(174): Show |
183 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(180): Show |
intron_variant | MODIFIER | c.839-1751_839-1750d others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130487581 | ||||||
| chr9:130487690 | G | A | 1 | a0001c0003t0001g0048 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.839-1643G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130487690 | |||||||
| chr9:130487757 | C | CT | 153 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(150): Show |
159 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(156): Show |
intron_variant | MODIFIER | c.839-1564dupT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130487757 | ||||||
| chr9:130487757 | CT | C | 105 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(102): Show |
110 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.839-1564delT | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr9 | 130487757 | ||||||
| chr9:130487864 | C | T | 17 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0326 others(14): Show |
19 | HG01884.hp1 HG01943.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.839-1469C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130487864 | |||||||
| chr9:130488076 | G | A | 1 | a0001c0001t0001g0122 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.839-1257G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130488076 | |||||||
| chr9:130488097 | A | G | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.839-1236A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130488097 | |||||||
| chr9:130488199 | A | G | 3 | a0001c0001t0001g0161 a0001c0001t0001g0316 a0001c0001t0001g0318 |
3 | HG00323.hp1 HG01175.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.839-1134A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130488199 | |||||||
| chr9:130488289 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.839-1044C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130488289 | |||||||
| chr9:130488424 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.839-909A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130488424 | |||||||
| chr9:130488455 | T | G | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(90): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.839-878T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130488455 | |||||||
| chr9:130488636 | C | T | 2 | a0001c0001t0001g0073 a0001c0001t0001g0219 |
2 | HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.839-697C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130488636 | |||||||
| chr9:130488985 | C | T | 1 | a0001c0001t0001g0238 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.839-348C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130488985 | |||||||
| chr9:130488992 | G | A | 1 | a0001c0001t0001g0121 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.839-341G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130488992 | |||||||
| chr9:130489031 | G | A | 22 | a0001c0003t0001g0048 a0001c0003t0001g0131 a0001c0003t0001g0135 others(19): Show |
22 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(19): Show |
intron_variant | MODIFIER | c.839-302G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130489031 | |||||||
| chr9:130489033 | A | G | 1 | a0001c0001t0001g0239 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.839-300A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130489033 | |||||||
| chr9:130489058 | G | A | 1 | a0001c0001t0001g0085 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.839-275G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130489058 | |||||||
| chr9:130489199 | G | A | 1 | a0001c0001t0001g0323 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.839-134G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130489199 | |||||||
| chr9:130489245 | A | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(233): Show |
244 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.839-88A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130489245 | |||||||
| chr9:130489248 | T | A | 3 | a0001c0001t0001g0169 a0001c0001t0001g0204 a0001c0003t0001g0319 |
3 | HG01261.hp2 HG02258.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.839-85T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130489248 | |||||||
| chr9:130489256 | T | G | 7 | a0001c0001t0001g0301 a0001c0001t0001g0302 a0001c0001t0001g0303 others(4): Show |
7 | HG00741.hp1 HG01074.hp1 HG01106.hp1 others(4): Show |
intron_variant | MODIFIER | c.839-77T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 11/14 | chr9 | 130489256 | |||||||
| chr9:130489533 | C | T | 9 | a0001c0001t0001g0158 a0001c0001t0001g0160 a0001c0001t0001g0162 others(6): Show |
9 | HG00280.hp2 HG00558.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.970+69C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130489533 | |||||||
| chr9:130489672 | C | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0198 a0001c0001t0001g0330 |
3 | HG02615.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.970+208C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130489672 | |||||||
| chr9:130489707 | C | T | 91 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(88): Show |
95 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(92): Show |
intron_variant | MODIFIER | c.970+243C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130489707 | |||||||
| chr9:130489729 | G | T | 23 | a0001c0003t0001g0048 a0001c0003t0001g0131 a0001c0003t0001g0135 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.970+265G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130489729 | |||||||
| chr9:130489959 | T | C | 1 | a0001c0002t0001g0187 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.970+495T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130489959 | |||||||
| chr9:130490251 | C | T | 3 | a0001c0001t0001g0240 a0001c0001t0001g0254 a0001c0001t0001g0313 |
3 | HG00673.hp1 NA18940.hp2 NA19080.hp2 |
intron_variant | MODIFIER | c.970+787C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130490251 | |||||||
| chr9:130490252 | G | A | 23 | a0001c0003t0001g0048 a0001c0003t0001g0131 a0001c0003t0001g0135 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.970+788G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130490252 | |||||||
| chr9:130490433 | C | G | 1 | a0001c0001t0001g0281 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.970+969C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130490433 | |||||||
| chr9:130490560 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.970+1096C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130490560 | |||||||
| chr9:130490604 | C | G | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.970+1140C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130490604 | |||||||
| chr9:130490651 | T | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0326 others(14): Show |
19 | HG01884.hp1 HG01943.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.970+1187T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130490651 | |||||||
| chr9:130490714 | T | C | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.970+1250T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130490714 | |||||||
| chr9:130490727 | G | T | 1 | a0001c0001t0001g0134 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.970+1263G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130490727 | |||||||
| chr9:130490853 | C | T | 4 | a0001c0001t0001g0014 a0001c0001t0001g0242 a0001c0001t0001g0262 others(1): Show |
5 | NA18952.hp2 NA18957.hp1 NA18962.hp2 others(2): Show |
intron_variant | MODIFIER | c.970+1389C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130490853 | |||||||
| chr9:130490900 | A | G | 3 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0344 |
5 | HG02280.hp1 HG02630.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.970+1436A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130490900 | |||||||
| chr9:130491241 | C | G | 1 | a0001c0001t0001g0075 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.970+1777C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491241 | |||||||
| chr9:130491241 | C | T | 30 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(27): Show |
30 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(27): Show |
intron_variant | MODIFIER | c.970+1777C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491241 | |||||||
| chr9:130491242 | G | C | 1 | a0001c0001t0001g0075 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.970+1778G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491242 | |||||||
| chr9:130491366 | G | A | 2 | a0001c0002t0001g0145 a0001c0002t0001g0146 |
2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.970+1902G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491366 | |||||||
| chr9:130491472 | C | A | 2 | a0001c0001t0001g0126 a0001c0001t0001g0197 |
2 | HG02630.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.970+2008C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491472 | |||||||
| chr9:130491555 | A | T | 1 | a0001c0001t0001g0075 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.970+2091A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491555 | |||||||
| chr9:130491565 | T | C | 2 | a0001c0002t0001g0145 a0001c0002t0001g0146 |
2 | HG03195.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.970+2101T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491565 | |||||||
| chr9:130491589 | C | T | 1 | a0001c0001t0001g0102 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.970+2125C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491589 | |||||||
| chr9:130491604 | C | T | 23 | a0001c0003t0001g0048 a0001c0003t0001g0131 a0001c0003t0001g0135 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.970+2140C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491604 | |||||||
| chr9:130491715 | C | T | 1 | a0001c0001t0001g0212 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.970+2251C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491715 | |||||||
| chr9:130491796 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.970+2332G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491796 | |||||||
| chr9:130491806 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0326 others(14): Show |
19 | HG01884.hp1 HG01943.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.970+2342G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491806 | |||||||
| chr9:130491909 | A | G | 1 | a0001c0001t0001g0304 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.970+2445A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491909 | |||||||
| chr9:130491981 | C | T | 302 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(299): Show |
315 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(312): Show |
intron_variant | MODIFIER | c.970+2517C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130491981 | |||||||
| chr9:130492177 | C | T | 3 | a0001c0002t0001g0184 a0001c0002t0001g0187 a0001c0002t0001g0225 |
3 | HG02602.hp2 HG02683.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.971-2690C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130492177 | |||||||
| chr9:130492232 | T | G | 23 | a0001c0003t0001g0048 a0001c0003t0001g0131 a0001c0003t0001g0135 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.971-2635T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130492232 | |||||||
| chr9:130492243 | C | G | 23 | a0001c0003t0001g0048 a0001c0003t0001g0131 a0001c0003t0001g0135 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.971-2624C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130492243 | |||||||
| chr9:130492317 | G | T | 23 | a0001c0003t0001g0048 a0001c0003t0001g0131 a0001c0003t0001g0135 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.971-2550G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130492317 | |||||||
| chr9:130492525 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.971-2342C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130492525 | |||||||
| chr9:130492610 | C | CA | 3 | a0001c0001t0001g0139 a0001c0001t0001g0198 a0001c0001t0001g0330 |
3 | HG02615.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.971-2256dupA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr9 | 130492610 | ||||||
| chr9:130492779 | G | A | 1 | a0001c0001t0001g0195 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.971-2088G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130492779 | |||||||
| chr9:130492902 | G | A | 2 | a0001c0001t0001g0213 a0001c0001t0001g0214 |
2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.971-1965G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130492902 | |||||||
| chr9:130493494 | C | T | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.971-1373C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130493494 | |||||||
| chr9:130493589 | G | T | 3 | a0001c0003t0001g0292 a0001c0003t0001g0321 a0001c0003t0001g0322 |
3 | HG02895.hp1 HG02897.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.971-1278G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130493589 | |||||||
| chr9:130493689 | T | C | 7 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.971-1178T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130493689 | |||||||
| chr9:130493748 | G | GGCCT | 17 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0326 others(14): Show |
19 | HG01884.hp1 HG01943.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.971-1095_971-1092d others(6): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr9 | 130493748 | ||||||
| chr9:130493911 | C | G | 95 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(92): Show |
100 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(97): Show |
intron_variant | MODIFIER | c.971-956C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130493911 | |||||||
| chr9:130494022 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.971-845C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130494022 | |||||||
| chr9:130494023 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0326 others(14): Show |
19 | HG01884.hp1 HG01943.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.971-844G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130494023 | |||||||
| chr9:130494033 | A | C | 17 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0326 others(14): Show |
19 | HG01884.hp1 HG01943.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.971-834A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130494033 | |||||||
| chr9:130494393 | A | C | 23 | a0001c0003t0001g0048 a0001c0003t0001g0131 a0001c0003t0001g0135 others(20): Show |
23 | HG00738.hp2 HG01070.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.971-474A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130494393 | |||||||
| chr9:130494501 | T | G | 2 | a0001c0001t0001g0073 a0001c0001t0001g0219 |
2 | HG00642.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.971-366T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130494501 | |||||||
| chr9:130494743 | C | G | 1 | a0001c0001t0001g0052 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.971-124C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130494743 | |||||||
| chr9:130494769 | G | A | 3 | a0001c0001t0001g0085 a0001c0001t0001g0234 a0001c0001t0001g0324 |
3 | HG03927.hp2 HG04199.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.971-98G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130494769 | |||||||
| chr9:130494832 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.971-35G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 12/14 | chr9 | 130494832 | |||||||
| chr9:130495267 | C | T | 1 | a0001c0002t0001g0019 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1127+244C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495267 | |||||||
| chr9:130495402 | G | A | 89 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(86): Show |
93 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(90): Show |
intron_variant | MODIFIER | c.1127+379G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495402 | |||||||
| chr9:130495436 | C | A | 1 | a0001c0002t0001g0181 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1127+413C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495436 | |||||||
| chr9:130495444 | C | CAT | 6 | a0001c0001t0001g0104 a0001c0001t0001g0204 a0001c0001t0001g0205 others(3): Show |
6 | HG01109.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1127+437_1127+438d others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495444 | ||||||
| chr9:130495444 | C | CATATAT | 3 | a0001c0001t0001g0148 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1127+433_1127+438d others(8): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495444 | ||||||
| chr9:130495444 | C | CATATATA others(7): Show |
1 | a0001c0001t0001g0143 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1127+425_1127+438d others(16): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495444 | ||||||
| chr9:130495444 | C | CATATATA others(9): Show |
3 | a0001c0001t0001g0021 a0001c0001t0001g0144 a0001c0001t0001g0166 |
3 | HG02886.hp1 HG02895.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1127+423_1127+438d others(18): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495444 | ||||||
| chr9:130495460 | T | C | 27 | a0001c0001t0001g0023 a0001c0001t0001g0067 a0001c0001t0001g0078 others(24): Show |
27 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.1127+437T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495460 | |||||||
| chr9:130495462 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1127+439C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495462 | |||||||
| chr9:130495464 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1127+441C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495464 | |||||||
| chr9:130495468 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1127+445C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495468 | |||||||
| chr9:130495470 | T | C | 1 | a0001c0001t0001g0067 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1127+447T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495470 | |||||||
| chr9:130495470 | T | TAC | 6 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0001t0001g0095 others(3): Show |
6 | HG01515.hp1 HG02040.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.1127+448_1127+449i others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495470 | ||||||
| chr9:130495470 | T | TACAC | 73 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0014 others(70): Show |
77 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(74): Show |
intron_variant | MODIFIER | c.1127+448_1127+449i others(6): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495470 | ||||||
| chr9:130495470 | T | TACACAC | 9 | a0001c0001t0001g0023 a0001c0001t0001g0029 a0001c0001t0001g0094 others(6): Show |
9 | HG01069.hp1 HG01074.hp1 HG01099.hp2 others(6): Show |
intron_variant | MODIFIER | c.1127+448_1127+449i others(8): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495470 | ||||||
| chr9:130495470 | T | TACACACA others(1): Show |
3 | a0001c0001t0001g0025 a0001c0001t0001g0246 a0001c0001t0001g0302 |
3 | HG01346.hp1 HG02083.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.1127+448_1127+449i others(10): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495470 | ||||||
| chr9:130495470 | T | TACACACA others(3): Show |
39 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0024 others(36): Show |
40 | HG00642.hp1 HG00642.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.1127+448_1127+449i others(12): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495470 | ||||||
| chr9:130495470 | T | TACACACA others(5): Show |
1 | a0001c0001t0001g0038 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1127+448_1127+449i others(14): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495470 | ||||||
| chr9:130495470 | T | TACACACA others(7): Show |
2 | a0001c0001t0001g0274 a0001c0001t0001g0317 |
2 | HG03654.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.1127+448_1127+449i others(16): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495470 | ||||||
| chr9:130495470 | T | TACACACA others(9): Show |
2 | a0001c0001t0001g0223 a0001c0001t0001g0233 |
2 | HG00408.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.1127+448_1127+449i others(18): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495470 | ||||||
| chr9:130495472 | T | C | 147 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(144): Show |
153 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(150): Show |
intron_variant | MODIFIER | c.1127+449T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495472 | |||||||
| chr9:130495472 | T | TAC | 4 | a0001c0001t0001g0026 a0001c0001t0001g0197 a0001c0001t0001g0267 others(1): Show |
4 | HG00738.hp1 HG02273.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+477_1127+478d others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495472 | ||||||
| chr9:130495472 | T | TACACAC | 88 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(85): Show |
92 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1127+473_1127+478d others(8): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495472 | ||||||
| chr9:130495472 | T | TACACACA others(1): Show |
7 | a0001c0001t0001g0020 a0001c0001t0001g0055 a0001c0001t0001g0170 others(4): Show |
8 | HG01981.hp1 HG02080.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.1127+471_1127+478d others(10): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495472 | ||||||
| chr9:130495472 | T | TACACACA others(5): Show |
5 | a0001c0001t0001g0158 a0001c0001t0001g0162 a0001c0001t0001g0249 others(2): Show |
5 | HG02735.hp2 HG03492.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.1127+467_1127+478d others(14): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495472 | ||||||
| chr9:130495472 | T | TACACACA others(7): Show |
4 | a0001c0001t0001g0160 a0001c0001t0001g0241 a0001c0001t0001g0338 others(1): Show |
4 | HG00280.hp2 HG02683.hp2 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.1127+465_1127+478d others(16): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495472 | ||||||
| chr9:130495472 | TAC | T | 18 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0143 others(15): Show |
20 | HG01884.hp1 HG01943.hp2 HG02280.hp1 others(17): Show |
intron_variant | MODIFIER | c.1127+477_1127+478d others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495472 | ||||||
| chr9:130495478 | C | T | 3 | a0001c0001t0001g0148 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1127+455C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495478 | |||||||
| chr9:130495480 | C | CATAT | 3 | a0001c0001t0001g0148 a0001c0001t0001g0213 a0001c0001t0001g0214 |
3 | HG02896.hp1 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1127+458_1127+459i others(6): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495480 | ||||||
| chr9:130495500 | C | CACACACA others(1): Show |
4 | a0001c0001t0001g0034 a0001c0001t0001g0152 a0001c0001t0001g0258 others(1): Show |
4 | HG01346.hp2 HG01358.hp2 HG02027.hp2 others(1): Show |
intron_variant | MODIFIER | c.1127+478_1127+479i others(10): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495500 | ||||||
| chr9:130495500 | CAT | C | 3 | a0001c0001t0001g0342 a0001c0001t0001g0346 a0001c0001t0001g0347 |
3 | HG02717.hp1 HG02723.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1127+487_1127+488d others(4): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130495500 | ||||||
| chr9:130495502 | T | C | 93 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(90): Show |
98 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(95): Show |
intron_variant | MODIFIER | c.1127+479T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495502 | |||||||
| chr9:130495504 | T | C | 1 | a0001c0001t0001g0072 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1127+481T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495504 | |||||||
| chr9:130495512 | A | T | 2 | a0001c0001t0001g0193 a0001c0001t0001g0194 |
2 | HG02015.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.1127+489A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495512 | |||||||
| chr9:130495581 | G | T | 1 | a0001c0001t0001g0170 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1127+558G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495581 | |||||||
| chr9:130495713 | G | A | 2 | a0001c0001t0001g0223 a0001c0001t0001g0274 |
2 | HG02135.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.1127+690G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495713 | |||||||
| chr9:130495741 | G | A | 2 | a0001c0001t0001g0206 a0001c0001t0001g0207 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1127+718G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495741 | |||||||
| chr9:130495824 | A | T | 2 | a0001c0001t0001g0308 a0003c0008t0001g0201 |
2 | HG00639.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.1127+801A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495824 | |||||||
| chr9:130495994 | G | A | 3 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0036 |
3 | HG02083.hp1 HG02523.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.1127+971G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130495994 | |||||||
| chr9:130496008 | A | G | 3 | a0001c0001t0001g0066 a0001c0001t0001g0071 a0001c0001t0001g0072 |
3 | HG02040.hp2 NA18944.hp2 NA18965.hp2 |
intron_variant | MODIFIER | c.1127+985A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496008 | |||||||
| chr9:130496009 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1127+986C>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496009 | |||||||
| chr9:130496114 | C | T | 303 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
316 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(313): Show |
intron_variant | MODIFIER | c.1127+1091C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496114 | |||||||
| chr9:130496155 | G | A | 1 | a0001c0001t0001g0037 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1127+1132G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496155 | |||||||
| chr9:130496298 | G | A | 1 | a0001c0003t0001g0296 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1127+1275G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496298 | |||||||
| chr9:130496332 | C | T | 1 | a0001c0001t0001g0230 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1127+1309C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496332 | |||||||
| chr9:130496358 | G | T | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1127+1335G>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496358 | |||||||
| chr9:130496439 | G | A | 17 | a0001c0001t0001g0004 a0001c0001t0001g0164 a0001c0001t0001g0326 others(14): Show |
19 | HG01884.hp1 HG01943.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.1127+1416G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496439 | |||||||
| chr9:130496468 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1127+1445G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496468 | |||||||
| chr9:130496550 | C | T | 3 | a0001c0001t0001g0349 a0001c0001t0001g0350 a0001c0002t0001g0136 |
3 | HG03041.hp1 HG03540.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1127+1527C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496550 | |||||||
| chr9:130496593 | T | TA | 21 | a0001c0001t0001g0074 a0001c0001t0001g0079 a0001c0001t0001g0090 others(18): Show |
21 | HG00673.hp2 HG02148.hp2 HG02602.hp1 others(18): Show |
intron_variant | MODIFIER | c.1127+1594dupA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130496593 | ||||||
| chr9:130496593 | TA | T | 46 | a0001c0001t0001g0004 a0001c0001t0001g0021 a0001c0001t0001g0032 others(43): Show |
48 | HG00099.hp2 HG00323.hp1 HG01070.hp2 others(45): Show |
intron_variant | MODIFIER | c.1127+1594delA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130496593 | ||||||
| chr9:130496593 | TAA | T | 7 | a0001c0001t0001g0148 a0001c0001t0001g0166 a0001c0001t0001g0213 others(4): Show |
7 | HG01943.hp2 HG02717.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127+1593_1127+159 others(6): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130496593 | ||||||
| chr9:130496673 | C | T | 7 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127+1650C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496673 | |||||||
| chr9:130496683 | C | T | 3 | a0001c0001t0001g0268 a0001c0001t0001g0312 a0001c0001t0001g0314 |
3 | HG01255.hp1 HG01993.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.1127+1660C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496683 | |||||||
| chr9:130496702 | GC | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1127+1682delC | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130496702 | ||||||
| chr9:130496710 | G | A | 1 | a0001c0001t0001g0155 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1127+1687G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496710 | |||||||
| chr9:130496789 | C | T | 1 | a0001c0001t0001g0283 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1127+1766C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496789 | |||||||
| chr9:130496945 | C | T | 1 | a0001c0001t0001g0172 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1127+1922C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496945 | |||||||
| chr9:130496996 | A | G | 88 | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0009 others(85): Show |
92 | HG00280.hp1 HG00438.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1127+1973A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130496996 | |||||||
| chr9:130497321 | C | T | 1 | a0001c0001t0001g0193 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1128-2184C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497321 | |||||||
| chr9:130497343 | A | C | 2 | a0001c0001t0001g0008 a0001c0001t0001g0283 |
3 | HG03471.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1128-2162A>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497343 | |||||||
| chr9:130497345 | C | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0283 |
3 | HG03471.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1128-2160C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497345 | |||||||
| chr9:130497346 | A | T | 2 | a0001c0001t0001g0008 a0001c0001t0001g0283 |
3 | HG03471.hp2 HG03486.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1128-2159A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497346 | |||||||
| chr9:130497386 | T | C | 343 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(340): Show |
361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1128-2119T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497386 | |||||||
| chr9:130497488 | T | TA | 18 | a0001c0001t0001g0004 a0001c0001t0001g0140 a0001c0001t0001g0164 others(15): Show |
20 | HG01884.hp1 HG01943.hp2 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1128-2004dupA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130497488 | ||||||
| chr9:130497488 | TA | T | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1128-2004delA | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr9 | 130497488 | ||||||
| chr9:130497537 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1128-1968C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497537 | |||||||
| chr9:130497675 | A | T | 1 | a0001c0001t0001g0274 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1128-1830A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497675 | |||||||
| chr9:130497747 | G | C | 1 | a0001c0001t0001g0020 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1128-1758G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497747 | |||||||
| chr9:130497777 | A | G | 7 | a0001c0001t0001g0021 a0001c0001t0001g0143 a0001c0001t0001g0144 others(4): Show |
7 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.1128-1728A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497777 | |||||||
| chr9:130497779 | G | C | 2 | a0001c0001t0001g0043 a0001c0002t0001g0019 |
2 | HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1128-1726G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497779 | |||||||
| chr9:130497836 | G | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0008 others(89): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.1128-1669G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130497836 | |||||||
| chr9:130498008 | G | A | 342 | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(339): Show |
360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1128-1497G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130498008 | |||||||
| chr9:130498047 | T | C | 1 | a0001c0001t0001g0333 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1128-1458T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130498047 | |||||||
| chr9:130498204 | G | A | 3 | a0001c0001t0001g0139 a0001c0001t0001g0198 a0001c0001t0001g0330 |
3 | HG02615.hp2 HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1128-1301G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130498204 | |||||||
| chr9:130498410 | C | T | 1 | a0001c0001t0001g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1128-1095C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130498410 | |||||||
| chr9:130498501 | G | A | 6 | a0001c0001t0001g0342 a0001c0001t0001g0346 a0001c0001t0001g0347 others(3): Show |
6 | HG02717.hp1 HG02723.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1128-1004G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130498501 | |||||||
| chr9:130498763 | C | T | 3 | a0001c0001t0001g0076 a0001c0002t0001g0180 a0001c0002t0002g0179 |
3 | NA19067.hp1 NA19070.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.1128-742C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130498763 | |||||||
| chr9:130498799 | G | A | 4 | a0001c0001t0001g0148 a0001c0001t0001g0212 a0001c0001t0001g0213 others(1): Show |
4 | HG02258.hp1 HG02896.hp1 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1128-706G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130498799 | |||||||
| chr9:130498894 | G | A | 19 | a0001c0003t0001g0048 a0001c0003t0001g0131 a0001c0003t0001g0135 others(16): Show |
19 | HG00738.hp2 HG01261.hp2 HG01361.hp2 others(16): Show |
intron_variant | MODIFIER | c.1128-611G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130498894 | |||||||
| chr9:130499058 | A | G | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1128-447A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130499058 | |||||||
| chr9:130499307 | G | A | 1 | a0001c0001t0001g0332 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1128-198G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130499307 | |||||||
| chr9:130499469 | C | G | 1 | a0001c0005t0001g0031 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1128-36C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 13/14 | chr9 | 130499469 | |||||||
| chr9:130499649 | G | C | 1 | a0001c0001t0001g0233 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1193+79G>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130499649 | |||||||
| chr9:130499731 | C | T | 1 | a0001c0001t0001g0125 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1193+161C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130499731 | |||||||
| chr9:130499764 | C | T | 1 | a0001c0001t0001g0277 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.1193+194C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130499764 | |||||||
| chr9:130499909 | T | C | 1 | a0001c0001t0001g0029 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1193+339T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130499909 | |||||||
| chr9:130500112 | G | A | 4 | a0001c0001t0001g0143 a0001c0001t0001g0144 a0001c0001t0001g0166 others(1): Show |
4 | HG02818.hp2 HG02886.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193+542G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500112 | |||||||
| chr9:130500263 | T | G | 1 | a0001c0001t0001g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1193+693T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500263 | |||||||
| chr9:130500276 | T | A | 1 | a0001c0001t0001g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1194-700T>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500276 | |||||||
| chr9:130500285 | A | ACGAACTG others(22): Show |
1 | a0001c0001t0001g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1194-691_1194-690i others(31): Show |
ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500285 | |||||||
| chr9:130500286 | T | C | 1 | a0001c0001t0001g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1194-690T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500286 | |||||||
| chr9:130500290 | T | G | 1 | a0001c0001t0001g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1194-686T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500290 | |||||||
| chr9:130500299 | T | G | 1 | a0001c0001t0001g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1194-677T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500299 | |||||||
| chr9:130500305 | A | T | 1 | a0001c0001t0001g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1194-671A>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500305 | |||||||
| chr9:130500313 | T | G | 1 | a0001c0001t0001g0270 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1194-663T>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500313 | |||||||
| chr9:130500360 | T | C | 2 | a0001c0001t0001g0043 a0001c0002t0001g0019 |
2 | HG03471.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1194-616T>C | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500360 | |||||||
| chr9:130500392 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1194-584G>A | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500392 | |||||||
| chr9:130500559 | C | T | 1 | a0001c0001t0001g0087 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.1194-417C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500559 | |||||||
| chr9:130500699 | C | G | 1 | a0001c0001t0001g0130 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1194-277C>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500699 | |||||||
| chr9:130500766 | A | G | 46 | a0001c0001t0001g0012 a0001c0001t0001g0022 a0001c0001t0001g0023 others(43): Show |
47 | HG00408.hp1 HG00639.hp2 HG00642.hp1 others(44): Show |
intron_variant | MODIFIER | c.1194-210A>G | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500766 | |||||||
| chr9:130500813 | C | T | 1 | a0001c0001t0001g0140 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1194-163C>T | ASS1 | ENSG00000130707.18 | transcript | ENST00000352480.10 | protein_coding | 14/14 | chr9 | 130500813 |