Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 81502 |
| ensemblid | ENSG00000101294.19 |
| hgncid | 16435 |
| symbol | HM13 |
| name | histocompatibility minor 13 |
| refseq_nuc | NM_178581.3 |
| refseq_prot | NP_848696.1 |
| ensembl_nuc | ENST00000398174.9 |
| ensembl_prot | ENSP00000381237.3 |
| mane_status | MANE Select |
| chr | chr20 |
| start | 31514442 |
| end | 31569543 |
| strand | + |
| ver | v1.2 |
| region | chr20:31514442-31569543 |
| region5000 | chr20:31509442-31574543 |
| regionname0 | HM13_chr20_31514442_31569543 |
| regionname5000 | HM13_chr20_31509442_31574543 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 426 | 201 | 77 | 54 | 46 | 10 | 12 | 26 | HM13_chr20_31509442_31574543 | HM13 | MDSAL others(421): Show |
chr20 | 31509442 | 31574543 |
| a0002 | 0/0 | 426 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | MDSAL others(421): Show |
chr20 | 31509442 | 31574543 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1278 | 199 | 76 | 53 | 46 | 10 | 12 | HM13_chr20_31509442_31574543 | HM13 | ATGGA others(1273): Show |
chr20 | 31509442 | 31574543 | ||
| a0001c0002 | 0/0 | 1278 | 2 | 1 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ATGGA others(1273): Show |
chr20 | 31509442 | 31574543 | ||
| a0002c0003 | 0/0 | 1278 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ATGGA others(1273): Show |
chr20 | 31509442 | 31574543 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 1715 | 109 | 15 | 32 | 45 | 7 | 8 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0001t0002 | 0/0 | 1715 | 71 | 47 | 19 | 0 | 3 | 2 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0001t0003 | 0/0 | 1715 | 7 | 6 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0001t0004 | 0/0 | 1715 | 2 | 2 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0001t0005 | 0/0 | 1715 | 2 | 0 | 0 | 0 | 0 | 2 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0001t0006 | 0/0 | 1715 | 2 | 2 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0001t0007 | 0/0 | 1715 | 2 | 2 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0001t0008 | 0/0 | 1715 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0001t0009 | 0/0 | 1715 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0001t0010 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0001t0011 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0001c0002t0002 | 0/0 | 1715 | 2 | 1 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| a0002c0003t0003 | 0/0 | 1715 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | ACTTC others(1710): Show |
chr20 | 31509442 | 31574543 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 4 | 0 | 2 | 2 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0002 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0103 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0146 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0003 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0004 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0002g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0005g0008 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0006g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0006g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0007g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0007g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0008g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0009g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0010g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0001t0011g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0002t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0001c0002t0002g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| a0002c0003t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0087 | EUR | GBR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0109 | EUR | GBR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00140 | hp1 | a0001 | c0001 | t0002 | g0006 | EUR | GBR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0012 | EUR | GBR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | CHS | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | CHS | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHS | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0175 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00738 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0018 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01069 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01070 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01071 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01074 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01167 | hp2 | a0001 | c0001 | t0002 | g0039 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01168 | hp2 | a0001 | c0001 | t0002 | g0038 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01169 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01175 | hp1 | a0001 | c0001 | t0008 | g0111 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01192 | hp2 | a0001 | c0001 | t0002 | g0084 | AMR | PUR | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0125 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01256 | hp2 | a0001 | c0001 | t0002 | g0050 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01258 | hp1 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01346 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01496 | hp2 | a0001 | c0002 | t0002 | g0029 | AMR | CLM | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0132 | EUR | IBS | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01515 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | IBS | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0089 | EUR | IBS | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01516 | hp2 | a0001 | c0001 | t0002 | g0067 | EUR | IBS | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01884 | hp1 | a0001 | c0001 | t0003 | g0019 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01993 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02040 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | KHV | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0172 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02055 | hp2 | a0001 | c0001 | t0002 | g0054 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | KHV | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02145 | hp2 | a0001 | c0001 | t0011 | g0024 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CDX | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02257 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02280 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02300 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02451 | hp1 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | KHV | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0055 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02572 | hp2 | a0001 | c0001 | t0002 | g0053 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02622 | hp1 | a0001 | c0001 | t0002 | g0180 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02622 | hp2 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02630 | hp1 | a0001 | c0001 | t0002 | g0041 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02630 | hp2 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02717 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02723 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02723 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02809 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0071 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02818 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02818 | hp2 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02895 | hp2 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02896 | hp1 | a0001 | c0001 | t0002 | g0073 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02896 | hp2 | a0001 | c0001 | t0002 | g0046 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02897 | hp1 | a0001 | c0001 | t0002 | g0005 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02897 | hp2 | a0001 | c0001 | t0002 | g0182 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02922 | hp1 | a0001 | c0001 | t0002 | g0070 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02922 | hp2 | a0001 | c0001 | t0002 | g0059 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02965 | hp1 | a0001 | c0001 | t0002 | g0030 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02965 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02976 | hp1 | a0001 | c0001 | t0002 | g0083 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02976 | hp2 | a0001 | c0001 | t0002 | g0037 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0177 | SAS | PJL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03041 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03041 | hp2 | a0002 | c0003 | t0003 | g0016 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03098 | hp1 | a0001 | c0001 | t0002 | g0036 | AFR | MSL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03098 | hp2 | a0001 | c0001 | t0007 | g0077 | AFR | MSL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03139 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03139 | hp2 | a0001 | c0001 | t0010 | g0075 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03209 | hp1 | a0001 | c0001 | t0002 | g0082 | AFR | MSL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03209 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | MSL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03453 | hp1 | a0001 | c0001 | t0002 | g0086 | AFR | MSL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03453 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | MSL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03491 | hp2 | a0001 | c0001 | t0005 | g0008 | SAS | PJL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0008 | SAS | PJL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03516 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03516 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | ESN | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03540 | hp1 | a0001 | c0002 | t0002 | g0179 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03540 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | GWD | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03579 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | MSL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03579 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | MSL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | BEB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03834 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | BEB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | STU | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | STU | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18522 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | YRI | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18522 | hp2 | a0001 | c0001 | t0006 | g0085 | AFR | YRI | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | CHB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18906 | hp1 | a0001 | c0001 | t0002 | g0078 | AFR | YRI | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18906 | hp2 | a0001 | c0001 | t0007 | g0076 | AFR | YRI | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18965 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | LWK | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19030 | hp2 | a0001 | c0001 | t0002 | g0045 | AFR | LWK | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19055 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19079 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19087 | hp2 | a0001 | c0001 | t0009 | g0142 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19240 | hp1 | a0001 | c0001 | t0003 | g0021 | AFR | YRI | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA19240 | hp2 | a0001 | c0001 | t0003 | g0022 | AFR | YRI | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0174 | EUR | TSI | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA20805 | hp2 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0066 | SAS | GIH | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0167 | SAS | GIH | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02109 | hp1 | a0001 | c0001 | t0003 | g0017 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02486 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02559 | hp1 | a0001 | c0001 | t0004 | g0025 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03471 | hp1 | a0001 | c0001 | t0002 | g0040 | AFR | MSL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG03471 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | MSL | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG06807 | hp1 | a0001 | c0001 | t0003 | g0023 | AFR | USA | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| HG06807 | hp2 | a0001 | c0001 | t0002 | g0004 | AFR | USA | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | USA | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | USA | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA21309 | hp1 | a0001 | c0001 | t0006 | g0015 | AFR | LWK | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | LWK | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0146 | REF | REF | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0103 | REF | REF | HM13_chr20_31509442_31574543 | HM13 | chr20 | 31509442 | 31574543 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:31569140 | A | C | 1 | a0002 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.1202A>C | p.Lys401Thr | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 13/13 | 1312/1715 | 1202/1281 | 401/426 | chr20 | 31569140 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:31514728 | C | T | 1 | a0001c0002 | 2 | HG01496.hp2 HG03540.hp1 |
synonymous_variant | LOW | c.177C>T | p.Arg59Arg | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/13 | 287/1715 | 177/1281 | 59/426 | chr20 | 31514728 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:31514457 | A | G | 1 | a0001c0001t0007 | 2 | HG03098.hp2 NA18906.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-95A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/13 | chr20 | 31514457 | |||||||
| chr20:31514467 | G | T | 1 | a0001c0001t0011 | 1 | HG02145.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-85G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/13 | chr20 | 31514467 | |||||||
| chr20:31514503 | C | T | 2 | a0001c0001t0006 a0001c0001t0010 |
3 | HG03139.hp2 NA18522.hp2 NA21309.hp1 |
5_prime_UTR_variant | MODIFIER | c.-49C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/13 | 49 | chr20 | 31514503 | ||||||
| chr20:31569223 | A | G | 8 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0005 others(5): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
3_prime_UTR_variant | MODIFIER | c.*4A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 13/13 | 4 | chr20 | 31569223 | ||||||
| chr20:31569290 | G | A | 1 | a0001c0001t0008 | 1 | HG01175.hp1 | 3_prime_UTR_variant | MODIFIER | c.*71G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 13/13 | 71 | chr20 | 31569290 | ||||||
| chr20:31569361 | C | A | 3 | a0001c0001t0003 a0001c0001t0011 a0002c0003t0003 |
9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*142C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 13/13 | 142 | chr20 | 31569361 | ||||||
| chr20:31569419 | C | T | 1 | a0001c0001t0005 | 2 | HG03491.hp2 HG03492.hp2 |
3_prime_UTR_variant | MODIFIER | c.*200C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 13/13 | 200 | chr20 | 31569419 | ||||||
| chr20:31569450 | C | T | 1 | a0001c0001t0009 | 1 | NA19087.hp2 | 3_prime_UTR_variant | MODIFIER | c.*231C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 13/13 | 231 | chr20 | 31569450 | ||||||
| chr20:31569491 | A | G | 1 | a0001c0001t0004 | 2 | HG02559.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*272A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 13/13 | 272 | chr20 | 31569491 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr20:31514745 | C | CG | 4 | a0001c0001t0002g0180 a0001c0001t0002g0181 a0001c0001t0002g0182 others(1): Show |
4 | HG02257.hp2 HG02622.hp1 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.183+14dupG | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31514745 | ||||||
| chr20:31514816 | A | ACCT | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.183+84_183+86dupCT others(1): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31514816 | ||||||
| chr20:31514939 | G | A | 1 | a0001c0001t0006g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.183+205G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31514939 | |||||||
| chr20:31514995 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.183+261C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31514995 | |||||||
| chr20:31515067 | C | G | 1 | a0001c0001t0001g0178 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.183+333C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31515067 | |||||||
| chr20:31515084 | A | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.183+350A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31515084 | |||||||
| chr20:31515198 | C | T | 1 | a0001c0001t0002g0084 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.183+464C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31515198 | |||||||
| chr20:31515564 | C | A | 9 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(6): Show |
9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.183+830C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31515564 | |||||||
| chr20:31515605 | G | T | 1 | a0001c0001t0001g0177 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.183+871G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31515605 | |||||||
| chr20:31515770 | G | A | 6 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(3): Show |
6 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.183+1036G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31515770 | |||||||
| chr20:31515810 | T | C | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.183+1076T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31515810 | |||||||
| chr20:31515841 | G | C | 1 | a0001c0001t0002g0027 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.183+1107G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31515841 | |||||||
| chr20:31516043 | A | G | 3 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0176 |
3 | HG00733.hp2 HG01168.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.183+1309A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31516043 | |||||||
| chr20:31516233 | G | C | 60 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
68 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.183+1499G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31516233 | |||||||
| chr20:31516434 | C | T | 5 | a0001c0001t0002g0071 a0001c0001t0002g0072 a0001c0001t0002g0073 others(2): Show |
5 | HG02723.hp1 HG02809.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.183+1700C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31516434 | |||||||
| chr20:31516614 | G | C | 1 | a0001c0001t0001g0087 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.183+1880G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31516614 | |||||||
| chr20:31517001 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.183+2267C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31517001 | |||||||
| chr20:31517004 | A | G | 130 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(127): Show |
143 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.183+2270A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31517004 | |||||||
| chr20:31517497 | A | G | 1 | a0001c0001t0001g0132 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.183+2763A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31517497 | |||||||
| chr20:31517796 | G | GT | 83 | a0001c0001t0001g0172 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.183+3063dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31517796 | ||||||
| chr20:31517968 | G | A | 1 | a0001c0001t0010g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.183+3234G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31517968 | |||||||
| chr20:31518028 | T | C | 83 | a0001c0001t0001g0172 a0001c0001t0002g0003 a0001c0001t0002g0004 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.183+3294T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31518028 | |||||||
| chr20:31518037 | AT | A | 77 | a0001c0001t0001g0174 a0001c0001t0002g0003 a0001c0001t0002g0004 others(74): Show |
85 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(82): Show |
intron_variant | MODIFIER | c.183+3318delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31518037 | ||||||
| chr20:31518326 | C | T | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.183+3592C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31518326 | |||||||
| chr20:31518866 | T | G | 48 | a0001c0001t0001g0133 a0001c0001t0001g0134 a0001c0001t0001g0135 others(45): Show |
53 | HG00140.hp1 HG00408.hp2 HG00738.hp1 others(50): Show |
intron_variant | MODIFIER | c.183+4132T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31518866 | |||||||
| chr20:31518866 | T | TATAGAGA others(1): Show |
2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.183+4133_183+4134i others(10): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31518866 | ||||||
| chr20:31518868 | G | T | 42 | a0001c0001t0001g0012 a0001c0001t0001g0014 a0001c0001t0001g0087 others(39): Show |
46 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(43): Show |
intron_variant | MODIFIER | c.183+4134G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31518868 | |||||||
| chr20:31518870 | G | T | 11 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 others(8): Show |
11 | HG01106.hp1 HG02145.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.183+4136G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31518870 | |||||||
| chr20:31518872 | G | T | 3 | a0001c0001t0002g0082 a0001c0001t0002g0083 a0001c0001t0006g0015 |
3 | HG02976.hp1 HG03209.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.183+4138G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31518872 | |||||||
| chr20:31518909 | G | A | 1 | a0001c0001t0003g0022 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.183+4175G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31518909 | |||||||
| chr20:31519311 | G | A | 1 | a0001c0001t0002g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.183+4577G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31519311 | |||||||
| chr20:31519550 | C | G | 1 | a0001c0001t0010g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.183+4816C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31519550 | |||||||
| chr20:31519592 | T | C | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.183+4858T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31519592 | |||||||
| chr20:31519710 | C | CATTTAGG others(5): Show |
1 | a0001c0001t0001g0157 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.183+4977_183+4988d others(14): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31519710 | ||||||
| chr20:31519843 | C | CT | 33 | a0001c0001t0001g0014 a0001c0001t0001g0087 a0001c0001t0001g0123 others(30): Show |
34 | HG00099.hp1 HG00408.hp1 HG00597.hp2 others(31): Show |
intron_variant | MODIFIER | c.183+5128dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31519843 | ||||||
| chr20:31519843 | CT | C | 73 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(70): Show |
81 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.183+5128delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31519843 | ||||||
| chr20:31520460 | C | T | 1 | a0001c0001t0003g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.183+5726C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31520460 | |||||||
| chr20:31520730 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.183+5996A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31520730 | |||||||
| chr20:31520843 | T | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.183+6109T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31520843 | |||||||
| chr20:31520972 | C | T | 7 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0071 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.183+6238C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31520972 | |||||||
| chr20:31521090 | A | G | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+6356A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31521090 | |||||||
| chr20:31521106 | A | T | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.183+6372A>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31521106 | |||||||
| chr20:31521248 | T | G | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.184-6236T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31521248 | |||||||
| chr20:31521404 | C | T | 1 | a0001c0001t0002g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.184-6080C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31521404 | |||||||
| chr20:31521479 | A | G | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.184-6005A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31521479 | |||||||
| chr20:31521558 | T | G | 3 | a0001c0001t0006g0015 a0001c0001t0006g0085 a0001c0001t0010g0075 |
3 | HG03139.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.184-5926T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31521558 | |||||||
| chr20:31521600 | A | C | 1 | a0001c0001t0002g0056 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.184-5884A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31521600 | |||||||
| chr20:31521715 | C | T | 6 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0156 others(3): Show |
6 | HG01192.hp1 HG01257.hp1 HG01346.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-5769C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31521715 | |||||||
| chr20:31521728 | C | CAA | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(74): Show |
intron_variant | MODIFIER | c.184-5740_184-5739d others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31521728 | ||||||
| chr20:31521728 | C | CAAA | 6 | a0001c0001t0002g0057 a0001c0001t0002g0181 a0001c0001t0010g0075 others(3): Show |
6 | HG01496.hp2 HG02257.hp2 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-5741_184-5739d others(5): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31521728 | ||||||
| chr20:31521854 | C | CT | 72 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(69): Show |
80 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(77): Show |
intron_variant | MODIFIER | c.184-5611dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31521854 | ||||||
| chr20:31521854 | C | CTT | 5 | a0001c0001t0002g0054 a0001c0001t0002g0061 a0001c0001t0002g0079 others(2): Show |
5 | HG02055.hp2 HG02145.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-5612_184-5611d others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31521854 | ||||||
| chr20:31521854 | CT | C | 7 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0001g0090 others(4): Show |
7 | HG00738.hp2 HG01106.hp2 HG01256.hp1 others(4): Show |
intron_variant | MODIFIER | c.184-5611delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31521854 | ||||||
| chr20:31521964 | G | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-5520G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31521964 | |||||||
| chr20:31522026 | G | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.184-5458G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522026 | |||||||
| chr20:31522126 | G | A | 1 | a0001c0001t0010g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.184-5358G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522126 | |||||||
| chr20:31522191 | C | T | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(65): Show |
76 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.184-5293C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522191 | |||||||
| chr20:31522272 | C | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.184-5212C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522272 | |||||||
| chr20:31522287 | G | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-5197G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522287 | |||||||
| chr20:31522392 | A | C | 1 | a0001c0001t0001g0159 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.184-5092A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522392 | |||||||
| chr20:31522457 | G | T | 1 | a0001c0001t0001g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.184-5027G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522457 | |||||||
| chr20:31522544 | T | TA | 5 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0006g0015 others(2): Show |
5 | HG02559.hp1 HG03139.hp2 NA18522.hp1 others(2): Show |
intron_variant | MODIFIER | c.184-4931dupA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31522544 | ||||||
| chr20:31522544 | T | TAA | 60 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0006 others(57): Show |
67 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(64): Show |
intron_variant | MODIFIER | c.184-4932_184-4931d others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31522544 | ||||||
| chr20:31522544 | T | TAAA | 8 | a0001c0001t0002g0005 a0001c0001t0002g0030 a0001c0001t0002g0031 others(5): Show |
9 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(6): Show |
intron_variant | MODIFIER | c.184-4933_184-4931d others(5): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31522544 | ||||||
| chr20:31522552 | A | AAAC | 7 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(4): Show |
7 | HG00741.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-4931_184-4930i others(5): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31522552 | ||||||
| chr20:31522554 | C | A | 9 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(6): Show |
9 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(6): Show |
intron_variant | MODIFIER | c.184-4930C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522554 | |||||||
| chr20:31522624 | CTG | C | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(65): Show |
76 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.184-4857_184-4856d others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31522624 | ||||||
| chr20:31522673 | C | T | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.184-4811C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522673 | |||||||
| chr20:31522674 | T | C | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.184-4810T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522674 | |||||||
| chr20:31522719 | G | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.184-4765G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522719 | |||||||
| chr20:31522829 | T | A | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.184-4655T>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31522829 | |||||||
| chr20:31522861 | G | GA | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(65): Show |
76 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.184-4613dupA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31522861 | ||||||
| chr20:31523035 | G | GT | 6 | a0001c0001t0001g0128 a0001c0001t0002g0028 a0001c0001t0002g0049 others(3): Show |
6 | HG02257.hp2 HG02572.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-4441dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31523035 | ||||||
| chr20:31523043 | T | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.184-4441T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523043 | |||||||
| chr20:31523043 | T | TG | 10 | a0001c0001t0002g0038 a0001c0001t0002g0071 a0001c0001t0002g0072 others(7): Show |
10 | HG00741.hp2 HG01168.hp2 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.184-4438dupG | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31523043 | ||||||
| chr20:31523043 | T | TGG | 30 | a0001c0001t0002g0004 a0001c0001t0002g0006 a0001c0001t0002g0007 others(27): Show |
35 | HG00140.hp1 HG01069.hp2 HG01070.hp1 others(32): Show |
intron_variant | MODIFIER | c.184-4439_184-4438d others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31523043 | ||||||
| chr20:31523043 | T | TTG | 16 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0033 others(13): Show |
19 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.184-4441_184-4440i others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523043 | |||||||
| chr20:31523043 | T | TTGG | 6 | a0001c0001t0002g0031 a0001c0001t0002g0054 a0001c0001t0002g0057 others(3): Show |
6 | HG01516.hp2 HG02055.hp2 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.184-4441_184-4440i others(5): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523043 | |||||||
| chr20:31523047 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.184-4437A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523047 | |||||||
| chr20:31523054 | C | T | 2 | a0001c0001t0002g0074 a0001c0001t0003g0020 |
2 | HG02809.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.184-4430C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523054 | |||||||
| chr20:31523212 | G | C | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.184-4272G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523212 | |||||||
| chr20:31523214 | C | G | 1 | a0001c0001t0001g0157 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.184-4270C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523214 | |||||||
| chr20:31523268 | C | CT | 22 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0028 others(19): Show |
25 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(22): Show |
intron_variant | MODIFIER | c.184-4203dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31523268 | ||||||
| chr20:31523307 | G | A | 1 | a0001c0001t0002g0057 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.184-4177G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523307 | |||||||
| chr20:31523377 | C | T | 1 | a0001c0001t0001g0122 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.184-4107C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523377 | |||||||
| chr20:31523436 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0160 |
2 | HG00408.hp1 NA18965.hp2 |
intron_variant | MODIFIER | c.184-4048T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523436 | |||||||
| chr20:31523543 | A | G | 20 | a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0060 others(17): Show |
23 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.184-3941A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523543 | |||||||
| chr20:31523681 | A | C | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | NA18747.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.184-3803A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523681 | |||||||
| chr20:31523748 | G | A | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.184-3736G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523748 | |||||||
| chr20:31523837 | T | C | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.184-3647T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31523837 | |||||||
| chr20:31524027 | G | C | 1 | a0001c0001t0001g0161 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.184-3457G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31524027 | |||||||
| chr20:31524076 | C | CT | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.184-3405dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31524076 | ||||||
| chr20:31524190 | TG | T | 2 | a0001c0001t0001g0091 a0001c0001t0001g0132 |
2 | HG01515.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.184-3293delG | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31524190 | |||||||
| chr20:31524287 | G | A | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.184-3197G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31524287 | |||||||
| chr20:31524315 | G | A | 4 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0052 others(1): Show |
6 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.184-3169G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31524315 | |||||||
| chr20:31524361 | C | T | 1 | a0001c0001t0003g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.184-3123C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31524361 | |||||||
| chr20:31524499 | G | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | NA18747.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.184-2985G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31524499 | |||||||
| chr20:31524710 | C | CT | 11 | a0001c0001t0001g0090 a0001c0001t0001g0117 a0001c0001t0001g0118 others(8): Show |
11 | HG00408.hp1 HG00738.hp2 HG01175.hp2 others(8): Show |
intron_variant | MODIFIER | c.184-2752dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31524710 | ||||||
| chr20:31524710 | CT | C | 7 | a0001c0001t0001g0092 a0001c0001t0001g0133 a0001c0001t0001g0150 others(4): Show |
7 | HG01070.hp1 HG01074.hp2 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.184-2752delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31524710 | ||||||
| chr20:31524753 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.184-2731G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31524753 | |||||||
| chr20:31524795 | G | A | 1 | a0001c0001t0003g0018 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.184-2689G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31524795 | |||||||
| chr20:31524955 | C | T | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.184-2529C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31524955 | |||||||
| chr20:31525159 | A | G | 1 | a0001c0001t0002g0028 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.184-2325A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31525159 | |||||||
| chr20:31525314 | G | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.184-2170G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31525314 | |||||||
| chr20:31525855 | A | G | 5 | a0001c0001t0001g0133 a0001c0001t0001g0138 a0001c0001t0001g0139 others(2): Show |
5 | HG02129.hp1 HG02132.hp2 NA18939.hp2 others(2): Show |
intron_variant | MODIFIER | c.184-1629A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31525855 | |||||||
| chr20:31525900 | T | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.184-1584T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31525900 | |||||||
| chr20:31525944 | T | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.184-1540T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31525944 | |||||||
| chr20:31526066 | C | A | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.184-1418C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31526066 | |||||||
| chr20:31526160 | CT | C | 76 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(73): Show |
84 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.184-1309delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31526160 | ||||||
| chr20:31526217 | T | G | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.184-1267T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31526217 | |||||||
| chr20:31526316 | G | A | 1 | a0001c0001t0001g0093 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.184-1168G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31526316 | |||||||
| chr20:31526409 | G | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.184-1075G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31526409 | |||||||
| chr20:31526522 | C | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.184-962C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31526522 | |||||||
| chr20:31527337 | CA | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.184-134delA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr20 | 31527337 | ||||||
| chr20:31527448 | G | T | 1 | a0001c0001t0003g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.184-36G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 1/12 | chr20 | 31527448 | |||||||
| chr20:31527825 | GT | G | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.282+246delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 31527825 | ||||||
| chr20:31527830 | A | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.282+248A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31527830 | |||||||
| chr20:31527896 | C | CT | 5 | a0001c0001t0001g0013 a0001c0001t0001g0116 a0001c0001t0002g0004 others(2): Show |
8 | HG01069.hp2 HG01192.hp2 HG01934.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+328dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 31527896 | ||||||
| chr20:31527896 | CT | C | 5 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0132 others(2): Show |
5 | HG01069.hp1 HG01070.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.282+328delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 31527896 | ||||||
| chr20:31528050 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.282+468G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31528050 | |||||||
| chr20:31528152 | A | G | 1 | a0001c0001t0002g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.282+570A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31528152 | |||||||
| chr20:31528184 | T | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.282+602T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31528184 | |||||||
| chr20:31528312 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.282+730C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31528312 | |||||||
| chr20:31528573 | G | C | 2 | a0001c0001t0001g0088 a0001c0001t0001g0096 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.282+991G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31528573 | |||||||
| chr20:31528625 | C | T | 3 | a0001c0001t0002g0070 a0001c0001t0003g0018 a0001c0001t0003g0019 |
3 | HG00741.hp2 HG01884.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.282+1043C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31528625 | |||||||
| chr20:31528626 | G | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.282+1044G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31528626 | |||||||
| chr20:31528827 | C | T | 7 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0071 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+1245C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31528827 | |||||||
| chr20:31528829 | C | T | 7 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0071 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.282+1247C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31528829 | |||||||
| chr20:31529090 | C | A | 2 | a0001c0001t0002g0040 a0001c0001t0002g0048 |
2 | HG03130.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.282+1508C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31529090 | |||||||
| chr20:31529302 | A | G | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.282+1720A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31529302 | |||||||
| chr20:31529349 | G | A | 19 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
20 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.282+1767G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31529349 | |||||||
| chr20:31529538 | C | A | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+1956C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31529538 | |||||||
| chr20:31529545 | C | T | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(65): Show |
76 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.282+1963C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31529545 | |||||||
| chr20:31529596 | T | C | 1 | a0001c0001t0001g0123 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.282+2014T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31529596 | |||||||
| chr20:31529859 | C | T | 1 | a0001c0001t0001g0137 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.282+2277C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31529859 | |||||||
| chr20:31529966 | A | G | 1 | a0001c0001t0001g0154 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.282+2384A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31529966 | |||||||
| chr20:31530153 | T | G | 1 | a0001c0001t0002g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.282+2571T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31530153 | |||||||
| chr20:31530414 | CT | C | 79 | a0001c0001t0001g0087 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
87 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(84): Show |
intron_variant | MODIFIER | c.282+2845delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 31530414 | ||||||
| chr20:31530475 | A | C | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.282+2893A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31530475 | |||||||
| chr20:31530643 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.282+3061T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31530643 | |||||||
| chr20:31530650 | C | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.282+3068C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31530650 | |||||||
| chr20:31530699 | G | A | 8 | a0001c0001t0001g0087 a0001c0001t0001g0152 a0001c0001t0001g0154 others(5): Show |
8 | HG00099.hp1 HG01081.hp1 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.282+3117G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31530699 | |||||||
| chr20:31530815 | C | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.282+3233C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31530815 | |||||||
| chr20:31530987 | A | G | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.282+3405A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31530987 | |||||||
| chr20:31531024 | C | G | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(65): Show |
76 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.282+3442C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31531024 | |||||||
| chr20:31531051 | T | G | 1 | a0001c0001t0001g0117 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.282+3469T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31531051 | |||||||
| chr20:31531072 | T | C | 1 | a0001c0001t0001g0097 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.282+3490T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31531072 | |||||||
| chr20:31531133 | C | T | 6 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(3): Show |
6 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+3551C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31531133 | |||||||
| chr20:31531331 | G | A | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(65): Show |
76 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.282+3749G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31531331 | |||||||
| chr20:31531490 | G | A | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+3908G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31531490 | |||||||
| chr20:31531537 | T | C | 1 | a0001c0001t0002g0069 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.282+3955T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31531537 | |||||||
| chr20:31531572 | TTTTTTTG others(3): Show |
T | 1 | a0001c0001t0001g0177 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.282+4003_282+4012d others(12): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 31531572 | ||||||
| chr20:31531627 | T | A | 1 | a0001c0001t0001g0120 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.282+4045T>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31531627 | |||||||
| chr20:31531654 | C | A | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.282+4072C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31531654 | |||||||
| chr20:31531978 | C | G | 1 | a0001c0001t0005g0008 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.282+4396C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31531978 | |||||||
| chr20:31532096 | A | AT | 18 | a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0060 others(15): Show |
21 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(18): Show |
intron_variant | MODIFIER | c.282+4526dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 31532096 | ||||||
| chr20:31532128 | G | A | 6 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(3): Show |
6 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.282+4546G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532128 | |||||||
| chr20:31532155 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.282+4573G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532155 | |||||||
| chr20:31532222 | C | G | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.282+4640C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532222 | |||||||
| chr20:31532230 | T | G | 1 | a0001c0001t0002g0055 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.282+4648T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532230 | |||||||
| chr20:31532262 | TGAAAATA others(27): Show |
T | 1 | a0001c0001t0001g0134 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.282+4681_282+4714d others(36): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532262 | |||||||
| chr20:31532323 | G | T | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.282+4741G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532323 | |||||||
| chr20:31532506 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.282+4924C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532506 | |||||||
| chr20:31532522 | T | C | 2 | a0001c0001t0001g0126 a0001c0001t0001g0127 |
2 | HG03834.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.282+4940T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532522 | |||||||
| chr20:31532534 | C | T | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.282+4952C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532534 | |||||||
| chr20:31532750 | C | T | 1 | a0001c0001t0001g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.282+5168C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532750 | |||||||
| chr20:31532979 | G | A | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(65): Show |
76 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.283-5200G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31532979 | |||||||
| chr20:31533035 | G | T | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-5144G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31533035 | |||||||
| chr20:31533066 | G | A | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.283-5113G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31533066 | |||||||
| chr20:31533086 | C | G | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.283-5093C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31533086 | |||||||
| chr20:31533123 | C | T | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283-5056C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31533123 | |||||||
| chr20:31533427 | C | G | 7 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0052 others(4): Show |
9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.283-4752C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31533427 | |||||||
| chr20:31533560 | A | T | 1 | a0001c0001t0001g0114 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.283-4619A>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31533560 | |||||||
| chr20:31533612 | G | T | 2 | a0001c0001t0002g0078 a0001c0001t0002g0081 |
2 | HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.283-4567G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31533612 | |||||||
| chr20:31533620 | C | T | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.283-4559C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31533620 | |||||||
| chr20:31533943 | G | A | 1 | a0001c0001t0001g0177 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.283-4236G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31533943 | |||||||
| chr20:31534036 | C | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-4143C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31534036 | |||||||
| chr20:31534093 | T | TGA | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.283-4086_283-4085i others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31534093 | |||||||
| chr20:31534095 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.283-4084C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31534095 | |||||||
| chr20:31534513 | G | T | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.283-3666G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31534513 | |||||||
| chr20:31534526 | G | A | 3 | a0001c0001t0006g0015 a0001c0001t0006g0085 a0001c0001t0010g0075 |
3 | HG03139.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-3653G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31534526 | |||||||
| chr20:31534534 | A | G | 6 | a0001c0001t0002g0078 a0001c0001t0002g0081 a0001c0001t0002g0082 others(3): Show |
6 | HG02818.hp2 HG02976.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.283-3645A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31534534 | |||||||
| chr20:31534628 | C | G | 1 | a0001c0001t0002g0053 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.283-3551C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31534628 | |||||||
| chr20:31535003 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.283-3176G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535003 | |||||||
| chr20:31535017 | C | T | 1 | a0001c0001t0002g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-3162C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535017 | |||||||
| chr20:31535080 | C | G | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283-3099C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535080 | |||||||
| chr20:31535172 | G | A | 1 | a0001c0001t0001g0160 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.283-3007G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535172 | |||||||
| chr20:31535381 | C | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.283-2798C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535381 | |||||||
| chr20:31535386 | A | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-2793A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535386 | |||||||
| chr20:31535424 | G | T | 1 | a0001c0001t0003g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.283-2755G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535424 | |||||||
| chr20:31535464 | A | G | 60 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(57): Show |
68 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(65): Show |
intron_variant | MODIFIER | c.283-2715A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535464 | |||||||
| chr20:31535497 | G | C | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0021 |
3 | HG00741.hp2 HG01884.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.283-2682G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535497 | |||||||
| chr20:31535745 | G | C | 3 | a0001c0001t0006g0015 a0001c0001t0006g0085 a0001c0001t0010g0075 |
3 | HG03139.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-2434G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535745 | |||||||
| chr20:31535785 | T | TCAAGAAG others(20): Show |
1 | a0001c0001t0001g0134 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.283-2393_283-2367d others(29): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr20 | 31535785 | ||||||
| chr20:31535964 | C | G | 1 | a0001c0001t0002g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.283-2215C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535964 | |||||||
| chr20:31535970 | T | C | 2 | a0001c0001t0007g0076 a0001c0001t0007g0077 |
2 | HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.283-2209T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31535970 | |||||||
| chr20:31536101 | G | A | 1 | a0001c0001t0002g0031 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.283-2078G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31536101 | |||||||
| chr20:31536137 | T | G | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.283-2042T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31536137 | |||||||
| chr20:31536144 | A | G | 1 | a0001c0001t0001g0134 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.283-2035A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31536144 | |||||||
| chr20:31536220 | G | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-1959G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31536220 | |||||||
| chr20:31536425 | C | T | 1 | a0001c0001t0006g0085 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.283-1754C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31536425 | |||||||
| chr20:31536441 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18939.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.283-1738G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31536441 | |||||||
| chr20:31536442 | C | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18939.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.283-1737C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31536442 | |||||||
| chr20:31536458 | C | A | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(65): Show |
76 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.283-1721C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31536458 | |||||||
| chr20:31536803 | C | A | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283-1376C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31536803 | |||||||
| chr20:31536956 | G | A | 3 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 |
3 | HG00741.hp2 HG01884.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.283-1223G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31536956 | |||||||
| chr20:31537048 | G | A | 6 | a0001c0001t0002g0005 a0001c0001t0002g0031 a0001c0001t0002g0034 others(3): Show |
7 | HG02055.hp2 HG02451.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.283-1131G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31537048 | |||||||
| chr20:31537216 | T | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-963T>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31537216 | |||||||
| chr20:31537333 | G | A | 1 | a0001c0001t0001g0009 | 2 | HG02080.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.283-846G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31537333 | |||||||
| chr20:31537402 | C | G | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.283-777C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31537402 | |||||||
| chr20:31537484 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0001g0096 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.283-695C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31537484 | |||||||
| chr20:31537560 | A | G | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.283-619A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31537560 | |||||||
| chr20:31537617 | G | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-562G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31537617 | |||||||
| chr20:31537841 | C | T | 1 | a0001c0001t0001g0128 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.283-338C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31537841 | |||||||
| chr20:31537873 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.283-306C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31537873 | |||||||
| chr20:31537978 | A | G | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.283-201A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31537978 | |||||||
| chr20:31538060 | T | C | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.283-119T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 2/12 | chr20 | 31538060 | |||||||
| chr20:31538955 | A | G | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.365+694A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31538955 | |||||||
| chr20:31539111 | T | G | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.365+850T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31539111 | |||||||
| chr20:31539381 | C | G | 3 | a0001c0001t0001g0088 a0001c0001t0001g0096 a0001c0001t0001g0112 |
3 | HG01257.hp2 HG01258.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.365+1120C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31539381 | |||||||
| chr20:31539405 | G | A | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | NA18939.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.365+1144G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31539405 | |||||||
| chr20:31539589 | A | C | 69 | a0001c0001t0001g0143 a0001c0001t0002g0003 a0001c0001t0002g0004 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.365+1328A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31539589 | |||||||
| chr20:31539743 | C | T | 1 | a0001c0001t0001g0152 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.365+1482C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31539743 | |||||||
| chr20:31539908 | C | A | 1 | a0001c0001t0001g0161 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.365+1647C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31539908 | |||||||
| chr20:31539924 | T | G | 19 | a0001c0001t0001g0014 a0001c0001t0001g0150 a0001c0001t0001g0151 others(16): Show |
20 | HG00408.hp1 HG00597.hp2 HG00621.hp2 others(17): Show |
intron_variant | MODIFIER | c.365+1663T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31539924 | |||||||
| chr20:31540211 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.365+1950G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31540211 | |||||||
| chr20:31540456 | G | T | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+2195G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31540456 | |||||||
| chr20:31540457 | C | T | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+2196C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31540457 | |||||||
| chr20:31540582 | C | G | 3 | a0001c0001t0002g0039 a0001c0001t0002g0047 a0001c0001t0002g0180 |
3 | HG01167.hp2 HG01361.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.365+2321C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31540582 | |||||||
| chr20:31540633 | C | T | 2 | a0001c0001t0002g0063 a0001c0001t0002g0065 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.365+2372C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31540633 | |||||||
| chr20:31540738 | C | T | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.365+2477C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31540738 | |||||||
| chr20:31540750 | T | G | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(78): Show |
89 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.365+2489T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31540750 | |||||||
| chr20:31540782 | G | A | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(78): Show |
89 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.365+2521G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31540782 | |||||||
| chr20:31540880 | T | G | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.365+2619T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31540880 | |||||||
| chr20:31540979 | C | CAA | 6 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(3): Show |
6 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.365+2731_365+2732d others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 31540979 | ||||||
| chr20:31541177 | T | C | 1 | a0001c0001t0002g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.365+2916T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31541177 | |||||||
| chr20:31541243 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.365+2982A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31541243 | |||||||
| chr20:31541296 | C | A | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.365+3035C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31541296 | |||||||
| chr20:31541350 | G | C | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.365+3089G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31541350 | |||||||
| chr20:31541396 | G | A | 1 | a0001c0001t0003g0018 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.365+3135G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31541396 | |||||||
| chr20:31541398 | G | A | 13 | a0001c0001t0002g0006 a0001c0001t0002g0027 a0001c0001t0002g0032 others(10): Show |
14 | HG00140.hp1 HG01074.hp1 HG01167.hp2 others(11): Show |
intron_variant | MODIFIER | c.365+3137G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31541398 | |||||||
| chr20:31541444 | C | T | 3 | a0001c0001t0001g0129 a0001c0001t0001g0130 a0001c0001t0001g0131 |
3 | NA18939.hp1 NA19060.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.365+3183C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31541444 | |||||||
| chr20:31541489 | AT | A | 2 | a0001c0001t0002g0079 a0001c0001t0002g0080 |
2 | HG02486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.365+3229delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31541489 | |||||||
| chr20:31541490 | TA | T | 124 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(121): Show |
137 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.365+3245delA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr20 | 31541490 | ||||||
| chr20:31542245 | C | A | 1 | a0001c0001t0001g0087 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.366-2702C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31542245 | |||||||
| chr20:31542423 | C | G | 2 | a0001c0001t0002g0032 a0001c0001t0002g0038 |
2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.366-2524C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31542423 | |||||||
| chr20:31542430 | GA | G | 3 | a0001c0001t0001g0150 a0001c0001t0001g0155 a0001c0001t0001g0173 |
3 | HG02040.hp1 NA18957.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.366-2516delA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31542430 | |||||||
| chr20:31542479 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.366-2468G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31542479 | |||||||
| chr20:31542497 | A | C | 1 | a0001c0001t0002g0070 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.366-2450A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31542497 | |||||||
| chr20:31542526 | A | G | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.366-2421A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31542526 | |||||||
| chr20:31542720 | G | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.366-2227G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31542720 | |||||||
| chr20:31542926 | T | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(78): Show |
89 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.366-2021T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31542926 | |||||||
| chr20:31542927 | G | A | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.366-2020G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31542927 | |||||||
| chr20:31542972 | A | C | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.366-1975A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31542972 | |||||||
| chr20:31543001 | G | T | 2 | a0001c0001t0002g0073 a0001c0001t0002g0182 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.366-1946G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543001 | |||||||
| chr20:31543004 | G | A | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.366-1943G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543004 | |||||||
| chr20:31543129 | C | T | 6 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(3): Show |
6 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.366-1818C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543129 | |||||||
| chr20:31543379 | G | A | 1 | a0001c0001t0001g0120 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.366-1568G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543379 | |||||||
| chr20:31543431 | A | T | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(78): Show |
89 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.366-1516A>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543431 | |||||||
| chr20:31543446 | G | A | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.366-1501G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543446 | |||||||
| chr20:31543509 | G | A | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.366-1438G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543509 | |||||||
| chr20:31543553 | T | C | 1 | a0001c0001t0001g0099 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.366-1394T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543553 | |||||||
| chr20:31543727 | C | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.366-1220C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543727 | |||||||
| chr20:31543807 | G | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.366-1140G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543807 | |||||||
| chr20:31543883 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.366-1064G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543883 | |||||||
| chr20:31543913 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.366-1034G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31543913 | |||||||
| chr20:31544132 | G | C | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(78): Show |
89 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.366-815G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31544132 | |||||||
| chr20:31544163 | T | C | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.366-784T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31544163 | |||||||
| chr20:31544413 | C | G | 1 | a0001c0001t0001g0136 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.366-534C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31544413 | |||||||
| chr20:31544598 | A | T | 1 | a0001c0001t0001g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.366-349A>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31544598 | |||||||
| chr20:31544823 | G | T | 61 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(58): Show |
69 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.366-124G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 3/12 | chr20 | 31544823 | |||||||
| chr20:31545371 | C | CTCAA | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.454+337_454+340dup others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr20 | 31545371 | ||||||
| chr20:31545401 | C | T | 1 | a0001c0001t0001g0130 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.454+366C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31545401 | |||||||
| chr20:31545498 | C | T | 5 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0097 others(2): Show |
7 | HG01175.hp2 HG01981.hp2 HG01993.hp2 others(4): Show |
intron_variant | MODIFIER | c.454+463C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31545498 | |||||||
| chr20:31545611 | G | T | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.454+576G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31545611 | |||||||
| chr20:31545961 | C | T | 1 | a0001c0001t0002g0086 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.454+926C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31545961 | |||||||
| chr20:31546015 | A | G | 133 | a0001c0001t0001g0002 a0001c0001t0001g0013 a0001c0001t0001g0014 others(130): Show |
146 | HG00099.hp1 HG00140.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.454+980A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31546015 | |||||||
| chr20:31546025 | G | A | 1 | a0001c0001t0003g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.454+990G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31546025 | |||||||
| chr20:31546044 | C | CT | 12 | a0001c0001t0001g0095 a0001c0001t0001g0099 a0001c0001t0001g0118 others(9): Show |
12 | HG00741.hp1 HG01070.hp2 HG01192.hp1 others(9): Show |
intron_variant | MODIFIER | c.454+1031dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr20 | 31546044 | ||||||
| chr20:31546044 | CT | C | 7 | a0001c0001t0001g0153 a0001c0001t0002g0035 a0001c0001t0002g0036 others(4): Show |
7 | HG02109.hp1 HG02895.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.454+1031delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr20 | 31546044 | ||||||
| chr20:31546044 | CTT | C | 71 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(68): Show |
79 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(76): Show |
intron_variant | MODIFIER | c.454+1030_454+1031d others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr20 | 31546044 | ||||||
| chr20:31546089 | G | A | 2 | a0001c0001t0003g0023 a0001c0001t0011g0024 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.454+1054G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31546089 | |||||||
| chr20:31546491 | C | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.454+1456C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31546491 | |||||||
| chr20:31546531 | A | G | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.454+1496A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31546531 | |||||||
| chr20:31546619 | T | C | 1 | a0001c0001t0002g0081 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.454+1584T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31546619 | |||||||
| chr20:31546726 | G | T | 1 | a0001c0001t0001g0164 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.454+1691G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31546726 | |||||||
| chr20:31546754 | CA | C | 76 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(73): Show |
84 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(81): Show |
intron_variant | MODIFIER | c.454+1735delA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr20 | 31546754 | ||||||
| chr20:31547054 | T | C | 6 | a0001c0001t0003g0017 a0001c0001t0003g0018 a0001c0001t0003g0019 others(3): Show |
6 | HG00741.hp2 HG01884.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.455-1975T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31547054 | |||||||
| chr20:31547497 | C | T | 3 | a0001c0001t0002g0006 a0001c0001t0002g0050 a0001c0001t0002g0051 |
4 | HG00140.hp1 HG01074.hp1 HG01256.hp2 others(1): Show |
intron_variant | MODIFIER | c.455-1532C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31547497 | |||||||
| chr20:31548187 | A | G | 56 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(53): Show |
63 | HG00738.hp1 HG01069.hp2 HG01070.hp1 others(60): Show |
intron_variant | MODIFIER | c.455-842A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31548187 | |||||||
| chr20:31548416 | T | C | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.455-613T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31548416 | |||||||
| chr20:31548510 | G | T | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.455-519G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31548510 | |||||||
| chr20:31548662 | A | AT | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.455-366dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr20 | 31548662 | ||||||
| chr20:31548674 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.455-355C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31548674 | |||||||
| chr20:31548913 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.455-116G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31548913 | |||||||
| chr20:31548958 | C | T | 1 | a0001c0001t0010g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.455-71C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 4/12 | chr20 | 31548958 | |||||||
| chr20:31549429 | A | G | 3 | a0001c0001t0006g0015 a0001c0001t0006g0085 a0001c0001t0010g0075 |
3 | HG03139.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.666+97A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 6/12 | chr20 | 31549429 | |||||||
| chr20:31549629 | A | G | 70 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(67): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.666+297A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 6/12 | chr20 | 31549629 | |||||||
| chr20:31549671 | C | T | 57 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(54): Show |
64 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(61): Show |
intron_variant | MODIFIER | c.666+339C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 6/12 | chr20 | 31549671 | |||||||
| chr20:31549754 | A | G | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.667-310A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 6/12 | chr20 | 31549754 | |||||||
| chr20:31550168 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.724+47G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31550168 | |||||||
| chr20:31550307 | G | A | 1 | a0001c0001t0001g0131 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.724+186G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31550307 | |||||||
| chr20:31550373 | G | A | 2 | a0001c0001t0002g0070 a0001c0001t0002g0147 |
2 | HG01346.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.724+252G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31550373 | |||||||
| chr20:31550532 | T | C | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.724+411T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31550532 | |||||||
| chr20:31550685 | G | A | 1 | a0001c0001t0002g0040 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.724+564G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31550685 | |||||||
| chr20:31550928 | T | C | 7 | a0001c0001t0002g0060 a0001c0001t0002g0061 a0001c0001t0002g0071 others(4): Show |
7 | HG02630.hp2 HG02723.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.724+807T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31550928 | |||||||
| chr20:31551009 | T | G | 6 | a0001c0001t0002g0006 a0001c0001t0002g0032 a0001c0001t0002g0038 others(3): Show |
7 | HG00140.hp1 HG01074.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.724+888T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551009 | |||||||
| chr20:31551205 | A | T | 2 | a0001c0001t0002g0060 a0001c0001t0002g0061 |
2 | HG02630.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.724+1084A>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551205 | |||||||
| chr20:31551241 | T | C | 1 | a0001c0001t0001g0128 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.724+1120T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551241 | |||||||
| chr20:31551349 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0178 |
2 | HG01192.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.724+1228C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551349 | |||||||
| chr20:31551434 | C | G | 1 | a0001c0001t0001g0149 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.724+1313C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551434 | |||||||
| chr20:31551521 | A | C | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.724+1400A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551521 | |||||||
| chr20:31551527 | C | T | 1 | a0001c0001t0003g0017 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.724+1406C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551527 | |||||||
| chr20:31551670 | G | A | 1 | a0001c0001t0001g0164 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.724+1549G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551670 | |||||||
| chr20:31551748 | G | A | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.724+1627G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551748 | |||||||
| chr20:31551821 | C | A | 1 | a0001c0001t0001g0162 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.724+1700C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551821 | |||||||
| chr20:31551842 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.724+1721A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31551842 | |||||||
| chr20:31552045 | T | C | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.724+1924T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552045 | |||||||
| chr20:31552050 | G | A | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0006 others(65): Show |
75 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.724+1929G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552050 | |||||||
| chr20:31552051 | C | T | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0006 others(65): Show |
75 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.724+1930C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552051 | |||||||
| chr20:31552073 | G | A | 2 | a0001c0001t0002g0049 a0001c0001t0002g0055 |
2 | HG02572.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.724+1952G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552073 | |||||||
| chr20:31552075 | G | A | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0006 others(65): Show |
75 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.724+1954G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552075 | |||||||
| chr20:31552078 | G | T | 68 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0006 others(65): Show |
75 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.724+1957G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552078 | |||||||
| chr20:31552083 | T | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.724+1962T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552083 | |||||||
| chr20:31552466 | C | T | 1 | a0001c0001t0001g0113 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.725-2280C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552466 | |||||||
| chr20:31552557 | A | G | 9 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0097 others(6): Show |
11 | HG01175.hp2 HG01981.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.725-2189A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552557 | |||||||
| chr20:31552558 | G | A | 1 | a0001c0001t0010g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.725-2188G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552558 | |||||||
| chr20:31552667 | G | C | 1 | a0001c0001t0001g0108 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.725-2079G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552667 | |||||||
| chr20:31552749 | G | A | 4 | a0001c0001t0002g0007 a0001c0001t0002g0041 a0001c0001t0002g0044 others(1): Show |
5 | HG02451.hp2 HG02622.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.725-1997G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552749 | |||||||
| chr20:31552946 | G | A | 1 | a0001c0001t0011g0024 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.725-1800G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31552946 | |||||||
| chr20:31553067 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.725-1679G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31553067 | |||||||
| chr20:31553153 | A | T | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.725-1593A>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31553153 | |||||||
| chr20:31553188 | CAG | C | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.725-1557_725-1556d others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31553188 | |||||||
| chr20:31553195 | C | A | 1 | a0001c0001t0002g0070 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.725-1551C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31553195 | |||||||
| chr20:31553265 | C | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.725-1481C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31553265 | |||||||
| chr20:31553295 | C | CA | 82 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0009 others(79): Show |
92 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(89): Show |
intron_variant | MODIFIER | c.725-1432dupA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr20 | 31553295 | ||||||
| chr20:31553295 | C | CAA | 12 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0097 others(9): Show |
14 | HG01175.hp2 HG01981.hp2 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.725-1433_725-1432d others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr20 | 31553295 | ||||||
| chr20:31553530 | G | A | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.725-1216G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31553530 | |||||||
| chr20:31553571 | C | G | 1 | a0001c0001t0002g0147 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.725-1175C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31553571 | |||||||
| chr20:31553657 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.725-1089C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31553657 | |||||||
| chr20:31553710 | A | T | 1 | a0001c0001t0010g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.725-1036A>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31553710 | |||||||
| chr20:31553839 | G | T | 3 | a0001c0001t0006g0015 a0001c0001t0006g0085 a0001c0001t0010g0075 |
3 | HG03139.hp2 NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.725-907G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31553839 | |||||||
| chr20:31554015 | G | A | 2 | a0001c0001t0001g0010 a0001c0001t0001g0119 |
3 | NA18979.hp2 NA19060.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.725-731G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554015 | |||||||
| chr20:31554218 | G | A | 81 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(78): Show |
89 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.725-528G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554218 | |||||||
| chr20:31554240 | C | T | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.725-506C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554240 | |||||||
| chr20:31554375 | C | T | 4 | a0001c0001t0003g0018 a0001c0001t0003g0019 a0001c0001t0003g0020 others(1): Show |
4 | HG00741.hp2 HG01884.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.725-371C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554375 | |||||||
| chr20:31554377 | C | CA | 80 | a0001c0001t0001g0165 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.725-355dupA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr20 | 31554377 | ||||||
| chr20:31554405 | G | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.725-341G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554405 | |||||||
| chr20:31554442 | G | A | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.725-304G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554442 | |||||||
| chr20:31554587 | C | T | 20 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0027 others(17): Show |
22 | HG00140.hp1 HG01074.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.725-159C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554587 | |||||||
| chr20:31554618 | C | T | 1 | a0001c0001t0001g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.725-128C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554618 | |||||||
| chr20:31554621 | G | T | 1 | a0001c0001t0001g0120 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.725-125G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554621 | |||||||
| chr20:31554677 | G | A | 20 | a0001c0001t0002g0006 a0001c0001t0002g0007 a0001c0001t0002g0027 others(17): Show |
22 | HG00140.hp1 HG01074.hp1 HG01167.hp2 others(19): Show |
intron_variant | MODIFIER | c.725-69G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554677 | |||||||
| chr20:31554701 | A | T | 2 | a0001c0001t0003g0023 a0001c0001t0011g0024 |
2 | HG02145.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.725-45A>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554701 | |||||||
| chr20:31554729 | C | A | 1 | a0001c0001t0001g0092 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.725-17C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 7/12 | chr20 | 31554729 | |||||||
| chr20:31555359 | G | A | 8 | a0001c0001t0002g0078 a0001c0001t0002g0079 a0001c0001t0002g0080 others(5): Show |
8 | HG02486.hp1 HG02818.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.808+530G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31555359 | |||||||
| chr20:31555436 | C | CAG | 82 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(79): Show |
90 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(87): Show |
intron_variant | MODIFIER | c.808+607_808+608ins others(2): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31555436 | |||||||
| chr20:31555436 | C | T | 1 | a0001c0001t0001g0159 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.808+607C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31555436 | |||||||
| chr20:31555444 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.808+615G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31555444 | |||||||
| chr20:31555475 | C | T | 78 | a0001c0001t0001g0095 a0001c0001t0001g0118 a0001c0001t0002g0003 others(75): Show |
86 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(83): Show |
intron_variant | MODIFIER | c.808+646C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31555475 | |||||||
| chr20:31555521 | A | G | 1 | a0001c0001t0001g0153 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.808+692A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31555521 | |||||||
| chr20:31555805 | C | CA | 5 | a0001c0001t0001g0101 a0001c0001t0003g0017 a0001c0001t0003g0021 others(2): Show |
5 | HG02109.hp1 HG03041.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.808+991dupA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr20 | 31555805 | ||||||
| chr20:31555826 | C | G | 2 | a0001c0002t0002g0029 a0001c0002t0002g0179 |
2 | HG01496.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.808+997C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31555826 | |||||||
| chr20:31555931 | C | T | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.808+1102C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31555931 | |||||||
| chr20:31556036 | C | CT | 66 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0006 others(63): Show |
73 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.808+1222dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr20 | 31556036 | ||||||
| chr20:31556135 | G | A | 1 | a0001c0001t0001g0168 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.808+1306G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31556135 | |||||||
| chr20:31556145 | TCTCCTGC others(30): Show |
T | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.808+1318_808+1354d others(39): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr20 | 31556145 | ||||||
| chr20:31556183 | C | G | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.808+1354C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31556183 | |||||||
| chr20:31556190 | C | A | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.808+1361C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31556190 | |||||||
| chr20:31556192 | C | A | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.808+1363C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31556192 | |||||||
| chr20:31556193 | C | A | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.808+1364C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31556193 | |||||||
| chr20:31556194 | A | T | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.808+1365A>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31556194 | |||||||
| chr20:31556195 | C | T | 1 | a0001c0001t0001g0155 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.808+1366C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31556195 | |||||||
| chr20:31556321 | G | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.808+1492G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31556321 | |||||||
| chr20:31556739 | G | A | 1 | a0001c0001t0003g0020 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.808+1910G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31556739 | |||||||
| chr20:31556933 | G | A | 1 | a0001c0001t0002g0066 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.808+2104G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31556933 | |||||||
| chr20:31557018 | C | CA | 5 | a0001c0001t0001g0110 a0001c0001t0001g0138 a0001c0001t0001g0148 others(2): Show |
5 | HG01081.hp1 HG01081.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.808+2206dupA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr20 | 31557018 | ||||||
| chr20:31557018 | CA | C | 79 | a0001c0001t0001g0132 a0001c0001t0002g0003 a0001c0001t0002g0004 others(76): Show |
87 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(84): Show |
intron_variant | MODIFIER | c.808+2206delA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr20 | 31557018 | ||||||
| chr20:31557092 | G | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.808+2263G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557092 | |||||||
| chr20:31557182 | A | G | 2 | a0001c0001t0002g0063 a0001c0001t0002g0065 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.808+2353A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557182 | |||||||
| chr20:31557310 | A | C | 1 | a0001c0001t0010g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.809-2301A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557310 | |||||||
| chr20:31557417 | C | T | 1 | a0001c0001t0001g0145 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.809-2194C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557417 | |||||||
| chr20:31557702 | T | G | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.809-1909T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557702 | |||||||
| chr20:31557703 | C | CT | 23 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0102 others(20): Show |
25 | HG00621.hp2 HG01175.hp1 HG01175.hp2 others(22): Show |
intron_variant | MODIFIER | c.809-1884dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr20 | 31557703 | ||||||
| chr20:31557703 | C | CTTT | 67 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(64): Show |
75 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(72): Show |
intron_variant | MODIFIER | c.809-1886_809-1884d others(5): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr20 | 31557703 | ||||||
| chr20:31557703 | C | CTTTT | 8 | a0001c0001t0002g0053 a0001c0001t0002g0056 a0001c0001t0002g0058 others(5): Show |
8 | HG01070.hp1 HG02145.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.809-1887_809-1884d others(6): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr20 | 31557703 | ||||||
| chr20:31557703 | CT | C | 6 | a0001c0001t0001g0105 a0001c0001t0001g0125 a0001c0001t0001g0132 others(3): Show |
6 | HG01256.hp1 HG01515.hp1 HG02040.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-1884delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr20 | 31557703 | ||||||
| chr20:31557743 | T | C | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.809-1868T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557743 | |||||||
| chr20:31557847 | A | G | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.809-1764A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557847 | |||||||
| chr20:31557859 | C | T | 1 | a0001c0001t0001g0151 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.809-1752C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557859 | |||||||
| chr20:31557895 | C | T | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.809-1716C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557895 | |||||||
| chr20:31557928 | G | A | 4 | a0001c0001t0002g0006 a0001c0001t0002g0042 a0001c0001t0002g0050 others(1): Show |
5 | HG00140.hp1 HG01074.hp1 HG01256.hp2 others(2): Show |
intron_variant | MODIFIER | c.809-1683G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557928 | |||||||
| chr20:31557998 | G | A | 1 | a0001c0001t0010g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.809-1613G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31557998 | |||||||
| chr20:31558065 | G | C | 6 | a0001c0001t0003g0017 a0001c0001t0003g0020 a0001c0001t0004g0025 others(3): Show |
6 | HG02109.hp1 HG02559.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.809-1546G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31558065 | |||||||
| chr20:31558332 | C | A | 1 | a0001c0001t0001g0144 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.809-1279C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31558332 | |||||||
| chr20:31558347 | G | T | 1 | a0001c0001t0001g0089 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.809-1264G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31558347 | |||||||
| chr20:31558396 | A | G | 4 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0052 others(1): Show |
6 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(3): Show |
intron_variant | MODIFIER | c.809-1215A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31558396 | |||||||
| chr20:31558549 | TCTC | T | 76 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(73): Show |
84 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(81): Show |
intron_variant | MODIFIER | c.809-1056_809-1054d others(5): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | INFO_REALIGN_3_PRIME | chr20 | 31558549 | ||||||
| chr20:31558560 | C | T | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.809-1051C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31558560 | |||||||
| chr20:31558728 | G | T | 1 | a0001c0001t0001g0160 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.809-883G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31558728 | |||||||
| chr20:31558763 | G | A | 1 | a0001c0001t0001g0099 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.809-848G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31558763 | |||||||
| chr20:31558869 | G | T | 1 | a0001c0001t0003g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.809-742G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31558869 | |||||||
| chr20:31558971 | T | C | 7 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0052 others(4): Show |
9 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.809-640T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31558971 | |||||||
| chr20:31559059 | C | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0010g0075 |
3 | HG02559.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.809-552C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31559059 | |||||||
| chr20:31559099 | A | C | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.809-512A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31559099 | |||||||
| chr20:31559221 | G | A | 1 | a0001c0001t0001g0139 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.809-390G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31559221 | |||||||
| chr20:31559241 | A | G | 2 | a0001c0001t0002g0035 a0001c0001t0002g0048 |
2 | HG03130.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.809-370A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31559241 | |||||||
| chr20:31559326 | A | G | 73 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(70): Show |
81 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(78): Show |
intron_variant | MODIFIER | c.809-285A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31559326 | |||||||
| chr20:31559342 | C | G | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.809-269C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31559342 | |||||||
| chr20:31559422 | G | A | 2 | a0001c0001t0001g0108 a0001c0001t0001g0109 |
2 | HG00099.hp2 HG00733.hp1 |
intron_variant | MODIFIER | c.809-189G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31559422 | |||||||
| chr20:31559467 | T | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.809-144T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31559467 | |||||||
| chr20:31559471 | T | C | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.809-140T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 8/12 | chr20 | 31559471 | |||||||
| chr20:31559751 | C | A | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.845+104C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31559751 | |||||||
| chr20:31559835 | G | C | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.845+188G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31559835 | |||||||
| chr20:31559856 | G | A | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.845+209G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31559856 | |||||||
| chr20:31560023 | C | A | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.845+376C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31560023 | |||||||
| chr20:31560149 | T | C | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.845+502T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31560149 | |||||||
| chr20:31560223 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.845+576A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31560223 | |||||||
| chr20:31560296 | C | T | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.845+649C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31560296 | |||||||
| chr20:31560304 | C | T | 1 | a0001c0001t0003g0018 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.845+657C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31560304 | |||||||
| chr20:31560521 | A | G | 2 | a0001c0001t0001g0165 a0001c0001t0001g0171 |
2 | HG01106.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.845+874A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31560521 | |||||||
| chr20:31560720 | C | A | 1 | a0001c0001t0001g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.846-914C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31560720 | |||||||
| chr20:31560733 | G | T | 1 | a0001c0001t0003g0018 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.846-901G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31560733 | |||||||
| chr20:31561283 | A | T | 2 | a0001c0001t0003g0017 a0002c0003t0003g0016 |
2 | HG02109.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.846-351A>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31561283 | |||||||
| chr20:31561343 | T | C | 1 | a0001c0001t0006g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.846-291T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31561343 | |||||||
| chr20:31561344 | A | G | 1 | a0001c0001t0002g0079 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.846-290A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31561344 | |||||||
| chr20:31561464 | C | G | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.846-170C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31561464 | |||||||
| chr20:31561475 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.846-159G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31561475 | |||||||
| chr20:31561535 | C | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.846-99C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31561535 | |||||||
| chr20:31561535 | C | T | 1 | a0001c0001t0001g0009 | 2 | HG02080.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.846-99C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 9/12 | chr20 | 31561535 | |||||||
| chr20:31561836 | C | T | 3 | a0001c0001t0004g0025 a0001c0001t0004g0026 a0001c0001t0010g0075 |
3 | HG02559.hp1 HG03139.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.948+100C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31561836 | |||||||
| chr20:31561840 | C | G | 3 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0153 |
3 | HG02717.hp1 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.948+104C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31561840 | |||||||
| chr20:31561931 | C | T | 2 | a0001c0001t0001g0174 a0001c0001t0001g0175 |
2 | HG00733.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.948+195C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31561931 | |||||||
| chr20:31561932 | G | A | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.948+196G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31561932 | |||||||
| chr20:31561957 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.948+221C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31561957 | |||||||
| chr20:31562274 | T | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.948+538T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562274 | |||||||
| chr20:31562339 | A | G | 1 | a0001c0001t0001g0091 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.948+603A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562339 | |||||||
| chr20:31562476 | G | A | 61 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(58): Show |
69 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(66): Show |
intron_variant | MODIFIER | c.948+740G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562476 | |||||||
| chr20:31562501 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.948+765C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562501 | |||||||
| chr20:31562521 | G | A | 4 | a0001c0001t0001g0149 a0001c0001t0001g0156 a0001c0001t0001g0158 others(1): Show |
4 | HG01192.hp1 HG01257.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.948+785G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562521 | |||||||
| chr20:31562526 | G | A | 2 | a0001c0001t0001g0102 a0001c0001t0001g0128 |
2 | HG02132.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.948+790G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562526 | |||||||
| chr20:31562705 | C | G | 1 | a0001c0001t0001g0126 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.948+969C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562705 | |||||||
| chr20:31562890 | C | G | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.948+1154C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562890 | |||||||
| chr20:31562926 | A | G | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.948+1190A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562926 | |||||||
| chr20:31562936 | T | C | 10 | a0001c0001t0001g0010 a0001c0001t0001g0011 a0001c0001t0001g0097 others(7): Show |
12 | HG01175.hp2 HG01981.hp2 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.948+1200T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562936 | |||||||
| chr20:31562955 | C | T | 69 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(66): Show |
77 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(74): Show |
intron_variant | MODIFIER | c.948+1219C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31562955 | |||||||
| chr20:31563200 | C | A | 2 | a0001c0001t0001g0169 a0001c0001t0001g0170 |
2 | HG02486.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.948+1464C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563200 | |||||||
| chr20:31563304 | G | A | 1 | a0001c0001t0003g0019 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.948+1568G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563304 | |||||||
| chr20:31563366 | C | T | 2 | a0001c0002t0002g0029 a0001c0002t0002g0179 |
2 | HG01496.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.948+1630C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563366 | |||||||
| chr20:31563386 | G | A | 1 | a0001c0001t0001g0136 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.948+1650G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563386 | |||||||
| chr20:31563410 | G | A | 5 | a0001c0001t0002g0003 a0001c0001t0002g0033 a0001c0001t0002g0052 others(2): Show |
7 | HG00738.hp1 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.948+1674G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563410 | |||||||
| chr20:31563506 | T | C | 1 | a0001c0001t0001g0177 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.948+1770T>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563506 | |||||||
| chr20:31563770 | G | C | 1 | a0001c0001t0001g0106 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.948+2034G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563770 | |||||||
| chr20:31563777 | G | A | 3 | a0001c0001t0001g0143 a0001c0001t0001g0145 a0001c0001t0001g0153 |
3 | HG02717.hp1 HG02895.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.948+2041G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563777 | |||||||
| chr20:31563795 | G | A | 2 | a0001c0001t0001g0088 a0001c0001t0001g0096 |
2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.948+2059G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563795 | |||||||
| chr20:31563866 | C | T | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.948+2130C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563866 | |||||||
| chr20:31563933 | G | A | 21 | a0001c0001t0002g0004 a0001c0001t0002g0058 a0001c0001t0002g0060 others(18): Show |
24 | HG01069.hp2 HG01070.hp1 HG01071.hp2 others(21): Show |
intron_variant | MODIFIER | c.948+2197G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31563933 | |||||||
| chr20:31564016 | A | G | 1 | a0001c0001t0001g0148 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.949-2194A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31564016 | |||||||
| chr20:31564077 | GA | G | 9 | a0001c0001t0001g0094 a0001c0001t0001g0104 a0001c0001t0001g0166 others(6): Show |
10 | HG01069.hp1 HG01346.hp2 HG01496.hp1 others(7): Show |
intron_variant | MODIFIER | c.949-2118delA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr20 | 31564077 | ||||||
| chr20:31564242 | G | A | 1 | a0001c0001t0002g0041 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.949-1968G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31564242 | |||||||
| chr20:31564344 | A | C | 2 | a0001c0001t0002g0045 a0001c0001t0002g0056 |
2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.949-1866A>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31564344 | |||||||
| chr20:31564478 | G | A | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.949-1732G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31564478 | |||||||
| chr20:31564547 | C | T | 1 | a0001c0001t0002g0062 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.949-1663C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31564547 | |||||||
| chr20:31564851 | CA | C | 80 | a0001c0001t0001g0093 a0001c0001t0002g0003 a0001c0001t0002g0004 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.949-1344delA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr20 | 31564851 | ||||||
| chr20:31564862 | A | G | 1 | a0001c0001t0010g0075 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.949-1348A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31564862 | |||||||
| chr20:31565165 | C | CA | 11 | a0001c0001t0001g0125 a0001c0001t0002g0027 a0001c0001t0002g0039 others(8): Show |
11 | HG00741.hp2 HG01167.hp2 HG01256.hp1 others(8): Show |
intron_variant | MODIFIER | c.949-1029dupA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr20 | 31565165 | ||||||
| chr20:31565178 | A | G | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.949-1032A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565178 | |||||||
| chr20:31565197 | G | A | 1 | a0001c0001t0003g0021 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.949-1013G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565197 | |||||||
| chr20:31565264 | A | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.949-946A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565264 | |||||||
| chr20:31565277 | G | A | 1 | a0001c0001t0002g0078 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.949-933G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565277 | |||||||
| chr20:31565337 | G | A | 1 | a0001c0001t0001g0161 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.949-873G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565337 | |||||||
| chr20:31565339 | C | T | 1 | a0001c0001t0004g0026 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.949-871C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565339 | |||||||
| chr20:31565340 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.949-870G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565340 | |||||||
| chr20:31565471 | G | A | 1 | a0001c0001t0001g0098 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.949-739G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565471 | |||||||
| chr20:31565481 | C | CA | 5 | a0001c0001t0001g0117 a0001c0001t0002g0027 a0001c0001t0002g0052 others(2): Show |
5 | HG01175.hp2 HG02723.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.949-710dupA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr20 | 31565481 | ||||||
| chr20:31565481 | C | CAA | 65 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(62): Show |
73 | HG00140.hp1 HG00738.hp1 HG01069.hp2 others(70): Show |
intron_variant | MODIFIER | c.949-711_949-710dup others(2): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr20 | 31565481 | ||||||
| chr20:31565506 | G | T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0056 |
2 | HG03130.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.949-704G>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565506 | |||||||
| chr20:31565754 | G | A | 6 | a0001c0001t0002g0006 a0001c0001t0002g0032 a0001c0001t0002g0038 others(3): Show |
7 | HG00140.hp1 HG01074.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.949-456G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565754 | |||||||
| chr20:31565760 | C | A | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.949-450C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565760 | |||||||
| chr20:31565844 | GCAT | G | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.949-365_949-363del others(3): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565844 | |||||||
| chr20:31565848 | T | A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.949-362T>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31565848 | |||||||
| chr20:31566131 | A | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.949-79A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 10/12 | chr20 | 31566131 | |||||||
| chr20:31566312 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1034+17G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31566312 | |||||||
| chr20:31566434 | G | C | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.1034+139G>C | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31566434 | |||||||
| chr20:31566528 | C | A | 1 | a0001c0001t0003g0018 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1034+233C>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31566528 | |||||||
| chr20:31566678 | CA | C | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1034+384delA | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31566678 | |||||||
| chr20:31566778 | C | T | 1 | a0001c0001t0002g0067 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1034+483C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31566778 | |||||||
| chr20:31566871 | C | T | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1034+576C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31566871 | |||||||
| chr20:31566950 | C | T | 2 | a0001c0001t0001g0120 a0001c0001t0001g0121 |
2 | NA18747.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.1034+655C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31566950 | |||||||
| chr20:31566986 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1034+691G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31566986 | |||||||
| chr20:31567351 | G | A | 1 | a0001c0001t0001g0158 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1035-727G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31567351 | |||||||
| chr20:31567473 | C | G | 2 | a0001c0001t0006g0015 a0001c0001t0006g0085 |
2 | NA18522.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1035-605C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31567473 | |||||||
| chr20:31567478 | C | T | 1 | a0001c0001t0006g0015 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1035-600C>T | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31567478 | |||||||
| chr20:31567507 | A | ATC | 12 | a0001c0001t0001g0002 a0001c0001t0001g0124 a0001c0001t0001g0133 others(9): Show |
15 | HG00408.hp2 HG01433.hp1 HG01934.hp2 others(12): Show |
intron_variant | MODIFIER | c.1035-552_1035-551d others(4): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr20 | 31567507 | ||||||
| chr20:31567517 | C | G | 83 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(80): Show |
91 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(88): Show |
intron_variant | MODIFIER | c.1035-561C>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31567517 | |||||||
| chr20:31567527 | C | CT | 2 | a0001c0001t0001g0113 a0001c0001t0001g0141 |
2 | HG02129.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.1035-551_1035-550i others(3): Show |
HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31567527 | |||||||
| chr20:31567944 | A | G | 2 | a0001c0001t0004g0025 a0001c0001t0004g0026 |
2 | HG02559.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1035-134A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 11/12 | chr20 | 31567944 | |||||||
| chr20:31568339 | G | A | 2 | a0001c0001t0002g0082 a0001c0001t0002g0083 |
2 | HG02976.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1181+115G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 12/12 | chr20 | 31568339 | |||||||
| chr20:31568359 | A | G | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1181+135A>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 12/12 | chr20 | 31568359 | |||||||
| chr20:31568575 | T | G | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.1181+351T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 12/12 | chr20 | 31568575 | |||||||
| chr20:31568687 | G | A | 80 | a0001c0001t0002g0003 a0001c0001t0002g0004 a0001c0001t0002g0005 others(77): Show |
88 | HG00140.hp1 HG00738.hp1 HG00741.hp2 others(85): Show |
intron_variant | MODIFIER | c.1182-433G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 12/12 | chr20 | 31568687 | |||||||
| chr20:31569049 | G | A | 3 | a0001c0001t0003g0022 a0001c0001t0003g0023 a0001c0001t0011g0024 |
3 | HG02145.hp2 HG06807.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1182-71G>A | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 12/12 | chr20 | 31569049 | |||||||
| chr20:31569096 | T | G | 1 | a0001c0001t0001g0110 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1182-24T>G | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 12/12 | chr20 | 31569096 | |||||||
| chr20:31569100 | G | GT | 50 | a0001c0001t0002g0003 a0001c0001t0002g0005 a0001c0001t0002g0006 others(47): Show |
55 | HG00140.hp1 HG00738.hp1 HG01074.hp1 others(52): Show |
splice_region_variant&intron_variant | LOW | c.1182-7dupT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr20 | 31569100 | ||||||
| chr20:31569100 | GT | G | 11 | a0001c0001t0001g0125 a0001c0001t0001g0137 a0001c0001t0003g0017 others(8): Show |
11 | HG00741.hp2 HG01256.hp1 HG01884.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.1182-7delT | HM13 | ENSG00000101294.19 | transcript | ENST00000398174.9 | protein_coding | 12/12 | INFO_REALIGN_3_PRIME | chr20 | 31569100 |