Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 8725 |
| ensemblid | ENSG00000105176.18 |
| hgncid | 13236 |
| symbol | URI1 |
| name | URI1 prefoldin like chaperone |
| refseq_nuc | NM_003796.3 |
| refseq_prot | NP_003787.2 |
| ensembl_nuc | ENST00000392271.6 |
| ensembl_prot | ENSP00000376097.2 |
| mane_status | MANE Select |
| chr | chr19 |
| start | 29942239 |
| end | 30016612 |
| strand | + |
| ver | v1.2 |
| region | chr19:29942239-30016612 |
| region5000 | chr19:29937239-30021612 |
| regionname0 | URI1_chr19_29942239_30016612 |
| regionname5000 | URI1_chr19_29937239_30021612 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 0/1 | 534 | 203 | 41 | 41 | 85 | 10 | 25 | 66 | URI1_chr19_29937239_30021612 | URI1 | MEAPT others(529): Show |
chr19 | 29937239 | 30021612 |
| a0002 | 1/0 | 535 | 109 | 28 | 19 | 52 | 0 | 9 | 39 | URI1_chr19_29937239_30021612 | URI1 | MEAPT others(530): Show |
chr19 | 29937239 | 30021612 |
| a0003 | 0/0 | 535 | 13 | 13 | 0 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | MEAPT others(530): Show |
chr19 | 29937239 | 30021612 |
| a0004 | 0/0 | 534 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | MEAPT others(529): Show |
chr19 | 29937239 | 30021612 |
| a0005 | 0/0 | 534 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | MEAPT others(529): Show |
chr19 | 29937239 | 30021612 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/1 | 1602 | 197 | 41 | 40 | 82 | 10 | 23 | URI1_chr19_29937239_30021612 | URI1 | ATGGA others(1597): Show |
chr19 | 29937239 | 30021612 | ||
| a0001c0004 | 0/0 | 1602 | 3 | 0 | 0 | 3 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | ATGGA others(1597): Show |
chr19 | 29937239 | 30021612 | ||
| a0001c0006 | 0/0 | 1602 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | ATGGA others(1597): Show |
chr19 | 29937239 | 30021612 | ||
| a0001c0007 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | ATGGA others(1597): Show |
chr19 | 29937239 | 30021612 | ||
| a0001c0008 | 0/0 | 1602 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | ATGGA others(1597): Show |
chr19 | 29937239 | 30021612 | ||
| a0002c0002 | 1/0 | 1605 | 108 | 28 | 18 | 52 | 0 | 9 | URI1_chr19_29937239_30021612 | URI1 | ATGGA others(1600): Show |
chr19 | 29937239 | 30021612 | ||
| a0002c0009 | 0/0 | 1605 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | ATGGA others(1600): Show |
chr19 | 29937239 | 30021612 | ||
| a0003c0003 | 0/0 | 1605 | 13 | 13 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | ATGGA others(1600): Show |
chr19 | 29937239 | 30021612 | ||
| a0004c0005 | 0/0 | 1602 | 2 | 2 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | ATGGA others(1597): Show |
chr19 | 29937239 | 30021612 | ||
| a0005c0010 | 0/0 | 1602 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | ATGGA others(1597): Show |
chr19 | 29937239 | 30021612 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/1 | 3457 | 189 | 35 | 39 | 81 | 10 | 23 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0001c0001t0005 | 0/0 | 3457 | 4 | 3 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0001c0001t0011 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0001c0001t0012 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0001c0001t0013 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0001c0001t0015 | 0/0 | 3457 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0001c0004t0001 | 0/0 | 3457 | 3 | 0 | 0 | 3 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0001c0006t0001 | 0/0 | 3457 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0001c0007t0001 | 0/0 | 3457 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0001c0008t0001 | 0/0 | 3457 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0002c0002t0001 | 1/0 | 3460 | 27 | 15 | 6 | 5 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0002c0002t0002 | 0/0 | 3460 | 64 | 0 | 9 | 46 | 0 | 9 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0002c0002t0003 | 0/0 | 3460 | 7 | 6 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0002c0002t0004 | 0/0 | 3460 | 5 | 3 | 2 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0002c0002t0007 | 0/0 | 3460 | 2 | 2 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0002c0002t0008 | 0/0 | 3460 | 2 | 2 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0002c0002t0014 | 0/0 | 3460 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0002c0009t0002 | 0/0 | 3460 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0003c0003t0001 | 0/0 | 3460 | 9 | 9 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0003c0003t0006 | 0/0 | 3460 | 2 | 2 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0003c0003t0009 | 0/0 | 3460 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0003c0003t0010 | 0/0 | 3460 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3455): Show |
chr19 | 29937239 | 30021612 |
| a0004c0005t0001 | 0/0 | 3457 | 2 | 2 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| a0005c0010t0001 | 0/0 | 3457 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | GTGTG others(3452): Show |
chr19 | 29937239 | 30021612 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0107 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0005g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0011g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0012g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0013g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0001t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0004t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0004t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0004t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0006t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0007t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0001c0008t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0027 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0005 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0002g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0003g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0003g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0004g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0004g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0008g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0002t0014g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0002c0009t0002g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0001g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0006g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0006g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0009g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0003c0003t0010g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0004c0005t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0004c0005t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| a0005c0010t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0212 | EUR | GBR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0098 | EUR | GBR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00408 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00408 | hp2 | a0002 | c0002 | t0002 | g0304 | EAS | CHS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | CHS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00609 | hp1 | a0002 | c0002 | t0002 | g0320 | EAS | CHS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00642 | hp1 | a0002 | c0002 | t0001 | g0032 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00735 | hp1 | a0002 | c0002 | t0002 | g0293 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00741 | hp1 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01070 | hp1 | a0002 | c0002 | t0001 | g0035 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01070 | hp2 | a0002 | c0002 | t0002 | g0290 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01071 | hp2 | a0002 | c0002 | t0001 | g0036 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01074 | hp1 | a0002 | c0002 | t0002 | g0300 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01074 | hp2 | a0002 | c0002 | t0001 | g0026 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01081 | hp2 | a0001 | c0001 | t0005 | g0046 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01109 | hp2 | a0002 | c0002 | t0003 | g0018 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01167 | hp2 | a0002 | c0002 | t0004 | g0255 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01169 | hp1 | a0002 | c0002 | t0004 | g0254 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01175 | hp1 | a0001 | c0006 | t0001 | g0221 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01175 | hp2 | a0002 | c0009 | t0002 | g0307 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0122 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01257 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01261 | hp2 | a0002 | c0002 | t0001 | g0030 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01358 | hp1 | a0002 | c0002 | t0002 | g0272 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0219 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01361 | hp1 | a0002 | c0002 | t0001 | g0080 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | CLM | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01516 | hp1 | a0001 | c0001 | t0001 | g0171 | EUR | IBS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0234 | EUR | IBS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0210 | EUR | IBS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0170 | EUR | IBS | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01884 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01891 | hp2 | a0002 | c0002 | t0001 | g0008 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0141 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0211 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01981 | hp1 | a0002 | c0002 | t0002 | g0271 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0229 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02004 | hp2 | a0002 | c0002 | t0002 | g0275 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02015 | hp1 | a0002 | c0002 | t0002 | g0281 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02015 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02027 | hp1 | a0002 | c0002 | t0002 | g0321 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02040 | hp2 | a0002 | c0002 | t0002 | g0295 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02055 | hp1 | a0003 | c0003 | t0010 | g0039 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02055 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02056 | hp2 | a0002 | c0002 | t0002 | g0310 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02071 | hp2 | a0002 | c0002 | t0002 | g0289 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02074 | hp1 | a0002 | c0002 | t0001 | g0137 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02080 | hp1 | a0002 | c0002 | t0002 | g0305 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02083 | hp2 | a0002 | c0002 | t0014 | g0284 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02129 | hp2 | a0002 | c0002 | t0002 | g0302 | EAS | KHV | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02145 | hp1 | a0002 | c0002 | t0003 | g0016 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02145 | hp2 | a0003 | c0003 | t0006 | g0006 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02148 | hp2 | a0002 | c0002 | t0002 | g0298 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02155 | hp1 | a0002 | c0002 | t0002 | g0279 | EAS | CDX | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | CDX | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | CDX | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CDX | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02257 | hp1 | a0002 | c0002 | t0004 | g0021 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02258 | hp2 | a0002 | c0002 | t0001 | g0084 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02293 | hp2 | a0002 | c0002 | t0002 | g0274 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02300 | hp1 | a0002 | c0002 | t0002 | g0273 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | PEL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02451 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02572 | hp1 | a0002 | c0002 | t0001 | g0028 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02572 | hp2 | a0002 | c0002 | t0003 | g0020 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0214 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02615 | hp1 | a0002 | c0002 | t0001 | g0011 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02622 | hp2 | a0001 | c0001 | t0015 | g0007 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02630 | hp1 | a0002 | c0002 | t0004 | g0257 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02630 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02647 | hp1 | a0001 | c0001 | t0012 | g0203 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02647 | hp2 | a0002 | c0002 | t0001 | g0010 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02683 | hp1 | a0002 | c0002 | t0002 | g0311 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02698 | hp2 | a0002 | c0002 | t0002 | g0309 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02886 | hp1 | a0002 | c0002 | t0001 | g0081 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02896 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02897 | hp1 | a0002 | c0002 | t0001 | g0034 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02922 | hp1 | a0002 | c0002 | t0007 | g0253 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02965 | hp2 | a0001 | c0001 | t0011 | g0217 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02970 | hp1 | a0002 | c0002 | t0001 | g0031 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02970 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0247 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0202 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03017 | hp2 | a0002 | c0002 | t0002 | g0283 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03098 | hp2 | a0002 | c0002 | t0001 | g0111 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03130 | hp1 | a0003 | c0003 | t0001 | g0038 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03130 | hp2 | a0002 | c0002 | t0003 | g0023 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03195 | hp1 | a0002 | c0002 | t0007 | g0256 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03195 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03209 | hp1 | a0003 | c0003 | t0001 | g0042 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03209 | hp2 | a0002 | c0002 | t0008 | g0024 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03225 | hp2 | a0003 | c0003 | t0001 | g0001 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03239 | hp1 | a0002 | c0002 | t0002 | g0291 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03239 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0143 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03453 | hp2 | a0002 | c0002 | t0001 | g0116 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0163 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03486 | hp2 | a0002 | c0002 | t0001 | g0009 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03490 | hp1 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0192 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03491 | hp1 | a0002 | c0002 | t0002 | g0318 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03491 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03492 | hp1 | a0002 | c0002 | t0002 | g0319 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03492 | hp2 | a0002 | c0002 | t0002 | g0005 | SAS | PJL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03516 | hp1 | a0002 | c0002 | t0003 | g0019 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03516 | hp2 | a0003 | c0003 | t0001 | g0043 | AFR | ESN | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03540 | hp1 | a0003 | c0003 | t0001 | g0040 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03540 | hp2 | a0002 | c0002 | t0003 | g0015 | AFR | GWD | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03579 | hp1 | a0002 | c0002 | t0001 | g0012 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | BEB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0065 | SAS | BEB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | BEB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | BEB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG04115 | hp1 | a0001 | c0007 | t0001 | g0136 | SAS | STU | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0232 | SAS | STU | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0060 | SAS | BEB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0223 | SAS | STU | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG04199 | hp2 | a0001 | c0008 | t0001 | g0085 | SAS | STU | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0189 | SAS | STU | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG04204 | hp2 | a0002 | c0002 | t0002 | g0294 | SAS | STU | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0194 | SAS | STU | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | STU | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | YRI | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18522 | hp2 | a0003 | c0003 | t0001 | g0041 | AFR | YRI | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18747 | hp1 | a0002 | c0002 | t0002 | g0265 | EAS | CHB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | CHB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18906 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | YRI | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | YRI | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18939 | hp1 | a0002 | c0002 | t0002 | g0270 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18943 | hp2 | a0002 | c0002 | t0002 | g0280 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18946 | hp2 | a0002 | c0002 | t0002 | g0264 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18948 | hp2 | a0002 | c0002 | t0002 | g0267 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18950 | hp2 | a0002 | c0002 | t0002 | g0308 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18959 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18960 | hp1 | a0002 | c0002 | t0002 | g0263 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18962 | hp2 | a0002 | c0002 | t0002 | g0282 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18963 | hp1 | a0002 | c0002 | t0002 | g0317 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18963 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18964 | hp2 | a0002 | c0002 | t0002 | g0288 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18968 | hp1 | a0002 | c0002 | t0002 | g0277 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18968 | hp2 | a0001 | c0001 | t0013 | g0074 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18970 | hp2 | a0002 | c0002 | t0001 | g0139 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18971 | hp1 | a0002 | c0002 | t0002 | g0266 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18971 | hp2 | a0005 | c0010 | t0001 | g0058 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18984 | hp2 | a0002 | c0002 | t0002 | g0278 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18985 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18986 | hp1 | a0002 | c0002 | t0002 | g0303 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18986 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18987 | hp1 | a0002 | c0002 | t0002 | g0313 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18989 | hp2 | a0001 | c0004 | t0001 | g0089 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18991 | hp1 | a0002 | c0002 | t0002 | g0261 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18991 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18992 | hp2 | a0002 | c0002 | t0002 | g0262 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18994 | hp1 | a0002 | c0002 | t0002 | g0299 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18994 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18995 | hp1 | a0002 | c0002 | t0002 | g0296 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18999 | hp1 | a0002 | c0002 | t0002 | g0316 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19003 | hp2 | a0002 | c0002 | t0002 | g0287 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19005 | hp1 | a0002 | c0002 | t0002 | g0285 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19007 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19010 | hp2 | a0002 | c0002 | t0001 | g0138 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19011 | hp1 | a0001 | c0004 | t0001 | g0096 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19011 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19012 | hp2 | a0002 | c0002 | t0002 | g0268 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | LWK | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19030 | hp2 | a0002 | c0002 | t0003 | g0017 | AFR | LWK | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19054 | hp1 | a0002 | c0002 | t0002 | g0259 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19054 | hp2 | a0002 | c0002 | t0001 | g0246 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19057 | hp1 | a0002 | c0002 | t0002 | g0292 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19058 | hp2 | a0002 | c0002 | t0002 | g0269 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19063 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19066 | hp1 | a0002 | c0002 | t0002 | g0306 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19067 | hp2 | a0002 | c0002 | t0002 | g0314 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19070 | hp2 | a0002 | c0002 | t0002 | g0315 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19075 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19077 | hp1 | a0002 | c0002 | t0002 | g0276 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19077 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19078 | hp1 | a0002 | c0002 | t0002 | g0260 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19078 | hp2 | a0001 | c0004 | t0001 | g0091 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19079 | hp2 | a0002 | c0002 | t0002 | g0258 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19082 | hp1 | a0002 | c0002 | t0002 | g0301 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19084 | hp1 | a0002 | c0002 | t0002 | g0312 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19084 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19087 | hp2 | a0002 | c0002 | t0002 | g0286 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19090 | hp1 | a0002 | c0002 | t0001 | g0245 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19090 | hp2 | a0002 | c0002 | t0002 | g0297 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | YRI | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA19240 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | YRI | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA20129 | hp1 | a0003 | c0003 | t0006 | g0322 | AFR | ASW | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA20129 | hp2 | a0004 | c0005 | t0001 | g0014 | AFR | ASW | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0220 | EUR | TSI | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0188 | EUR | TSI | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | GIH | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0215 | SAS | GIH | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02109 | hp1 | a0003 | c0003 | t0009 | g0037 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02109 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02486 | hp1 | a0002 | c0002 | t0001 | g0238 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0142 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| HG03471 | hp2 | a0002 | c0002 | t0004 | g0022 | AFR | MSL | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA18955 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA20300 | hp1 | a0004 | c0005 | t0001 | g0013 | AFR | USA | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA20300 | hp2 | a0003 | c0003 | t0001 | g0044 | AFR | USA | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA21309 | hp1 | a0002 | c0002 | t0001 | g0029 | AFR | LWK | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| NA21309 | hp2 | a0002 | c0002 | t0008 | g0025 | AFR | LWK | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0107 | REF | REF | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| homoSapiens | grch38p0 | a0002 | c0002 | t0001 | g0027 | REF | REF | URI1_chr19_29937239_30021612 | URI1 | chr19 | 29937239 | 30021612 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:29942612 | T | C | 2 | a0003 a0004 |
15 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
missense_variant | MODERATE | c.65T>C | p.Leu22Pro | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/11 | 374/3460 | 65/1608 | 22/535 | chr19 | 29942612 | |||
| chr19:29942629 | C | G | 1 | a0005 | 1 | NA18971.hp2 | missense_variant | MODERATE | c.82C>G | p.Pro28Ala | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/11 | 391/3460 | 82/1608 | 28/535 | chr19 | 29942629 | |||
| chr19:30009211 | GTGA | G | 3 | a0001 a0004 a0005 |
205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
disruptive_inframe_deletion | MODERATE | c.918_920delTGA | p.Asp307del | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/11 | 1227/3460 | 918/1608 | 306/535 | INFO_REALIGN_3_PRIME | chr19 | 30009211 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:29942649 | C | G | 1 | a0002c0009 | 1 | HG01175.hp2 | synonymous_variant | LOW | c.102C>G | p.Arg34Arg | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/11 | 411/3460 | 102/1608 | 34/535 | chr19 | 29942649 | |||
| chr19:30009014 | T | C | 1 | a0001c0004 | 3 | NA18989.hp2 NA19011.hp1 NA19078.hp2 |
synonymous_variant | LOW | c.696T>C | p.Asp232Asp | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/11 | 1005/3460 | 696/1608 | 232/535 | chr19 | 30009014 | |||
| chr19:30009191 | T | C | 1 | a0001c0006 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.873T>C | p.Asn291Asn | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/11 | 1182/3460 | 873/1608 | 291/535 | chr19 | 30009191 | |||
| chr19:30014892 | T | C | 1 | a0001c0007 | 1 | HG04115.hp1 | synonymous_variant | LOW | c.1431T>C | p.Phe477Phe | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 1740/3460 | 1431/1608 | 477/535 | chr19 | 30014892 | |||
| chr19:30014922 | A | G | 1 | a0001c0008 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1461A>G | p.Val487Val | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 1770/3460 | 1461/1608 | 487/535 | chr19 | 30014922 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:29942245 | G | A | 1 | a0003c0003t0009 | 1 | HG02109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-303G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/11 | 303 | chr19 | 29942245 | ||||||
| chr19:29942433 | C | A | 1 | a0002c0002t0003 | 7 | HG01109.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-115C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/11 | 115 | chr19 | 29942433 | ||||||
| chr19:29942477 | C | G | 1 | a0001c0001t0015 | 1 | HG02622.hp2 | 5_prime_UTR_variant | MODIFIER | c.-71C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/11 | 71 | chr19 | 29942477 | ||||||
| chr19:30015209 | C | A | 2 | a0003c0003t0006 a0003c0003t0010 |
3 | HG02055.hp1 HG02145.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*140C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 140 | chr19 | 30015209 | ||||||
| chr19:30015210 | G | A | 1 | a0002c0002t0007 | 2 | HG02922.hp1 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*141G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 141 | chr19 | 30015210 | ||||||
| chr19:30015246 | A | G | 1 | a0002c0002t0014 | 1 | HG02083.hp2 | 3_prime_UTR_variant | MODIFIER | c.*177A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 177 | chr19 | 30015246 | ||||||
| chr19:30015283 | C | T | 1 | a0001c0001t0013 | 1 | NA18968.hp2 | 3_prime_UTR_variant | MODIFIER | c.*214C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 214 | chr19 | 30015283 | ||||||
| chr19:30015399 | T | A | 3 | a0002c0002t0002 a0002c0002t0014 a0002c0009t0002 |
66 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*330T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 330 | chr19 | 30015399 | ||||||
| chr19:30016281 | G | A | 1 | a0001c0001t0011 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1212G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 1212 | chr19 | 30016281 | ||||||
| chr19:30016302 | A | C | 1 | a0002c0002t0008 | 2 | HG03209.hp2 NA21309.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1233A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 1233 | chr19 | 30016302 | ||||||
| chr19:30016314 | A | G | 6 | a0002c0002t0002 a0002c0002t0003 a0002c0002t0004 others(3): Show |
80 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*1245A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 1245 | chr19 | 30016314 | ||||||
| chr19:30016354 | A | T | 1 | a0001c0001t0005 | 4 | HG01081.hp2 HG02109.hp2 NA18906.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1285A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 1285 | chr19 | 30016354 | ||||||
| chr19:30016376 | A | T | 1 | a0003c0003t0010 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 1307 | chr19 | 30016376 | ||||||
| chr19:30016452 | C | T | 1 | a0001c0001t0012 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1383C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 1383 | chr19 | 30016452 | ||||||
| chr19:30016583 | T | A | 1 | a0003c0003t0010 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1514T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 11/11 | 1514 | chr19 | 30016583 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr19:29942676 | C | T | 1 | a0003c0003t0006g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.117+12C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29942676 | |||||||
| chr19:29942711 | C | T | 69 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(66): Show |
69 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.117+47C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29942711 | |||||||
| chr19:29942755 | G | T | 4 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+91G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29942755 | |||||||
| chr19:29942761 | C | T | 211 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(208): Show |
215 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(212): Show |
intron_variant | MODIFIER | c.117+97C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29942761 | |||||||
| chr19:29942860 | C | A | 5 | a0001c0001t0001g0048 a0001c0001t0005g0045 a0001c0001t0005g0046 others(2): Show |
5 | HG01081.hp2 HG02109.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+196C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29942860 | |||||||
| chr19:29942903 | C | A | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.117+239C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29942903 | |||||||
| chr19:29942926 | G | A | 25 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(22): Show |
25 | HG02040.hp1 HG02080.hp2 HG02165.hp2 others(22): Show |
intron_variant | MODIFIER | c.117+262G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29942926 | |||||||
| chr19:29942951 | A | G | 2 | a0002c0002t0002g0320 a0002c0002t0002g0321 |
2 | HG00609.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.117+287A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29942951 | |||||||
| chr19:29943047 | C | T | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+383C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943047 | |||||||
| chr19:29943068 | C | T | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.117+404C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943068 | |||||||
| chr19:29943098 | C | T | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.117+434C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943098 | |||||||
| chr19:29943120 | A | AT | 5 | a0001c0001t0001g0048 a0001c0001t0005g0045 a0001c0001t0005g0046 others(2): Show |
5 | HG01081.hp2 HG02109.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+458dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29943120 | ||||||
| chr19:29943156 | G | C | 217 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(214): Show |
221 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(218): Show |
intron_variant | MODIFIER | c.117+492G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943156 | |||||||
| chr19:29943382 | T | C | 215 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(212): Show |
219 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(216): Show |
intron_variant | MODIFIER | c.117+718T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943382 | |||||||
| chr19:29943500 | T | C | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+836T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943500 | |||||||
| chr19:29943508 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.117+844C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943508 | |||||||
| chr19:29943946 | G | A | 1 | a0001c0001t0001g0050 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.117+1282G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943946 | |||||||
| chr19:29943947 | C | T | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+1283C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943947 | |||||||
| chr19:29943970 | T | C | 1 | a0001c0001t0001g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.117+1306T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943970 | |||||||
| chr19:29943986 | A | G | 1 | a0001c0001t0001g0243 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.117+1322A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29943986 | |||||||
| chr19:29944000 | A | G | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+1336A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944000 | |||||||
| chr19:29944140 | C | CAT | 22 | a0001c0001t0001g0003 a0001c0001t0001g0060 a0001c0001t0001g0158 others(19): Show |
23 | HG00558.hp2 HG00741.hp2 HG01516.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+1528_117+1529d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | C | CATAT | 21 | a0001c0001t0001g0061 a0001c0001t0001g0062 a0001c0001t0001g0063 others(18): Show |
21 | HG00733.hp1 HG01167.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.117+1526_117+1529d others(6): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | C | CATATAT | 20 | a0001c0001t0001g0004 a0001c0001t0001g0065 a0001c0001t0001g0066 others(17): Show |
21 | HG00609.hp2 HG00741.hp1 HG01168.hp1 others(18): Show |
intron_variant | MODIFIER | c.117+1524_117+1529d others(8): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | C | CATATATA others(1): Show |
20 | a0001c0001t0001g0069 a0001c0001t0001g0070 a0001c0001t0001g0204 others(17): Show |
21 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(18): Show |
intron_variant | MODIFIER | c.117+1522_117+1529d others(10): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | C | CATATATA others(3): Show |
20 | a0001c0001t0001g0071 a0001c0001t0001g0072 a0001c0001t0001g0219 others(17): Show |
20 | HG00642.hp1 HG01071.hp1 HG01175.hp1 others(17): Show |
intron_variant | MODIFIER | c.117+1520_117+1529d others(12): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | C | CATATATA others(5): Show |
7 | a0001c0001t0001g0073 a0001c0001t0001g0234 a0001c0001t0001g0235 others(4): Show |
7 | HG01070.hp1 HG01071.hp2 HG01516.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+1518_117+1529d others(14): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | C | CATATATA others(9): Show |
4 | a0001c0001t0001g0239 a0001c0001t0001g0240 a0002c0002t0001g0238 others(1): Show |
4 | HG00140.hp1 HG02486.hp1 HG03942.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+1514_117+1529d others(18): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | C | CATATATA others(11): Show |
3 | a0001c0001t0001g0241 a0001c0001t0001g0242 a0001c0001t0013g0074 |
3 | HG01433.hp2 NA18943.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.117+1512_117+1529d others(20): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | C | CATATATA others(146): Show |
1 | a0003c0003t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.117+1484_117+1485i others(155): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CAT | C | 13 | a0001c0001t0001g0056 a0001c0001t0001g0126 a0001c0001t0001g0127 others(10): Show |
13 | HG00558.hp1 HG01081.hp2 HG01192.hp2 others(10): Show |
intron_variant | MODIFIER | c.117+1528_117+1529d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATAT | C | 11 | a0001c0001t0001g0055 a0001c0001t0001g0117 a0001c0001t0001g0118 others(8): Show |
11 | HG01257.hp1 HG01496.hp2 HG01934.hp1 others(8): Show |
intron_variant | MODIFIER | c.117+1526_117+1529d others(6): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATAT | C | 8 | a0001c0001t0001g0054 a0001c0001t0001g0112 a0001c0001t0001g0113 others(5): Show |
8 | HG01074.hp2 HG01891.hp1 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+1524_117+1529d others(8): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(1): Show |
C | 11 | a0001c0001t0001g0101 a0001c0001t0001g0102 a0001c0001t0001g0103 others(8): Show |
11 | HG00438.hp2 HG01884.hp1 HG02155.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+1522_117+1529d others(10): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(3): Show |
C | 4 | a0001c0001t0001g0002 a0001c0001t0001g0099 a0001c0001t0001g0100 others(1): Show |
5 | HG00733.hp2 HG02055.hp1 NA18950.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+1520_117+1529d others(12): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(5): Show |
C | 8 | a0001c0001t0001g0050 a0001c0001t0001g0092 a0001c0001t0001g0093 others(5): Show |
8 | HG00140.hp2 HG02015.hp2 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+1518_117+1529d others(14): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(7): Show |
C | 6 | a0001c0001t0001g0052 a0001c0001t0001g0053 a0001c0001t0001g0088 others(3): Show |
6 | NA18984.hp1 NA18989.hp2 NA18998.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+1516_117+1529d others(16): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(9): Show |
C | 3 | a0001c0001t0001g0051 a0001c0001t0001g0087 a0001c0001t0001g0248 |
3 | HG02451.hp2 HG02602.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.117+1514_117+1529d others(18): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(11): Show |
C | 2 | a0001c0001t0001g0086 a0001c0001t0001g0247 |
2 | HG02698.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.117+1512_117+1529d others(20): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(13): Show |
C | 1 | a0001c0008t0001g0085 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.117+1510_117+1529d others(22): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(15): Show |
C | 7 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0249 others(4): Show |
7 | HG00642.hp2 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+1508_117+1529d others(24): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(17): Show |
C | 1 | a0001c0001t0001g0243 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.117+1506_117+1529d others(26): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(19): Show |
C | 3 | a0001c0001t0001g0079 a0002c0002t0001g0080 a0002c0002t0001g0081 |
3 | HG00639.hp1 HG01361.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.117+1504_117+1529d others(28): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(23): Show |
C | 8 | a0002c0002t0002g0312 a0002c0002t0002g0313 a0002c0002t0002g0314 others(5): Show |
8 | HG03491.hp1 HG03492.hp1 NA18963.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+1500_117+1529d others(32): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(25): Show |
C | 71 | a0001c0001t0001g0078 a0002c0002t0002g0258 a0002c0002t0002g0259 others(68): Show |
71 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(68): Show |
intron_variant | MODIFIER | c.117+1498_117+1529d others(34): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(27): Show |
C | 1 | a0001c0001t0001g0077 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.117+1496_117+1529d others(36): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(29): Show |
C | 5 | a0001c0001t0001g0076 a0001c0001t0015g0007 a0002c0002t0001g0008 others(2): Show |
5 | HG01255.hp1 HG01891.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+1494_117+1529d others(38): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944140 | CATATATA others(33): Show |
C | 3 | a0003c0003t0009g0037 a0004c0005t0001g0013 a0004c0005t0001g0014 |
3 | HG02109.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.117+1490_117+1529d others(42): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944140 | ||||||
| chr19:29944143 | A | ATATATTA others(155): Show |
1 | a0003c0003t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.117+1484_117+1485i others(164): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944143 | ||||||
| chr19:29944143 | A | ATATATTA others(178): Show |
1 | a0003c0003t0001g0043 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.117+1484_117+1485i others(187): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944143 | ||||||
| chr19:29944143 | A | ATATATTA others(179): Show |
1 | a0003c0003t0001g0001 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.117+1484_117+1485i others(188): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944143 | ||||||
| chr19:29944143 | A | ATATATTA others(179): Show |
1 | a0003c0003t0001g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.117+1484_117+1485i others(188): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944143 | ||||||
| chr19:29944143 | A | ATATATTA others(177): Show |
1 | a0003c0003t0001g0041 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.117+1484_117+1485i others(186): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944143 | ||||||
| chr19:29944143 | A | ATATATTA others(179): Show |
1 | a0003c0003t0001g0001 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.117+1484_117+1485i others(188): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944143 | ||||||
| chr19:29944143 | A | ATATATTA others(177): Show |
1 | a0003c0003t0001g0001 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+1484_117+1485i others(186): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944143 | ||||||
| chr19:29944157 | A | AT | 5 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(2): Show |
7 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+1494dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944157 | ||||||
| chr19:29944169 | A | AT | 5 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(2): Show |
7 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+1506dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29944169 | ||||||
| chr19:29944193 | A | ATATATAT others(8): Show |
1 | a0001c0001t0001g0141 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.117+1529_117+1530i others(17): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944193 | |||||||
| chr19:29944194 | A | T | 1 | a0001c0001t0001g0176 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.117+1530A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944194 | |||||||
| chr19:29944195 | A | G | 2 | a0001c0001t0001g0157 a0001c0001t0001g0177 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.117+1531A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944195 | |||||||
| chr19:29944215 | T | A | 4 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0092 others(1): Show |
4 | HG02015.hp2 NA18955.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+1551T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944215 | |||||||
| chr19:29944309 | C | A | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+1645C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944309 | |||||||
| chr19:29944431 | C | T | 3 | a0003c0003t0009g0037 a0004c0005t0001g0013 a0004c0005t0001g0014 |
3 | HG02109.hp1 NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.117+1767C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944431 | |||||||
| chr19:29944606 | A | G | 1 | a0001c0001t0001g0156 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.117+1942A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944606 | |||||||
| chr19:29944659 | A | T | 1 | a0001c0001t0001g0064 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.117+1995A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944659 | |||||||
| chr19:29944759 | C | T | 67 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0002c0002t0002g0258 others(64): Show |
67 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(64): Show |
intron_variant | MODIFIER | c.117+2095C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944759 | |||||||
| chr19:29944774 | T | G | 2 | a0001c0001t0001g0204 a0001c0001t0001g0219 |
2 | HG01257.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.117+2110T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944774 | |||||||
| chr19:29944817 | C | G | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+2153C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944817 | |||||||
| chr19:29944920 | A | G | 4 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+2256A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29944920 | |||||||
| chr19:29945472 | C | T | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+2808C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29945472 | |||||||
| chr19:29945565 | A | G | 1 | a0002c0002t0002g0311 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.117+2901A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29945565 | |||||||
| chr19:29945860 | G | A | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0220 |
3 | HG01168.hp2 HG01169.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.117+3196G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29945860 | |||||||
| chr19:29945861 | AT | A | 8 | a0001c0001t0001g0178 a0002c0002t0001g0245 a0002c0002t0001g0246 others(5): Show |
8 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+3208delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29945861 | ||||||
| chr19:29945928 | C | T | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+3264C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29945928 | |||||||
| chr19:29945939 | A | G | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 |
3 | HG01361.hp1 HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.117+3275A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29945939 | |||||||
| chr19:29946067 | TC | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.117+3412delC | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29946067 | ||||||
| chr19:29946075 | C | A | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.117+3411C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29946075 | |||||||
| chr19:29946381 | C | T | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+3717C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29946381 | |||||||
| chr19:29946528 | T | C | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+3864T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29946528 | |||||||
| chr19:29946589 | C | G | 1 | a0002c0002t0001g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.117+3925C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29946589 | |||||||
| chr19:29946869 | C | T | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+4205C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29946869 | |||||||
| chr19:29946996 | A | G | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.117+4332A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29946996 | |||||||
| chr19:29947036 | A | G | 1 | a0002c0002t0004g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.117+4372A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29947036 | |||||||
| chr19:29947158 | C | G | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.117+4494C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29947158 | |||||||
| chr19:29947181 | T | C | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+4517T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29947181 | |||||||
| chr19:29947204 | G | A | 3 | a0002c0002t0001g0111 a0002c0002t0001g0116 a0002c0002t0001g0238 |
3 | HG02486.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.117+4540G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29947204 | |||||||
| chr19:29947222 | G | A | 1 | a0002c0002t0004g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.117+4558G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29947222 | |||||||
| chr19:29947228 | A | G | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+4564A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29947228 | |||||||
| chr19:29947718 | G | A | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+5054G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29947718 | |||||||
| chr19:29947883 | A | G | 1 | a0002c0002t0002g0310 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.117+5219A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29947883 | |||||||
| chr19:29948010 | T | C | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+5346T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948010 | |||||||
| chr19:29948012 | C | T | 1 | a0001c0001t0001g0175 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.117+5348C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948012 | |||||||
| chr19:29948016 | C | T | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+5352C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948016 | |||||||
| chr19:29948141 | A | G | 1 | a0001c0001t0012g0203 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.117+5477A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948141 | |||||||
| chr19:29948248 | C | T | 4 | a0001c0001t0001g0059 a0001c0001t0001g0067 a0001c0001t0001g0068 others(1): Show |
4 | NA18968.hp2 NA19067.hp1 NA19075.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+5584C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948248 | |||||||
| chr19:29948317 | G | A | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+5653G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948317 | |||||||
| chr19:29948323 | C | G | 7 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0066 others(4): Show |
7 | HG02040.hp1 NA18953.hp1 NA19002.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+5659C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948323 | |||||||
| chr19:29948406 | T | C | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+5742T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948406 | |||||||
| chr19:29948418 | G | C | 1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.117+5754G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948418 | |||||||
| chr19:29948550 | C | CTTTTTTT | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+5888_117+5894d others(9): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29948550 | ||||||
| chr19:29948694 | G | T | 2 | a0002c0002t0001g0011 a0002c0002t0001g0012 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.117+6030G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948694 | |||||||
| chr19:29948734 | C | G | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+6070C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948734 | |||||||
| chr19:29948833 | T | C | 13 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0003c0003t0001g0001 others(10): Show |
15 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.117+6169T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948833 | |||||||
| chr19:29948867 | C | CG | 6 | a0001c0001t0001g0083 a0001c0001t0001g0094 a0001c0001t0001g0101 others(3): Show |
6 | HG00642.hp2 HG00735.hp2 HG01109.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+6207dupG | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29948867 | ||||||
| chr19:29948916 | C | T | 78 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.117+6252C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948916 | |||||||
| chr19:29948927 | A | AC | 11 | a0001c0001t0001g0206 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG01168.hp2 HG02055.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.117+6269dupC | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29948927 | ||||||
| chr19:29948944 | C | T | 3 | a0003c0003t0001g0038 a0003c0003t0006g0006 a0003c0003t0006g0322 |
3 | HG02145.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.117+6280C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948944 | |||||||
| chr19:29948952 | C | T | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.117+6288C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948952 | |||||||
| chr19:29948980 | C | T | 1 | a0004c0005t0001g0014 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.117+6316C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948980 | |||||||
| chr19:29948990 | GGCTGGCC others(39): Show |
G | 4 | a0001c0001t0001g0190 a0002c0002t0001g0008 a0002c0002t0001g0009 others(1): Show |
4 | HG00733.hp1 HG01891.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+6334_117+6379d others(48): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29948990 | ||||||
| chr19:29948997 | C | T | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+6333C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948997 | |||||||
| chr19:29948998 | A | G | 305 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(302): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.117+6334A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29948998 | |||||||
| chr19:29949030 | C | T | 1 | a0001c0001t0001g0079 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.117+6366C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949030 | |||||||
| chr19:29949079 | T | G | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.117+6415T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949079 | |||||||
| chr19:29949089 | G | A | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.117+6425G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949089 | |||||||
| chr19:29949157 | C | T | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.117+6493C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949157 | |||||||
| chr19:29949210 | G | A | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.117+6546G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949210 | |||||||
| chr19:29949220 | C | G | 1 | a0002c0002t0001g0081 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+6556C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949220 | |||||||
| chr19:29949242 | C | T | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.117+6578C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949242 | |||||||
| chr19:29949252 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.117+6588C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949252 | |||||||
| chr19:29949277 | G | A | 2 | a0002c0002t0001g0111 a0002c0002t0001g0116 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.117+6613G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949277 | |||||||
| chr19:29949294 | C | T | 25 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(22): Show |
25 | HG02040.hp1 HG02080.hp2 HG02165.hp2 others(22): Show |
intron_variant | MODIFIER | c.117+6630C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949294 | |||||||
| chr19:29949310 | C | T | 1 | a0001c0001t0001g0243 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.117+6646C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949310 | |||||||
| chr19:29949315 | C | T | 1 | a0002c0002t0003g0023 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.117+6651C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949315 | |||||||
| chr19:29949329 | T | C | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+6665T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949329 | |||||||
| chr19:29949331 | C | T | 1 | a0002c0002t0002g0309 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.117+6667C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949331 | |||||||
| chr19:29949423 | A | G | 1 | a0002c0002t0002g0308 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.117+6759A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949423 | |||||||
| chr19:29949435 | C | T | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+6771C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949435 | |||||||
| chr19:29949526 | G | A | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.117+6862G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949526 | |||||||
| chr19:29949563 | G | A | 1 | a0002c0002t0002g0310 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.117+6899G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949563 | |||||||
| chr19:29949594 | C | T | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+6930C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949594 | |||||||
| chr19:29949614 | G | A | 1 | a0002c0002t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.117+6950G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949614 | |||||||
| chr19:29949847 | C | T | 1 | a0002c0009t0002g0307 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.117+7183C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949847 | |||||||
| chr19:29949907 | A | G | 2 | a0001c0001t0001g0174 a0001c0001t0001g0242 |
2 | HG01433.hp2 HG01934.hp2 |
intron_variant | MODIFIER | c.117+7243A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29949907 | |||||||
| chr19:29949911 | AGAGGGAG others(21): Show |
A | 1 | a0002c0002t0002g0306 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.117+7253_117+7280d others(30): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29949911 | ||||||
| chr19:29949931 | C | CGGGAGG | 9 | a0001c0001t0001g0048 a0001c0001t0005g0045 a0001c0001t0005g0046 others(6): Show |
9 | HG01081.hp2 HG02055.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+7281_117+7286d others(8): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29949931 | ||||||
| chr19:29949962 | A | AT | 77 | a0002c0002t0002g0259 a0002c0002t0002g0260 a0002c0002t0002g0261 others(74): Show |
77 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(74): Show |
intron_variant | MODIFIER | c.117+7304dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29949962 | ||||||
| chr19:29950002 | G | C | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117+7338G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29950002 | |||||||
| chr19:29950202 | A | AT | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.117+7541dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29950202 | ||||||
| chr19:29950395 | T | G | 3 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0003c0003t0009g0037 |
3 | HG02109.hp1 NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.117+7731T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29950395 | |||||||
| chr19:29950396 | G | A | 1 | a0002c0002t0002g0259 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.117+7732G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29950396 | |||||||
| chr19:29950400 | CA | C | 46 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(43): Show |
47 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.117+7738delA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29950400 | ||||||
| chr19:29950404 | C | T | 46 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(43): Show |
47 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(44): Show |
intron_variant | MODIFIER | c.117+7740C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29950404 | |||||||
| chr19:29950535 | C | T | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.117+7871C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29950535 | |||||||
| chr19:29950596 | A | G | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+7932A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29950596 | |||||||
| chr19:29950624 | A | G | 11 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.117+7960A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29950624 | |||||||
| chr19:29950786 | G | A | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+8122G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29950786 | |||||||
| chr19:29951409 | C | CG | 6 | a0001c0001t0001g0094 a0001c0001t0001g0158 a0001c0001t0001g0159 others(3): Show |
6 | HG01981.hp2 HG02738.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+8745_117+8746i others(3): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951409 | |||||||
| chr19:29951410 | A | C | 8 | a0001c0001t0001g0072 a0001c0001t0001g0094 a0001c0001t0001g0158 others(5): Show |
8 | HG01981.hp2 HG02055.hp1 HG02738.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+8746A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951410 | |||||||
| chr19:29951410 | A | G | 303 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.117+8746A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951410 | |||||||
| chr19:29951456 | A | G | 2 | a0001c0001t0001g0167 a0001c0001t0001g0230 |
2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.117+8792A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951456 | |||||||
| chr19:29951525 | C | A | 26 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(23): Show |
28 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.117+8861C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951525 | |||||||
| chr19:29951601 | C | T | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.117+8937C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951601 | |||||||
| chr19:29951621 | A | G | 4 | a0003c0003t0001g0001 a0003c0003t0001g0041 a0003c0003t0001g0042 others(1): Show |
6 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+8957A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951621 | |||||||
| chr19:29951717 | T | A | 69 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(66): Show |
69 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.117+9053T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951717 | |||||||
| chr19:29951777 | A | G | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.117+9113A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951777 | |||||||
| chr19:29951799 | T | C | 11 | a0001c0001t0015g0007 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.117+9135T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951799 | |||||||
| chr19:29951913 | C | A | 1 | a0002c0009t0002g0307 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.117+9249C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951913 | |||||||
| chr19:29951961 | T | C | 5 | a0002c0002t0004g0254 a0002c0002t0004g0255 a0002c0002t0004g0257 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+9297T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951961 | |||||||
| chr19:29951992 | A | G | 1 | a0001c0001t0001g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.117+9328A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29951992 | |||||||
| chr19:29952050 | T | A | 1 | a0001c0001t0001g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.117+9386T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29952050 | |||||||
| chr19:29952253 | C | T | 9 | a0002c0002t0003g0015 a0002c0002t0003g0016 a0002c0002t0003g0017 others(6): Show |
9 | HG01109.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.117+9589C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29952253 | |||||||
| chr19:29952663 | G | A | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.117+9999G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29952663 | |||||||
| chr19:29952663 | G | C | 1 | a0003c0003t0001g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.117+9999G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29952663 | |||||||
| chr19:29952821 | G | A | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.117+10157G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29952821 | |||||||
| chr19:29952872 | C | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.117+10208C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29952872 | |||||||
| chr19:29952877 | C | T | 5 | a0002c0002t0002g0301 a0002c0002t0002g0302 a0002c0002t0002g0303 others(2): Show |
5 | HG00408.hp2 HG02080.hp1 HG02129.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+10213C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29952877 | |||||||
| chr19:29953051 | T | C | 5 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(2): Show |
7 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+10387T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29953051 | |||||||
| chr19:29953525 | G | A | 78 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.117+10861G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29953525 | |||||||
| chr19:29953541 | A | G | 4 | a0001c0001t0001g0048 a0001c0001t0005g0045 a0001c0001t0005g0046 others(1): Show |
4 | HG01081.hp2 HG02109.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+10877A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29953541 | |||||||
| chr19:29953562 | A | T | 9 | a0002c0002t0002g0259 a0002c0002t0002g0295 a0002c0002t0002g0296 others(6): Show |
9 | HG01074.hp1 HG02040.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+10898A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29953562 | |||||||
| chr19:29953691 | G | GT | 206 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(203): Show |
210 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(207): Show |
intron_variant | MODIFIER | c.117+11039dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29953691 | ||||||
| chr19:29953691 | G | GTT | 7 | a0001c0001t0001g0071 a0001c0001t0001g0124 a0001c0001t0001g0149 others(4): Show |
7 | HG00099.hp2 HG00639.hp2 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+11038_117+1103 others(6): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29953691 | ||||||
| chr19:29953709 | G | A | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+11045G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29953709 | |||||||
| chr19:29953869 | A | T | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.117+11205A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29953869 | |||||||
| chr19:29953922 | G | T | 1 | a0003c0003t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.117+11258G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29953922 | |||||||
| chr19:29954037 | T | C | 1 | a0002c0002t0002g0260 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.117+11373T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29954037 | |||||||
| chr19:29954152 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.117+11488A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29954152 | |||||||
| chr19:29954425 | A | C | 1 | a0002c0002t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.117+11761A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29954425 | |||||||
| chr19:29954488 | T | G | 56 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(53): Show |
56 | HG00408.hp2 HG00609.hp1 HG01070.hp2 others(53): Show |
intron_variant | MODIFIER | c.117+11824T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29954488 | |||||||
| chr19:29954511 | C | CT | 195 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(192): Show |
199 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(196): Show |
intron_variant | MODIFIER | c.117+11867dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29954511 | ||||||
| chr19:29954511 | C | CTT | 10 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0094 others(7): Show |
10 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.117+11866_117+1186 others(6): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29954511 | ||||||
| chr19:29954511 | CT | C | 13 | a0001c0001t0015g0007 a0002c0002t0002g0262 a0002c0002t0002g0263 others(10): Show |
15 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.117+11867delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29954511 | ||||||
| chr19:29954575 | C | T | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+11911C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29954575 | |||||||
| chr19:29954670 | A | T | 1 | a0003c0003t0001g0040 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.117+12006A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29954670 | |||||||
| chr19:29954676 | G | A | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+12012G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29954676 | |||||||
| chr19:29954741 | C | A | 1 | a0002c0002t0001g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.117+12077C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29954741 | |||||||
| chr19:29954765 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.117+12101G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29954765 | |||||||
| chr19:29954929 | T | A | 11 | a0001c0001t0015g0007 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.117+12265T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29954929 | |||||||
| chr19:29955003 | A | AT | 7 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(4): Show |
7 | HG01361.hp1 HG01884.hp2 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+12349dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29955003 | ||||||
| chr19:29955050 | G | C | 1 | a0002c0002t0001g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.117+12386G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955050 | |||||||
| chr19:29955121 | A | AT | 9 | a0001c0001t0001g0068 a0001c0001t0001g0105 a0001c0001t0001g0106 others(6): Show |
9 | HG00438.hp2 HG02083.hp1 HG02683.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+12473dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29955121 | ||||||
| chr19:29955121 | AT | A | 10 | a0001c0001t0001g0048 a0001c0001t0001g0108 a0001c0001t0001g0179 others(7): Show |
10 | HG01070.hp1 HG01081.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+12473delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29955121 | ||||||
| chr19:29955137 | T | A | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+12473T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955137 | |||||||
| chr19:29955155 | G | A | 78 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.117+12491G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955155 | |||||||
| chr19:29955259 | C | T | 2 | a0002c0002t0004g0021 a0002c0002t0004g0022 |
2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.117+12595C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955259 | |||||||
| chr19:29955556 | A | G | 5 | a0001c0001t0015g0007 a0002c0009t0002g0307 a0003c0003t0001g0038 others(2): Show |
5 | HG01175.hp2 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+12892A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955556 | |||||||
| chr19:29955611 | G | T | 1 | a0001c0001t0001g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.117+12947G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955611 | |||||||
| chr19:29955640 | C | T | 1 | a0002c0002t0001g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.117+12976C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955640 | |||||||
| chr19:29955647 | C | T | 1 | a0001c0001t0013g0074 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.117+12983C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955647 | |||||||
| chr19:29955661 | CT | C | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.117+13008delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29955661 | ||||||
| chr19:29955767 | T | C | 1 | a0002c0002t0001g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.117+13103T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955767 | |||||||
| chr19:29955937 | G | C | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.117+13273G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955937 | |||||||
| chr19:29955981 | C | CT | 7 | a0001c0001t0001g0100 a0001c0001t0005g0047 a0002c0002t0001g0138 others(4): Show |
7 | HG01070.hp2 NA18964.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+13330dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29955981 | ||||||
| chr19:29955987 | T | A | 1 | a0002c0002t0002g0265 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.117+13323T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29955987 | |||||||
| chr19:29956088 | G | A | 1 | a0001c0001t0001g0235 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.117+13424G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956088 | |||||||
| chr19:29956176 | G | GGTTT | 11 | a0001c0001t0015g0007 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.117+13512_117+1351 others(8): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956176 | |||||||
| chr19:29956230 | CT | C | 11 | a0001c0001t0015g0007 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.117+13568delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29956230 | ||||||
| chr19:29956285 | C | CT | 65 | a0001c0001t0001g0158 a0001c0001t0001g0204 a0001c0001t0001g0219 others(62): Show |
65 | HG00408.hp2 HG00735.hp1 HG01074.hp1 others(62): Show |
intron_variant | MODIFIER | c.117+13641dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29956285 | ||||||
| chr19:29956285 | CT | C | 30 | a0001c0001t0001g0051 a0001c0001t0001g0060 a0001c0001t0001g0061 others(27): Show |
30 | HG00639.hp1 HG01070.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.117+13641delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29956285 | ||||||
| chr19:29956312 | G | T | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.117+13648G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956312 | |||||||
| chr19:29956321 | A | C | 1 | a0001c0001t0001g0071 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.117+13657A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956321 | |||||||
| chr19:29956373 | T | C | 1 | a0001c0001t0001g0087 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.117+13709T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956373 | |||||||
| chr19:29956413 | G | A | 2 | a0002c0002t0001g0111 a0002c0002t0001g0116 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.117+13749G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956413 | |||||||
| chr19:29956453 | A | G | 78 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.117+13789A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956453 | |||||||
| chr19:29956620 | C | T | 6 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0160 others(3): Show |
6 | HG01975.hp1 HG02004.hp1 HG02129.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+13956C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956620 | |||||||
| chr19:29956621 | G | C | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.117+13957G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956621 | |||||||
| chr19:29956678 | C | T | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+14014C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956678 | |||||||
| chr19:29956682 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.117+14018G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956682 | |||||||
| chr19:29956767 | A | G | 208 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(205): Show |
212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.117+14103A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956767 | |||||||
| chr19:29956778 | G | A | 7 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(4): Show |
7 | HG02074.hp1 HG02109.hp1 NA18970.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+14114G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956778 | |||||||
| chr19:29956781 | C | A | 9 | a0001c0001t0001g0102 a0001c0001t0001g0117 a0001c0001t0001g0129 others(6): Show |
9 | HG02647.hp1 HG02886.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.117+14117C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956781 | |||||||
| chr19:29956794 | C | G | 1 | a0001c0001t0001g0233 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.117+14130C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956794 | |||||||
| chr19:29956807 | G | C | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.117+14143G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956807 | |||||||
| chr19:29956861 | A | G | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.117+14197A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956861 | |||||||
| chr19:29956921 | C | T | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.117+14257C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29956921 | |||||||
| chr19:29957092 | A | G | 3 | a0002c0002t0001g0111 a0002c0002t0001g0116 a0002c0002t0001g0238 |
3 | HG02486.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-14101A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29957092 | |||||||
| chr19:29957110 | C | T | 1 | a0003c0003t0006g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.118-14083C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29957110 | |||||||
| chr19:29957255 | G | C | 1 | a0001c0001t0001g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.118-13938G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29957255 | |||||||
| chr19:29957291 | G | GCCGCTTT others(297): Show |
47 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(44): Show |
48 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.118-13888_118-1388 others(308): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29957291 | ||||||
| chr19:29957383 | G | T | 1 | a0001c0001t0001g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.118-13810G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29957383 | |||||||
| chr19:29957545 | A | G | 1 | a0002c0002t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.118-13648A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29957545 | |||||||
| chr19:29957655 | A | G | 1 | a0002c0002t0002g0310 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.118-13538A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29957655 | |||||||
| chr19:29957693 | T | G | 11 | a0001c0001t0015g0007 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-13500T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29957693 | |||||||
| chr19:29957764 | A | G | 1 | a0001c0001t0001g0131 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.118-13429A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29957764 | |||||||
| chr19:29957873 | G | C | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-13320G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29957873 | |||||||
| chr19:29957891 | A | AG | 4 | a0002c0002t0001g0138 a0002c0002t0001g0139 a0002c0002t0001g0245 others(1): Show |
4 | NA18970.hp2 NA19010.hp2 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-13302_118-1330 others(5): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29957891 | |||||||
| chr19:29957891 | A | AT | 9 | a0001c0001t0001g0131 a0001c0001t0001g0241 a0001c0001t0001g0252 others(6): Show |
9 | HG01070.hp1 HG01071.hp2 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-13285dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29957891 | ||||||
| chr19:29958121 | C | T | 1 | a0001c0001t0001g0189 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.118-13072C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29958121 | |||||||
| chr19:29958161 | T | A | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-13032T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29958161 | |||||||
| chr19:29958205 | G | GT | 11 | a0001c0001t0015g0007 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-12979dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29958205 | ||||||
| chr19:29958222 | T | G | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.118-12971T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29958222 | |||||||
| chr19:29958349 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.118-12844C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29958349 | |||||||
| chr19:29958374 | G | A | 1 | a0001c0001t0001g0192 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.118-12819G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29958374 | |||||||
| chr19:29958454 | G | A | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-12739G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29958454 | |||||||
| chr19:29958535 | T | A | 1 | a0004c0005t0001g0014 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.118-12658T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29958535 | |||||||
| chr19:29958606 | G | A | 1 | a0002c0002t0002g0306 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.118-12587G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29958606 | |||||||
| chr19:29958689 | G | T | 9 | a0001c0001t0001g0102 a0001c0001t0001g0117 a0001c0001t0001g0129 others(6): Show |
9 | HG02647.hp1 HG02886.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-12504G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29958689 | |||||||
| chr19:29958955 | C | CA | 212 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(209): Show |
216 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(213): Show |
intron_variant | MODIFIER | c.118-12228dupA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29958955 | ||||||
| chr19:29959051 | G | A | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-12142G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959051 | |||||||
| chr19:29959077 | G | A | 1 | a0002c0002t0001g0031 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.118-12116G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959077 | |||||||
| chr19:29959099 | C | T | 3 | a0002c0002t0004g0257 a0002c0002t0007g0253 a0002c0002t0007g0256 |
3 | HG02630.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-12094C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959099 | |||||||
| chr19:29959226 | G | A | 11 | a0001c0001t0015g0007 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-11967G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959226 | |||||||
| chr19:29959250 | C | G | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 |
3 | HG01361.hp1 HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.118-11943C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959250 | |||||||
| chr19:29959251 | G | A | 36 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0052 others(33): Show |
36 | HG01167.hp1 HG01257.hp2 HG01358.hp2 others(33): Show |
intron_variant | MODIFIER | c.118-11942G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959251 | |||||||
| chr19:29959415 | C | T | 7 | a0002c0002t0003g0015 a0002c0002t0003g0016 a0002c0002t0003g0017 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-11778C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959415 | |||||||
| chr19:29959544 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0011g0217 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.118-11649A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959544 | |||||||
| chr19:29959583 | T | C | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-11610T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959583 | |||||||
| chr19:29959766 | A | G | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-11427A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959766 | |||||||
| chr19:29959804 | A | AT | 214 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(211): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.118-11382dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29959804 | ||||||
| chr19:29959832 | T | G | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.118-11361T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29959832 | |||||||
| chr19:29959849 | TTCTC | T | 3 | a0002c0002t0001g0111 a0002c0002t0001g0116 a0002c0002t0001g0238 |
3 | HG02486.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-11340_118-1133 others(8): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29959849 | ||||||
| chr19:29960030 | C | T | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-11163C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960030 | |||||||
| chr19:29960142 | T | C | 1 | a0001c0001t0001g0125 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.118-11051T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960142 | |||||||
| chr19:29960370 | T | A | 1 | a0001c0001t0015g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-10823T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960370 | |||||||
| chr19:29960391 | A | G | 202 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(199): Show |
206 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(203): Show |
intron_variant | MODIFIER | c.118-10802A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960391 | |||||||
| chr19:29960410 | CTCTT | C | 11 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0092 others(8): Show |
11 | HG01255.hp2 HG02015.hp2 HG02602.hp2 others(8): Show |
intron_variant | MODIFIER | c.118-10781_118-1077 others(8): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29960410 | ||||||
| chr19:29960481 | A | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.118-10712A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960481 | |||||||
| chr19:29960484 | C | T | 4 | a0002c0002t0002g0312 a0002c0002t0002g0315 a0002c0002t0002g0316 others(1): Show |
4 | NA18963.hp1 NA18999.hp1 NA19070.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-10709C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960484 | |||||||
| chr19:29960528 | C | T | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-10665C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960528 | |||||||
| chr19:29960594 | C | T | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-10599C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960594 | |||||||
| chr19:29960633 | C | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.118-10560C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960633 | |||||||
| chr19:29960728 | A | T | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-10465A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960728 | |||||||
| chr19:29960893 | A | G | 22 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(19): Show |
24 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.118-10300A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960893 | |||||||
| chr19:29960908 | C | T | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.118-10285C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29960908 | |||||||
| chr19:29961080 | C | T | 2 | a0001c0001t0001g0141 a0001c0001t0001g0229 |
2 | HG01975.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.118-10113C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961080 | |||||||
| chr19:29961247 | CT | C | 31 | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0072 others(28): Show |
33 | HG00558.hp1 HG01167.hp1 HG01169.hp1 others(30): Show |
intron_variant | MODIFIER | c.118-9927delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29961247 | ||||||
| chr19:29961477 | A | G | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.118-9716A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961477 | |||||||
| chr19:29961527 | A | G | 1 | a0001c0001t0001g0200 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.118-9666A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961527 | |||||||
| chr19:29961587 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.118-9606G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961587 | |||||||
| chr19:29961674 | TG | T | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-9518delG | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961674 | |||||||
| chr19:29961675 | G | T | 4 | a0002c0002t0002g0268 a0003c0003t0001g0038 a0003c0003t0006g0006 others(1): Show |
4 | HG02145.hp2 HG03130.hp1 NA19012.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-9518G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961675 | |||||||
| chr19:29961675 | GT | G | 285 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(282): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.118-9503delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29961675 | ||||||
| chr19:29961676 | T | G | 7 | a0002c0002t0002g0268 a0002c0002t0002g0293 a0002c0002t0002g0294 others(4): Show |
7 | HG00735.hp1 HG02145.hp2 HG02683.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-9517T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961676 | |||||||
| chr19:29961677 | T | G | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-9516T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961677 | |||||||
| chr19:29961688 | T | G | 5 | a0002c0002t0001g0028 a0002c0002t0001g0031 a0002c0002t0001g0245 others(2): Show |
5 | HG02109.hp1 HG02572.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.118-9505T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961688 | |||||||
| chr19:29961690 | T | G | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-9503T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961690 | |||||||
| chr19:29961691 | G | T | 9 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(6): Show |
11 | HG02055.hp2 HG02145.hp2 HG02970.hp2 others(8): Show |
intron_variant | MODIFIER | c.118-9502G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961691 | |||||||
| chr19:29961810 | C | T | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.118-9383C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961810 | |||||||
| chr19:29961891 | G | A | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-9302G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961891 | |||||||
| chr19:29961905 | G | C | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.118-9288G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29961905 | |||||||
| chr19:29962116 | A | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.118-9077A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29962116 | |||||||
| chr19:29962209 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(1): Show |
4 | HG01168.hp1 HG01516.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-8984A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29962209 | |||||||
| chr19:29962260 | C | T | 1 | a0001c0001t0001g0186 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.118-8933C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29962260 | |||||||
| chr19:29962263 | CT | C | 9 | a0001c0001t0001g0102 a0001c0001t0001g0117 a0001c0001t0001g0129 others(6): Show |
9 | HG02647.hp1 HG02886.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-8919delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29962263 | ||||||
| chr19:29962402 | C | CTT | 7 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(4): Show |
9 | HG02055.hp1 HG02055.hp2 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.118-8773_118-8772d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29962402 | ||||||
| chr19:29962402 | CT | C | 282 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(279): Show |
286 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(283): Show |
intron_variant | MODIFIER | c.118-8772delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29962402 | ||||||
| chr19:29962402 | CTT | C | 6 | a0001c0001t0001g0072 a0001c0001t0001g0133 a0001c0001t0001g0179 others(3): Show |
6 | HG00099.hp1 HG01167.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-8773_118-8772d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29962402 | ||||||
| chr19:29962527 | T | C | 1 | a0003c0003t0006g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.118-8666T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29962527 | |||||||
| chr19:29962591 | T | C | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-8602T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29962591 | |||||||
| chr19:29962598 | CT | C | 6 | a0002c0002t0001g0111 a0002c0002t0001g0116 a0002c0002t0001g0238 others(3): Show |
6 | HG02257.hp1 HG02486.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-8582delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29962598 | ||||||
| chr19:29962746 | A | C | 1 | a0001c0001t0001g0176 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.118-8447A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29962746 | |||||||
| chr19:29962866 | A | G | 1 | a0001c0001t0001g0128 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.118-8327A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29962866 | |||||||
| chr19:29963002 | A | G | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-8191A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963002 | |||||||
| chr19:29963006 | C | T | 1 | a0002c0002t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.118-8187C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963006 | |||||||
| chr19:29963249 | C | T | 1 | a0001c0001t0001g0222 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.118-7944C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963249 | |||||||
| chr19:29963382 | C | A | 1 | a0002c0002t0004g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.118-7811C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963382 | |||||||
| chr19:29963419 | T | C | 1 | a0003c0003t0001g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.118-7774T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963419 | |||||||
| chr19:29963420 | T | A | 1 | a0003c0003t0001g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.118-7773T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963420 | |||||||
| chr19:29963421 | G | A | 1 | a0003c0003t0001g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.118-7772G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963421 | |||||||
| chr19:29963422 | T | A | 1 | a0003c0003t0001g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.118-7771T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963422 | |||||||
| chr19:29963435 | G | T | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.118-7758G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963435 | |||||||
| chr19:29963510 | A | G | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.118-7683A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963510 | |||||||
| chr19:29963573 | G | C | 2 | a0001c0001t0001g0112 a0001c0001t0001g0209 |
2 | HG00438.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.118-7620G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29963573 | |||||||
| chr19:29964086 | G | T | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.118-7107G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964086 | |||||||
| chr19:29964115 | A | G | 3 | a0001c0001t0001g0149 a0001c0001t0001g0200 a0001c0001t0001g0215 |
3 | HG00639.hp2 HG03834.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.118-7078A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964115 | |||||||
| chr19:29964373 | C | T | 30 | a0001c0001t0001g0076 a0001c0001t0001g0078 a0001c0001t0001g0079 others(27): Show |
31 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(28): Show |
intron_variant | MODIFIER | c.118-6820C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964373 | |||||||
| chr19:29964459 | G | GT | 4 | a0003c0003t0001g0001 a0003c0003t0001g0041 a0003c0003t0001g0042 others(1): Show |
6 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-6730dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29964459 | ||||||
| chr19:29964459 | G | T | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-6734G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964459 | |||||||
| chr19:29964464 | G | GT | 82 | a0001c0001t0001g0077 a0001c0001t0001g0112 a0001c0001t0001g0127 others(79): Show |
82 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.118-6712dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29964464 | ||||||
| chr19:29964464 | G | T | 14 | a0001c0001t0001g0075 a0001c0001t0001g0120 a0001c0001t0001g0135 others(11): Show |
16 | HG00099.hp1 HG01109.hp1 HG01261.hp1 others(13): Show |
intron_variant | MODIFIER | c.118-6729G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964464 | |||||||
| chr19:29964469 | T | G | 1 | a0001c0001t0001g0066 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.118-6724T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964469 | |||||||
| chr19:29964485 | A | ACGGAGTT others(18): Show |
1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.118-6706_118-6682d others(27): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29964485 | ||||||
| chr19:29964510 | G | T | 78 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.118-6683G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964510 | |||||||
| chr19:29964521 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.118-6672A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964521 | |||||||
| chr19:29964557 | C | T | 1 | a0001c0001t0001g0165 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.118-6636C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964557 | |||||||
| chr19:29964617 | C | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.118-6576C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964617 | |||||||
| chr19:29964645 | A | G | 1 | a0002c0002t0001g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.118-6548A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964645 | |||||||
| chr19:29964650 | T | G | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.118-6543T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964650 | |||||||
| chr19:29964855 | G | GT | 16 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(13): Show |
18 | HG01884.hp2 HG02055.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.118-6323dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29964855 | ||||||
| chr19:29964855 | GT | G | 11 | a0001c0001t0001g0076 a0001c0001t0001g0121 a0001c0001t0001g0122 others(8): Show |
11 | HG01255.hp1 HG01257.hp1 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.118-6323delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29964855 | ||||||
| chr19:29964856 | T | G | 2 | a0002c0002t0001g0111 a0002c0002t0001g0238 |
2 | HG02486.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.118-6337T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964856 | |||||||
| chr19:29964857 | T | G | 1 | a0002c0002t0001g0116 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-6336T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964857 | |||||||
| chr19:29964934 | C | G | 1 | a0001c0001t0015g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-6259C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964934 | |||||||
| chr19:29964998 | G | C | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 |
3 | HG01361.hp1 HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.118-6195G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29964998 | |||||||
| chr19:29965065 | G | C | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.118-6128G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29965065 | |||||||
| chr19:29965383 | A | C | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.118-5810A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29965383 | |||||||
| chr19:29965446 | C | T | 1 | a0001c0001t0001g0197 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.118-5747C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29965446 | |||||||
| chr19:29965472 | C | T | 1 | a0002c0002t0001g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.118-5721C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29965472 | |||||||
| chr19:29965657 | C | A | 1 | a0001c0001t0001g0233 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.118-5536C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29965657 | |||||||
| chr19:29965945 | A | C | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.118-5248A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29965945 | |||||||
| chr19:29966087 | A | G | 1 | a0002c0002t0002g0005 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.118-5106A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966087 | |||||||
| chr19:29966137 | G | T | 1 | a0001c0001t0001g0194 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.118-5056G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966137 | |||||||
| chr19:29966329 | G | A | 2 | a0001c0001t0001g0162 a0001c0001t0001g0207 |
2 | HG00735.hp2 HG01928.hp1 |
intron_variant | MODIFIER | c.118-4864G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966329 | |||||||
| chr19:29966335 | C | T | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.118-4858C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966335 | |||||||
| chr19:29966341 | G | C | 1 | a0001c0001t0001g0053 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.118-4852G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966341 | |||||||
| chr19:29966404 | A | G | 3 | a0001c0001t0001g0095 a0001c0001t0001g0126 a0001c0001t0001g0127 |
3 | NA18955.hp2 NA18959.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.118-4789A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966404 | |||||||
| chr19:29966415 | C | T | 3 | a0003c0003t0001g0038 a0003c0003t0006g0006 a0003c0003t0006g0322 |
3 | HG02145.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.118-4778C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966415 | |||||||
| chr19:29966523 | A | C | 1 | a0003c0003t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.118-4670A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966523 | |||||||
| chr19:29966787 | A | G | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.118-4406A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966787 | |||||||
| chr19:29966839 | C | T | 1 | a0001c0001t0001g0146 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.118-4354C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966839 | |||||||
| chr19:29966872 | A | G | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.118-4321A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29966872 | |||||||
| chr19:29967081 | G | A | 13 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0003c0003t0001g0001 others(10): Show |
15 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.118-4112G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29967081 | |||||||
| chr19:29967456 | A | G | 64 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(61): Show |
64 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.118-3737A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29967456 | |||||||
| chr19:29967578 | T | C | 78 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.118-3615T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29967578 | |||||||
| chr19:29967622 | C | T | 1 | a0003c0003t0001g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.118-3571C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29967622 | |||||||
| chr19:29967888 | C | T | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-3305C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29967888 | |||||||
| chr19:29967892 | C | T | 1 | a0001c0001t0001g0114 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.118-3301C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29967892 | |||||||
| chr19:29967946 | C | G | 4 | a0001c0001t0015g0007 a0003c0003t0001g0038 a0003c0003t0006g0006 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-3247C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29967946 | |||||||
| chr19:29968122 | A | T | 1 | a0001c0001t0001g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.118-3071A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968122 | |||||||
| chr19:29968124 | A | G | 4 | a0001c0001t0015g0007 a0003c0003t0001g0038 a0003c0003t0006g0006 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-3069A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968124 | |||||||
| chr19:29968289 | A | G | 11 | a0001c0001t0015g0007 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-2904A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968289 | |||||||
| chr19:29968458 | C | G | 2 | a0001c0001t0001g0228 a0001c0001t0001g0237 |
2 | NA18960.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.118-2735C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968458 | |||||||
| chr19:29968462 | C | T | 1 | a0001c0001t0001g0199 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.118-2731C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968462 | |||||||
| chr19:29968565 | CT | C | 30 | a0001c0001t0001g0068 a0001c0001t0001g0100 a0001c0001t0001g0101 others(27): Show |
30 | HG01070.hp1 HG01109.hp2 HG01168.hp1 others(27): Show |
intron_variant | MODIFIER | c.118-2604delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29968565 | ||||||
| chr19:29968565 | CTT | C | 194 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(191): Show |
200 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(197): Show |
intron_variant | MODIFIER | c.118-2605_118-2604d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29968565 | ||||||
| chr19:29968565 | CTTT | C | 16 | a0001c0001t0001g0077 a0001c0001t0001g0141 a0001c0001t0001g0145 others(13): Show |
16 | HG01975.hp1 HG02004.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.118-2606_118-2604d others(5): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29968565 | ||||||
| chr19:29968569 | T | C | 2 | a0002c0002t0007g0253 a0002c0002t0007g0256 |
2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.118-2624T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968569 | |||||||
| chr19:29968571 | T | C | 2 | a0001c0001t0001g0201 a0001c0001t0011g0217 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.118-2622T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968571 | |||||||
| chr19:29968572 | T | C | 4 | a0001c0001t0015g0007 a0003c0003t0001g0038 a0003c0003t0006g0006 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-2621T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968572 | |||||||
| chr19:29968573 | T | C | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-2620T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968573 | |||||||
| chr19:29968574 | T | C | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-2619T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968574 | |||||||
| chr19:29968576 | T | C | 1 | a0002c0002t0001g0116 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.118-2617T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968576 | |||||||
| chr19:29968707 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.118-2486G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968707 | |||||||
| chr19:29968806 | C | T | 3 | a0002c0002t0001g0111 a0002c0002t0001g0116 a0002c0002t0001g0238 |
3 | HG02486.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.118-2387C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968806 | |||||||
| chr19:29968985 | T | A | 1 | a0002c0002t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.118-2208T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29968985 | |||||||
| chr19:29969028 | C | T | 1 | a0001c0001t0001g0072 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.118-2165C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969028 | |||||||
| chr19:29969151 | A | G | 1 | a0001c0001t0015g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-2042A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969151 | |||||||
| chr19:29969220 | T | C | 1 | a0001c0001t0001g0148 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.118-1973T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969220 | |||||||
| chr19:29969251 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.118-1942A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969251 | |||||||
| chr19:29969277 | A | T | 1 | a0001c0001t0001g0088 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.118-1916A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969277 | |||||||
| chr19:29969281 | A | G | 1 | a0002c0002t0002g0308 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.118-1912A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969281 | |||||||
| chr19:29969300 | T | C | 1 | a0001c0001t0015g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-1893T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969300 | |||||||
| chr19:29969382 | A | C | 1 | a0001c0001t0001g0179 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.118-1811A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969382 | |||||||
| chr19:29969473 | C | T | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.118-1720C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969473 | |||||||
| chr19:29969511 | G | C | 3 | a0002c0002t0002g0293 a0002c0002t0002g0294 a0002c0002t0002g0311 |
3 | HG00735.hp1 HG02683.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.118-1682G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969511 | |||||||
| chr19:29969659 | A | G | 1 | a0001c0001t0001g0160 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.118-1534A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969659 | |||||||
| chr19:29969982 | G | T | 1 | a0001c0001t0001g0212 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.118-1211G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29969982 | |||||||
| chr19:29970128 | A | AT | 48 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0065 others(45): Show |
48 | HG00639.hp2 HG00735.hp2 HG00741.hp1 others(45): Show |
intron_variant | MODIFIER | c.118-1037dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29970128 | ||||||
| chr19:29970128 | ATTTTTTT others(3): Show |
A | 4 | a0002c0002t0002g0289 a0002c0002t0003g0017 a0002c0002t0003g0018 others(1): Show |
4 | HG01109.hp2 HG02071.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-1046_118-1037d others(12): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29970128 | ||||||
| chr19:29970128 | ATTTTTTT others(4): Show |
A | 78 | a0001c0001t0001g0099 a0001c0001t0001g0112 a0001c0001t0001g0243 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00733.hp2 others(75): Show |
intron_variant | MODIFIER | c.118-1047_118-1037d others(13): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29970128 | ||||||
| chr19:29970128 | ATTTTTTT others(5): Show |
A | 22 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(19): Show |
24 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(21): Show |
intron_variant | MODIFIER | c.118-1048_118-1037d others(14): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29970128 | ||||||
| chr19:29970128 | ATTTTTTT others(6): Show |
A | 1 | a0002c0002t0001g0010 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.118-1049_118-1037d others(15): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29970128 | ||||||
| chr19:29970128 | ATTTTTTT others(7): Show |
A | 2 | a0002c0002t0001g0008 a0002c0002t0001g0009 |
2 | HG01891.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.118-1050_118-1037d others(16): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29970128 | ||||||
| chr19:29970128 | ATTTTTTT others(8): Show |
A | 1 | a0001c0001t0001g0105 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.118-1051_118-1037d others(17): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr19 | 29970128 | ||||||
| chr19:29970186 | T | C | 4 | a0001c0001t0001g0249 a0001c0001t0001g0250 a0001c0001t0001g0251 others(1): Show |
4 | HG01884.hp2 HG02280.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-1007T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29970186 | |||||||
| chr19:29970202 | T | C | 6 | a0002c0002t0002g0271 a0002c0002t0002g0272 a0002c0002t0002g0273 others(3): Show |
6 | HG01070.hp2 HG01358.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.118-991T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29970202 | |||||||
| chr19:29970752 | A | G | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.118-441A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29970752 | |||||||
| chr19:29970755 | T | C | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-438T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29970755 | |||||||
| chr19:29970783 | A | C | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.118-410A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29970783 | |||||||
| chr19:29970865 | T | C | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.118-328T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29970865 | |||||||
| chr19:29970881 | T | C | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.118-312T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29970881 | |||||||
| chr19:29971085 | A | G | 2 | a0002c0002t0002g0287 a0002c0002t0002g0288 |
2 | NA18964.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.118-108A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29971085 | |||||||
| chr19:29971118 | T | A | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.118-75T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 1/10 | chr19 | 29971118 | |||||||
| chr19:29971432 | G | A | 4 | a0002c0002t0001g0012 a0002c0002t0001g0245 a0002c0002t0001g0246 others(1): Show |
4 | HG02109.hp1 HG03579.hp1 NA19054.hp2 others(1): Show |
intron_variant | MODIFIER | c.152+205G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29971432 | |||||||
| chr19:29971463 | C | CCTT | 11 | a0001c0001t0015g0007 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.152+237_152+239dup others(3): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29971463 | ||||||
| chr19:29971689 | C | CT | 6 | a0001c0001t0001g0232 a0001c0001t0005g0047 a0002c0002t0001g0245 others(3): Show |
6 | HG02055.hp1 HG04115.hp2 NA18971.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+475dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29971689 | ||||||
| chr19:29971703 | A | T | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152+476A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29971703 | |||||||
| chr19:29972370 | T | G | 1 | a0002c0002t0001g0008 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.152+1143T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29972370 | |||||||
| chr19:29972480 | C | T | 2 | a0001c0001t0001g0181 a0001c0001t0001g0197 |
2 | NA19057.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.152+1253C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29972480 | |||||||
| chr19:29972712 | G | A | 3 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0003c0003t0009g0037 |
3 | HG02109.hp1 NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.152+1485G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29972712 | |||||||
| chr19:29972824 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.152+1597A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29972824 | |||||||
| chr19:29973031 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.152+1804A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29973031 | |||||||
| chr19:29973286 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0234 |
2 | HG01168.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.152+2059C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29973286 | |||||||
| chr19:29973307 | G | A | 1 | a0001c0007t0001g0136 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.152+2080G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29973307 | |||||||
| chr19:29973337 | G | A | 1 | a0001c0001t0001g0127 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.152+2110G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29973337 | |||||||
| chr19:29973371 | C | G | 5 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0003c0003t0001g0038 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+2144C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29973371 | |||||||
| chr19:29973466 | G | T | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.152+2239G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29973466 | |||||||
| chr19:29973616 | T | C | 1 | a0002c0002t0002g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.152+2389T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29973616 | |||||||
| chr19:29973863 | T | C | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 |
3 | HG01361.hp1 HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.152+2636T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29973863 | |||||||
| chr19:29974223 | G | A | 9 | a0001c0001t0001g0050 a0001c0001t0001g0054 a0001c0001t0001g0063 others(6): Show |
9 | HG02040.hp1 HG03834.hp2 NA18953.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+2996G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974223 | |||||||
| chr19:29974240 | GCACTCAA others(5): Show |
G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3014_152+3025d others(14): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974240 | |||||||
| chr19:29974253 | A | T | 2 | a0002c0002t0003g0015 a0002c0002t0003g0020 |
2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.152+3026A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974253 | |||||||
| chr19:29974262 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3035A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974262 | |||||||
| chr19:29974271 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3044A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974271 | |||||||
| chr19:29974281 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3054A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974281 | |||||||
| chr19:29974285 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3058T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974285 | |||||||
| chr19:29974288 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3061T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974288 | |||||||
| chr19:29974289 | A | C | 24 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0087 others(21): Show |
26 | HG00438.hp1 HG00558.hp1 HG00609.hp2 others(23): Show |
intron_variant | MODIFIER | c.152+3062A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974289 | |||||||
| chr19:29974291 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3064T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974291 | |||||||
| chr19:29974292 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3065T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974292 | |||||||
| chr19:29974293 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3066G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974293 | |||||||
| chr19:29974295 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3068C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974295 | |||||||
| chr19:29974296 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3069A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974296 | |||||||
| chr19:29974297 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3070G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974297 | |||||||
| chr19:29974325 | G | A | 1 | a0001c0001t0001g0218 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.152+3098G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974325 | |||||||
| chr19:29974335 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3108G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974335 | |||||||
| chr19:29974337 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3110G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974337 | |||||||
| chr19:29974347 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3120T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974347 | |||||||
| chr19:29974354 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3127T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974354 | |||||||
| chr19:29974359 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3132T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974359 | |||||||
| chr19:29974383 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3156T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974383 | |||||||
| chr19:29974386 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3159G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974386 | |||||||
| chr19:29974402 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3175T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974402 | |||||||
| chr19:29974403 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3176G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974403 | |||||||
| chr19:29974406 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3179A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974406 | |||||||
| chr19:29974448 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3221G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974448 | |||||||
| chr19:29974463 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3236G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974463 | |||||||
| chr19:29974475 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3248G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974475 | |||||||
| chr19:29974492 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3265G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974492 | |||||||
| chr19:29974499 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3272T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974499 | |||||||
| chr19:29974502 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3275G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974502 | |||||||
| chr19:29974504 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3277C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974504 | |||||||
| chr19:29974505 | G | C | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3278G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974505 | |||||||
| chr19:29974506 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3279G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974506 | |||||||
| chr19:29974512 | A | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3285A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974512 | |||||||
| chr19:29974514 | A | G | 1 | a0002c0002t0002g0270 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.152+3287A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974514 | |||||||
| chr19:29974522 | A | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3295A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974522 | |||||||
| chr19:29974524 | T | C | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3297T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974524 | |||||||
| chr19:29974527 | T | G | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3300T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974527 | |||||||
| chr19:29974528 | G | A | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3301G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974528 | |||||||
| chr19:29974554 | C | A | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3327C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974554 | |||||||
| chr19:29974582 | C | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3355C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974582 | |||||||
| chr19:29974584 | A | C | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.152+3357A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974584 | |||||||
| chr19:29974636 | T | C | 12 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0003c0003t0001g0001 others(9): Show |
14 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.152+3409T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974636 | |||||||
| chr19:29974748 | G | A | 4 | a0002c0002t0001g0029 a0003c0003t0001g0038 a0003c0003t0006g0006 others(1): Show |
4 | HG02145.hp2 HG03130.hp1 NA20129.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+3521G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974748 | |||||||
| chr19:29974928 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.152+3701G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974928 | |||||||
| chr19:29974998 | T | C | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152+3771T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29974998 | |||||||
| chr19:29975108 | T | C | 78 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.152+3881T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975108 | |||||||
| chr19:29975143 | C | G | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.152+3916C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975143 | |||||||
| chr19:29975233 | G | A | 69 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(66): Show |
69 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.152+4006G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975233 | |||||||
| chr19:29975288 | A | T | 1 | a0001c0001t0001g0162 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.152+4061A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975288 | |||||||
| chr19:29975356 | CTATA | C | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 |
3 | HG01361.hp1 HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.152+4133_152+4136d others(6): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29975356 | ||||||
| chr19:29975396 | A | C | 216 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(213): Show |
220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.152+4169A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975396 | |||||||
| chr19:29975469 | A | C | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.152+4242A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975469 | |||||||
| chr19:29975500 | CT | C | 293 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(290): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.152+4294delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29975500 | ||||||
| chr19:29975500 | CTT | C | 8 | a0001c0001t0001g0063 a0001c0001t0001g0073 a0001c0001t0001g0077 others(5): Show |
8 | HG01070.hp1 HG01167.hp2 HG02040.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+4293_152+4294d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29975500 | ||||||
| chr19:29975648 | C | T | 1 | a0001c0001t0001g0127 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.152+4421C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975648 | |||||||
| chr19:29975651 | G | A | 4 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG01081.hp2 HG02109.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+4424G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975651 | |||||||
| chr19:29975658 | C | T | 1 | a0001c0001t0001g0143 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.152+4431C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975658 | |||||||
| chr19:29975718 | C | A | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.152+4491C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975718 | |||||||
| chr19:29975806 | C | T | 1 | a0002c0002t0002g0288 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.152+4579C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975806 | |||||||
| chr19:29975977 | A | G | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.152+4750A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975977 | |||||||
| chr19:29975986 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.152+4759G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29975986 | |||||||
| chr19:29976009 | C | T | 3 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 |
3 | HG01361.hp1 HG02258.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.152+4782C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29976009 | |||||||
| chr19:29976079 | T | C | 1 | a0003c0003t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.152+4852T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29976079 | |||||||
| chr19:29976107 | A | AT | 18 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0002c0002t0001g0137 others(15): Show |
20 | HG02055.hp1 HG02055.hp2 HG02074.hp1 others(17): Show |
intron_variant | MODIFIER | c.152+4889dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29976107 | ||||||
| chr19:29976136 | G | C | 12 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0003c0003t0001g0001 others(9): Show |
14 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.152+4909G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29976136 | |||||||
| chr19:29976366 | G | T | 8 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(5): Show |
8 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.152+5139G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29976366 | |||||||
| chr19:29976470 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.152+5243T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29976470 | |||||||
| chr19:29976484 | A | T | 4 | a0002c0002t0002g0262 a0002c0002t0002g0285 a0002c0002t0002g0286 others(1): Show |
4 | HG02083.hp2 NA18992.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+5257A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29976484 | |||||||
| chr19:29976727 | T | C | 1 | a0002c0002t0002g0268 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.152+5500T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29976727 | |||||||
| chr19:29977495 | A | G | 1 | a0001c0001t0001g0159 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.152+6268A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29977495 | |||||||
| chr19:29977551 | A | C | 1 | a0001c0001t0001g0057 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.152+6324A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29977551 | |||||||
| chr19:29977558 | C | CT | 6 | a0001c0001t0001g0112 a0001c0001t0001g0182 a0001c0007t0001g0136 others(3): Show |
6 | HG01192.hp1 HG01361.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.152+6348dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29977558 | ||||||
| chr19:29977558 | CT | C | 74 | a0001c0001t0001g0140 a0001c0001t0001g0168 a0001c0001t0015g0007 others(71): Show |
74 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(71): Show |
intron_variant | MODIFIER | c.152+6348delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29977558 | ||||||
| chr19:29977562 | T | C | 2 | a0001c0001t0001g0178 a0001c0001t0001g0184 |
2 | NA18939.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.152+6335T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29977562 | |||||||
| chr19:29977575 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0005g0045 a0001c0001t0005g0046 others(2): Show |
5 | HG01081.hp2 HG02109.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+6348T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29977575 | |||||||
| chr19:29977585 | T | TGAGTG | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.152+6361_152+6362i others(7): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29977585 | ||||||
| chr19:29977683 | G | C | 1 | a0001c0001t0001g0129 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.152+6456G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29977683 | |||||||
| chr19:29977706 | C | T | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+6479C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29977706 | |||||||
| chr19:29977781 | G | A | 9 | a0001c0001t0001g0082 a0001c0001t0001g0088 a0001c0001t0001g0092 others(6): Show |
9 | HG01255.hp2 HG02015.hp2 NA18955.hp1 others(6): Show |
intron_variant | MODIFIER | c.152+6554G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29977781 | |||||||
| chr19:29977942 | GAT | G | 3 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 |
3 | HG02074.hp1 NA18970.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.152+6717_152+6718d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29977942 | ||||||
| chr19:29978019 | T | C | 5 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0003c0003t0001g0038 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+6792T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29978019 | |||||||
| chr19:29978068 | C | T | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.152+6841C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29978068 | |||||||
| chr19:29978069 | A | T | 9 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0002c0002t0001g0245 others(6): Show |
9 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.152+6842A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29978069 | |||||||
| chr19:29978080 | C | T | 5 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0003c0003t0001g0038 others(2): Show |
5 | HG02145.hp2 HG02622.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.152+6853C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29978080 | |||||||
| chr19:29978100 | A | G | 1 | a0001c0001t0001g0065 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.152+6873A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29978100 | |||||||
| chr19:29978174 | C | G | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.152+6947C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29978174 | |||||||
| chr19:29978497 | A | AT | 18 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0178 others(15): Show |
18 | HG00558.hp2 HG01891.hp2 HG02165.hp1 others(15): Show |
intron_variant | MODIFIER | c.153-6717dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29978497 | ||||||
| chr19:29979096 | A | C | 199 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(196): Show |
203 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(200): Show |
intron_variant | MODIFIER | c.153-6127A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29979096 | |||||||
| chr19:29979348 | G | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.153-5875G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29979348 | |||||||
| chr19:29979424 | T | C | 2 | a0001c0001t0001g0228 a0001c0001t0001g0237 |
2 | NA18960.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.153-5799T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29979424 | |||||||
| chr19:29979504 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-5719A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29979504 | |||||||
| chr19:29979665 | C | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.153-5558C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29979665 | |||||||
| chr19:29979864 | A | T | 1 | a0003c0003t0006g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.153-5359A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29979864 | |||||||
| chr19:29980175 | A | G | 1 | a0002c0002t0002g0276 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.153-5048A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980175 | |||||||
| chr19:29980378 | A | G | 1 | a0002c0002t0002g0283 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.153-4845A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980378 | |||||||
| chr19:29980501 | T | G | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.153-4722T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980501 | |||||||
| chr19:29980529 | C | A | 6 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0003c0003t0001g0038 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-4694C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980529 | |||||||
| chr19:29980572 | T | A | 1 | a0002c0002t0002g0303 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.153-4651T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980572 | |||||||
| chr19:29980601 | AT | A | 6 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0003c0003t0001g0038 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-4614delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29980601 | ||||||
| chr19:29980612 | T | TA | 17 | a0001c0001t0001g0077 a0001c0001t0001g0247 a0001c0001t0001g0248 others(14): Show |
18 | HG01081.hp2 HG01891.hp2 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.153-4584dupA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29980612 | ||||||
| chr19:29980612 | T | TAA | 150 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(147): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.153-4585_153-4584d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29980612 | ||||||
| chr19:29980612 | T | TAAA | 55 | a0001c0001t0001g0048 a0001c0001t0001g0052 a0001c0001t0001g0059 others(52): Show |
55 | HG00735.hp2 HG01109.hp1 HG01255.hp1 others(52): Show |
intron_variant | MODIFIER | c.153-4586_153-4584d others(5): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29980612 | ||||||
| chr19:29980612 | TA | T | 60 | a0002c0002t0001g0034 a0002c0002t0001g0035 a0002c0002t0002g0258 others(57): Show |
60 | HG00735.hp1 HG01070.hp1 HG01074.hp1 others(57): Show |
intron_variant | MODIFIER | c.153-4584delA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29980612 | ||||||
| chr19:29980612 | TAA | T | 11 | a0002c0002t0001g0029 a0002c0002t0002g0264 a0002c0002t0002g0283 others(8): Show |
11 | HG01070.hp2 HG01109.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.153-4585_153-4584d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29980612 | ||||||
| chr19:29980626 | A | C | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.153-4597A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980626 | |||||||
| chr19:29980659 | T | G | 1 | a0001c0001t0001g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.153-4564T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980659 | |||||||
| chr19:29980751 | G | A | 222 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(219): Show |
228 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(225): Show |
intron_variant | MODIFIER | c.153-4472G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980751 | |||||||
| chr19:29980778 | C | T | 4 | a0001c0001t0001g0075 a0001c0001t0001g0120 a0001c0001t0001g0135 others(1): Show |
4 | HG01109.hp1 HG01928.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-4445C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980778 | |||||||
| chr19:29980790 | C | T | 1 | a0001c0001t0001g0244 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.153-4433C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980790 | |||||||
| chr19:29980806 | C | T | 1 | a0001c0001t0001g0179 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.153-4417C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980806 | |||||||
| chr19:29980884 | G | A | 6 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0003c0003t0001g0038 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-4339G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29980884 | |||||||
| chr19:29980922 | CA | C | 279 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(276): Show |
285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.153-4279delA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29980922 | ||||||
| chr19:29981094 | CT | C | 10 | a0001c0001t0001g0075 a0001c0001t0001g0120 a0001c0001t0001g0135 others(7): Show |
10 | HG00099.hp1 HG00099.hp2 HG01109.hp1 others(7): Show |
intron_variant | MODIFIER | c.153-4118delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29981094 | ||||||
| chr19:29981225 | T | C | 4 | a0002c0002t0001g0028 a0002c0002t0001g0031 a0002c0002t0008g0024 others(1): Show |
4 | HG02572.hp1 HG02970.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-3998T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29981225 | |||||||
| chr19:29981308 | T | C | 1 | a0001c0001t0001g0078 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.153-3915T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29981308 | |||||||
| chr19:29981386 | A | G | 9 | a0001c0001t0001g0102 a0001c0001t0001g0117 a0001c0001t0001g0129 others(6): Show |
9 | HG02647.hp1 HG02886.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.153-3837A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29981386 | |||||||
| chr19:29981386 | A | T | 1 | a0001c0001t0001g0065 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.153-3837A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29981386 | |||||||
| chr19:29981915 | C | G | 3 | a0001c0001t0001g0191 a0001c0001t0001g0194 a0001c0001t0001g0234 |
3 | HG01168.hp1 HG01516.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.153-3308C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29981915 | |||||||
| chr19:29982049 | A | G | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.153-3174A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29982049 | |||||||
| chr19:29982265 | C | T | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.153-2958C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29982265 | |||||||
| chr19:29982287 | T | G | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.153-2936T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29982287 | |||||||
| chr19:29982392 | GT | G | 78 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.153-2825delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29982392 | ||||||
| chr19:29982467 | A | G | 13 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0178 others(10): Show |
13 | HG00558.hp2 HG02165.hp1 NA18939.hp2 others(10): Show |
intron_variant | MODIFIER | c.153-2756A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29982467 | |||||||
| chr19:29982602 | G | C | 3 | a0003c0003t0001g0038 a0003c0003t0006g0006 a0003c0003t0006g0322 |
3 | HG02145.hp2 HG03130.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.153-2621G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29982602 | |||||||
| chr19:29982679 | C | T | 1 | a0001c0001t0001g0226 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.153-2544C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29982679 | |||||||
| chr19:29982687 | T | C | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0220 |
3 | HG01168.hp2 HG01169.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.153-2536T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29982687 | |||||||
| chr19:29982968 | A | G | 1 | a0003c0003t0001g0044 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.153-2255A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29982968 | |||||||
| chr19:29983004 | A | G | 1 | a0001c0001t0001g0220 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.153-2219A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29983004 | |||||||
| chr19:29983617 | C | A | 201 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(198): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.153-1606C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29983617 | |||||||
| chr19:29984129 | T | C | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153-1094T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984129 | |||||||
| chr19:29984205 | C | T | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.153-1018C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984205 | |||||||
| chr19:29984206 | G | A | 2 | a0002c0002t0001g0080 a0002c0002t0001g0081 |
2 | HG01361.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.153-1017G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984206 | |||||||
| chr19:29984237 | C | G | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.153-986C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984237 | |||||||
| chr19:29984263 | T | C | 1 | a0001c0001t0001g0146 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.153-960T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984263 | |||||||
| chr19:29984403 | T | C | 9 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 others(6): Show |
11 | HG01361.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.153-820T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984403 | |||||||
| chr19:29984414 | G | C | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.153-809G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984414 | |||||||
| chr19:29984544 | A | G | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153-679A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984544 | |||||||
| chr19:29984556 | A | G | 1 | a0002c0002t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.153-667A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984556 | |||||||
| chr19:29984562 | T | C | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.153-661T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984562 | |||||||
| chr19:29984629 | G | T | 5 | a0002c0002t0001g0029 a0003c0003t0001g0038 a0003c0003t0006g0006 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-594G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984629 | |||||||
| chr19:29984704 | T | A | 4 | a0001c0001t0015g0007 a0003c0003t0001g0038 a0003c0003t0006g0006 others(1): Show |
4 | HG02145.hp2 HG02622.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-519T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984704 | |||||||
| chr19:29984757 | C | A | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.153-466C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984757 | |||||||
| chr19:29984790 | G | A | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.153-433G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984790 | |||||||
| chr19:29984802 | A | C | 12 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0002c0002t0001g0137 others(9): Show |
12 | HG02055.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.153-421A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984802 | |||||||
| chr19:29984859 | C | T | 2 | a0001c0001t0001g0188 a0001c0001t0001g0208 |
2 | HG01361.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.153-364C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29984859 | |||||||
| chr19:29985107 | G | A | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.153-116G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29985107 | |||||||
| chr19:29985119 | C | CAAAAAAA others(6): Show |
1 | a0002c0002t0001g0026 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.153-58_153-46dupAA others(11): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | C | CAAAAAAA others(13): Show |
1 | a0002c0002t0002g0297 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.153-65_153-46dupAA others(18): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(3): Show |
C | 1 | a0002c0002t0001g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.153-55_153-46delAA others(8): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(4): Show |
C | 4 | a0002c0002t0002g0279 a0002c0002t0002g0308 a0002c0002t0004g0254 others(1): Show |
4 | HG01167.hp2 HG01169.hp1 HG02155.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-56_153-46delAA others(9): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(5): Show |
C | 3 | a0002c0002t0002g0310 a0002c0002t0002g0314 a0002c0002t0003g0015 |
3 | HG02056.hp2 HG03540.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.153-57_153-46delAA others(10): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(6): Show |
C | 4 | a0002c0002t0002g0260 a0002c0002t0002g0263 a0002c0002t0002g0269 others(1): Show |
4 | NA18960.hp1 NA18968.hp1 NA19058.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-58_153-46delAA others(11): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(7): Show |
C | 4 | a0002c0002t0001g0012 a0002c0002t0001g0081 a0002c0002t0002g0293 others(1): Show |
4 | HG00735.hp1 HG02698.hp2 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-59_153-46delAA others(12): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(8): Show |
C | 3 | a0002c0002t0002g0294 a0002c0002t0002g0299 a0002c0002t0003g0018 |
3 | HG01109.hp2 HG04204.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.153-60_153-46delAA others(13): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(9): Show |
C | 6 | a0002c0002t0001g0034 a0002c0002t0002g0270 a0002c0002t0002g0295 others(3): Show |
6 | HG00609.hp1 HG02027.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.153-61_153-46delAA others(14): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(10): Show |
C | 8 | a0002c0002t0001g0033 a0002c0002t0002g0258 a0002c0002t0002g0268 others(5): Show |
8 | HG02071.hp2 HG02896.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.153-62_153-46delAA others(15): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(11): Show |
C | 19 | a0002c0002t0001g0011 a0002c0002t0001g0137 a0002c0002t0001g0138 others(16): Show |
19 | HG01358.hp1 HG01981.hp1 HG02074.hp1 others(16): Show |
intron_variant | MODIFIER | c.153-63_153-46delAA others(16): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(12): Show |
C | 22 | a0001c0001t0001g0048 a0001c0001t0001g0163 a0001c0001t0001g0186 others(19): Show |
22 | HG00408.hp2 HG01070.hp2 HG02004.hp2 others(19): Show |
intron_variant | MODIFIER | c.153-64_153-46delAA others(17): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(14): Show |
C | 1 | a0002c0002t0001g0116 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.153-66_153-46delAA others(19): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(15): Show |
C | 2 | a0001c0001t0001g0077 a0002c0002t0001g0028 |
2 | HG02572.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.153-67_153-46delAA others(20): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(16): Show |
C | 4 | a0001c0001t0001g0145 a0002c0002t0001g0009 a0002c0002t0001g0031 others(1): Show |
4 | HG02970.hp1 HG03139.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.153-68_153-46delAA others(21): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(17): Show |
C | 3 | a0001c0001t0001g0065 a0002c0002t0001g0008 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.153-69_153-46delAA others(22): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(18): Show |
C | 8 | a0001c0001t0001g0051 a0001c0001t0001g0069 a0001c0001t0001g0184 others(5): Show |
8 | HG03209.hp1 HG03471.hp2 HG03516.hp2 others(5): Show |
intron_variant | MODIFIER | c.153-70_153-46delAA others(23): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(19): Show |
C | 26 | a0001c0001t0001g0052 a0001c0001t0001g0054 a0001c0001t0001g0067 others(23): Show |
28 | HG00642.hp2 HG01175.hp1 HG01358.hp2 others(25): Show |
intron_variant | MODIFIER | c.153-71_153-46delAA others(24): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(20): Show |
C | 72 | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0053 others(69): Show |
74 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(71): Show |
intron_variant | MODIFIER | c.153-72_153-46delAA others(25): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(21): Show |
C | 79 | a0001c0001t0001g0002 a0001c0001t0001g0050 a0001c0001t0001g0062 others(76): Show |
81 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(78): Show |
intron_variant | MODIFIER | c.153-73_153-46delAA others(26): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(22): Show |
C | 17 | a0001c0001t0001g0102 a0001c0001t0001g0108 a0001c0001t0001g0109 others(14): Show |
17 | HG01081.hp1 HG01884.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.153-74_153-46delAA others(27): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(23): Show |
C | 2 | a0001c0001t0005g0045 a0001c0001t0005g0046 |
2 | HG01081.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.153-75_153-46delAA others(28): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(24): Show |
C | 1 | a0002c0002t0007g0253 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.153-76_153-46delAA others(29): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(25): Show |
C | 4 | a0002c0002t0007g0256 a0003c0003t0001g0038 a0003c0003t0006g0006 others(1): Show |
4 | HG02145.hp2 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.153-77_153-46delAA others(30): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(26): Show |
C | 2 | a0001c0001t0015g0007 a0002c0002t0002g0311 |
2 | HG02622.hp2 HG02683.hp1 |
intron_variant | MODIFIER | c.153-78_153-46delAA others(31): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(27): Show |
C | 2 | a0002c0002t0001g0029 a0002c0002t0003g0023 |
2 | HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.153-79_153-46delAA others(32): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(31): Show |
C | 1 | a0001c0001t0001g0063 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.153-83_153-46delAA others(36): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(33): Show |
C | 2 | a0001c0001t0001g0131 a0001c0001t0001g0252 |
2 | HG02280.hp1 HG02280.hp2 |
intron_variant | MODIFIER | c.153-85_153-46delAA others(38): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985119 | CAAAAAAA others(35): Show |
C | 1 | a0002c0002t0001g0084 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.153-87_153-46delAA others(40): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985119 | ||||||
| chr19:29985151 | AAAAAAAA others(20): Show |
A | 1 | a0001c0001t0001g0223 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.153-66_153-40delAA others(25): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr19 | 29985151 | ||||||
| chr19:29985172 | A | G | 1 | a0001c0001t0001g0003 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.153-51A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29985172 | |||||||
| chr19:29985173 | A | G | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.153-50A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 2/10 | chr19 | 29985173 | |||||||
| chr19:29985492 | AAT | A | 4 | a0001c0001t0005g0045 a0001c0001t0005g0046 a0001c0001t0005g0047 others(1): Show |
4 | HG01081.hp2 HG02109.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.231+198_231+199del others(2): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr19 | 29985492 | ||||||
| chr19:29985591 | T | C | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.231+290T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 3/10 | chr19 | 29985591 | |||||||
| chr19:29985594 | T | C | 12 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0002c0002t0001g0137 others(9): Show |
12 | HG02055.hp1 HG02074.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.231+293T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 3/10 | chr19 | 29985594 | |||||||
| chr19:29985852 | A | G | 1 | a0002c0002t0001g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.232-430A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 3/10 | chr19 | 29985852 | |||||||
| chr19:29985991 | A | G | 1 | a0001c0001t0001g0231 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.232-291A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 3/10 | chr19 | 29985991 | |||||||
| chr19:29986150 | T | C | 5 | a0001c0001t0015g0007 a0003c0003t0001g0038 a0003c0003t0006g0006 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.232-132T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 3/10 | chr19 | 29986150 | |||||||
| chr19:29986475 | C | T | 1 | a0001c0001t0001g0240 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.367+58C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29986475 | |||||||
| chr19:29986513 | G | A | 1 | a0002c0002t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.367+96G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29986513 | |||||||
| chr19:29986607 | C | T | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.367+190C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29986607 | |||||||
| chr19:29986664 | C | T | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.367+247C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29986664 | |||||||
| chr19:29986746 | A | G | 1 | a0002c0002t0002g0283 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.367+329A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29986746 | |||||||
| chr19:29986802 | C | G | 1 | a0001c0001t0001g0101 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.367+385C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29986802 | |||||||
| chr19:29986871 | A | T | 6 | a0001c0001t0015g0007 a0002c0002t0001g0029 a0003c0003t0001g0038 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.367+454A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29986871 | |||||||
| chr19:29986963 | C | A | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.367+546C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29986963 | |||||||
| chr19:29986983 | G | A | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.367+566G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29986983 | |||||||
| chr19:29987181 | C | T | 1 | a0002c0002t0007g0253 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.367+764C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987181 | |||||||
| chr19:29987295 | G | C | 1 | a0001c0001t0001g0182 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.367+878G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987295 | |||||||
| chr19:29987419 | T | C | 2 | a0002c0002t0001g0080 a0002c0002t0001g0081 |
2 | HG01361.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.367+1002T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987419 | |||||||
| chr19:29987454 | T | C | 2 | a0002c0002t0004g0021 a0002c0002t0004g0022 |
2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.367+1037T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987454 | |||||||
| chr19:29987524 | T | C | 42 | a0001c0001t0001g0002 a0001c0001t0001g0102 a0001c0001t0001g0103 others(39): Show |
43 | HG00558.hp2 HG00639.hp2 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.367+1107T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987524 | |||||||
| chr19:29987649 | A | G | 25 | a0001c0001t0001g0082 a0001c0001t0001g0083 a0001c0001t0001g0086 others(22): Show |
25 | HG00140.hp1 HG00642.hp2 HG00735.hp2 others(22): Show |
intron_variant | MODIFIER | c.367+1232A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987649 | |||||||
| chr19:29987712 | G | A | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.367+1295G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987712 | |||||||
| chr19:29987861 | A | G | 11 | a0002c0002t0001g0029 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.367+1444A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987861 | |||||||
| chr19:29987876 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.367+1459A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987876 | |||||||
| chr19:29987890 | G | A | 2 | a0002c0002t0001g0080 a0002c0002t0001g0081 |
2 | HG01361.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.367+1473G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987890 | |||||||
| chr19:29987894 | G | C | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.367+1477G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987894 | |||||||
| chr19:29987916 | C | T | 9 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0160 others(6): Show |
9 | HG01975.hp1 HG02004.hp1 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.367+1499C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987916 | |||||||
| chr19:29987934 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.367+1517A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29987934 | |||||||
| chr19:29988025 | G | A | 1 | a0001c0001t0001g0071 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.367+1608G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988025 | |||||||
| chr19:29988060 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1643T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988060 | |||||||
| chr19:29988072 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1655A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988072 | |||||||
| chr19:29988082 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1665C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988082 | |||||||
| chr19:29988083 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1666A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988083 | |||||||
| chr19:29988085 | T | G | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1668T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988085 | |||||||
| chr19:29988093 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1676A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988093 | |||||||
| chr19:29988097 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1680G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988097 | |||||||
| chr19:29988099 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1682T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988099 | |||||||
| chr19:29988104 | G | C | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1687G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988104 | |||||||
| chr19:29988114 | G | A | 1 | a0001c0001t0001g0202 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.367+1697G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988114 | |||||||
| chr19:29988116 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1699T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988116 | |||||||
| chr19:29988124 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1707T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988124 | |||||||
| chr19:29988134 | C | G | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1717C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988134 | |||||||
| chr19:29988138 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1721A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988138 | |||||||
| chr19:29988151 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1734A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988151 | |||||||
| chr19:29988157 | A | G | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1740A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988157 | |||||||
| chr19:29988159 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1742T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988159 | |||||||
| chr19:29988161 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1744T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988161 | |||||||
| chr19:29988162 | T | C | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1745T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988162 | |||||||
| chr19:29988167 | C | CA | 266 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(263): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.367+1766dupA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29988167 | ||||||
| chr19:29988167 | C | CAA | 13 | a0001c0001t0001g0117 a0001c0001t0001g0118 a0001c0001t0001g0161 others(10): Show |
13 | HG01109.hp2 HG02074.hp2 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.367+1765_367+1766d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29988167 | ||||||
| chr19:29988167 | CA | C | 10 | a0003c0003t0001g0001 a0003c0003t0001g0038 a0003c0003t0001g0040 others(7): Show |
12 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.367+1766delA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29988167 | ||||||
| chr19:29988184 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1767T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988184 | |||||||
| chr19:29988185 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1768T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988185 | |||||||
| chr19:29988187 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1770C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988187 | |||||||
| chr19:29988188 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1771G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988188 | |||||||
| chr19:29988189 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1772T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988189 | |||||||
| chr19:29988192 | AGCTCTTT others(1808): Show |
A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+1776_367+3590d others(2): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988192 | |||||||
| chr19:29988277 | G | T | 3 | a0002c0002t0001g0245 a0002c0002t0001g0246 a0003c0003t0009g0037 |
3 | HG02109.hp1 NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.367+1860G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988277 | |||||||
| chr19:29988333 | A | G | 1 | a0002c0002t0001g0080 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.367+1916A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988333 | |||||||
| chr19:29988404 | C | T | 6 | a0003c0003t0001g0001 a0003c0003t0001g0040 a0003c0003t0001g0041 others(3): Show |
8 | HG02055.hp2 HG02970.hp2 HG03209.hp1 others(5): Show |
intron_variant | MODIFIER | c.367+1987C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988404 | |||||||
| chr19:29988451 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.367+2034C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988451 | |||||||
| chr19:29988662 | G | T | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.367+2245G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988662 | |||||||
| chr19:29988667 | G | A | 3 | a0002c0002t0001g0111 a0002c0002t0001g0116 a0002c0002t0001g0238 |
3 | HG02486.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.367+2250G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988667 | |||||||
| chr19:29988711 | T | A | 1 | a0001c0001t0001g0198 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.367+2294T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988711 | |||||||
| chr19:29988800 | T | C | 2 | a0002c0002t0001g0033 a0002c0002t0001g0034 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.367+2383T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988800 | |||||||
| chr19:29988862 | T | C | 11 | a0002c0002t0001g0029 a0003c0003t0001g0001 a0003c0003t0001g0038 others(8): Show |
13 | HG02055.hp1 HG02055.hp2 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.367+2445T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988862 | |||||||
| chr19:29988966 | G | A | 2 | a0002c0002t0001g0011 a0002c0002t0001g0012 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.367+2549G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29988966 | |||||||
| chr19:29989071 | A | C | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.367+2654A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989071 | |||||||
| chr19:29989360 | G | A | 2 | a0001c0001t0001g0114 a0001c0001t0001g0144 |
2 | HG03017.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.367+2943G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989360 | |||||||
| chr19:29989402 | T | C | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.367+2985T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989402 | |||||||
| chr19:29989484 | C | T | 4 | a0003c0003t0001g0038 a0003c0003t0006g0006 a0003c0003t0006g0322 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.367+3067C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989484 | |||||||
| chr19:29989508 | C | T | 1 | a0001c0001t0001g0242 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.367+3091C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989508 | |||||||
| chr19:29989525 | G | A | 1 | a0002c0002t0002g0264 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.367+3108G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989525 | |||||||
| chr19:29989551 | T | G | 3 | a0001c0004t0001g0089 a0001c0004t0001g0091 a0001c0004t0001g0096 |
3 | NA18989.hp2 NA19011.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.367+3134T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989551 | |||||||
| chr19:29989569 | C | T | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.367+3152C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989569 | |||||||
| chr19:29989650 | T | A | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.367+3233T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989650 | |||||||
| chr19:29989690 | G | A | 6 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(3): Show |
6 | HG02074.hp1 HG02109.hp1 NA18970.hp2 others(3): Show |
intron_variant | MODIFIER | c.367+3273G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989690 | |||||||
| chr19:29989769 | GT | G | 295 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(292): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.367+3365delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29989769 | ||||||
| chr19:29989769 | GTT | G | 11 | a0001c0001t0001g0123 a0001c0001t0001g0140 a0001c0001t0001g0141 others(8): Show |
11 | HG01975.hp1 HG02004.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.367+3364_367+3365d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29989769 | ||||||
| chr19:29989916 | T | G | 2 | a0002c0002t0001g0033 a0002c0002t0001g0034 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.367+3499T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29989916 | |||||||
| chr19:29990008 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3591T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990008 | |||||||
| chr19:29990010 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3593T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990010 | |||||||
| chr19:29990012 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3595C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990012 | |||||||
| chr19:29990013 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3596T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990013 | |||||||
| chr19:29990014 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3597T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990014 | |||||||
| chr19:29990015 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3598T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990015 | |||||||
| chr19:29990016 | G | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3599G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990016 | |||||||
| chr19:29990018 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3601T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990018 | |||||||
| chr19:29990020 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3603T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990020 | |||||||
| chr19:29990021 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3604T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990021 | |||||||
| chr19:29990022 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3605T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990022 | |||||||
| chr19:29990023 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3606T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990023 | |||||||
| chr19:29990025 | C | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3608C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990025 | |||||||
| chr19:29990027 | A | G | 1 | a0002c0002t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.367+3610A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990027 | |||||||
| chr19:29990028 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3611T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990028 | |||||||
| chr19:29990029 | T | A | 1 | a0001c0001t0001g0060 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.367+3612T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990029 | |||||||
| chr19:29990083 | A | G | 1 | a0001c0001t0001g0151 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.367+3666A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990083 | |||||||
| chr19:29990090 | A | C | 2 | a0001c0001t0001g0183 a0001c0001t0001g0236 |
2 | HG02165.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.367+3673A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990090 | |||||||
| chr19:29990160 | T | C | 7 | a0002c0002t0003g0015 a0002c0002t0003g0016 a0002c0002t0003g0017 others(4): Show |
7 | HG01109.hp2 HG02145.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+3743T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990160 | |||||||
| chr19:29990542 | G | A | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.367+4125G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990542 | |||||||
| chr19:29990847 | A | T | 9 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 others(6): Show |
11 | HG01361.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+4430A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990847 | |||||||
| chr19:29990943 | C | G | 1 | a0001c0001t0001g0242 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.367+4526C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29990943 | |||||||
| chr19:29991052 | C | G | 1 | a0002c0002t0002g0308 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.367+4635C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29991052 | |||||||
| chr19:29991121 | C | G | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.367+4704C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29991121 | |||||||
| chr19:29991126 | C | G | 10 | a0001c0001t0001g0054 a0001c0001t0001g0063 a0001c0001t0001g0066 others(7): Show |
10 | HG02040.hp1 NA18953.hp1 NA18955.hp2 others(7): Show |
intron_variant | MODIFIER | c.367+4709C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29991126 | |||||||
| chr19:29991343 | A | C | 2 | a0004c0005t0001g0013 a0004c0005t0001g0014 |
2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.367+4926A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29991343 | |||||||
| chr19:29991344 | A | C | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+4927A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29991344 | |||||||
| chr19:29991456 | C | G | 78 | a0002c0002t0002g0258 a0002c0002t0002g0259 a0002c0002t0002g0260 others(75): Show |
78 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.367+5039C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29991456 | |||||||
| chr19:29991744 | A | T | 2 | a0001c0001t0001g0109 a0001c0001t0001g0155 |
2 | HG02922.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.367+5327A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29991744 | |||||||
| chr19:29991790 | T | A | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.367+5373T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29991790 | |||||||
| chr19:29991836 | G | A | 319 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(316): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.367+5419G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29991836 | |||||||
| chr19:29991935 | G | C | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+5518G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29991935 | |||||||
| chr19:29992056 | A | G | 3 | a0001c0001t0001g0165 a0001c0001t0001g0183 a0001c0001t0001g0236 |
3 | HG02165.hp1 NA19060.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.367+5639A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29992056 | |||||||
| chr19:29992701 | C | G | 5 | a0001c0001t0015g0007 a0003c0003t0001g0038 a0003c0003t0006g0006 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+6284C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29992701 | |||||||
| chr19:29992701 | C | T | 1 | a0002c0002t0002g0310 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.367+6284C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29992701 | |||||||
| chr19:29992848 | C | T | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.367+6431C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29992848 | |||||||
| chr19:29992914 | A | G | 1 | a0001c0008t0001g0085 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.367+6497A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29992914 | |||||||
| chr19:29993012 | T | C | 1 | a0001c0001t0001g0252 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.367+6595T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29993012 | |||||||
| chr19:29993033 | G | A | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.367+6616G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29993033 | |||||||
| chr19:29993354 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.367+6937A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29993354 | |||||||
| chr19:29993565 | T | C | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.367+7148T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29993565 | |||||||
| chr19:29993684 | G | T | 2 | a0002c0002t0001g0111 a0002c0002t0001g0116 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.367+7267G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29993684 | |||||||
| chr19:29993687 | G | C | 1 | a0002c0002t0001g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.367+7270G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29993687 | |||||||
| chr19:29993957 | A | G | 2 | a0001c0001t0001g0201 a0001c0001t0011g0217 |
2 | HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.367+7540A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29993957 | |||||||
| chr19:29993998 | C | T | 1 | a0002c0002t0002g0315 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.367+7581C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29993998 | |||||||
| chr19:29994063 | A | ATG | 3 | a0001c0001t0001g0077 a0001c0001t0001g0145 a0001c0001t0001g0186 |
3 | HG02622.hp1 HG02897.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.367+7666_367+7667d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29994063 | ||||||
| chr19:29994063 | ATG | A | 88 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0002c0002t0001g0028 others(85): Show |
88 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(85): Show |
intron_variant | MODIFIER | c.367+7666_367+7667d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29994063 | ||||||
| chr19:29994063 | ATGTG | A | 4 | a0001c0001t0015g0007 a0003c0003t0006g0006 a0003c0003t0006g0322 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.367+7664_367+7667d others(6): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29994063 | ||||||
| chr19:29994100 | G | T | 1 | a0003c0003t0009g0037 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.367+7683G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994100 | |||||||
| chr19:29994327 | C | T | 2 | a0002c0002t0003g0018 a0002c0002t0003g0023 |
2 | HG01109.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.367+7910C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994327 | |||||||
| chr19:29994329 | C | T | 2 | a0001c0001t0001g0122 a0001c0001t0001g0219 |
2 | HG01257.hp1 HG01358.hp2 |
intron_variant | MODIFIER | c.367+7912C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994329 | |||||||
| chr19:29994389 | A | G | 5 | a0001c0001t0015g0007 a0003c0003t0001g0038 a0003c0003t0006g0006 others(2): Show |
5 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+7972A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994389 | |||||||
| chr19:29994516 | A | G | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.367+8099A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994516 | |||||||
| chr19:29994618 | G | A | 1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.367+8201G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994618 | |||||||
| chr19:29994733 | G | A | 9 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 others(6): Show |
11 | HG01361.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.367+8316G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994733 | |||||||
| chr19:29994748 | G | A | 2 | a0001c0001t0001g0191 a0001c0001t0001g0234 |
2 | HG01168.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.367+8331G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994748 | |||||||
| chr19:29994781 | A | AT | 16 | a0001c0001t0001g0132 a0001c0001t0001g0158 a0001c0001t0001g0167 others(13): Show |
16 | HG01168.hp1 HG01192.hp1 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.367+8381dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29994781 | ||||||
| chr19:29994781 | AT | A | 7 | a0001c0001t0001g0072 a0001c0001t0015g0007 a0003c0003t0001g0038 others(4): Show |
7 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.367+8381delT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29994781 | ||||||
| chr19:29994846 | A | G | 2 | a0001c0001t0001g0129 a0001c0001t0001g0130 |
2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.367+8429A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994846 | |||||||
| chr19:29994895 | C | T | 1 | a0001c0001t0001g0141 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.367+8478C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994895 | |||||||
| chr19:29994904 | C | A | 3 | a0002c0002t0001g0111 a0002c0002t0001g0116 a0002c0002t0001g0238 |
3 | HG02486.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.367+8487C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994904 | |||||||
| chr19:29994941 | C | T | 19 | a0002c0002t0002g0259 a0002c0002t0002g0261 a0002c0002t0002g0263 others(16): Show |
19 | HG01074.hp1 HG02040.hp2 HG02056.hp2 others(16): Show |
intron_variant | MODIFIER | c.367+8524C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29994941 | |||||||
| chr19:29995181 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.367+8764A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29995181 | |||||||
| chr19:29995282 | A | T | 11 | a0001c0001t0015g0007 a0002c0002t0001g0137 a0002c0002t0001g0138 others(8): Show |
11 | HG02055.hp1 HG02074.hp1 HG02109.hp1 others(8): Show |
intron_variant | MODIFIER | c.367+8865A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29995282 | |||||||
| chr19:29995352 | T | C | 2 | a0001c0001t0001g0087 a0001c0001t0001g0094 |
2 | HG02602.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.367+8935T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29995352 | |||||||
| chr19:29995443 | G | C | 2 | a0002c0002t0001g0011 a0002c0002t0001g0012 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.367+9026G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29995443 | |||||||
| chr19:29995552 | T | TA | 303 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(300): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.367+9146dupA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29995552 | ||||||
| chr19:29995691 | A | G | 1 | a0002c0002t0002g0310 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.367+9274A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29995691 | |||||||
| chr19:29995725 | G | GT | 10 | a0002c0002t0001g0029 a0002c0002t0001g0111 a0002c0002t0001g0116 others(7): Show |
10 | HG00408.hp2 HG02074.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.367+9319dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29995725 | ||||||
| chr19:29995808 | A | G | 1 | a0002c0002t0001g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.367+9391A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29995808 | |||||||
| chr19:29995847 | G | A | 10 | a0001c0001t0001g0102 a0001c0001t0001g0117 a0001c0001t0001g0129 others(7): Show |
10 | HG02258.hp2 HG02647.hp1 HG02886.hp2 others(7): Show |
intron_variant | MODIFIER | c.367+9430G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29995847 | |||||||
| chr19:29995964 | C | T | 9 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 others(6): Show |
11 | HG01361.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-9397C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29995964 | |||||||
| chr19:29996252 | A | C | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.368-9109A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29996252 | |||||||
| chr19:29996409 | T | G | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.368-8952T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29996409 | |||||||
| chr19:29996418 | T | G | 4 | a0001c0001t0015g0007 a0003c0003t0006g0006 a0003c0003t0006g0322 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-8943T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29996418 | |||||||
| chr19:29996470 | A | G | 300 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(297): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.368-8891A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29996470 | |||||||
| chr19:29996479 | T | TTG | 97 | a0001c0001t0001g0066 a0001c0001t0001g0076 a0001c0001t0001g0121 others(94): Show |
98 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(95): Show |
intron_variant | MODIFIER | c.368-8862_368-8861d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29996479 | ||||||
| chr19:29996479 | T | TTGTG | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-8864_368-8861d others(6): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29996479 | ||||||
| chr19:29996479 | T | TTGTGTGT others(1): Show |
5 | a0001c0001t0015g0007 a0003c0003t0001g0038 a0003c0003t0006g0006 others(2): Show |
5 | HG02055.hp1 HG02109.hp1 HG02145.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-8868_368-8861d others(10): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29996479 | ||||||
| chr19:29996479 | T | TTGTGTGT others(3): Show |
1 | a0003c0003t0006g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.368-8870_368-8861d others(12): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29996479 | ||||||
| chr19:29996479 | TTG | T | 5 | a0001c0001t0001g0123 a0001c0001t0001g0127 a0001c0001t0001g0171 others(2): Show |
5 | HG01516.hp1 NA18959.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-8862_368-8861d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29996479 | ||||||
| chr19:29996518 | G | A | 4 | a0001c0001t0015g0007 a0003c0003t0006g0006 a0003c0003t0006g0322 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-8843G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29996518 | |||||||
| chr19:29996692 | G | A | 1 | a0002c0002t0001g0011 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.368-8669G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29996692 | |||||||
| chr19:29996797 | G | GT | 6 | a0001c0001t0001g0167 a0001c0001t0015g0007 a0002c0002t0002g0314 others(3): Show |
6 | HG02055.hp1 HG02145.hp2 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.368-8553dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29996797 | ||||||
| chr19:29997035 | A | G | 3 | a0002c0002t0001g0111 a0002c0002t0001g0116 a0002c0002t0001g0238 |
3 | HG02486.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.368-8326A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29997035 | |||||||
| chr19:29997160 | G | A | 3 | a0001c0001t0005g0046 a0001c0001t0005g0047 a0001c0001t0005g0049 |
3 | HG01081.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.368-8201G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29997160 | |||||||
| chr19:29997369 | A | C | 1 | a0002c0002t0001g0026 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.368-7992A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29997369 | |||||||
| chr19:29997441 | T | G | 2 | a0001c0001t0001g0212 a0001c0001t0001g0235 |
2 | HG00099.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.368-7920T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29997441 | |||||||
| chr19:29997480 | G | C | 2 | a0001c0001t0001g0191 a0001c0001t0001g0234 |
2 | HG01168.hp1 HG01516.hp2 |
intron_variant | MODIFIER | c.368-7881G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29997480 | |||||||
| chr19:29997581 | T | C | 1 | a0001c0001t0001g0193 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.368-7780T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29997581 | |||||||
| chr19:29997786 | A | G | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.368-7575A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29997786 | |||||||
| chr19:29997846 | C | T | 1 | a0002c0002t0002g0260 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.368-7515C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29997846 | |||||||
| chr19:29998245 | T | C | 3 | a0003c0003t0006g0006 a0003c0003t0006g0322 a0003c0003t0010g0039 |
3 | HG02055.hp1 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.368-7116T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29998245 | |||||||
| chr19:29998472 | T | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-6889T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29998472 | |||||||
| chr19:29998679 | T | G | 1 | a0001c0001t0001g0075 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.368-6682T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29998679 | |||||||
| chr19:29999242 | T | C | 9 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 others(6): Show |
11 | HG01361.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-6119T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29999242 | |||||||
| chr19:29999321 | G | T | 1 | a0003c0003t0006g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.368-6040G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29999321 | |||||||
| chr19:29999327 | C | G | 9 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 others(6): Show |
11 | HG01361.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.368-6034C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29999327 | |||||||
| chr19:29999411 | C | A | 204 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(201): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.368-5950C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29999411 | |||||||
| chr19:29999577 | G | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.368-5784G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29999577 | |||||||
| chr19:29999681 | T | C | 3 | a0002c0002t0004g0257 a0002c0002t0007g0253 a0002c0002t0007g0256 |
3 | HG02630.hp1 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.368-5680T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29999681 | |||||||
| chr19:29999705 | G | A | 1 | a0003c0003t0006g0006 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.368-5656G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29999705 | |||||||
| chr19:29999708 | CCTTATCA others(104): Show |
C | 1 | a0002c0002t0002g0277 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.368-5652_368-5542d others(2): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29999708 | |||||||
| chr19:29999810 | C | A | 1 | a0001c0001t0001g0231 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.368-5551C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29999810 | |||||||
| chr19:29999828 | C | T | 3 | a0003c0003t0006g0006 a0003c0003t0006g0322 a0003c0003t0010g0039 |
3 | HG02055.hp1 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.368-5533C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 29999828 | |||||||
| chr19:29999980 | C | CT | 290 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(287): Show |
296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.368-5371dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29999980 | ||||||
| chr19:29999980 | C | CTT | 8 | a0001c0001t0001g0071 a0001c0001t0001g0113 a0001c0001t0001g0198 others(5): Show |
8 | HG02074.hp1 HG02451.hp1 NA18970.hp2 others(5): Show |
intron_variant | MODIFIER | c.368-5372_368-5371d others(4): Show |
URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 29999980 | ||||||
| chr19:30000001 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-5360A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30000001 | |||||||
| chr19:30000137 | G | A | 213 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(210): Show |
218 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(215): Show |
intron_variant | MODIFIER | c.368-5224G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30000137 | |||||||
| chr19:30000225 | A | G | 2 | a0001c0001t0001g0082 a0001c0001t0001g0093 |
2 | NA18955.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.368-5136A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30000225 | |||||||
| chr19:30000596 | T | TA | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(1): Show |
4 | HG01168.hp1 HG01516.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-4764dupA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr19 | 30000596 | ||||||
| chr19:30000702 | C | G | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.368-4659C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30000702 | |||||||
| chr19:30000748 | C | T | 1 | a0001c0001t0001g0112 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.368-4613C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30000748 | |||||||
| chr19:30000971 | C | T | 2 | a0001c0001t0001g0149 a0001c0001t0001g0215 |
2 | HG00639.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.368-4390C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30000971 | |||||||
| chr19:30001142 | C | T | 1 | a0001c0001t0001g0163 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.368-4219C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30001142 | |||||||
| chr19:30001301 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.368-4060G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30001301 | |||||||
| chr19:30001328 | A | T | 4 | a0001c0001t0015g0007 a0003c0003t0006g0006 a0003c0003t0006g0322 others(1): Show |
4 | HG02055.hp1 HG02145.hp2 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-4033A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30001328 | |||||||
| chr19:30001473 | A | G | 203 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(200): Show |
207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.368-3888A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30001473 | |||||||
| chr19:30001492 | A | G | 1 | a0002c0009t0002g0307 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.368-3869A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30001492 | |||||||
| chr19:30001518 | C | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0204 |
2 | HG01257.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.368-3843C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30001518 | |||||||
| chr19:30001539 | T | A | 1 | a0001c0001t0001g0104 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.368-3822T>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30001539 | |||||||
| chr19:30001778 | G | T | 1 | a0001c0001t0001g0209 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.368-3583G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30001778 | |||||||
| chr19:30001825 | G | A | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-3536G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30001825 | |||||||
| chr19:30001996 | G | T | 1 | a0002c0002t0002g0271 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.368-3365G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30001996 | |||||||
| chr19:30002120 | A | C | 1 | a0001c0001t0001g0067 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.368-3241A>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30002120 | |||||||
| chr19:30002174 | G | A | 1 | a0001c0001t0001g0142 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.368-3187G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30002174 | |||||||
| chr19:30002211 | A | G | 7 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(4): Show |
7 | HG02074.hp1 HG02109.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.368-3150A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30002211 | |||||||
| chr19:30002216 | A | G | 1 | a0002c0002t0001g0008 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.368-3145A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30002216 | |||||||
| chr19:30002217 | T | G | 2 | a0001c0001t0001g0131 a0001c0001t0001g0250 |
2 | HG02280.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.368-3144T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30002217 | |||||||
| chr19:30002311 | G | A | 3 | a0001c0001t0005g0046 a0001c0001t0005g0047 a0001c0001t0005g0049 |
3 | HG01081.hp2 NA18906.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.368-3050G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30002311 | |||||||
| chr19:30002551 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-2810A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30002551 | |||||||
| chr19:30002802 | T | G | 5 | a0002c0002t0004g0254 a0002c0002t0004g0255 a0002c0002t0004g0257 others(2): Show |
5 | HG01167.hp2 HG01169.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.368-2559T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30002802 | |||||||
| chr19:30002833 | A | G | 1 | a0003c0003t0006g0322 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.368-2528A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30002833 | |||||||
| chr19:30002876 | C | T | 2 | a0003c0003t0001g0038 a0003c0003t0009g0037 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.368-2485C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30002876 | |||||||
| chr19:30003178 | T | C | 9 | a0002c0002t0003g0015 a0002c0002t0003g0016 a0002c0002t0003g0017 others(6): Show |
9 | HG01109.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.368-2183T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30003178 | |||||||
| chr19:30003189 | G | A | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.368-2172G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30003189 | |||||||
| chr19:30003253 | C | T | 1 | a0003c0003t0001g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.368-2108C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30003253 | |||||||
| chr19:30003283 | A | G | 4 | a0001c0001t0001g0191 a0001c0001t0001g0192 a0001c0001t0001g0194 others(1): Show |
4 | HG01168.hp1 HG01516.hp2 HG03490.hp2 others(1): Show |
intron_variant | MODIFIER | c.368-2078A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30003283 | |||||||
| chr19:30003290 | C | T | 2 | a0003c0003t0001g0038 a0003c0003t0009g0037 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.368-2071C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30003290 | |||||||
| chr19:30003382 | C | T | 1 | a0001c0001t0001g0088 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.368-1979C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30003382 | |||||||
| chr19:30003688 | A | G | 2 | a0001c0001t0001g0121 a0001c0001t0001g0204 |
2 | HG01257.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.368-1673A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30003688 | |||||||
| chr19:30003837 | T | C | 2 | a0001c0001t0001g0078 a0001c0001t0001g0123 |
2 | HG00408.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.368-1524T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30003837 | |||||||
| chr19:30003891 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.368-1470A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30003891 | |||||||
| chr19:30004217 | C | G | 1 | a0002c0002t0001g0238 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.368-1144C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30004217 | |||||||
| chr19:30004350 | A | G | 2 | a0001c0001t0001g0102 a0001c0001t0012g0203 |
2 | HG02647.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.368-1011A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30004350 | |||||||
| chr19:30004467 | T | C | 1 | a0001c0001t0001g0243 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.368-894T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30004467 | |||||||
| chr19:30004514 | T | G | 1 | a0001c0001t0001g0160 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.368-847T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30004514 | |||||||
| chr19:30004624 | T | C | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.368-737T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30004624 | |||||||
| chr19:30004628 | A | G | 205 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(202): Show |
209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.368-733A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30004628 | |||||||
| chr19:30005028 | A | G | 308 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(305): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.368-333A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 4/10 | chr19 | 30005028 | |||||||
| chr19:30006257 | C | T | 2 | a0002c0002t0001g0111 a0002c0002t0001g0116 |
2 | HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.517+549C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30006257 | |||||||
| chr19:30006303 | A | G | 2 | a0002c0002t0004g0021 a0002c0002t0004g0022 |
2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.517+595A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30006303 | |||||||
| chr19:30006373 | G | A | 1 | a0002c0002t0002g0317 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.517+665G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30006373 | |||||||
| chr19:30006490 | A | G | 3 | a0001c0004t0001g0089 a0001c0004t0001g0091 a0001c0004t0001g0096 |
3 | NA18989.hp2 NA19011.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.517+782A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30006490 | |||||||
| chr19:30006516 | A | G | 11 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(8): Show |
11 | HG01884.hp1 HG01891.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.517+808A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30006516 | |||||||
| chr19:30006694 | T | C | 5 | a0001c0001t0001g0048 a0001c0001t0005g0045 a0001c0001t0005g0046 others(2): Show |
5 | HG01081.hp2 HG02109.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.518-776T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30006694 | |||||||
| chr19:30006769 | A | G | 1 | a0001c0001t0001g0208 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.518-701A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30006769 | |||||||
| chr19:30006793 | T | C | 1 | a0002c0002t0002g0266 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.518-677T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30006793 | |||||||
| chr19:30006979 | C | T | 9 | a0001c0001t0001g0075 a0001c0001t0001g0135 a0001c0001t0001g0159 others(6): Show |
9 | HG00099.hp1 HG01109.hp1 HG01192.hp1 others(6): Show |
intron_variant | MODIFIER | c.518-491C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30006979 | |||||||
| chr19:30007027 | C | T | 309 | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(306): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.518-443C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30007027 | |||||||
| chr19:30007134 | T | C | 2 | a0001c0001t0001g0157 a0001c0001t0001g0177 |
2 | HG02615.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.518-336T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30007134 | |||||||
| chr19:30007234 | T | C | 1 | a0001c0001t0001g0149 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.518-236T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30007234 | |||||||
| chr19:30007405 | A | G | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.518-65A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30007405 | |||||||
| chr19:30007448 | G | A | 2 | a0001c0001t0001g0171 a0001c0001t0001g0210 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.518-22G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 6/10 | chr19 | 30007448 | |||||||
| chr19:30007944 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.686+306A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 7/10 | chr19 | 30007944 | |||||||
| chr19:30008004 | G | A | 3 | a0003c0003t0006g0006 a0003c0003t0006g0322 a0003c0003t0010g0039 |
3 | HG02055.hp1 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.686+366G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 7/10 | chr19 | 30008004 | |||||||
| chr19:30008231 | C | T | 1 | a0002c0009t0002g0307 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.686+593C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 7/10 | chr19 | 30008231 | |||||||
| chr19:30008318 | T | C | 1 | a0001c0001t0001g0233 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.686+680T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 7/10 | chr19 | 30008318 | |||||||
| chr19:30008375 | T | G | 2 | a0001c0001t0001g0247 a0001c0001t0001g0248 |
2 | HG02451.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.687-630T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 7/10 | chr19 | 30008375 | |||||||
| chr19:30008599 | A | G | 1 | a0001c0001t0001g0090 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.687-406A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 7/10 | chr19 | 30008599 | |||||||
| chr19:30009457 | G | A | 1 | a0001c0001t0001g0230 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1035+104G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30009457 | |||||||
| chr19:30009833 | T | C | 11 | a0001c0001t0001g0164 a0001c0001t0001g0165 a0001c0001t0001g0178 others(8): Show |
11 | HG00558.hp2 HG02165.hp1 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.1035+480T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30009833 | |||||||
| chr19:30010090 | G | A | 2 | a0002c0002t0002g0318 a0002c0002t0002g0319 |
2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1035+737G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30010090 | |||||||
| chr19:30010535 | C | T | 1 | a0002c0002t0003g0017 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1036-559C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30010535 | |||||||
| chr19:30010628 | T | C | 2 | a0002c0002t0001g0033 a0002c0002t0001g0034 |
2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1036-466T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30010628 | |||||||
| chr19:30010640 | C | T | 2 | a0002c0002t0001g0245 a0002c0002t0001g0246 |
2 | NA19054.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.1036-454C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30010640 | |||||||
| chr19:30010741 | A | G | 1 | a0003c0003t0001g0038 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1036-353A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30010741 | |||||||
| chr19:30010745 | T | C | 2 | a0002c0002t0004g0021 a0002c0002t0004g0022 |
2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1036-349T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30010745 | |||||||
| chr19:30010781 | T | C | 9 | a0002c0002t0001g0080 a0002c0002t0001g0081 a0002c0002t0001g0084 others(6): Show |
11 | HG01361.hp1 HG02055.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1036-313T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30010781 | |||||||
| chr19:30010829 | G | T | 1 | a0002c0002t0001g0029 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1036-265G>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30010829 | |||||||
| chr19:30011023 | G | C | 2 | a0002c0002t0001g0011 a0002c0002t0001g0012 |
2 | HG02615.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1036-71G>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 8/10 | chr19 | 30011023 | |||||||
| chr19:30011576 | G | A | 3 | a0002c0002t0001g0008 a0002c0002t0001g0009 a0002c0002t0001g0010 |
3 | HG01891.hp2 HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1178+340G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 9/10 | chr19 | 30011576 | |||||||
| chr19:30011619 | G | GT | 18 | a0001c0001t0001g0108 a0001c0001t0001g0109 a0001c0001t0001g0110 others(15): Show |
18 | HG01884.hp1 HG01891.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1178+397dupT | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr19 | 30011619 | ||||||
| chr19:30011620 | T | C | 1 | a0001c0001t0001g0101 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1178+384T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 9/10 | chr19 | 30011620 | |||||||
| chr19:30011754 | T | G | 2 | a0002c0002t0001g0035 a0002c0002t0001g0036 |
2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1178+518T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 9/10 | chr19 | 30011754 | |||||||
| chr19:30012090 | G | A | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1179-195G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 9/10 | chr19 | 30012090 | |||||||
| chr19:30012255 | G | A | 79 | a0002c0002t0002g0005 a0002c0002t0002g0258 a0002c0002t0002g0259 others(76): Show |
80 | HG00408.hp2 HG00609.hp1 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.1179-30G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 9/10 | chr19 | 30012255 | |||||||
| chr19:30012817 | C | T | 2 | a0003c0003t0001g0038 a0003c0003t0009g0037 |
2 | HG02109.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1425+286C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30012817 | |||||||
| chr19:30012842 | A | G | 5 | a0002c0002t0001g0137 a0002c0002t0001g0138 a0002c0002t0001g0139 others(2): Show |
5 | HG02074.hp1 NA18970.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.1425+311A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30012842 | |||||||
| chr19:30012897 | C | A | 1 | a0002c0002t0001g0012 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1425+366C>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30012897 | |||||||
| chr19:30013274 | A | T | 1 | a0001c0001t0001g0134 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1425+743A>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30013274 | |||||||
| chr19:30013353 | A | G | 1 | a0001c0001t0001g0212 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1425+822A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30013353 | |||||||
| chr19:30013425 | C | T | 1 | a0001c0001t0001g0188 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1425+894C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30013425 | |||||||
| chr19:30013439 | C | G | 3 | a0002c0002t0001g0111 a0002c0002t0001g0116 a0002c0002t0001g0238 |
3 | HG02486.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1425+908C>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30013439 | |||||||
| chr19:30013544 | A | G | 1 | a0002c0002t0002g0291 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1425+1013A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30013544 | |||||||
| chr19:30013692 | A | G | 3 | a0003c0003t0006g0006 a0003c0003t0006g0322 a0003c0003t0010g0039 |
3 | HG02055.hp1 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1425+1161A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30013692 | |||||||
| chr19:30013909 | T | C | 120 | a0001c0001t0001g0002 a0001c0001t0001g0048 a0001c0001t0001g0050 others(117): Show |
121 | HG00099.hp1 HG00140.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.1426-978T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30013909 | |||||||
| chr19:30013978 | A | G | 2 | a0002c0002t0004g0021 a0002c0002t0004g0022 |
2 | HG02257.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.1426-909A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30013978 | |||||||
| chr19:30014003 | T | C | 1 | a0001c0001t0015g0007 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1426-884T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30014003 | |||||||
| chr19:30014006 | A | G | 1 | a0003c0003t0010g0039 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1426-881A>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30014006 | |||||||
| chr19:30014048 | G | A | 3 | a0001c0001t0001g0098 a0001c0001t0001g0132 a0001c0001t0001g0153 |
3 | HG00140.hp2 HG01192.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1426-839G>A | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30014048 | |||||||
| chr19:30014075 | TA | T | 15 | a0001c0001t0001g0057 a0001c0001t0001g0059 a0001c0001t0001g0092 others(12): Show |
15 | HG00558.hp2 HG00639.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1426-796delA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr19 | 30014075 | ||||||
| chr19:30014381 | T | C | 3 | a0003c0003t0006g0006 a0003c0003t0006g0322 a0003c0003t0010g0039 |
3 | HG02055.hp1 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1426-506T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30014381 | |||||||
| chr19:30014489 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1426-398C>T | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30014489 | |||||||
| chr19:30014520 | T | G | 3 | a0002c0002t0001g0111 a0002c0002t0001g0116 a0002c0002t0001g0238 |
3 | HG02486.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1426-367T>G | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30014520 | |||||||
| chr19:30014681 | TA | T | 3 | a0003c0003t0006g0006 a0003c0003t0006g0322 a0003c0003t0010g0039 |
3 | HG02055.hp1 HG02145.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.1426-201delA | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr19 | 30014681 | ||||||
| chr19:30014790 | T | C | 2 | a0001c0001t0001g0159 a0001c0001t0001g0182 |
2 | HG01192.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.1426-97T>C | URI1 | ENSG00000105176.18 | transcript | ENST00000392271.6 | protein_coding | 10/10 | chr19 | 30014790 |